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Int. J. Mol. Sci. 2014, 15(6), 10424-10445; doi:10.3390/ijms150610424
Published: 10 June 2014
Abstract: Alternative splicing (AS) occurs widely in plants and can provide the main source of transcriptome and proteome diversity in an organism. AS functions in a range of physiological processes, including plant disease resistance, but its biological roles and functional mechanisms remain poorly understood. Many plant disease resistance (R) genes undergo AS, and several R genes require alternatively spliced transcripts to produce R proteins that can specifically recognize pathogen invasion. In the finely-tuned process of R protein activation, the truncated isoforms generated by AS may participate in plant disease resistance either by suppressing the negative regulation of initiation of immunity, or by directly engaging in effector-triggered signaling. Although emerging research has shown the functional significance of AS in plant biotic stress responses, many aspects of this topic remain to be understood. Several interesting issues surrounding the AS of R genes, especially regarding its functional roles and regulation, will require innovative techniques and additional research to unravel.
Alternative splicing (AS) describes the processing of a single pre-mRNA to produce multiple transcript isoforms . Genome-wide studies have shown that AS is prevalent in eukaryotes and that more than 95% of human multi-exon genes undergo AS [2,3]. One of the most impressive examples of AS is the Drosophila melanogaster gene down syndrome cell adhesion molecule (Dscam), which contains 95 exons, and can generate 38,016 distinct alternative transcript isoforms, a number in excess of the total number of genes (14,500) in the genome . AS appears to serve as the primary source for transcriptome and proteome diversity in many eukaryotes [2,5,6,7]. In plants, analysis of Arabidopsis EST/cDNA libraries initially gave rise to estimates of AS rates as low as 1.2% . Subsequently, improved EST coverage led to estimates of 11.6% , 21.8% , and 30% . More recently, high-throughput sequencing has revealed that about 61% of intron-containing genes in Arabidopsis undergo AS . Considering that these data were obtained from plants growing under normal conditions, the actual value for AS frequency is likely to be even higher. Environmental and biotic stresses can induce AS, and novel splicing sites have been identified in studies of AS under stress conditions [13,14,15]. A recent RNA-seq study of Pseudomonas syringae-infected Arabidopsis indicated that over 90% of the expressed genes (23,385 out of 25,619) underwent AS . Moreover, differential expression of alternative transcript isoforms in different tissues and at different development stages adds another layer of complexity to AS mechanisms and transcriptome annotation [16,17,18,19].
Proteins encoded by AS isoforms can have different activities, tissue distributions, or intracellular localizations [17,20,21,22,23]. Although its biological function is not fully understood in plants, AS is involved in many physiological processes, including defense responses [24,25,26,27]. Plants have evolved sophisticated systems to detect pathogen attacks and trigger innate immunity. Recently, AS has been recognized as a crucial regulatory mechanism in plant defense against pathogen infections [28,29,30,31,32]. This review begins with an overview of disease resistance in plants and then discusses current knowledge about the involvement of AS in plant immunity, as well as the prospects for future research.
2. Plant Disease Resistance
Two types of plant immunity operate to restrict pathogen colonization in the host. The first, a basal level of plant defense responses are activated by the pathogen (or microbe)-associated molecular patterns (PAMPs or MAMPs), such as chitin, flagellin, and Elongation Factor-Tu (EF-Tu). The perception of structurally conserved PAMPs by plant transmembrane pattern recognition receptors (PRRs) induces PAMP-triggered immunity (PTI). However, pathogens can suppress PTI with secreted effector proteins. Accordingly, in the second line of defense, the plant deploys resistance (R) proteins to recognize corresponding effector proteins called Avirulence (Avr) proteins, leading to the stronger disease resistance, called effector-triggered immunity (ETI). R proteins recognize Avr proteins either directly or indirectly. Direct R-Avr interaction is exemplified by the direct binding of the Linum usitatissimum (flax) L. protein with its cognate effectors . Indirect R-Avr interaction can be explained by the proposed “guard hypothesis” ; in this model, R proteins detect pathogens indirectly, by the effects of Avr proteins on other cellular proteins, termed guardees.
The co-evolution or “arms race” between host and pathogen has been extensively studied in the interaction between Arabidopsis and pathogenic P. syringae expressing EF-Tu. Direct binding of EF-Tu to its receptor EFR induces phosphorylation on the tyrosine residues of EFR, and activates PTI . However, the P. syringae-secreted effector HopA1 has phosphatase activity and reduces EFR phosphorylation, thus blocking EF-Tu-triggered PTI . The Arabidopsis R protein RPS6 (Resistance to P. syringae 6) specifically recognizes HopA1 . The HopA1 target guarded by RPS6 is believed to be EDS1 (Enhanced disease susceptibility 1), a pivotal signal transducer in RPS6-mediated ETI, although EDS1 also functions downstream of pathogen detection .
PTI cannot completely inhibit pathogen colonization, but can retard pathogen invasion . By contrast, ETI can be viewed as intensified and long-lasting PTI that includes the development of systemic acquired resistance and rapid, localized programmed cell death known as the hypersensitive response (HR) . A chain of defense responses occur concomitant with the HR, including oxidative burst, accumulation of salicylic acid (SA), expression of pathogenesis-related (PR) genes, and defensin biosynthesis. PTI involves mitogen-activated protein kinase-signaling cascades and the accumulation of reactive oxygen species [41,42], and constitutive activation of PTI in the absence of pathogen results deleterious effects on plant development. As a long-lasting, systemic response, ETI must be fine-tuned to protect the plant from pathogen attack without excessive fitness costs.
2.1. R Genes
The majority of cloned R genes encode proteins containing a central nucleotide-binding site (NBS) and a C-terminal leucine-rich repeat (LRR) region. The NBS region normally consists of three subdomains, NBS, ARC1, and ARC2. The characteristic NBS subdomain includes a binding site for ATP or GTP and is active in initiation of signaling cascades leading to resistance responses . The ARC subdomains (named for their presence in Apaf-1, R proteins, and CED-4) are highly conserved and essential for intramolecular interactions of R proteins . By contrast, the LRR motif confers recognition specificity to the plant defense response [45,46,47,48].
Based on their N-terminal structures, members of the NBS-LRR family of R genes can be further subdivided into two subfamilies. One subfamily comprises members with a domain homologous to the intracellular signaling domains of the Drosophila Toll and mammalian Interleukin (IL)-1 receptor (TIR-NBS-LRR). TIR-NBS-LRR genes are exclusively present in dicot species. Members of this subfamily include tobacco N, flax L6 and M, Arabidopsis RPP1, RPP4 and RPS4, and Medicago truncatula RCT1. Another subfamily is characterized by a putative coiled-coil domain in the N-terminal region (CC-NBS-LRR). CC-NBS-LRR genes are widely distributed in both dicots and monocots. Both the CC and TIR domains likely function in interaction with downstream factors in ETI signaling . Although most TIR- and CC-NBS-LRRs lack putative transmembrane domains or organelle-targeting signals and are predicted to be cytosolic, some show dynamic changes in subcellular localization [42,50].
2.2. Signaling Components in ETI
In addition to their structural differences, TIR-NBS-LRR and CC-NBS-LRR genes generally function through distinct signaling pathways, requiring either EDS1 or NDR1 (Non-race-specific disease resistance 1), respectively . One exception is the Arabidopsis HRT gene that confers resistance to TCV (Turnip crinkle virus). HRT is a CC-NBS-LRR gene but its signaling is dependent on EDS1 . Moreover, a few CC-NBS-LRR genes including RPP7, RPP8, and RPP13 can activate defense signaling independent of EDS1 and NDR1 [51,53,54]. Venugopal et al.  proposed, however, that EDS1 and SA act redundantly to regulate ETI to viral, bacterial, and oomycete pathogens. As such, participation of EDS1 in signaling triggered by CC-NBS-LRR R proteins may be masked by SA, and vice versa. In such cases, the requirement for EDS1 would be observed only when disease resistance does not require SA accumulation. PAD4 (Phytoalexin deficient 4) and SGA101 are indispensable for EDS1-required signaling to restrict pathogen growth [56,57]. EDS1, PAD4, SAG101 function independently, as well as in a ternary complex of SAG101-EDS1-PAD4, serving as signal transducers in HRT-mediated resistance to TCV . However, the HR associated with TCV resistance conferred by HRT requires only EDS1, whereas the SA signaling induced by HRT requires only PAD4.
Genetic analysis of Arabidopsis mutants defective in systemic acquired resistance led to the isolation of NPR1 (Non-expresser of PR genes 1), which encodes a putative transcription factor regulating PR gene expression downstream of SA production . Further investigation of the regulator of NPR1 in Arabidopsis resulted in identification of the gain-of-function mutant snc1 (Suppressor of npr1-1, constitutive 1) , which exhibits a dwarfed phenotype caused by constitutive activation of defense signaling in the absence of pathogen infection. Based on these mutants it can be concluded that wild type SNC1 suppresses NPR1 and to finely control autoimmune responses. Interestingly, snc1 encodes a TIR-NBS-LRR R protein, and the snc1 mutant morphology is restored or suppressed to different extents in a series of mos (Modifier of snc1) mutants. Thus far, 13 MOS genes have been cloned, the gene products of which act in various cellular and molecular processes, including pre-mRNA splicing, nuclear trafficking of serine-arginine rich (SR) proteins and protein modification, which is indicative of a highly complex network for regulation of R protein-mediated ETI [61,62,63,64,65,66,67,68,69,70,71,72].
3. AS of R Genes
3.1. AS of TIR-NBS-LRR Genes
Most TIR-NBS-LRR genes have conserved gene structures in the coding region, which generally contains three or four introns. The first exon encodes the TIR domain, the second exon encodes the NBS domain, and the remaining exons encode the LRR region. AS of TIR-NBS-LRR genes can result from intron retention, selection of alternative exons, or usage of alternative 5' or 3' splicing sites. Alternative isoforms have been reported for many TIR-NBS-LRR genes, such as tobacco N , flax L, and M loci , Arabidopsis SNC1, RPS4, RPS6, RPP5, and RAC1 [37,75,76,77,78], tomato Bs4 , potato Y-1 , and M. truncatula RCT1 . The functional consequences of AS events have been characterized for only a few TIR-NBS-LRR R genes, including Arabidopsis RPS4, tobacco N, and M. truncatula RCT1.
3.1.1. Arabidopsis RPS4
The Arabidopsis RPS4 gene confers resistance to Pseudomonas syringae pv. tomato strain DC3000 (DC3000) expressing AvrRps4. AS produces six transcript isoforms of RPS4 via retention of intron 2 and/or intron 3, and splicing of a cryptic intron in exon 3 (Figure 1A) . Due to premature stop codons introduced by frame shifts, the alternatively spliced isoforms encode no or fewer LRR repeats. Experiments involving stable transformation of RPS4 genomic constructs lacking intron 2 and/or intron 3, under the control of the RPS4 promoter, showed that deletion of a single intron was sufficient to abolish RPS4 function, even though splicing of remaining intron was unaffected and the normally spliced transcript was also expressed . Therefore, resistance to DC3000 requires AS of RPS4.
A role for these alternatively spliced isoforms as regulatory RNAs remains possible, but there is evidence that they encode truncated proteins that regulate the activity of full-length RPS4. An artificial combination of normal and alternatively spliced isoforms only partially restored RPS4-mediated resistance . The molar ratio of RPS4 transcript isoforms in that experiment was altered compared to those naturally occurring, suggesting that the ratio is of functional importance. The abundance of the various AS isoforms of RPS4, particularly the isoform retaining intron 3 (RPS4AT4), is under dynamic regulation in response to AvrRps4. Whereas the full-length transcript including all exons is the predominant splicing product in uninoculated leaves, pathogen inoculation induces a rapid, >100-fold increase of RPS4AT4 . The truncated proteins encoded by RPS4 variants were detected in transient expression assays, confirming that the aberrant transcripts are functional.
3.1.2. Tobacco N
Tobacco N specifically recognizes a 50-kDa helicase protein (p50) of tobacco mosaic virus (TMV), and the N gene is alternatively spliced [73,82]. In addition to the major isoform (NRT), an alternative isoform (NAT) is generated via AS of a hidden exon containing a stop codon within intron 3, which yields a putative product lacking 13 of 14 LRR repeats (Figure 1B). Similar to RPS4, a dynamic abundance ratio of NRT to NAT is also observed during TMV infection . Although NRT is predominant before infection, NAT is the more abundant isoform 6 h after TMV inoculation, and the original isoform ratio reappears 9 h after inoculation. Perturbing the ratio of NRT to NAT resulted in compromised TMV resistance. The boost in NAT production may result from a signaling cascade induced by interaction between NRT and p50. Because the accumulation of spliced variants occurs rapidly, the induced AS may regulate N function via feedback inhibition. Tobacco transformants expressing only NRT displayed incomplete resistance manifested by delayed HR, which suggests that NAT is required for full N-mediated resistance . However, NAT expressed alone was not sufficient for TMV-dependent HR.
3.1.3. M. truncatula RCT1
RCT1 confers resistance against multiple races of Colletotrichum trifolii, a hemi-biotrophic fungal pathogen that causes anthracnose disease in Medicago . AS of RCT1 results from the retention of intron 4, instead of intron 2 and/or intron 3 as in N and RPS4 (Figure 1C). The alternative isoform (RCT1AT) is predicted to encode a truncated protein consisting of the entire TIR, NBS, and LRR domains, but lacking the C-terminal domain of the normal RCT1 protein (RCT1RT). RCT1-mediated resistance requires RCT1AT and RCT1RT, as transformants containing only RCT1AT or RCT1RT showed no anthracnose resistance . Though the expression of RCT1 transcripts was stable and constitutive, and unaffected by pathogen infection, a certain expression threshold for RCT1AT seemed to be essential for effective resistance.
3.1.4. Flax L6 and Tomato Bs4
In contrast to RPS4, N and RCT1, alternatively spliced transcripts of flax L6 and tomato BS4 are not required for full resistance to the corresponding pathogens. For example, transgenic plants carrying an intronless L6 (L6RT) exhibited complete rust resistance, similar to plants carrying the wild-type L6 (Figure 1D) . L6 triggers flax rust resistance by direct interaction with its cognate effector AvrL567. The flax rust resistance gene M, which is homologous to L, is also alternatively spliced; therefore, it is possible that AS of the M locus could functionally substitute for AS of L6. This hypothesis was supported by trans-complementation of the Rx gene. Rx is a CC-NBS-LRR gene that confers resistance to potato virus X (PVX) elicited by a coat protein. The CC domains in Rx share 96% similarity with those of Gpa2, which is required for resistance to potato nematode [83,84]. The function of an NBS-LRR derivative of Rx (Rx NBS-LRR) lacking the CC domain can be complemented by Gpa2 to induce coat protein-dependent HR . Such trans-complementation appears to require high identity between the R proteins, because pepper Bs2 (Bacterial spot resistance gene 2), which is homologous to Rx, failed to functionally complement an Rx NBS-LRR derivative.
Transient co-expression of L6RT and AvrL6 in tobacco gives rise to apparent HR, which argues against any interference by the M locus . Likewise, transient expression of intronless Bs4 revealed that the normal Bs4 protein alone could mediate AvrBs4 recognition, which suggests that AS of Bs4 is functionally dispensable . Whereas such transient expression assays have served well for isolation of R genes , whether this system can reliably be used to analyze functional roles for AS of R genes remains to be established. It is possible that the observed HR could be due to partial resistance conferred by an endogenous full-length R protein, such as tobacco N. Recent analysis of truncated R genes containing TIR-NBS only (TN) in Arabidopsis showed that chlorosis was induced by transient overexpression of TN genes . The alternative L6 and Bs4 isoforms were not tested in transient assays; therefore, these transient expression experiments may not fully reflect the physiological roles of AS in the process.
A stunted phenotype caused by constitutive defense responses was observed in transgenic tobacco carrying an L6 genomic construct, as well as in transgenic tobacco plants in which L6RT was under the control of the 35S promoter . This evidence is suggestive that AS is irrelevant to L6-mediated resistance, with dwarfism serving as a reporter for activation of defense responses. However, the lack of tobacco transformants expressing L6RT from its native promoter precludes firm conclusions about this. Structural and functional analysis demonstrated that the TIR domain alone is necessary and sufficient for L6 immune signaling . More interestingly, with only one exception (L10-A), tobacco plants transformed with a genomic construct of L10 grew normally . Further analysis revealed that the stunted phenotype of L10-A is associated with the presence of an additional truncated L10 transcript resulting from an aberrant T-DNA integration . This truncated transcript is predicted to encode a protein containing the TIR and 39 amino acids of the NBS domain of L10. These findings point to the possibility that the functional significance of AS in L6 has been undervalued.
3.2. AS of CC-NBS-LRR Genes
AS has been identified in many CC-NBS-LRR R genes, including LR10 and Sr35 in wheat [90,91], Mla in barley [92,93], Pi-ta and RGA5 in rice [94,95], and JA1tr in common bean , but the functional importance of this post-transcriptional modification for full disease resistance is largely unknown. Only the alternative transcripts of RGA5 have been functionally characterized in a robust system .
Rice blast R protein RGA5 was found to cooperate with RGA4 in recognizing two sequence-unrelated effectors, Avr-pia and Avr1-CO39, through direct binding. Two transcript isoforms are generated by AS of the third of the three introns in the coding region of RGA5 . As in the case of M. truncatula RCT1, protein products of both the intronless, fully-spliced transcript (RGA5RT) and the AS version (RGA5AT) share the CC, NBS, and LRR domains, and differ only in the C-terminal region, which is related to the copper binding protein ATX1 (RATX1) . Transformants carrying RGA5AT are fully susceptible to Avr-pia- and Avr1-CO39-expressing Magnaporthe oryzae strains. Furthermore, in conjunction with RGA4, RGA5RT is necessary and sufficient to confer dual recognition specificity . Yeast two-hybrid assays demonstrated that Avr-pia and Avr1-CO39 physically interact with the C-terminal RATX1 domain, which is present only in RGA5RT. The disruption of the RATX1 domain consequently renders RGA5AT inactive. These findings highlight the importance of the non-LRR regions near the C-termini of R proteins, indicating that they may deserve more attention when exploring the functions of R proteins in disease resistance.
Another rice blast resistance gene, Pi-ta, confers resistance to strains of M. oryzae containing cognate avirulence gene Avr-Pita. A total of 12 distinct transcript isoforms were identified as resulting from AS and are predicted to encode 11 proteins. Some of these transcripts are constitutively expressed while others show differential expression upon blast infection . Their regulatory roles in disease resistance remain unknown.
The barley powdery mildew resistance genes Mla6 and Mla13 have very similar gene structures, including the conservation of two introns in the 5'-UTR and two introns in the coding region, as well as a large intron in the 3'-UTR. Notably, both genes exhibit AS of the 5'-UTR, which contains three upstream ORFs (uORFs); AS is also predicted to cause variation of one amino acid in the coding region of Mla13 . The expression of Mla13 transcripts is induced upon pathogen penetration, and a dynamic change in the relative abundance of transcript isoforms has been observed. Inactivation of uORF translation via mutagenesis suggests the uORFs in the 5'-UTR downregulate Mla13 synthesis . Hence, AS of uORFs may finely tune Mla13 expression to achieve effective resistance while minimizing host cell damage. However, it remains unknown whether full resistance mediated by Mla13 or Mla6 requires AS of the uORFs.
4. Possible Mechanisms of AS-Mediated Regulation of Defense Response
In the cases where AS is necessary for disease resistance, transgenic plants containing only the full-length transcript do not display auto-immunity or lesion mimic phenotypes induced by increased R protein activity, suggesting that AS is not likely to negatively regulate the R gene function. By contrast, the absence of AS impairs R gene-mediated resistance, which is indicative of positive roles for AS in defense responses. R protein isoforms therefore possibly function by suppressing the negative regulation of immunity activation, or by directly engaging in effector-trigged signaling, or by a combination of both.
4.1. Disruption of R Protein Autoinhibition
Whether an R protein is active or inactive is determined by the binding of ATP or ADP to the NBS domain . Since constitutive activation of R proteins leads to lethal effects on plant growth, negative regulation of R protein activity is essential [100,101,102]. Intramolecular interactions between R-protein domains may function as a regulatory switch, and several mechanistic models have been proposed to describe this R protein self-regulation, such as the “Jack-knife” model . These models are based largely on the trans-complementation of Rx CC-NBS and LRR domains . From the crystal structures of the TIR and CC domains [89,104], Takken and Goverse proposed a model in which the NBS domain interacts with the N-terminal half of the LRRs, maintaining the R protein as inactive in a closed conformation before pathogen invasion . An electrostatic interface that maintains the inactive conformation may be formed by interaction between the LRR and NBS domains. The C-terminal LRRs are exposed to serve as an antenna to detect charge changes induced by environmental perturbations. Since the TIR or CC domain can also interact with the NBS domain , the R protein is stabilized in a compact structure in the absence of pathogens. Studies on intramolecular interactions of Rx have provided evidence that the NBS domain alone is not sufficient for stable binding, but instead requires the CC domain. Notably, the CC domain could also interact with the NBS domain, unless N-terminal LRRs were bound to the NBS domain [44,85,106]. As such, the interaction of LRRs and NBS domains seems to cause conformational changes in the latter that facilitate NBS binding with CC domain. It has also been demonstrated that the ARC1 subdomain is necessary for binding of the Rx N-terminal LRR domain, while the ARC2 subdomain is required to maintain an autoinhibited state in the absence of elicitor, as well as for subsequent signaling . Mutation in LRRs or conserved ACR2 motifs of the NBS domain leads to the autoactivation of Rx and RPS5 [44,85,107]. The majority of truncated R protein variants generated by AS are presumably unstable, due to the lack of LRR domain, and it is thus speculated that the aberrant R protein isoforms induced by pathogen inoculation could form intermolecular interactions with their regular protein products. This would disrupt the closed conformation stabilized by intermolecular interactions and free active R proteins.
In addition to the autoinhibition, R proteins are also subjected to negative regulation by trans factors . RIN4, guarded by RPM1 and RPS2, is phosphorylated upon infection with P. syringae by AvrRpm1 and AvrB [108,109]. The rin4 mutants cannot survive in the presence of wild-type RPM1 and RPS2, due to strong activation of defense responses independent of pathogen infection. However, the rin4 defective phenotype is suppressed in the triple mutant rin4 rps2 rpm1 . It was deduced that interactions of RIN4 with RPM1 and RPS2 negatively regulate the activities of both of these R proteins. The down-regulation of R protein activity could also be achieved by limiting its accumulation to a steady level. SRFR1 (Suppressor of RPS4-RLD1) interacts with SNC1 to negatively regulate production of several R proteins, such as RPS2, RPS4 and RPS6 . Likewise, the F-box protein CPR1 (Constitutive expresser of PR genes 1) controls the stability of R proteins through SKP1-Cullin1-F-box (SCF)-mediated protein degradation . Loss-of-function cpr1 mutants displayed higher expression of SNC1 and RPS2, as well as autoimmunity responses. Excess R protein isoforms produced via AS upon effector recognition may compete with full-length R protein to interact with negative regulators and decrease the relative abundance of these suppressors, thereby releasing active R protein . This assumption is in line with observations that the overexpression of some R genes, including Rx, RPS2, and RPM1, leads to constitutive activation of resistance signaling.
4.2. Function as Signaling Factors
Overexpression of the TIR or CC domain of some R proteins (e.g., RPS4, RPP1, MLA10, and L6) can induce HR in the absence of cognate effectors [89,104,112,113,114]. In addition to the TIR-NBS-LRR-encoding R genes, plants also contain short pseudo-R gene homologs (TN and TX) . TN proteins contain the TIR and NBS domains, but lack the LRR domain, while TX proteins have only the TIR domain followed by a small and variable C-terminal domain. Arabidopsis contains 21 TN and 30 TX genes . Transient and stable overexpression of some TN and TX genes induced necrosis in tobacco leaves and reduced disease symptoms in P. syringae-infected Arabidopsis plants, respectively . This suggests that the truncated R proteins resulting from AS may also confer disease resistance with or without recognition specificity.
The crystal structures of the TIR domain of L6 and CC domain of MLA10 indicated that two activated R proteins form a homodimer at the CC or TIR domain to constitute a minimal functional unit [89,104]. In the presence of full-length R protein, the production of massive amounts of truncated proteins containing TIR or CC may serve as a rapid and energy-efficient mechanism to activate responses to pathogen infection. If so, the rapid increase of TIR or CC domain-dependent dimerization stimulated by AS of R genes might function to amplify the plant defense responses.
Protein function is associated with subcellular localization. It is possible that the alternative proteins generated by AS are localized to different compartments than the full-length R proteins, and numerous reports have demonstrated dynamic subcellular localization for R proteins such as RPS4 and N [42,117,118]. Distinct signaling pathways can be initiated by a single R protein in different subcellular localizations, and, thus, the coordinated trafficking of R proteins is required for the activation of full resistance . RPS4 is detected in both the endomembrane and nucleus in healthy and diseased leaves, with RPS4 accumulation in the nucleus appearing to be necessary for AvrRPS4-trigged immunity . AvrRPS4 also shows a nucleo-cytoplasmic distribution. Forcing AvrRPS4 to accumulate in cytoplasm through the C-terminal fusion of a nuclear export sequence led to moderate HR and partial suppression of bacterial growth. By contrast, sequestration of AvrRPS4 in the nucleus by fusion of nuclear localization sequence was sufficient for inhibition of bacterial growth, but cell death elicited by HR was abolished. HR signaling is therefore mediated by cytoplasmic RPS4-AvrRPS4 interaction, whereas the nuclear R-Avr interaction-induced resistance is not coupled to programmed cell death. This is in line with the findings that restriction of pathogen spread does not always correlate with HR [120,121,122]. However, because the construct used for examination of RPS4 subcellular localization consisted of its genomic sequence with an upstream fusion of the reporter gene under the control of the 35S promoter, any differential targeting of full-length RPS4 compared to truncated variants could not be distinguished . It is likely that the truncated RPS4 proteins would accumulate in the endomembrane system, since their C termini lack a bipartite nuclear localization sequence, which is necessary for accumulation of full-length RPS4 in the nucleus. This could explain why only 6%–10% of RPS4 was observed in the nuclei. The distinct types of signaling triggered by nucleo-cytoplasmic distribution of R-Avr interaction may be coordinated by AS and differential localization of the resultant protein isoforms.
Tobacco N is predicted to be cytoplasmic because it does not carry a recognizable nuclear localization signal. Unexpectedly, it was found to be localized to both the cytoplasm and the nucleus, and nuclear localization is required for N function . Different constructs, tagged with distinct fluorescence genes for different N transcript isoforms, are needed to test whether AS leads to diverse subcellular localizations for alternative N isoforms.
5. Regulation of AS of R Genes
AS dramatically increases the diversity of the transcriptome, and AS of R genes plays crucial roles in regulating plant defense responses; therefore, the mechanisms that regulate AS must be finely tuned to control the levels of different AS transcripts. Removal of introns within pre-mRNA in eukaryotes is catalyzed by the spliceosome, a highly dynamic and complex macromolecule comprising five (U1, U2, U4, U5, and U6) small ribonucleoproteins (snRNPs) and numerous RNA binding proteins (RBPs), such as serine/arginine-rich (SR) proteins and heterogeneous nuclear ribonucleoproteins (hnRNPs). The precise selection of intron/exons requires splicing factors to recognize four loosely conserved sequence features in pre-mRNA: (1) the 5' splicing site (SS) of GU paired with snRNP U1; (2) a branch point A for binding of splicing factor 1 at the 18 to 40 nucleotides upstream of the 3' SS; (3) the 3' SS of AG and (4) a poly-pyrimidine tract for recruitment of U2 auxiliary factor heterodimer [26,123]. It is noteworthy that a single intron may contain multiple sites for each of these four conserved sequence elements, adding more complexity in splicing site selection.
Differential selection of 5'- or 3'-SSs can be also affected by some short sequences of cis-elements in intronic and exonic region. According to the position and function, these cis-elements are grouped as exonic splicing enhancers, exonic splicing silencers, intronic splicing enhancers, and intronic splicing silencers. These splicing regulatory elements bind to trans-acting splicing factors, such as SR proteins and hnRNPs, playing critical roles in both constitutive and alternative splicing through either inducing or suppressing selection of nearby 5'- or 3'-splicing sites [124,125]. Interestingly, SR genes are also extensively alternatively spliced and AS of SR genes is affected by environmental stresses such as temperature, light and salt, which in turn induces splicing changes in the pre-mRNAs of other genes .
As mentioned above, screening for suppressors of the gain-of-function mutation snc1 led to the identification of a set of MOS genes, some of which function in pre-mRNA processing. For example, Arabidopsis mutants carrying a loss-of-function mutation for MOS4, MOS12, or MOS14 show altered splicing patterns for SNC1 and RPS4, which indicate that those genes have regulatory roles in AS of R genes [62,71,72]. MOS4, required for both ETI and PTI, is a nuclear localized CC homologous to human BCA2 (Breast cancer-amplified sequence 2). Together with the Myb-transcription factor CDC5L (Cell divison cycle 5 like protein) and the WD-40 repeat PLRG1 (Pleiotropic regulator 1), BCA2 was isolated from humans as an important component of a multiprotein spliceosome complex that includes the E3 ubiquitin ligase Prp19 (Precursor RNA processing 19) [127,128]. Yeast two-hybrid and in planta assays confirmed that MOS4 interacted with the Arabidopsis homologs of CDC5L and PRLG1 (AtCDC5 and PRL1, respectively) to constitute a core structure for a spliceosome-associated complex termed the MOS4-associated complex (MAC) . MAC3A and MAC3B, two functionally redundant homologs of Prp19, contribute to proper splicing of SNC1, though their effects on AS of RPS4 have not been investigated . Similarly, whether two other redundant homologs, MAC5A and MAC5B, function in R gene AS has not been tested . However, given that its counterpart in human is RBM22, which interacts with U6 snRNP, it is possible that MAC5 participates in pre-mRNA splicing in plants.
MOS12 encodes an SR protein homologous to human cyclin L . Co-immunoprecipitation of MOS12 with MOS4 indicates that MOS12 is also associated with the MAC. The mos12 mutant displays compromised RPS4-mediated resistance as well as an altered splicing pattern of RPS4, leading to a different abundance ratio of RPS4 transcript isoforms. However, the splicing pattern of RPS6 is normal in the mos12 mutant, as is RPS6-mediated resistance. This suggests that in addition to MAC, more spliceosomal complexes with distinct splicing specificities probably exist in plants.
Impaired SNC1- and RPS4-mediated PTI and ETI was also observed in the loss-of-function mutant of MOS14 . In addition to distorted splicing patterns, the mos14 mutants showed reduced expression of SNC1 and RPS4. MOS14 encodes a nuclear protein homologous to transportin-SR, which functions in nuclear trafficking of the SR protein. MOS14 interacts with four different SR proteins through its C-terminus, while the N-terminus interacts with a GTP-binding protein AtRAN1 (Ras-related nuclear protein 1) which functions in many processes, including nuclear transport of proteins. The nuclear localization of these four proteins was disrupted in mos14 mutants, which consequently affects the splicing profiles for their targets. Defective splicing resulting from mislocalization of MOS14 cargos may cause the reduction in SNC1 and RPS4 expression .
6. Future Prospects
The functional importance of AS in plant disease resistance has become increasingly clear. However, despite the substantial progress that has been made in the past decade, AS research in plant immunity is still in its infancy. The AS events characterized to date in CC-NBS-LRR genes appear not to be required for disease resistance. Therefore, more research on CC-NBS-LRR genes will be needed to confirm whether AS plays other functional roles. Some truncated TIR-NBS-LRR proteins encoded by alternative transcripts are required for full R-gene mediated resistance, which raises an interesting question of how they engage in R-Avr interactions. Neither the “elicitor-receptor” nor the “guard hypothesis” models explain how truncated R proteins function in triggering plant defense responses. The cognate Avr proteins for L6, RPS4 and N, and even their host targets [117,119,131] have been identified, providing an opportunity to discover biological roles for the aberrant R protein variants. Research in this direction will likely provide insights into the functional mechanisms of truncated R proteins, as well as their dynamic subcellular localization, and interactions with Avr proteins and their targets, thus extending our understanding of gene-for-gene resistance in plants.
The alternative transcript isoforms may be subjected to nonsense-mediated decay (NMD) , which is widespread in eukaryotes and serves as a quality control mechanism . NMD is coupled with AS to regulate the levels of functional mRNA transcripts through the specific degradation of alternatively spliced isoforms possessing a premature stop codon . However, it remains unclear that how the potential NMD targets derived from AS of R genes escape being destroyed. Although its functional roles are not clear and few targets have been identified, NMD regulation in disease resistance has been documented. nmd mutants display stunted phenotypes and curled leaves that resemble those of mutants with constitutive activation of defense responses , and the majority of transcripts enriched in nmd mutants are associated with the pathogen response .
The AS transcripts of R genes such as N and RPS4 are of low abundance in the absence of their corresponding effectors. It was first assumed that NMD activity was repressed during pathogen infection, resulting in the accumulation of alternative R gene transcripts , which is consistent with the weak NMD activity observed by RNA-seq analysis in P. syringae-infected Arabidopsis . Alternatively, the R gene transcript isoforms possessing premature stop codons may be insensitive to NMD. Generally, mRNAs targeted for NMD have uORFs or a larger 3'-UTR region . However, many transcripts displaying intron retention are not sensitive to NMD, although they appear to have the characteristics of transcripts affected by NMD. Whatever the mechanism, more evidence is required to clarify the molecular machinery that suppresses NMD of alternatively spliced transcripts of R genes.
The cloning of the MOS genes shed light onto spliceosomal regulation in the AS of R genes. However, the splicing factors and RNA-binding proteins responsible for pre-mRNA splicing of R genes other than SNC1 and RPS4 are completely unknown. One challenge is that mutations in these factors may cause inconspicuous phenotypes, because AS could be unnecessary for full disease resistance. In addition, even if defense signaling requires AS of an R gene, the mutant would likely grow normally in the absence of the pathogen expressing its cognate effector. We therefore have a long way to go before the full picture of regulation of R gene AS is revealed. Continuous advances in genomics, bioinformatics, transcriptomics, phenomics, and sequencing technologies, should facilitate our explorations of the complexity for generation and contribution of AS of R genes and elucidate new avenues to modify plant innate immunity.
apaf-1, R and ced-4
breast cancer-amplified sequence 2
bacterial spot resistance gene 4
cell divison cycle 5 like protein
constitutive expresser of PR genes 1
P. syringae pv tomato strain DC3000
down syndrome cell adhesion molecule
enhanced disease susceptibility 1
heterogeneous nuclear ribonucleoproteins
HR to TCV
leucine-rich repeat region
modifier of snc1
non-race-specific disease resistance 1
non-expresser of PR genes 1
50-kDa helicase protein
phytoalexin deficient 4
|PAMPs or MAMPs|
pathogen (or microbe)-associated molecular patterns
pleiotropic regulator 1
precursor RNA processing 19
pattern recognition receptors
resistance to Albugo candida isolated ACEM1
RAS-related nuclear protein 1
RNA binding proteins
recognition of Peronospora parasitica
resistance to P. Syringae
suppressor of npr1-1, constitutive 1
suppressor of RPS4-RLD1
turnip crinkle virus
Drosophila Toll and mammalian Interleukin-1 receptor
tobacco mosaic virus
truncated R proteins containing TIR-NBS only
truncated R proteins containing TIR only
This work was supported by United States Department of Agriculture-National Research Initiative Competitive Grants Program (2005-35301-15697 and 2005-35300-15461 to H.Z.) and the College of Agriculture of University of Kentucky. This article is published with the approval of the Director of the Kentucky Agricultural Experiment Station.
S.Y. and H.Z. wrote the manuscript; F.T and S.Y performed the experiments to characterize the role of alternative splicing in RCT1-mediated disease resistance in Medicago truncatula.
Conflicts of Interest
The authors declare no conflict of interest.
- Nilsen, T.W.; Graveley, B.R. Expansion of the eukaryotic proteome by alternative splicing. Nature 2010, 463, 457–463. [Google Scholar] [CrossRef]
- Pan, Q.; Shai, O.; Lee, L.J.; Frey, B.J.; Blencowe, B.J. Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing. Nat. Genet. 2008, 40, 1413–1415. [Google Scholar] [CrossRef]
- Wang, E.T.; Sandberg, R.; Luo, S.; Khrebtukova, I.; Zhang, L.; Mayr, C.; Kingsmore, S.F.; Schroth, G.P.; Burge, C.B. Alternative isoform regulation in human tissue transcriptomes. Nature 2008, 456, 470–476. [Google Scholar] [CrossRef]
- Graveley, B.R. Mutually exclusive splicing of the insect Dscam pre-mRNA directed by competing intronic RNA secondary structures. Cell 2005, 123, 65–73. [Google Scholar] [CrossRef]
- Brett, D.; Pospisil, H.; Valcarcel, J.; Reich, J.; Bork, P. Alternative splicing and genome complexity. Nat. Genet. 2002, 30, 29–30. [Google Scholar] [CrossRef]
- Kazan, K. Alternative splicing and proteome diversity in plants: The tip of the iceberg has just emerged. Trends Plant Sci. 2003, 8, 468–471. [Google Scholar] [CrossRef]
- Ramani, A.K.; Calarco, J.A.; Pan, Q.; Mavandadi, S.; Wang, Y.; Nelson, A.C.; Lee, L.J.; Morris, Q.; Blencowe, B.J.; Zhen, M. Genome-wide analysis of alternative splicing in Caenorhabditis elegans. Genome Res. 2011, 21, 342–348. [Google Scholar] [CrossRef]
- Zhu, W.; Schlueter, S.D.; Brendel, V. Refined annotation of the Arabidopsis genome by complete expressed sequence tag mapping. Plant Physiol. 2003, 132, 469–484. [Google Scholar] [CrossRef]
- Iida, K.; Seki, M.; Sakurai, T.; Satou, M.; Akiyama, K.; Toyoda, T.; Konagaya, A.; Shinozaki, K. Genome-wide analysis of alternative pre-mRNA splicing in Arabidopsis thaliana based on full-length cDNA sequences. Nucleic Acids Res. 2004, 32, 5096–5103. [Google Scholar] [CrossRef]
- Wang, B.B.; Brendel, V. Genomewide comparative analysis of alternative splicing in plants. Proc. Natl. Acad. Sci. USA 2006, 103, 7175–7180. [Google Scholar] [CrossRef]
- Campbell, M.A.; Haas, B.J.; Hamilton, J.P.; Mount, S.M.; Buell, C.R. Comprehensive analysis of alternative splicing in rice and comparative analyses with Arabidopsis. BioMed Cent. Genomics 2006, 7, 327. [Google Scholar]
- Marquez, Y.; Brown, J.W.; Simpson, C.; Barta, A.; Kalyna, M. Transcriptome survey reveals increased complexity of the alternative splicing landscape in Arabidopsis. Genome Res. 2012, 22, 1184–1195. [Google Scholar] [CrossRef]
- Ali, G.S.; Reddy, A.S. Regulation of alternative splicing of pre-mRNAs by stresses. Curr. Top. Microbiol. 2008, 326, 257–275. [Google Scholar]
- Mastrangelo, A.M.; Marone, D.; Laido, G.; de Leonardis, A.M.; de Vita, P. Alternative splicing: Enhancing ability to cope with stress via transcriptome plasticity. Plant Sci. 2012, 185–186, 40–49. [Google Scholar] [CrossRef]
- Howard, B.E.; Hu, Q.; Babaoglu, A.C.; Chandra, M.; Borghi, M.; Tan, X.; He, L.; Winter-Sederoff, H.; Gassmann, W.; Veronese, P. High-throughput RNA sequencing of pseudomonas-infected Arabidopsis reveals hidden transcriptome complexity and novel splice variants. PLoS One 2013, 8, e74183. [Google Scholar]
- Lopato, S.; Kalyna, M.; Dorner, S.; Kobayashi, R.; Krainer, A.R.; Barta, A. AtSRp30, one of two SF2/ASF-like proteins from Arabidopsis thaliana, regulates splicing of specific plant genes. Genes Dev. 1999, 13, 987–1001. [Google Scholar] [CrossRef]
- Lopato, S.; Waigmann, E.; Barta, A. Characterization of a novel arginine/serine-rich splicing factor in Arabidopsis. Plant Cell 1996, 8, 2255–2264. [Google Scholar] [CrossRef]
- Loraine, A.E.; McCormick, S.; Estrada, A.; Patel, K.; Qin, P. RNA-seq of Arabidopsis pollen uncovers novel transcription and alternative splicing. Plant Physiol. 2013, 162, 1092–1109. [Google Scholar] [CrossRef]
- Yoshimura, K.; Yabuta, Y.; Ishikawa, T.; Shigeoka, S. Identification of a cis element for tissue-specific alternative splicing of chloroplast ascorbate peroxidase pre-mRNA in higher plants. J. Biol. Chem. 2002, 277, 40623–40632. [Google Scholar] [CrossRef]
- De la Fuente van Bentem, S.; Vossen, J.H.; Vermeer, J.E.; de Vroomen, M.J.; Gadella, T.W., Jr.; Haring, M.A.; Cornelissen, B.J. The subcellular localization of plant protein phosphatase 5 isoforms is determined by alternative splicing. Plant Physiol. 2003, 133, 702–712. [Google Scholar] [CrossRef]
- Kriechbaumer, V.; Wang, P.; Hawes, C.; Abell, B.M. Alternative splicing of the auxin biosynthesis gene YUCCA4 determines its subcellular compartmentation. Plant J. 2012, 70, 292–302. [Google Scholar] [CrossRef]
- Remy, E.; Cabrito, T.R.; Baster, P.; Batista, R.A.; Teixeira, M.C.; Friml, J.; Sa-Correia, I.; Duque, P. A major facilitator superfamily transporter plays a dual role in polar auxin transport and drought stress tolerance in Arabidopsis. Plant Cell 2013, 25, 901–926. [Google Scholar] [CrossRef]
- Carvalho, S.D.; Saraiva, R.; Maia, T.M.; Abreu, I.A.; Duque, P. XBAT35, a novel Arabidopsis RING E3 ligase exhibiting dual targeting of its splice isoforms, is involved in ethylene-mediated regulation of apical hook curvature. Mol. Plant 2012, 5, 1295–1309. [Google Scholar] [CrossRef]
- Reddy, A.S.; Marquez, Y.; Kalyna, M.; Barta, A. Complexity of the alternative splicing landscape in plants. Plant Cell 2013, 25, 3657–3683. [Google Scholar] [CrossRef]
- Carvalho, R.F.; Feijao, C.V.; Duque, P. On the physiological significance of alternative splicing events in higher plants. Protoplasma 2013, 250, 639–650. [Google Scholar] [CrossRef]
- Reddy, A.S. Alternative splicing of pre-messenger RNAs in plants in the genomic era. Annu. Rev. Plant Biol. 2007, 58, 267–294. [Google Scholar] [CrossRef]
- Staiger, D.; Brown, J.W.S. Alternative splicing at the intersection of biological timing, development, and stress responses. Plant Cell 2013, 25, 3640–3656. [Google Scholar] [CrossRef]
- Zhang, X.C.; Gassmann, W. RPS4-mediated disease resistance requires the combined presence of RPS4 transcripts with full-length and truncated open reading frames. Plant Cell 2003, 15, 2333–2342. [Google Scholar] [CrossRef]
- Zhang, X.C.; Gassmann, W. Alternative splicing and mRNA levels of the disease resistance gene RPS4 are induced during defense responses. Plant Physiol. 2007, 145, 1577–1587. [Google Scholar] [CrossRef]
- Dinesh-Kumar, S.P.; Baker, B.J. Alternatively spliced N resistance gene transcripts: Their possible role in tobacco mosaic virus resistance. Proc. Natl. Acad. Sci. USA 2000, 97, 1908–1913. [Google Scholar] [CrossRef]
- Tang, F.; Yang, S.; Gao, M.; Zhu, H. Alternative splicing is required for RCT1-mediated disease resistance in Medicago truncatula. Plant Mol. Biol. 2013, 82, 367–374. [Google Scholar] [CrossRef]
- Staiger, D.; Korneli, C.; Lummer, M.; Navarro, L. Emerging role for RNA-based regulation in plant immunity. New Phytol. 2013, 197, 394–404. [Google Scholar] [CrossRef]
- Dodds, P.N.; Lawrence, G.J.; Catanzariti, A.M.; Teh, T.; Wang, C.I.; Ayliffe, M.A.; Kobe, B.; Ellis, J.G. Direct protein interaction underlies gene-for-gene specificity and coevolution of the flax resistance genes and flax rust avirulence genes. Proc. Natl. Acad. Sci. USA 2006, 103, 8888–8893. [Google Scholar] [CrossRef]
- Van der Biezen, E.A.; Jones, J.D. Plant disease-resistance proteins and the gene-for-gene concept. Trends Biochem. Sci. 1998, 23, 454–456. [Google Scholar] [CrossRef]
- Boller, T.; Felix, G. A renaissance of elicitors: Perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors. Annu. Rev. Plant Biol. 2009, 60, 379–406. [Google Scholar] [CrossRef]
- Macho, A.P.; Schwessinger, B.; Ntoukakis, V.; Brutus, A.; Segonzac, C.; Roy, S.; Kadota, Y.; Oh, M.H.; Sklenar, J.; Derbyshire, P. A bacterial tyrosine phosphatase inhibits plant pattern recognition receptor activation. Science 2014, 343, 1509–1512. [Google Scholar] [CrossRef]
- Kim, S.H.; Kwon, S.I.; Saha, D.; Anyanwu, N.C.; Gassmann, W. Resistance to the Pseudomonas syringae effector HopA1 is governed by the TIR-NBS-LRR protein RPS6 and is enhanced by mutations in SRFR1. Plant Physiol. 2009, 150, 1723–1732. [Google Scholar] [CrossRef]
- Bhattacharjee, S.; Halane, M.K.; Kim, S.H.; Gassmann, W. Pathogen effectors target Arabidopsis EDS1 and alter its interactions with immune regulators. Science 2011, 334, 1405–1408. [Google Scholar] [CrossRef]
- Glazebrook, J.; Rogers, E.E.; Ausubel, F.M. Use of Arabidopsis for genetic dissection of plant defense responses. Annu. Rev. Genet. 1997, 31, 547–569. [Google Scholar] [CrossRef]
- Goodman, R.N.; Novacky, A.J. The Hypersensitive Reaction in Plants to Pathogens: A Resistance Phenomenon; APS Press: St. Paul, MN, USA, 1994. [Google Scholar]
- Asai, T.; Tena, G.; Plotnikova, J.; Willmann, M.R.; Chiu, W.L.; Gomez-Gomez, L.; Boller, T.; Ausubel, F.M.; Sheen, J. MAP kinase signalling cascade in Arabidopsis innate immunity. Nature 2002, 415, 977–983. [Google Scholar] [CrossRef]
- Shen, Q.H.; Saijo, Y.; Mauch, S.; Biskup, C.; Bieri, S.; Keller, B.; Seki, H.; Ulker, B.; Somssich, I.E.; Schulze-Lefert, P. Nuclear activity of MLA immune receptors links isolate-specific and basal disease-resistance responses. Science 2007, 315, 1098–1103. [Google Scholar] [CrossRef]
- Traut, T.W. The functions and consensus motifs of nine types of peptide segments that form different types of nucleotide-binding sites. Eur. J. Biochem. 1994, 222, 9–19. [Google Scholar] [CrossRef]
- Rairdan, G.J.; Moffett, P. Distinct domains in the ARC region of the potato resistance protein Rx mediate LRR binding and inhibition of activation. Plant Cell 2006, 18, 2082–2093. [Google Scholar] [CrossRef]
- Kobe, B.; Deisenhofer, J. The leucine-rich repeat: A versatile binding motif. Trends Biochem. Sci. 1994, 19, 415–421. [Google Scholar] [CrossRef]
- Ellis, J.G.; Lawrence, G.J.; Luck, J.E.; Dodds, P.N. Identification of regions in alleles of the flax rust resistance gene L that determine differences in gene-for-gene specificity. Plant Cell 1999, 11, 495–506. [Google Scholar] [CrossRef]
- Leister, R.T.; Katagiri, F. A resistance gene product of the nucleotide binding site—Leucine rich repeats class can form a complex with bacterial avirulence proteins in vivo. Plant J. 2000, 22, 345–354. [Google Scholar] [CrossRef]
- Jia, Y.; McAdams, S.A.; Bryan, G.T.; Hershey, H.P.; Valent, B. Direct interaction of resistance gene and avirulence gene products confers rice blast resistance. Embo J. 2000, 19, 4004–4014. [Google Scholar] [CrossRef]
- Tao, Y.; Yuan, F.; Leister, R.T.; Ausubel, F.M.; Katagiri, F. Mutational analysis of the Arabidopsis nucleotide binding site-leucine-rich repeat resistance gene RPS2. Plant Cell 2000, 12, 2541–2554. [Google Scholar]
- Boyes, D.C.; Nam, J.; Dangl, J.L. The Arabidopsis thaliana RPM1 disease resistance gene product is a peripheral plasma membrane protein that is degraded coincident with the hypersensitive response. Proc. Natl. Acad. Sci. USA 1998, 95, 15849–15854. [Google Scholar] [CrossRef]
- Aarts, N.; Metz, M.; Holub, E.; Staskawicz, B.J.; Daniels, M.J.; Parker, J.E. Different requirements for EDS1 and NDR1 by disease resistance genes define at least two R gene-mediated signaling pathways in Arabidopsis. Proc. Natl. Acad. Sci. USA 1998, 95, 10306–10311. [Google Scholar]
- Chandra-Shekara, A.C.; Navarre, D.; Kachroo, A.; Kang, H.G.; Klessig, D.; Kachroo, P. Signaling requirements and role of salicylic acid in HRT- and rrt-mediated resistance to turnip crinkle virus in Arabidopsis. Plant J. 2004, 40, 647–659. [Google Scholar] [CrossRef]
- Bittner-Eddy, P.D.; Beynon, J.L. The Arabidopsis downy mildew resistance gene, RPP13-Nd, functions independently of NDR1 and EDS1 and does not require the accumulation of salicylic acid. Mol. Plant Microbe Interact. 2001, 14, 416–421. [Google Scholar] [CrossRef]
- McDowell, J.M.; Dhandaydham, M.; Long, T.A.; Aarts, M.G.; Goff, S.; Holub, E.B.; Dangl, J.L. Intragenic recombination and diversifying selection contribute to the evolution of downy mildew resistance at the RPP8 locus of Arabidopsis. Plant Cell 1998, 10, 1861–1874. [Google Scholar] [CrossRef]
- Venugopal, S.C.; Jeong, R.D.; Mandal, M.K.; Zhu, S.; Chandra-Shekara, A.C.; Xia, Y.; Hersh, M.; Stromberg, A.J.; Navarre, D.; Kachroo, A. Enhanced disease susceptibility 1 and salicylic acid act redundantly to regulate resistance gene-mediated signaling. PLoS Genet. 2009, 5, e1000545. [Google Scholar] [CrossRef]
- Falk, A.; Feys, B.J.; Frost, L.N.; Jones, J.D.; Daniels, M.J.; Parker, J.E. EDS1, an essential component of R gene-mediated disease resistance in Arabidopsis has homology to eukaryotic lipases. Proc. Natl. Acad. Sci. USA 1999, 96, 3292–3297. [Google Scholar] [CrossRef]
- Feys, B.J.; Wiermer, M.; Bhat, R.A.; Moisan, L.J.; Medina-Escobar, N.; Neu, C.; Cabral, A.; Parker, J.E. Arabidopsis senescence-associated gene101 stabilizes and signals within an enhanced disease susceptibility1 complex in plant innate immunity. Plant Cell 2005, 17, 2601–2613. [Google Scholar]
- Zhu, S.; Jeong, R.D.; Venugopal, S.C.; Lapchyk, L.; Navarre, D.; Kachroo, A.; Kachroo, P. SAG101 forms a ternary complex with EDS1 and PAD4 and is required for resistance signaling against turnip crinkle virus. PLoS Pathog. 2011, 7, e1002318. [Google Scholar] [CrossRef]
- Cao, H.; Glazebrook, J.; Clarke, J.D.; Volko, S.; Dong, X. The Arabidopsis NPR1 gene that controls systemic acquired resistance encodes a novel protein containing ankyrin repeats. Cell 1997, 88, 57–63. [Google Scholar] [CrossRef]
- Li, X.; Clarke, J.D.; Zhang, Y.; Dong, X. Activation of an EDS1-mediated R-gene pathway in the snc1 mutant leads to constitutive, NPR1-independent pathogen resistance. Mol. Plant Microbe Interact. 2001, 14, 1131–1139. [Google Scholar] [CrossRef]
- Palma, K.; Zhang, Y.; Li, X. An importin α homolog, MOS6, plays an important role in plant innate immunity. Curr. Biol. 2005, 15, 1129–1135. [Google Scholar]
- Palma, K.; Zhao, Q.; Cheng, Y.T.; Bi, D.; Monaghan, J.; Cheng, W.; Zhang, Y.; Li, X. Regulation of plant innate immunity by three proteins in a complex conserved across the plant and animal kingdoms. Genes Dev. 2007, 21, 1484–1493. [Google Scholar] [CrossRef]
- Zhang, Y.; Li, X. A putative nucleoporin 96 is required for both basal defense and constitutive resistance responses mediated by suppressor of npr1-1, constitutive 1. Plant Cell 2005, 17, 1306–1316. [Google Scholar] [CrossRef]
- Zhang, Y.; Cheng, Y.T.; Bi, D.; Palma, K.; Li, X. MOS2, a protein containing G-patch and KOW motifs, is essential for innate immunity in Arabidopsis thaliana. Curr. Biol. 2005, 15, 1936–1942. [Google Scholar] [CrossRef]
- Goritschnig, S.; Zhang, Y.; Li, X. The ubiquitin pathway is required for innate immunity in Arabidopsis. Plant J. 2007, 49, 540–551. [Google Scholar] [CrossRef]
- Wiermer, M.; Palma, K.; Zhang, Y.; Li, X. Should I stay or should I go? Nucleocytoplasmic trafficking in plant innate immunity. Cell. Microbiol. 2007, 9, 1880–1890. [Google Scholar] [CrossRef]
- Goritschnig, S.; Weihmann, T.; Zhang, Y.; Fobert, P.; McCourt, P.; Li, X. A novel role for protein farnesylation in plant innate immunity. Plant Physiol. 2008, 148, 348–357. [Google Scholar] [CrossRef]
- Cheng, Y.T.; Germain, H.; Wiermer, M.; Bi, D.; Xu, F.; Garcia, A.V.; Wirthmueller, L.; Despres, C.; Parker, J.E.; Zhang, Y. Nuclear pore complex component MOS7/Nup88 is required for innate immunity and nuclear accumulation of defense regulators in Arabidopsis. Plant Cell 2009, 21, 2503–2516. [Google Scholar] [CrossRef]
- Germain, H.; Qu, N.; Cheng, Y.T.; Lee, E.; Huang, Y.; Dong, O.X.; Gannon, P.; Huang, S.; Ding, P.; Li, Y. MOS11: A new component in the mRNA export pathway. PLoS Genet. 2010, 6, e1001250. [Google Scholar] [CrossRef]
- Li, Y.; Tessaro, M.J.; Li, X.; Zhang, Y. Regulation of the expression of plant resistance gene SNC1 by a protein with a conserved BAT2 domain. Plant Physiol. 2010, 153, 1425–1434. [Google Scholar] [CrossRef]
- Xu, S.; Zhang, Z.; Jing, B.; Gannon, P.; Ding, J.; Xu, F.; Li, X.; Zhang, Y. Transportin-SR is required for proper splicing of resistance genes and plant immunity. PLoS Genet. 2011, 7, e1002159. [Google Scholar] [CrossRef]
- Xu, F.; Xu, S.; Wiermer, M.; Zhang, Y.; Li, X. The cyclin L homolog MOS12 and the MOS4-associated complex are required for the proper splicing of plant resistance genes. Plant J. 2012, 70, 916–928. [Google Scholar] [CrossRef]
- Whitham, S.; Dinesh-Kumar, S.P.; Choi, D.; Hehl, R.; Corr, C.; Baker, B. The product of the tobacco mosaic virus resistance gene N: Similarity to toll and the interleukin-1 receptor. Cell 1994, 78, 1101–1115. [Google Scholar] [CrossRef]
- Ayliffe, M.A.; Frost, D.V.; Finnegan, E.J.; Lawrence, G.J.; Anderson, P.A.; Ellis, J.G. Analysis of alternative transcripts of the flax L6 rust resistance gene. Plant J. 1999, 17, 287–292. [Google Scholar] [CrossRef]
- Borhan, M.H.; Holub, E.B.; Beynon, J.L.; Rozwadowski, K.; Rimmer, S.R. The Arabidopsis TIR-NB-LRR gene RAC1 confers resistance to Albugo candida (white rust) and is dependent on EDS1 but not PAD4. Mol. Plant Microbe Interact. 2004, 17, 711–719. [Google Scholar] [CrossRef]
- Parker, J.E.; Coleman, M.J.; Szabo, V.; Frost, L.N.; Schmidt, R.; van der Biezen, E.A.; Moores, T.; Dean, C.; Daniels, M.J.; Jones, J.D. The Arabidopsis downy mildew resistance gene RPP5 shares similarity to the toll and interleukin-1 receptors with N and L6. Plant Cell 1997, 9, 879–894. [Google Scholar] [CrossRef]
- Gassmann, W.; Hinsch, M.E.; Staskawicz, B.J. The Arabidopsis RPS4 bacterial-resistance gene is a member of the TIR-NBS-LRR family of disease-resistance genes. Plant J. 1999, 20, 265–277. [Google Scholar] [CrossRef]
- Yi, H.; Richards, E.J. A cluster of disease resistance genes in Arabidopsis is coordinately regulated by transcriptional activation and RNA silencing. Plant Cell 2007, 19, 2929–2939. [Google Scholar] [CrossRef]
- Schornack, S.; Ballvora, A.; Gurlebeck, D.; Peart, J.; Baulcombe, D.; Ganal, M.; Baker, B.; Bonas, U.; Lahaye, T. The tomato resistance protein Bs4 is a predicted non-nuclear TIR-NB-LRR protein that mediates defense responses to severely truncated derivatives of AvrBs4 and overexpressed AvrBs3. Plant J. 2004, 37, 46–60. [Google Scholar] [CrossRef]
- Vidal, S.; Cabrera, H.; Andersson, R.A.; Fredriksson, A.; Valkonen, J.P. Potato gene Y-1 is an N gene homolog that confers cell death upon infection with potato virus Y. Mol. Plant Microbe Interact. 2002, 15, 717–727. [Google Scholar] [CrossRef]
- Yang, S.; Gao, M.; Xu, C.; Gao, J.; Deshpande, S.; Lin, S.; Roe, B.A.; Zhu, H. Alfalfa benefits from Medicago truncatula: The RCT1 gene from M. truncatula confers broad-spectrum resistance to anthracnose in alfalfa. Proc. Natl. Acad. Sci. USA 2008, 105, 12164–12169. [Google Scholar] [CrossRef]
- Erickson, F.L.; Holzberg, S.; Calderon-Urrea, A.; Handley, V.; Axtell, M.; Corr, C.; Baker, B. The helicase domain of the TMV replicase proteins induces the N-mediated defence response in tobacco. Plant J. 1999, 18, 67–75. [Google Scholar] [CrossRef]
- Bendahmane, A.; Querci, M.; Kanyuka, K.; Baulcombe, D.C. Agrobacterium transient expression system as a tool for the isolation of disease resistance genes: Application to the Rx2 locus in potato. Plant J. 2000, 21, 73–81. [Google Scholar] [CrossRef]
- Van der Vossen, E.A.; van der Voort, J.N.; Kanyuka, K.; Bendahmane, A.; Sandbrink, H.; Baulcombe, D.C.; Bakker, J.; Stiekema, W.J.; Klein-Lankhorst, R.M. Homologues of a single resistance-gene cluster in potato confer resistance to distinct pathogens: A virus and a nematode. Plant J. 2000, 23, 567–576. [Google Scholar] [CrossRef]
- Moffett, P.; Farnham, G.; Peart, J.; Baulcombe, D.C. Interaction between domains of a plant NBS-LRR protein in disease resistance-related cell death. Embo J. 2002, 21, 4511–4519. [Google Scholar] [CrossRef]
- Gassmann, W. Alternative splicing in plant defense. Curr. Top. Microbiol. 2008, 326, 219–233. [Google Scholar]
- Nandety, R.S.; Caplan, J.L.; Cavanaugh, K.; Perroud, B.; Wroblewski, T.; Michelmore, R.W.; Meyers, B.C. The role of TIR-NBS and TIR-X proteins in plant basal defense responses. Plant Physiol. 2013, 162, 1459–1472. [Google Scholar]
- Frost, D.; Way, H.; Howles, P.; Luck, J.; Manners, J.; Hardham, A.; Finnegan, J.; Ellis, J. Tobacco transgenic for the flax rust resistance gene L expresses allele-specific activation of defense responses. Mol. Plant Microbe Interact. 2004, 17, 224–232. [Google Scholar] [CrossRef]
- Bernoux, M.; Ve, T.; Williams, S.; Warren, C.; Hatters, D.; Valkov, E.; Zhang, X.; Ellis, J.G.; Kobe, B.; Dodds, P.N. Structural and functional analysis of a plant resistance protein TIR domain reveals interfaces for self-association, signaling, and autoregulation. Cell Host Microbe. 2011, 9, 200–211. [Google Scholar] [CrossRef]
- Sela, H.; Spiridon, L.N.; Petrescu, A.J.; Akerman, M.; Mandel-Gutfreund, Y.; Nevo, E.; Loutre, C.; Keller, B.; Schulman, A.H.; Fahima, T. Ancient diversity of splicing motifs and protein surfaces in the wild emmer wheat (Triticum dicoccoides) LR10 coiled coil (CC) and leucine-rich repeat (LRR) domains. Mol. Plant. Pathol. 2012, 13, 276–287. [Google Scholar] [CrossRef]
- Saintenac, C.; Zhang, W.; Salcedo, A.; Rouse, M.N.; Trick, H.N.; Akhunov, E.; Dubcovsky, J. Identification of wheat gene Sr35 that confers resistance to Ug99 stem rust race group. Science 2013, 341, 783–786. [Google Scholar] [CrossRef]
- Halterman, D.A.; Wei, F.; Wise, R.P. Powdery mildew-induced Mla mRNAs are alternatively spliced and contain multiple upstream open reading frames. Plant Physiol. 2003, 131, 558–567. [Google Scholar] [CrossRef]
- Halterman, D.; Zhou, F.; Wei, F.; Wise, R.P.; Schulze-Lefert, P. The MLA6 coiled-coil, NBS-LRR protein confers AvrMla6-dependent resistance specificity to Blumeria graminis f. sp. hordei in barley and wheat. Plant J. 2001, 25, 335–348. [Google Scholar] [CrossRef]
- Costanzo, S.; Jia, Y.L. Alternatively spliced transcripts of Pi-ta blast resistance gene in Oryza sativa. Plant Sci. 2009, 177, 468–478. [Google Scholar] [CrossRef]
- Cesari, S.; Thilliez, G.; Ribot, C.; Chalvon, V.; Michel, C.; Jauneau, A.; Rivas, S.; Alaux, L.; Kanzaki, H.; Okuyama, Y. The rice resistance protein pair RGA4/RGA5 recognizes the Magnaporthe oryzae effectors AVR-Pia and AVR1-CO39 by direct binding. Plant Cell 2013, 25, 1463–1481. [Google Scholar] [CrossRef]
- Ferrier-Cana, E.; Macadre, C.; Sevignac, M.; David, P.; Langin, T.; Geffroy, V. Distinct post-transcriptional modifications result into seven alternative transcripts of the CC-NBS-LRR gene JA1tr of Phaseolus vulgaris. Theor. Appl. Genet. 2005, 110, 895–905. [Google Scholar] [CrossRef]
- Okuyama, Y.; Kanzaki, H.; Abe, A.; Yoshida, K.; Tamiru, M.; Saitoh, H.; Fujibe, T.; Matsumura, H.; Shenton, M.; Galam, D.C. A multifaceted genomics approach allows the isolation of the rice Pia-blast resistance gene consisting of two adjacent NBS-LRR protein genes. Plant J. 2011, 66, 467–479. [Google Scholar] [CrossRef]
- Halterman, D.A.; Wise, R.P. Upstream open reading frames of the barley Mla13 powdery mildew resistance gene function co-operatively to down-regulate translation. Mol. Plant. Pathol. 2006, 7, 167–176. [Google Scholar] [CrossRef]
- Lukasik, E.; Takken, F.L. STANDing strong, resistance proteins instigators of plant defence. Curr. Opin. Plant Biol. 2009, 12, 427–436. [Google Scholar] [CrossRef]
- Bendahmane, A.; Farnham, G.; Moffett, P.; Baulcombe, D.C. Constitutive gain-of-function mutants in a nucleotide binding site-leucine rich repeat protein encoded at the Rx locus of potato. Plant J. 2002, 32, 195–204. [Google Scholar] [CrossRef]
- Shirano, Y.; Kachroo, P.; Shah, J.; Klessig, D.F. A gain-of-function mutation in an Arabidopsis toll interleukin1 receptor-nucleotide binding site-leucine-rich repeat type R gene triggers defense responses and results in enhanced disease resistance. Plant Cell 2002, 14, 3149–3162. [Google Scholar] [CrossRef]
- Zhang, Y.; Goritschnig, S.; Dong, X.; Li, X. A gain-of-function mutation in a plant disease resistance gene leads to constitutive activation of downstream signal transduction pathways in suppressor of npr1-1, constitutive 1. Plant Cell 2003, 15, 2636–2646. [Google Scholar] [CrossRef]
- Belkhadir, Y.; Subramaniam, R.; Dangl, J.L. Plant disease resistance protein signaling: NBS-LRR proteins and their partners. Curr. Opin. Plant Biol. 2004, 7, 391–399. [Google Scholar] [CrossRef]
- Maekawa, T.; Cheng, W.; Spiridon, L.N.; Toller, A.; Lukasik, E.; Saijo, Y.; Liu, P.; Shen, Q.H.; Micluta, M.A.; Somssich, I.E. Coiled-coil domain-dependent homodimerization of intracellular barley immune receptors defines a minimal functional module for triggering cell death. Cell Host Microbe. 2011, 9, 187–199. [Google Scholar] [CrossRef]
- Takken, F.L.; Goverse, A. How to build a pathogen detector: Structural basis of NB-LRR function. Curr. Opin. Plant Biol. 2012, 15, 375–384. [Google Scholar] [CrossRef]
- Rairdan, G.J.; Collier, S.M.; Sacco, M.A.; Baldwin, T.T.; Boettrich, T.; Moffett, P. The coiled-coil and nucleotide binding domains of the potato Rx disease resistance protein function in pathogen recognition and signaling. Plant Cell 2008, 20, 739–751. [Google Scholar] [CrossRef]
- Qi, D.; deYoung, B.J.; Innes, R.W. Structure-function analysis of the coiled-coil and leucine-rich repeat domains of the RPS5 disease resistance protein. Plant Physiol. 2012, 158, 1819–1832. [Google Scholar] [CrossRef]
- Mackey, D.; Belkhadir, Y.; Alonso, J.M.; Ecker, J.R.; Dangl, J.L. Arabidopsis RIN4 is a target of the type III virulence effector AvrRpt2 and modulates RPS2-mediated resistance. Cell 2003, 112, 379–389. [Google Scholar] [CrossRef]
- Mackey, D.; Holt, B.F., III; Wiig, A.; Dangl, J.L. RIN4 interacts with Pseudomonas syringae type III effector molecules and is required for RPM1-mediated resistance in Arabidopsis. Cell 2002, 108, 743–754. [Google Scholar] [CrossRef]
- Li, Y.; Li, S.; Bi, D.; Cheng, Y.T.; Li, X.; Zhang, Y. SRFR1 negatively regulates plant NB-LRR resistance protein accumulation to prevent autoimmunity. PLoS Pathog. 2010, 6, e1001111. [Google Scholar] [CrossRef]
- Cheng, Y.T.; Li, Y.; Huang, S.; Huang, Y.; Dong, X.; Zhang, Y.; Li, X. Stability of plant immune-receptor resistance proteins is controlled by SKP1-CULLIN1-F-box (SCF)-mediated protein degradation. Proc. Natl. Acad. Sci. USA 2011, 108, 14694–14699. [Google Scholar] [CrossRef]
- Zhang, Y.; Dorey, S.; Swiderski, M.; Jones, J.D. Expression of RPS4 in tobacco induces an AvrRps4-independent HR that requires EDS1, SGT1 and HSP90. Plant J. 2004, 40, 213–224. [Google Scholar] [CrossRef]
- Collier, S.M.; Hamel, L.P.; Moffett, P. Cell death mediated by the N-terminal domains of a unique and highly conserved class of NB-LRR protein. Mol. Plant Microbe Interact. 2011, 24, 918–931. [Google Scholar] [CrossRef]
- Swiderski, M.R.; Birker, D.; Jones, J.D.G. The TIR domain of TIR-NB-LRR resistance proteins is a signaling domain involved in cell death induction. Mol. Plant Microbe Interact. 2009, 22, 157–165. [Google Scholar] [CrossRef]
- Meyers, B.C.; Morgante, M.; Michelmore, R.W. TIR-X and TIR-NBS proteins: Two new families related to disease resistance TIR-NBS-LRR proteins encoded in Arabidopsis and other plant genomes. Plant J. 2002, 32, 77–92. [Google Scholar] [CrossRef]
- Meyers, B.C.; Kozik, A.; Griego, A.; Kuang, H.; Michelmore, R.W. Genome-wide analysis of NBS-LRR-encoding genes in Arabidopsis. Plant Cell 2003, 15, 809–834. [Google Scholar] [CrossRef]
- Burch-Smith, T.M.; Schiff, M.; Caplan, J.L.; Tsao, J.; Czymmek, K.; Dinesh-Kumar, S.P. A novel role for the TIR domain in association with pathogen-derived elicitors. PLoS Biol. 2007, 5, e68. [Google Scholar] [CrossRef]
- Wirthmueller, L.; Zhang, Y.; Jones, J.D.; Parker, J.E. Nuclear accumulation of the Arabidopsis immune receptor RPS4 is necessary for triggering EDS1-dependent defense. Curr. Biol. 2007, 17, 2023–2029. [Google Scholar] [CrossRef]
- Heidrich, K.; Wirthmueller, L.; Tasset, C.; Pouzet, C.; Deslandes, L.; Parker, J.E. Arabidopsis EDS1 connects pathogen effector recognition to cell compartment-specific immune responses. Science 2011, 334, 1401–1404. [Google Scholar] [CrossRef]
- Bendahmane, A.; Kanyuka, K.; Baulcombe, D.C. The Rx gene from potato controls separate virus resistance and cell death responses. Plant Cell 1999, 11, 781–792. [Google Scholar] [CrossRef]
- Coll, N.S.; Vercammen, D.; Smidler, A.; Clover, C.; van Breusegem, F.; Dangl, J.L.; Epple, P. Arabidopsis type I metacaspases control cell death. Science 2010, 330, 1393–1397. [Google Scholar] [CrossRef]
- Gassmann, W. Natural variation in the Arabidopsis response to the avirulence gene hopPsyA uncouples the hypersensitive response from disease resistance. Mol. Plant Microbe Interact. 2005, 18, 1054–1060. [Google Scholar] [CrossRef]
- Chen, M.; Manley, J.L. Mechanisms of alternative splicing regulation: Insights from molecular and genomics approaches. Nat. Rev. Mol. Cell Biol. 2009, 10, 741–754. [Google Scholar]
- Day, I.S.; Golovkin, M.; Palusa, S.G.; Link, A.; Ali, G.S.; Thomas, J.; Richardson, D.N.; Reddy, A.S. Interactions of SR45, an SR-like protein, with spliceosomal proteins and an intronic sequence: Insights into regulated splicing. Plant J. 2012, 71, 936–947. [Google Scholar] [CrossRef]
- Thomas, J.; Palusa, S.G.; Prasad, K.V.; Ali, G.S.; Surabhi, G.K.; Ben-Hur, A.; Abdel-Ghany, S.E.; Reddy, A.S. Identification of an intronic splicing regulatory element involved in auto-regulation of alternative splicing of SCL33 pre-mRNA. Plant J. 2012. [Google Scholar] [CrossRef]
- Palusa, S.G.; Ali, G.S.; Reddy, A.S. Alternative splicing of pre-mRNAs of Arabidopsis serine/arginine-rich proteins: Regulation by hormones and stresses. Plant J. 2007, 49, 1091–1107. [Google Scholar] [CrossRef]
- Ajuh, P.; Sleeman, J.; Chusainow, J.; Lamond, A.I. A direct interaction between the C-terminal region of CDC5L and the WD40 domain of PLRG1 is essential for pre-mRNA splicing. J. Biol. Chem. 2001, 276, 42370–42381. [Google Scholar] [CrossRef]
- Zhou, Z.; Licklider, L.J.; Gygi, S.P.; Reed, R. Comprehensive proteomic analysis of the human spliceosome. Nature 2002, 419, 182–185. [Google Scholar] [CrossRef]
- Monaghan, J.; Xu, F.; Gao, M.; Zhao, Q.; Palma, K.; Long, C.; Chen, S.; Zhang, Y.; Li, X. Two Prp19-like U-box proteins in the MOS4-associated complex play redundant roles in plant innate immunity. PLoS Pathog. 2009, 5, e1000526. [Google Scholar]
- Monaghan, J.; Xu, F.; Xu, S.; Zhang, Y.; Li, X. Two putative RNA-binding proteins function with unequal genetic redundancy in the MOS4-associated complex. Plant Physiol. 2010, 154, 1783–1793. [Google Scholar] [CrossRef]
- Caplan, J.L.; Mamillapalli, P.; Burch-Smith, T.M.; Czymmek, K.; Dinesh-Kumar, S.P. Chloroplastic protein NRIP1 mediates innate immune receptor recognition of a viral effector. Cell 2008, 132, 449–462. [Google Scholar]
- Maquat, L.E. Nonsense-mediated mRNA decay: Splicing, translation and mRNP dynamics. Nat. Rev. Mol. Cell Biol. 2004, 5, 89–99. [Google Scholar] [CrossRef]
- McGlincy, N.J.; Smith, C.W. Alternative splicing resulting in nonsense-mediated mRNA decay: What is the meaning of nonsense? Trends Biochem. Sci. 2008, 33, 385–393. [Google Scholar] [CrossRef]
- Jeong, H.J.; Kim, Y.J.; Kim, S.H.; Kim, Y.H.; Lee, I.J.; Kim, Y.K.; Shin, J.S. Nonsense-mediated mRNA decay factors, UPF1 and UPF3, contribute to plant defense. Plant Cell Physiol. 2011, 52, 2147–2156. [Google Scholar] [CrossRef]
- Rayson, S.; Arciga-Reyes, L.; Wootton, L.; de Torres Zabala, M.; Truman, W.; Graham, N.; Grant, M.; Davies, B. A role for nonsense-mediated mRNA decay in plants: Pathogen responses are induced in Arabidopsis thaliana NMD mutants. PLoS One 2012, 7, e31917. [Google Scholar]
- Kalyna, M.; Simpson, C.G.; Syed, N.H.; Lewandowska, D.; Marquez, Y.; Kusenda, B.; Marshall, J.; Fuller, J.; Cardle, L.; McNicol, J. Alternative splicing and nonsense-mediated decay modulate expression of important regulatory genes in Arabidopsis. Nucleic Acids Res. 2012, 40, 2454–2469. [Google Scholar] [CrossRef]
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