- freely available
Int. J. Mol. Sci. 2013, 14(1), 1119-1131; doi:10.3390/ijms14011119
Published: 8 January 2013
Abstract: The Crabs Claw (CRC) YABBY gene is required for regulating carpel development in angiosperms and has played an important role in nectary evolution during core eudicot speciation. The function or expression of CRC-like genes has been explored in two basal eudicots, Eschscholzia californica and Aquilegia formosa. To further investigate the function of CRC orthologous genes related to evolution of carpel and nectary development in basal eudicots, a CRC ortholog, EsCRC, was isolated and characterized from Epimedium sagittatum (Sieb. and Zucc.) Maxim. A phylogenetic analysis of EsCRC and previously identified CRC-like genes placed EsCRC within the basal eudicot lineage. Gene expression results suggest that EsCRC is involved in the development of sepals and carpels, but not nectaries. Phenotypic complementation of the Arabidopsis mutant crc-1 was achieved by constitutive expression of EsCRC. In addition, over-expression of EsCRC in Arabidopsis and tobacco gave rise to abaxially curled leaves. Transgenic results together with the gene expression analysis suggest that EsCRC may maintain a conserved function in carpel development and also play a novel role related to sepal formation. Absence of EsCRC and ElCRC expression in nectaries further indicates that nectary development in non-core eudicots is unrelated to expression of CRC-like genes.
Using integrative approaches, plant evolutionary developmental biology aims to study the molecular basis for the origin of novel traits during plant species evolution and diversification. Elucidation of the functions of important genes in different angiosperm lineages can enhance our understanding of plant evolution. For example, genomic and functional studies based on Arabidopsis thaliana and Antirrhinum majus have provided knowledge about transcription factors, such as MADS, MYB, bHLH, TCP, NAM/CUC and YABBY, which are responsible for regulating morphological development in angiosperms [1–5].
The YABBY gene family is a small class of transcription factors found exclusively in seed plants, with functions that have been well characterized in Arabidopsis and rice [6–15]. There are six members of the YABBY gene family in Arabidopsis: FILAMENTOUS FLOWER (FIL), CRABS CLAW (CRC), INNER NO OUTER (INO), YABBY2 (YAB2), YAB3 and YAB5 [7,11,16]. The proteins they encode are composed of an N-terminal zinc finger domain and a C-terminal helix-loop-helix (YABBY domain) [7,15]. Phylogenetic analysis of YABBY genes from extant angiosperm species strongly supports a sister relationship between INO-like genes and the common ancestor of CRC-like and FIL-like genes . In Arabidopsis, the “vegetative” YABBYs (FIL, YAB2, YAB3 and YAB5) are expressed in abaxial cells of lateral organ primordia, where they control leaflet initiation and laminar growth . INO expression occurs only in the abaxial domain of the ovule integument .
The expression or function of CRC-like genes has been reported for many angiosperms. The abaxial expression of a CRC-like ortholog in carpel walls of two basal angiosperm species, Amborella trichopoda and Cabomba caroliniana, suggests that an abaxial carpel wall expression pattern was primitively present in the common ancestor of angiosperms [17,18]. In the monocot rice, the CRC ortholog DROOPING LEAF (DL) specifies carpel and floral meristem identity and is also involved in leaf midrib development [9,12,13]. In the basal eudicot Eschscholzia californica (California poppy), EcCRC is involved in establishment of carpel polarity and ovule initiation . Abaxial expression in the carpel wall of Aquilegia formosa, another basal eudicot, has been detected through in situ hybridization, but CRC gene expression has not been observed in the nectary . In core eudicots, the Arabidopsis CRC is the major determinant of carpel growth and fusion and is responsible for floral meristem termination [7,15]. In addition, Arabidopsis CRC has the novel function of regulating nectary identity [7,15]. In other core-eudicot species, such as tobacco and petunia, CRC expression has been detected in both the nectary and the abaxial side of the ovary wall . The carpel development function of CRC orthologs thus appears to be conserved across angiosperms, whereas a role in nectary development has only been observed in core eudicot lineages .
The genus Epimedium belongs to the Berberidaceae family in Ranunculales, a basal eudicot order. Basal eudicots are a sister group to the core eudicots . Epimedium flowers show varying morphology in sepals and petals. Sepals in the outer floral whorl are ovate and not persistent; in contrast, second whorl sepals are notably petaloid and persistent, playing a major role in pollinator attraction. The petals, comprising the third and fourth whorls, are distinguished by a spur and sac. Nectar is made at the tip of the spur [21,22] (Supplementary Figure S1). In the present study, E. sagittatum (Sieb. & Zucc.) Maxim was selected to further investigate the function of CRC-like genes in basal eudicots and to examine the hypothesis that CRC exhibits a conserved function in carpels across angiosperms and that the co-option of orthologs in nectary development occurred after the emergence of Ranunculales . CRC orthologs from Epimedium were cloned and characterized in a series of experiments that included analysis of gene expression, mutant complementation in Arabidopsis and ectopic expression in Arabidopsis and tobacco.
2.1. Sequence Analyses and Phylogenetic Reconstruction of EsCRC
The full-length cDNA sequence of EsCRC, including a 534-bp ORF, was isolated from E. sagittatum. An orthologous gene, ElCRC, was also cloned from the closely-related E. leptorrhizum Stearn using the same primers as in EsCRC. Consistent with other CRC-like proteins from model species, both EsCRC and ElCRC were found to encode proteins possessing a typical zinc finger domain and a YABBY domain (Figure 1). Phylogenetic analysis closely grouped EsCRC and ElCRC with three other CRC-like genes from the basal eudicots Aquilegia formosa (AfCRC), Grevillea robusta (GrCRC) and Eschscholzia californica (EcCRC), indicating that EsCRC and ElCRC are orthologous CRC-like genes in the YABBY family (Figure 2).
2.2. EsCRC and ElCRC Expression Profiles
To investigate the putative role of CRC-like genes in basal eudicot Epimedium species, gene expression was analyzed in different organs of E. sagittatum and E. leptorrhizum using quantitative real-time PCR (qPCR). As shown in Figure 3A, EsCRC expression was detected in sepals and carpels, but not in leaves, petals or stamens. To verify the CRC-like gene expression observed in E. sagittatum sepals, ElCRC was analyzed in E. leptorrhizum: similar expression patterns were observed in sepals, but not in the petals, which possess nectaries at the end of blunt spurs (Figure 3B).
2.3. Ectopic Expression of EsCRC Can Rescue Nectary Development in the Arabidopsis crc-1 Mutant
Constitutive expression of genes from other species is carried out in Arabidopsis mutants to test gene functions [23–26]. To determine whether EsCRC biochemical functions are conserved relative to other CRC-like genes, EsCRC was overexpressed under the control of the cauliflower mosaic virus 35S promoter in the Arabidopsis crc-1 mutant. Of 10 independent transgenic plants tested, five lines with EsCRC expression (Figure 4A) showed full complementation of crc-1 carpel and nectary phenotypes and were subjected to further phenotypic characterization (Wild-type [C, E] and mutant crc-1 flowers [A, D] are shown for comparison in Figure 5). The Arabidopsis crc-1 mutant had broader gynoecia than the wild-type, an unfused apex of carpels (Figure 5D) and no nectary development (Figure 5A). An examination of the transgenic plants demonstrated that EsCRC rescued nectary development (Figure 5B) and carpel defects (Figure 5D) in the crc-1 mutant. These results suggest that EsCRC is biochemically equivalent in function to AtCRC. Furthermore, leaves in the transformed complementation lines exhibited abaxial curling as in wild-type Arabidopsis transformed with EsCRC.
2.4. EsCRC Influences Abaxial-Adaxial Leaf Formation in Transgenic Arabidopsis and Tobacco
It has been demonstrated that CRC orthologs from two monocots are expressed in leaves and can influence leaf development in transgenic Arabidopsis [27,28]. However, we cannot detect EsCRC expression in leaves. To test the possibility that the EsCRC coding region have the capability of affecting the leaf morphology in transgenic plants, we further examined overexpression of EsCRC in transgenic Arabidopsis and tobacco. Out of 10 kanamycin-resistant EsCRC-overexpressing transgenic lines with similar phenotypic changes in each construct, five lines in Arabidopsis and two lines in tobacco (Figure 4B,C) were chosen for detailed analysis. Compared with leaf phenotypes displayed in wild-type Arabidopsis (Figure 5F; left) and tobacco (Figure 5G; left), EsCRC overexpression in tobacco (Figure 5G; right) and Arabidopsis (Figure 5F; right) produced a phenotype with leaves curled towards the abaxial side. When compared with wild-type tobacco (Figure 5H; bottom), EsCRC-overexpressed tobacco exhibited abnormal petals with severely curled edges (Figure 5H; upper) and loss of anthocyanin (Figure 5H; middle and upper). To determine whether the ectopic expression of EsCRC affected epidermal cell morphology of adaxial and abaxial leaves, the abaxial and adaxial surfaces of transgenic and wild-type tobacco plants were examined using a scanning electron microscope. Compared with the abaxial (Figure 6A1,A2) and adaxial epidermis (Figure 6B1,B2) of wild-type tobacco, the transgenic overexpression lines showed more irregular cell surfaces and disordered cell arrangements on both the abaxial and adaxial epidermis (Figure 6C,D). Abaxial epidermis in transgenic lines displayed the most severe abnormalities (Figure 6C).
Functional studies and comparative expression analysis of CRC-like genes in different lineages, including monocots, early-diverging angiosperms, basal eudicots and core eudicots, indicate that CRC-like genes play crucial roles in gynoecium development [7,11,16–19]. For example, a CRC-like gene from the early-diverging angiosperm species Amborella trichopoda has been reported to partially complement carpel-related defects in the Arabidopsis crc-1 mutant . In addition, ectopic expression of OsDL, a CRC-like gene from rice, is fully capable of rescuing the severe crc-1 phenotype . Our complementation studies show that EsCRC can rescue carpel defects in the Arabidopsis crc-1 mutant. Collective evidence from heterologous expression of CRC orthologs from Amborella oryza and Epimedium demonstrate that the biochemical functions of CRC are reasonably well conserved. Furthermore, AtCRC, CcCRC, EcCRC and AfCRC expression has been detected in carpel primordia and abaxial walls of carpel primordia [15,17–19]. The expression of EsCRC in carpel tissue observed in our study further supports the notion that CRC-like gene expression in carpels is conserved in angiosperms [18–20]. Heterologous expression of homologous CRC-like genes from rice and Lilium longiflorum produce curled leaves in Arabidopsis, and changes in leaf cellular arrangement have been observed in a 35S::LlCRC transgenic Arabidopsis line [27,28]. Our results further confirm the involvement of CRC-like genes in leaf polarization in transgenic Arabidopsis. We were not able to detect EsCRC expression in Epimedium leaves, however, indicating that cis-regulatory changes may alter the role of EsCRC in Epimedium leaves.
In both E. leptorrhizum and E. sagittatum, transcripts of EsCRC and ElCRC were detected in sepals; this is in contrast to Eschscholzia californica, Aquilegia formosa, petunia, tobacco and Arabidopsis in which no such expression was observed [7,15,19]. Furthermore, no CRC-like gene expression has been observed in tepals of L. longiflorum or Asparagus asparagoides[28,29], nor are OsDL genes expressed in rice lemmas or paleae . Taking into consideration the existence of CRC expression in the early-diverging angiosperm C. caroliniana, we can suggest two explanations for the co-option of CRC-like gene expression in sepals of Epimedium. The first explanation assumes that CRC-like gene expression in sepals reflects the ancestral state, implying independent loss of expression in sepals of Eschscholzia californica, Aquilegia formosa and core eudicots, but not Epimedium. The second explanation is that EsCRC expression in sepals arose within Epimedium. More investigation of CRC-like gene expression in various species and further functional analysis using gene knock-down techniques, such as virus-induced gene silencing or stable gene transformation, should facilitate understanding of evolution of CRC-like genes.
Obvious nectary defects are observed in Arabidopsis CRC mutants  and in tobacco plants in which expression of CRC-like genes has been down-regulated . CRC-like gene expression has been detected in nectaries localized in either extrafloral (Capparis flexuosa and Gossypium hirsutum) or infloral (petunia and tobacco) organs of representative core eudicots . On the other hand, AfCRC is not transcribed in the tips of spur petals in the basal eudicot Aquilegia formosa. In our study, no EsCRC expression was observed in nectary petals, consistent with previous reports that CRC-like genes are not involved in nectary development outside of the core eudicots [19,20]. Moreover, a CRC-like gene from Amborella trichopoda has been reported to partially complement carpel-related defects, but not nectary development, in the Arabidopsis crc-1 mutant . However, the ectopic expression of OsDL  and EsCRC was able to rescue the severe crc-1 phenotype, suggesting that sequence divergence over time in CRC-like genes has somehow affected gene function in rice and E. sagittatum compared with Amborella trichopoda. Similar functional divergence within AP3-like genes with a paleoAP3 motif derived from gymnosperms and the basal eudicot Dicentra eximia resulted in only partial complementation in an experiment involving the Arabidopsis ap3-3 mutant [30,31]. Complementation testing of additional CRC-like gene orthologs from basal angiosperms should provide further insights into evolutionary conservation and divergence of CRC-like genes.
4. Experimental Section
4.1. Study System and Gene Isolation
Epimedium sagittatum and E. leptorrhizum were grown at the Wuhan Botanical Garden of the Chinese Academy of Sciences and identified by Dr. Yanjun Zhang from the Wuhan Botanical Garden Herbarium. Following extraction from a mixture of inflorescences, leaves and roots using Trizol regeant (Invitrogen, Carlsbad, CA, USA), total RNA was digested with RQ1 RNase-free DNase (Promega, Madison, WI, USA). The EsCRC gene was isolated using a combination of 3′- and 5′-RACE PCR. First-strand cDNA was transcribed from total RNA using Superscript III reverse transcriptase and the poly-T primer 3′-CDS (Invitrogen, Carlsbad, CA, USA). To isolate partial EsCRC, this was followed by 3′ rapid amplification of cDNA ends (3′-RACE) using the 3′-RACE adapter primer SMARTII and degenerate primer ABCRO6 . To obtain the 5′ partial cDNA end of EsCRC, first-strand synthesis was performed using total RNA with SMART II and 5′-CDS primers. Two rounds of 5′ RACE were performed using primer pairs UPM/5′CRCGSP1 for the first-strand PCR and NUP/5′CRCGSP2 for the second-strand PCR. The full-length EsCRC sequence was generated using CRCF and CRCR primers based on the 5′ UTR and 3′ UTR regions. All primers used for gene isolation and confirmation are listed in Supplementary Table S1.
4.2. Sequence Acquisition and Phylogenetic Analysis
Sequences of EsCRC, ElCRC and CRC orthologs from various species (Supplementary Table S2) were downloaded from the GenBank database and aligned based on deduced amino acid sequences using online MUSCLE software (EMBL) followed by manual adjustments. Alignments of full length nucleotide sequences were generated using aa2dna software based on the amino acid alignment . Maximum likelihood phylogenetic analyses were performed using Mega 5.0. A general time-reversible (GTR) model with a proportion of invariable sites was selected using Modeltest. Support for each branch was assessed using bootstrap analysis with 1000 bootstrap replicates.
4.3. Expression Analysis
To detect the expression of EsCRC and ElCRC, qPCR was performed on RNA from E. sagittatum and E. leptorrhizum following genomic-eraser purification (Takara, Dalian, China). RNA was obtained from leaves, sepals (outer sepals and inner sepals), petals, stamens and carpels of E. sagittatum and sepals and petals of E. leptorrhizum. Sepal samples included both outer sepals and inner petaloid sepals. All material was collected during the open flower stage, when nectary was present on petal spur tips. Prior to qPCR, first-strand synthesis and removal of DNA contamination were performed using a PrimeScript RT reagent kit (Takara, Dalian, Japan). qPCR was performed on an ABI7500 Real-Time PCR instrument (Life Technologies, Carlsbad, CA, USA) in 20-μL reaction volumes containing 10 ng cDNA, 10 μM each of primers qCRCF and qCRCR and SYBR Premix Ex Taq II (Takara, Dalian, Japan). The PCR protocol consisted of an initial denaturation stage (95 °C for 30 s, followed by 40 cycles at 94 °C for 3 s and 60 °C for 30 s) and a final dissociation stage (95 °C for 15 s, 60 °C for 1 min and 60 °C for 30 s). The two-delta CT relative quantification method with an EsActin internal control  was used to normalize expression levels of desired genes in different organs. All experiments were performed with three biological replicates, and three technical replicates were analyzed for each biological replicate. Data were analyzed using ABI7500 software.
4.4. Vector Construction and Plant Transformation
To construct the p35 Spro-EsCRC vector, full length EsCRC was excised from a PMD19-T vector (Takara, Dalian, Japan) using SalI and KpnI restriction enzymes and then ligated into a pMV binary vector (derived from pBI121) previously digested with XhoI and KpnI. The vectors were then confirmed using sequencing and enzyme digestion. Arabidopsis transformation was carried out using the classic Agrobacterium-mediated floral dip method . T0 seeds were harvested and screened on half-strength Murashige and Skoog medium supplemented with 50 μg/mL kanamycin, and EsCRC sequences in the resistant seedlings were identified using qPCR. For tobacco transformations, a p35 Spro-EsCRC vector was transferred into the tobacco genome using the Agrobacterium-mediated method . Transgenic tobacco plants were screened for further analysis using kanamycin and qPCR. The cDNA of leaf tissue from transgenic plants was used for qPCR.
4.5. Scanning Electron Microscopy (SEM) Analysis
Mature leaves from control and transgenic lines were fixed with 3% (w/v) paraformaldehyde and 0.25% glutaraldehyde in 0.2 N sodium phosphate buffer (pH 7.0) overnight at 4 °C. Fixed samples were rinsed three times with 0.1 M phosphate buffer (pH 7.0). After dehydration in different concentrations of acetone, material was stored overnight in 100% tert-butanol. Samples were dried in a JFD-310 drier (Joel, Tokoyo, Japan) and sputter-coated with carbon using a JFC-1600 anion sputter coating instrument (Joel, Tokoyo, Japan). SEM observations were performed with a JSM-6360LV scanning electron microscope (Joel, Tokoyo, Japan).
In this study, we isolated a putative CRC-like gene from the basal eudicot species E. sagittatum. EsCRC has high identity to other CRC orthologs and contains zinc finger and YABBY domains. As in monocots, basal angiosperms, basal eudicots and core eudicots, EsCRC expression was observed in carpels. In addition, expression was detected in sepals, suggesting a novel function for EsCRC. Functional experiments, including overexpression in Arabidopsis and tobacco and complementation of the crc-1 Arabidopsis mutant using p35 Spro-EsCRC demonstrated that EsCRC can influence leaf morphology in Arabidopsis and tobacco and also restore carpel defects and nectary formation in Arabidopsis. No expression was detected in nectary spurs of E. sagittatum. These results support a conserved role for CRC in carpel development and suggest that the pathway regulating nectary spur formation in Epimedium is different from the pathway controlling nectary development in Arabidopsis.
We thank John Bowman for sharing a sequence of Grevillea robusta, Mei Zhang for transforming Arabidopsis, Xiaoying Hu and Xiaomin Liu for assisting with scanning electron microscopy and Ling Yuan and Zubaida W. Yousaf for critically reviewing our manuscript. This work was supported by the National Natural Science Foundation of China (31000919 and 31270340), the CAS/SAFEA International Partnership Program for Creative Research Teams Project and the Knowledge Innovation Project of the Chinese Academy of Sciences (KSCX2-EW-J-20).
- Conflict of InterestThe authors declare no conflict of interest.
- Kaufmann, K.; Melzer, R.; Theissen, G. MIKC-type MADS-domain proteins: Structural modularity, protein interactions and network evolution in land plants. Gene 2005, 347, 183–198. [Google Scholar]
- Eckardt, N.A. YABBY genes and the development and origin of seed plant leaves. Plant Cell 2010, 22, 2103. [Google Scholar]
- Litt, A.; Kramer, E.M. The ABC model and the diversification of floral organ identity. Semin. Cell Dev. Biol 2010, 21, 129–137. [Google Scholar]
- Feller, A.; Machemer, K.; Braun, E.L.; Grotewold, E. Evolutionary and comparative analysis of MYB and bHLH plant transcription factors. Plant J 2011, 66, 94–116. [Google Scholar]
- Vialette-Guiraud, A.C.; Adam, H.; Finet, C.; Jasinski, S.; Jouannic, S.; Scutt, C.P. Insights from ANA-grade angiosperms into the early evolution of CUP-SHAPED COTYLEDON genes. Ann. Bot 2011, 107, 1511–1519. [Google Scholar]
- Siegfried, K.R.; Eshed, Y.; Baum, S.F.; Otsuga, D.; Drews, G.N.; Bowman, J.L. Members of the YABBY gene family specify abaxial cell fate in Arabidopsis. Development 1999, 126, 4117–4128. [Google Scholar]
- Bowman, J.L. The YABBY gene family and abaxial cell fate. Curr. Opin. Plant Biol 2000, 3, 17–22. [Google Scholar]
- Eshed, Y.; Baum, S.F.; Bowman, J.L. Distinct mechanisms promote polarity establishment in carpels of Arabidopsis. Cell 1999, 99, 199–209. [Google Scholar]
- Yamaguchi, T.; Nagasawa, N.; Kawasaki, S.; Matsuoka, M.; Nagato, Y.; Hirano, H.Y. The YABBY gene DROOPING LEAF regulates carpel specification and midrib development in Oryza sativa. Plant Cell 2004, 16, 500–509. [Google Scholar]
- Liu, H.L.; Xu, Y.Y.; Xu, Z.H.; Chong, K. A rice YABBY gene, OsYABBY4, preferentially expresses in developing vascular tissue. Dev. Genes Evol 2007, 217, 629–637. [Google Scholar]
- Goldshmidt, A.; Alvarez, J.P.; Bowman, J.L.; Eshed, Y. Signals derived from YABBY gene activities in organ primordia regulate growth and partitioning of Arabidopsis shoot apical meristems. Plant Cell 2008, 20, 1217–1230. [Google Scholar]
- Ohmori, Y.; Abiko, M.; Horibata, A.; Hirano, H.Y. A transposon, Ping, is integrated into intron 4 of the DROOPING LEAF gene of rice, weakly reducing its expression and causing a mild drooping leaf phenotype. Plant Cell Physiol 2008, 49, 1176–1184. [Google Scholar]
- Ohmori, Y.; Toriba, T.; Nakamura, H.; Ichikawa, H.; Hirano, H.Y. Temporal and spatial regulation of DROOPING LEAF gene expression that promotes midrib formation in rice. Plant J 2011, 65, 77–86. [Google Scholar]
- Tanaka, W.; Toriba, T.; Ohmori, Y.; Yoshida, A.; Kawai, A.; Mayama-Tsuchida, T.; Ichikawa, H.; Mitsuda, N.; Ohme-Takagi, M.; Hirano, H.Y. The YABBY gene TONGARI-BOUSHI1 is involved in lateral organ development and maintenance of meristem organization in the rice spikelet. Plant Cell 2012, 24, 80–95. [Google Scholar]
- Lee, J.Y.; Baum, S.F.; Alvarez, J.; Patel, A.; Chitwood, D.H.; Bowman, J.L. Activation of CRABS CLAW in the nectaries and carpels of Arabidopsis. Plant Cell 2005, 17, 25–36. [Google Scholar]
- Bartholmes, C.; Hidalgo, O.; Gleissberg, S. Evolution of the YABBY gene family with emphasis on the basal eudicot Eschscholzia californica (Papaveraceae). Plant Biol 2012, 14, 11–23. [Google Scholar]
- Fourquin, C.; Vinauger-Douard, M.; Fogliani, B.; Dumas, C.; Scutt, C.P. Evidence that CRABS CLAW and TOUSLED have conserved their roles in carpel development since the ancestor of the extant angiosperms. Proc. Natl. Acad. Sci. USA 2005, 102, 4649–4654. [Google Scholar]
- Yamada, T.; Yokota, S.; Hirayama, Y.; Imaichi, R.; Kato, M.; Gasser, C.S. Ancestral expression patterns and evolutionary diversification of YABBY genes in angiosperms. Plant J 2011, 67, 26–36. [Google Scholar]
- Orashakova, S.; Lange, M.; Lange, S.; Wege, S.; Becker, A. The CRABS CLAW ortholog from California poppy (Eschscholzia californica, Papaveraceae), EcCRC, is involved in floral meristem termination, gynoecium differentiation and ovule initiation. Plant J 2009, 58, 682–693. [Google Scholar]
- Lee, J.Y.; Baum, S.F.; Oh, S.H.; Jiang, C.Z.; Chen, J.C.; Bowman, J.L. Recruitment of CRABS CLAW to promote nectary development within the eudicot clade. Development 2005, 132, 5021–5032. [Google Scholar]
- Stearn, W.T. The Genus Epimedium and Other Herbaceous Berberidaceae; Timber Press: Portland, OR, USA, 2002. [Google Scholar]
- Hu, J.; Zhang, J.; Shan, H.; Chen, Z. Expression of floral MADS-box genes in Sinofranchetia chinensis (Lardizabalaceae): Implications for the nature of the nectar leaves. Ann. Bot 2012, 110, 57–69. [Google Scholar]
- Chen, M.K.; Lin, I.C.; Yang, C.H. Functional analysis of three lily (Lilium longiflorum) APETALA1-like MADS box genes in regulating floral transition and formation. Plant Cell Physiol 2008, 49, 704–717. [Google Scholar]
- Ferrario, S.; Immink, R.G.; Shchennikova, A.; Busscher-Lange, J.; Angenent, G.C. The MADS box gene FBP2 is required for SEPALLATA function in petunia. Plant Cell 2003, 15, 914–925. [Google Scholar]
- Hou, C.J.; Yang, C.H. Functional analysis of FT and TFL1 orthologs from orchid (Oncidium Gower Ramsey) that regulate the vegetative to reproductive transition. Plant Cell Physiol 2009, 50, 1544–1557. [Google Scholar]
- Wu, R.M.; Walton, E.F.; Richardson, A.C.; Wood, M.; Hellens, R.P.; Varkonyi-Gasic, E. Conservation and divergence of four kiwifruit SVP-like MADS-box genes suggest distinct roles in kiwifruit bud dormancy and flowering. J. Exp. Bot 2012, 63, 797–807. [Google Scholar]
- Fourquin, C.; Vinauger-Douard, M.; Chambrier, P.; Berne-Dedieu, A.; Scutt, C.P. Functional conservation between CRABS CLAW orthologues from widely diverged angiosperms. Ann. Bot 2007, 100, 651–657. [Google Scholar]
- Wang, A.; Tang, J.; Li, D.; Chen, C.; Zhao, X.; Zhu, L. Isolation and functional analysis of LiYAB1, a YABBY family gene, from lily (Lilium longiflorum). J. Plant Physiol 2009, 166, 988–995. [Google Scholar]
- Nakayama, H.; Yamaguchi, T.; Tsukaya, H. Expression patterns of AaDL, a CRABS CLAW ortholog in Asparagus asparagoides (Asparagaceae), demonstrate a stepwise evolution of CRC/DL subfamily of YABBY genes. Am. J. Bot 2010, 97, 591–600. [Google Scholar]
- Winter, K.U.; Saedler, H.; Theissen, G. On the origin of class B floral homeotic genes: Functional substitution and dominant inhibition in Arabidopsis by expression of an orthologue from the gymnosperm Gnetum. Plant J 2002, 31, 457–475. [Google Scholar]
- Lamb, R.S.; Irish, V.F. Functional divergence within the APETALA3/PISTILLATA floral homeotic gene lineages. Proc. Natl. Acad. Sci. USA 2003, 100, 6558–6563. [Google Scholar]
- Huang, W.; Sun, W.; Wang, Y. Isolation and molecular characterisation of flavonoid 3′-hydroxylase and flavonoid 3′,5′-hydroxylase genes from a traditional Chinese medicinal plant, Epimedium sagittatum. Gene 2012, 497, 125–130. [Google Scholar]
- Clough, S.J.; Bent, A.F. Floral dip: A simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J 1998, 16, 735–743. [Google Scholar]
- Glover, B.J.; Perez-Rodriguez, M.; Martin, C. Development of several epidermal cell types can be specified by the same MYB-related plant transcription factor. Development 1998, 125, 3497–3508. [Google Scholar]
© 2013 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).