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Int. J. Mol. Sci. 2013, 14(12), 24643-24655; doi:10.3390/ijms141224643
Published: 18 December 2013
Abstract: Class B gene APETALA3 (AP3) plays a key role in the development of petals and stamens. Here, we investigated the expression pattern of PAP3 gene (genbank accession number: HM104635) in the buds of cytoplasmic male sterility line 121A and its near-isogenic restorer line 121C at four developmental stages and analyzed the possible association between Class B genes and cytoplasmic male sterility of pepper. Semi-quantitative PCR and quantitative real-time RT-PCR (qRT-PCR) as well as RNA in situ hybridization showed increased expression of PAP3 at late phase of anther development and its higher expression in restorer line compared with sterility line indicating PAP3’s role at late developmental stage of anther and suppressed expression in sterility line. RNA in situ hybridization showed Class B gene features: high abundance in stamen and petal; lower expression in pistil; no expression in sepal. Results of transient expression in onion epidermal cells also showed PAP3 localized in the nucleus, which is consistent with the expression pattern of transcription factors of MADS-box gene family.
Pepper (Capsicum annuum L.), one of the world’s most important vegetable crops with remarkable food value and economic value, is a flowering plant belonging to Solanaceae. Production of hybrids using cytoplasmic male sterility (CMS) represents an ideal method in seed production of crops, including pepper, due to its low cost and the high purity of seeds [1–4]. Genes of cytoplasm and nucleus regulate CMS. Regulation on the CMS associated mitochondrial genes may lead to the expression change of nuclear genes, and expression of mitochondrial sterility genes themselves can be inhibited by nuclear genes [5–7]. Currently, two CMS genes, orf507 and atp6-2, were found in the pepper mitochondria . As for the fertility restorer gene (Rf), studies reported screening using analyses based on the differenced expression but no functional genes were identified [9–11].
Developmental abnormalities of stamens may disrupt the functions of anther or pollen and eventually lead to sterility. So far, our understanding on the genetic regulation of floral organ development is largely based on the studies using dicotyledonous plants, such as Arabidopsis, Antirrhinum, etc. Initially, the ABC model was proposed to explain floral organ development , which evolved to ABCDE model [13–19]. The model defines five classes of gene function which regulate floral organ development. Among them, the function of A and E regulate the development of sepals; the function of A, B and E determine the development of petals; the function of B, C and E determine the development of stamens; the function of C and E class genes regulate the development of carpel; the function of C, D and E regulate the development of ovule [9,13,15,17–19]. As the function of B class genes regulating floral organ development, MADS-box family members APETALA3 (AP3) and PISTILLATA (PI) are transcriptional factors to form AP3/PI heterodimers regulating the development of petal and stamen. Particularly, mutation of either gene may cause petals to transform sepals and stamens into carpels in some plants such as Arabidopsis and Antirrhinum [20,21]. In addition, AP3 and PI regulate other genes participating in the formations of petal and stamen, while the two genes are also regulated by other genes like LFY, AP1, UFO and ASK1 at different stages during flower development [22,23]. Currently, in plants, more than one AP3/PI homologous genes have been cloned and they appeared to execute different functions . However, we still poorly understand their functions, respectively . Though expression and function analyses of the genes may lay the foundation for revealing the stamen development process and illuminating the mechanism of male sterility, there are not any studies on peppers.
It has been shown that AP3 gene is essential for the development of stamen in higher plants. Exogenous gene interference, silence of AP3 and insertional mutation or deletion directional change of AP3 may lead to the conversion of stamen to carpel at varying degrees [25–29]; no pollen production or production of infertile pollen [30,31].
Accordingly, introduction of AP3 homolog to its mutant partially or fully restore the mutated stamens [32–34]. In addition, morphological changes may occur during development of cytoplasmic male sterile lines of these CMS model plants, such as tomatoes, carrots and tobacco . These changes normally occur at the late developmental stages of the buds with the conversion of stamen to carpel [36–41]. During this process, the CMS plants show striking similarities with the changes that had been previously reported in MADS-box family B-class gene AP3/PI-like mutants of Arabidopsis thaliana [36,39,42]. This suggests that the regulation of B-class gene is disturbed in many CMS systems. Studies on other plant CMS systems such as wheat, the low expression level of AP3 and PI genes might prevented stamens converting into pistil [43,44]. Actually, we have found the silence of PAP3 led to the phenotype of male sterility including shriveled anthers and reduced pollen numbers in restorer line 121C using pepper as a model plant .
To investigate the association between the expression of PAP3 and developmental abnormalities of anther, we analyzed the spatial and temporal expression pattern of PAP3, which was screened from a subtractive library of pepper, using buds of male infertility line 121A and near-isogenic restorer line 121C as test plants. This study may help us to further understand the relationship between stamen development and male sterility.
2.1. Comparison with Anther Transcriptome
Local blast showed PAP3 gene corresponds to comp54456_c0_seq1 in pepper anther transcriptome with a similarity of 99.85% and an E value of 0. There is no expression difference of comp54456_c0_seq1 between CMS line and restorer line based on the results of transcriptome sequencing.
2.2. Cloning of PAP3 in CMS Line 121A
PCR amplification based on PAP3 gene of restorer line produced 924 bp band (including ORF 681 bp) of the target gene (Figure 1A). Sequence alignment using DNAMAN version 6.0 software  showed no difference between the mRNA of this gene and PAP3 gene of restorer line indicating the PAP3 genes from the two resources are identical. Implicating the different phenotypes may result from difference of expressions instead of base sequence.
2.3. Construction of Transient Expressing Vector
The vector plasmid pCAMBIA1302 and target gene plasmid were digested using SpeI/BglII and target band was recovered to obtain the recombinant plasmid pCAMBIAl302-PAP3 by linking vector and target gene. The recombinant plasmid was subjected to validation using PCR and enzyme digestion (Figure 1B) showing a 683 bp band, which is consistent with the inserted target gene.
2.4. Subcellular Localization of Gene Expression
To investigate the subcellular distribution of PAP3 protein in the plant, we introduced the transient expression vector pCAMBIA1302-PAP3 fusion gene in the onion epidermal cells using gene gun bombardment and examined its expression of the green fluorescent protein (GFP) under laser confocal microscope. GFP signal could be observed throughout the cell membrane, cytoplasm and nucleus in the cells with expressing vector control pCAMBIA1302 (Figure 2c). However, GFP expression is only present in the nucleus (Figure 2f) indicating PAP3 is a nuclear gene, a feature shared with class B transcriptional factors of MADS-box family.
2.5. Expression of PAP3 Measured by Semi-Quantitative RT-PCR and qRT-PCR
In order to understand the expression of PAP3 in 121A and 121C, we initially applied RT-PCR and qRT-PCR for our research. As shown in Figure 3, PAP3 was present in each developmental stage of CMS line and restorer line with the highest abundance in the late stage (binucleate) during microspore development (Figure 3A(IV),B(IV)). Expression level in restorer line is higher than that of CMS line (Figure 3A(IV),B(IV)).
qRT-PCR showed the similar results as semi-quantitative RT-PCR. Specifically, PAP3 expression of restorer line in late-uninucleate and binucleate microspores was higher than that of CMS line (Figure 3C(III,IV)). However, the difference was not obvious at tetrad and early-or mid-uninucleate.
2.6. RNA in Situ Hybridization of PAP3
The apical meristem picked up from the 20 and 25 day seedling of pepper was used for RNA in situ hybridization. In restorer line, PAP3 is abundant in petals, stamen and pistil primordial at the early stage of flower bud differentiation (Figure 4b). Later on, PAP3 became abundant in stamen primordial and was poorly expressed in petal primordial and pistil primordial (Figure 4c). The expression pattern of PAP3 in 121A is similar with 121C (data not shown).
In microspores, PAP3 mainly localizes at anthers, it expresses during the development and achieves its abundance peaks at the late stage (Figure 5). There was no obvious difference between the CMS line and restorer line at early developmental stage (tetrad and early- or mid-uninucleate) (Figure 5a,b,e,f). However, The expression of PAP3 in restorer line is much higher than the CMS line (Figure 5c-1,d-1,g-1,h-1) at late developmental stage (late-uninucleate, binucleate). These results suggest PAP3 gene may be involved in the regulation of pollen development, especially the mature process of pollen.
In most studied angiosperms, AP3 and PI genes were shown to be expressed in petals and stamens except that they are occasionally present in the first and fourth whorls of flower and non-floral tissues . The class B gene expressed in the developmental petals and stamens of Brassica napus L. AP3 and PI expressed in floral tissue of Arabidopsis and seeds, leaves and roots of maize [48–50]. Class B genes were also shown to expressed in vascular bundle, stalk, embryonic primordial of developing tubes in aconite (Eranthis hyemalis) . These studies suggest expression patterns of class B genes such as AP3 and PI are not conservative and vary in different plants .
PAP3 expression sites of flower are similar in CMS line and restorer line. PAP3 is abundant in stamen but not in petal primordia at the early stage of flower bud development indicating PAP3 may regulate the development of petal and stamen. Besides, PAP3 is present in stamen, pistil and petals through the bud development with the highest abundance in stamen. However, PAP3 is not expressed in sepals. Our findings is consistent with early report showing continuous expression of developmental marker gene like PAP3 not only occurs in primordial of specific flora organ but also continues to the late stage of development .
Prior studies have shown that expression of AP3 and PI genes are suppressed in the flowers of sterile plants [42,44,54]. Other studies showed distinct expression levels of AP3 gene between sterile and fertile lines and its abundance in sterile line was lower than in fertile line at the late bud development stage [36,43,55]. In the present study, we found PAP3 expression is low at the early stage during microspore development and increased at late stage in both CMS line and restorer line indicating PAP3 is not only present in floral primordia but also may play a role in the pollen maturation process. In addition, PAP3 showed similar expression levels at early stages during microspore development between the CMS and restorer lines but expression of CMS line became much lower than the restorer line at late developmental stage. But PAP3’s counterpart unigene comp54456_c0_seq1 in pepper transcriptome showed similar expression levels in CMS and restorer lines, which could be explained by the sequencing of transcriptome using mixed anthers from different developmental stages .
During anther development, abnormity in any stage may affect the normal development of pollen microspore. We found pollen from male sterile line showed irregular shape, uneven size and emptiness and spallation at the late anther developmental stage (Figure 5d-1). However, restorer line appeared uniformed size, plump wall and free of shrinkage (Figure 5h-1) with lower expression level of CMS PAP3 compared with restorer line at late developmental stage of anther. Thus, the morphological difference may suggest PAP3 plays a role in the anther development, which warrants further studies for validation.
4. Experimental Section
4.1. Materials of Plants
Cytoplasmic male sterility line 121A and its isogenic restorer 121C were cultivated in the greenhouse of experimental station in China Agricultural University in 2012. Buds from the four developmental phases (tetrad, early-or mid-uninucleate, late-uninucleate, binucleate) in bud stage  were used for in situ hybridization and collected anther was used for semi-quantitative RT-PCR and qRT-PCR. Anther was harvested from the buds of 121A and 121C with white petals and used to clone PAP3 gene and analyze transient expression in onion epidermal cells. In addition, the apical meristem of the seedling was harvested from 20d and 25d cultivation of CMS line and restorer lines for in situ hybridization.
4.2. Gene Cloning and Blast
An EST showing 91% homology with class B gene TAP3 in Tomato flower was identified by screening using cDNA library induced by pepper CMS, which was constructed previously in our lab. We obtained 929 bp full length gene by RACE technology and named it as PAP3 (genbank accession number: HM104635). Phylogenetic analysis showed PAP3 is clustered into one group with the AP3 gene of Arabidopsis .
Blasting PAP3 in pepper anther transcriptome which was established in our lab  (with the same lines) was performed to identify the sequence with the highest similarity.
4.3. RNA Extraction and cDNA Synthesis
RNA was isolated using SV total RNA Isolation System Kit (Promega Inc., Madison, WI, USA) following instructions. cDNA was synthesized using PrimeScript 1st Strand cDNA synthesis kit (Takara, Dalian, China).
4.4. Cloning of PAP3 in CMS Line
PAP3 gene in CMS line was cloned used primers F and R (Table 1) designed based on PAP3 full length sequence. PCR was performed in total volumes of 25 μL containing 1 μL of cDNA, 5 μL of 5× PrimeSTAR® Buffer (Mg2+ plus; Takara, Dalian, China), 15.75 μL of ddH2O, 2 μL of dNTP mixture, 0.5 μL of specific F/R primers respectively, 0.25 μL of PrimeSTAR® HS DNA Polymerase. The PCR condition was as follows: 94 °C for 3 min; 35 cycles of 94 °C for 40 s, 55 °C 40 s, 72 °C for 1 min; finally 72 °C for 8 min. The product was separated on 1% agarose gel electrophoresis and purified using a DNA purification kit (BIOMED, Beijing, China) then sequenced. The clone and sequence were repeated 20 times.
4.5. Transient Expression of PAP3 in Onion Epidermal Cells
Based on the full length PAP3 sequence and pCAMBIA1302 vector’s restriction sites, two enzyme restrictions sites SpeI and BglII were picked up to design the primers SL-F and SL-R (Table 1 underlines indicate digestion sites of SpeI and BglII). Reverse transcription cDNA was used as template to amplify the coding region of the target gene (stop code was not included). The resulting PCR amplified products were inserted to the pCAMBIA1302 vector at the N-terminus of the GFP gene to generate pEGFP-PAP3. Verified by sequencing, pEGFP-PAP3 and an empty vector were transferred into onion epidermal cells using the particle bombardment method, respectively. The fluorescence signals were detected using laser confocal microscope.
4.6. Semi Quantitative RT-PCR and qRT-PCR
The pepper actin (GenBank: GQ339766.1) gene was served as the internal control of semi-quantittive RT-PCR and qRT-PCR. The cycling parameters of relative RT-PCR were: 94 °C for 3 min followed by 28 cycles of 94 °C for 30 s, 53 °C for 30 s, 72 °C for 30 s, and final elongation at 72 °C for 3 min. PCR products were visualized by 1% gel electrophoresis. qRT-PCR was performed using THUNDERBIRD SYBR qPCR Mix From BEIJING TINYOO Biotechnology Co., Ltd (Beijing, China). The primers for semi-quantitive RT-PCR and qRT-PCR were listed in Table 1 (PAP3-F and PAP3-R). Expression levels of the unigenes were calculated from the threshold cycle using the 2−ΔΔCT method .
4.7. In Situ Hybrization
Specific primers SH-F and SH-R were designed according to PAP3 gene (Table 1) to prepare probe template (product contains ORF excluded stop code). Digoxigenin-labeled sense and antisense probes of PAP3 gene were generated using SP6/T7 RNA polymerase through PCR amplification of cDNA and then kept in 50% formamide. Fixation of the samples and paraffin sectioning were previously described.
Before the hybridization, the sections were pretreated (dewaxing, rehydration and protease treatment). The glycine buffer was used to stop the reaction and the tissue was re-fixed. After acetic anhydride treatment following washing and dehydration, the class was kept in sealed plastic boxes at 4 °C for 4–5 h. The diluted probes were denatured at 80 °C for 2 min and kept on ice.
In situ hybridization was performed following a protocol described elsewhere .
Through expression analyses we confirmed the PAP3 gene as a class B gene of pepper, for its location in nucleus and highest expression in stamen. Our results also showed significantly higher expression in 121C than 121A during late-uninucleate and binucleate phases of microspore. Though preliminary functional verification by virus induced gene silencing has been implemented previously, transgenic experiments still need to be done for further verification of PAP3 gene for its effect on another development in the pepper cytoplasmic male sterile line.
Funded by National Natural Science Foundation project (project number: 31071806) and a grant for innovative team of fruit vegetables of modern agricultural technology in Beijing, China.
Conflicts of Interest
The authors declare no conflict of interest.
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|Table 1. Primers for expression analyses of PAP3.|
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