大豆质核互作雄性不育系NJCMS3A双亲雄性育性基因的SSR标记

利用大豆质核互作雄性不育系NJMCS3A的质、核供体亲本N21566和N21249构建F₂和BC₁F₁育性分离群体进行雄性育性的遗传分析与基因定位。结果表明, F₁正反交可育,F₂和BC₁F₁的可育株与不育株分离比例经χ²测验分别符合3∶1和1∶1,表明NJCMS3A供体亲本雄性育性由一对基因控制,可育等位基因为显性。该基因可能是NJCMS3A的一个恢复基因。选用793对SSR引物对F₂和BC₁F₁群体分别进行育性基因定位,发现该育性基因位于O连锁群上,在Satt331和Satt477标记之间,与Satt331、CSSR133和Satt477标记距离的次序一致,分别为8.1~10.4 cM、11.4~16.4 cM、13.3~19.2 cM。     

Inheritance of male fertility restoration of the cytoplasmic-nuclear male-sterile line NJCMS1A of soybean [Glycine max (L) Merr.]

At present, no report on inheritance of male fertility restoration has been released, yet more than 10 cytoplasmic-nuclear male-sterile soybean lines as well as their maintainers and restorers have been developed. Based on our previous work, 25 restorers for the male-sterile line NJCMS1A were identified and the inheritance of male fertility restoration for these restorers was studied. The results showed that F₁s between NJCMS1A and its restorers were completely male-fertile. The numbers of fertile and sterile plants in the F₂ population of Cross I (NJCMS1A × N23601) and Cross II (NJCMS1A × N23683) corresponded to a segregation ratio of 15:1, and the numbers of non-segregation lines, 3:1 segregation lines and 15:1 segregation lines in F_2:3 of the same two crosses fitted a 7:4:4 genotypic segregation ratio. The testcross BC₁F₁s between the F₁s of the above two crosses and NJCMS1A, NJCMS1B showed a 3:1 segregation ratio. Accordingly, it was inferred that two pairs of duplicate dominant genes controlled the male fertility restoration of NJCMS1A in both crosses. Meanwhile, F₂ of other 23 crosses between NJCMS1A and its 23 restorers showed a fertility segregation ratio of 3:1 or 15:1. The F₁s of the five testcrosses between NJCMS1A and the F₁s of five crosses selected from the above 23 crosses showed that fertility segregation was 3:1 in BC₁F₁s between NJCMS1A and F₁s of the crosses of which fertility segregation fitted 15:1 in F₂ population, while fertility segregation in BC₁F₁s was 1:1 for those fertility segregation fitted 3:1 in F₂ population. Allelism tests showed that restore genes of all restorers in the experiment were allelic to two pairs of dominant genes. All results showed that some restorers bore one pair of dominant restore gene and the others bore two pairs of duplicate dominant gene. The mechanism of F₁ male sterility of the cross N8855 × N2899 was discussed.     

Development of a cytoplasmic male‐sterile line NJCMS4A for hybrid soybean production

Cytoplasmic male‐sterile (CMS) lines are being used to produce hybrid seeds. Thus far, four CMS sources in soybean [Glycine max (L.) Merr.] have been reported in China. However, they are not sufficient or efficient in meeting the requirements of commercial soybean hybrid seed production. In this study, 33 varieties were tested for CMS using 45 crosses among 37 landraces and 17 annual wild soybean accessions (Glycine soja Sieb. et Zucc.). The cross of N23661 × N23658 showed partial to complete male sterility in backcross generations, while the corresponding reciprocal cross showed normal male fertility. Thus, the cytoplasm of N23661 is male‐sterile, the continuously backcrossed line is a male‐sterile line (designated NJCMS4A), and N23658 is its maintainer (designated NJCM4B). The male fertility of NJCMS4A was restored by another accession, Nansheng9403. Accordingly, NJCMS4A along with its maintainer and restorer composes a complete set of three lines for producing hybrid soybean. Using mitochondrial markers and sequence analyses, NJCMS4A is a CMS line with its cytoplasm not identical to the four previously reported CMS sources in soybean.     

Development of a cytoplasmic-nuclear male-sterile line of soybean

The F₁ of N8855 x N2899, a cross between two cultivars of G. max (L.) Merr., was found to be male-sterile. After it was back-crossed with the recurrent parent N2899 for four successive generations, a cytoplasmic-nuclear male-sterile line and its maintainer line, designated as NJCMS1A and NJCMS1B, respectively, were obtained. NJCMS1A was stable in male sterility with 98.29% plants being male-sterile at 0% pollen germination, while its female fertility was normal. The pollen abortion of NJCMS1A occurred at the binucleate stage. Then the vacuolation and disintegration of cytoplasm became further pronounced in NJCMS1A pollen. In addition, the abnormal phenomenon of 2 ∼ 3 styles surrounded by 20 ∼ 30 stamens was found in a few flowers of some male-sterile plants at BC₁F₁ and BC₂F₁. This revised version was published online in August 2006 with corrections to the Cover Date.     

Development of a new cytoplasmic-nuclear male-sterility line of soybean and inheritance of its male-fertility restorability

Based on previous work, a new cytoplasmic‐nuclear male‐sterile line NJCMS2A along with its maintainer NJCMS2B of soybean was released through four episodes of nuclear substitution backcrossing with male‐sterile plants of (N8855 × N1628)F₂ as donor parent and N1628 as recurrent parent. The male sterility of NJCMS2A was complete and female fertility was normal. A series of restorers from different sources were screened out and evaluated. It was found that from the crosses between NJCMS2A and its restorers, two pairs of duplicate dominant genes, allelic to those of NJCMS1A, controlled the inheritance of fertility restorability of NJCMS2A.     

Identification and characterization of new sources of cytoplasmic male sterility in rice

Search for male sterility-inducing cytoplasm in wild species of the genus Oryza was attempted with a view to diversify the base of the cytoplasmic genetic male sterility system currently used in the development of commercial rice hybrids. A total of 132 interspecific crosses were made involving accessions of four wild and two cultivated species, all belonging to the A genome. Wild accessions possessing sterility-inducing cytoplasms were identified following reciprocal and sterile F₂ backcross methods. Sterile segregants were pursued through substitution backcrosses to develop cytoplasmic male-sterile (CMS) lines. CMS lines were developed with the cytoplasm of either O. rufipogon (VNI) or O. nivara (DRW 21018, DRW 21001, DRW 21039, DRW 21030 and RPW 21111). Based on shape, staining, and abortive pattern of pollen and also on type of interaction with a set of restorers and maintainers for known cytoplasmic male steriles of WA source (V 20A), the newly-developed CMS lines were grouped into four classes. Of these, RPMS 1 and RPMS 2 showed gametophytic male sterility with a restorer reaction different from WA cytoplasmic male-sterile stocks.     

Cytoplasmic Systems in Different Male-Sterile Lines of Rice

In order to characterize the cytoplasmic system in seven cytoplasmic-genic male-sterile lines (CMS; A lines) of rice, viz., V 20A, ‘Zhenshan 97A’, IR 46831A, ‘Madhu A’ (cms-WA), ‘Yar-Ai-Zhao A’ (cms-Gam), ‘Pankhari 203A’ (cms-TN) and Wu 10A (cms-bo) and their isonuclear maintainers (B lines), all possible crosses were made between CMS lines and maintainers (A × B) as well as between the maintainers themselves (B × B). Based on F₁ pollen and spikelet fertility the CMS lines V 20A, ‘Zhenshan 97A’, IR 46831 A, ‘Madhu’ A possessing cms-WA cytoplasm were found to be genetically different from ‘Pankhari 203A’ (cms-TN), Wu 10A (cms- bo) and ‘Yar-Ai-Zhao A’ (cms-Gam) cytoplasms. Cms-bo and cms-TN cytoplasms appeared to be identical. Since the cytoplasms of the A lines are different from those of the B lines, the nuclear genes operating to cause the sterility might also be different in (A × B) and (B × B) crosses.     

Stability of male-sterile sources and fertility restoration of their hybrids in pearl millet

Genetic background has a significant effect on the expression of cytoplasmic-nuclear male sterility (CMS) in pearl millet (Pennisetum glaucum (L.) R. Br.). Therefore, a reliable characterization of CMS sources requires the use of near-isonuclear lines and their hybrids. We used this approach to characterize five CMS sources (A₁, A₂, A₃, A_v, and A₄). Male sterility of 81A₄ was the most stable, followed by 81A₁ and 81A_v, indicating the relative merits of these CMS sources in breeding stable male-sterile lines. Male-sterile lines 81A₂ and 81A₃ were highly unstable, indicating their minimal value. Differential male fertility restoration patterns of hybrids made on 81A_V and 81A₄ suggest that the A_v and A₄ cytoplasms represent CMS systems that are different from each other and from A₁, A₂ and A₃. An evaluation of topcross hybrids of 15 diverse populations made on 81A₁ and 81A₄ showed that each population had restorers and maintainers of both cytoplasms and that the frequency of maintainers of A₄ was as high as, or higher than, that of the A₁ cytoplasm. Thus, use of the A₄ cytoplasm can substantially increase the probability of breeding stable male-sterile lines based on inbreds developed from diverse genetic backgrounds, and also provide the opportunity for breeding restorers from each of these diverse genetic sources.     

Comparative genetic analysis and molecular mapping of fertility restoration genes for WA,Dissi, and Gambiaca cytoplasmic male sterility systems in rice

The genetic relationship among three cytoplasmic male sterility (CMS) systems, consisting of WA, Dissi, and Gambiaca, was studied. The results showed that the maintainers of one CMS system can also maintain sterility in other cytoplasmic backgrounds. The F₁ plants derived from crosses involving A and R lines of the respective cytoplasm and their cross-combination with other CMS systems showed similar pollen and spikelet fertility values, indicating that similar biological processes govern fertility restoration in these three CMS systems. The results from an inheritance study showed that the pollen fertility restoration in all three CMS systems was governed by two independent and dominant genes with classical duplicate gene action. Three F₂ populations, generated from the crosses between the parents of good-performing rice hybrids, that possess WA, Dissi, and Gambiaca CMS cytoplasm, were used to map the Rf genes. For the WA-CMS system, Rf3 was located at a distance of 2.8 cM from RM490 on chromosome 1 and Rf4 was located at 1.6 cM from RM1108 on chromosome 10. For the Dissi-CMS system, Rf3 was located on chromosome 1 at 1.9 cM from RM7466 and Rf4 on chromosome 10 was located at 2.3 cM from RM6100. The effect of Rf3 on pollen fertility appeared to be stronger than the effect of Rf4. In the Gambiaca-CMS system, only one major locus was mapped on chromosome 1 at 2.1 cM from RM576. These studies have led to the development of marker-assisted selection (MAS) for selecting putative restorer lines, new approaches to alloplasmic line breeding, and the transfer of Rf genes into adapted cultivars through a backcrossing program in an active hybrid rice breeding program.     

Inheritance and gene tagging of male fertility restoration of cytoplasmic-nuclear male-sterile line NJCMS1A in soybean

The F₁, F₂ and F_2:3 of the NJCMS1A × 'Zhongdou 5' cross were used to analyse the inheritance of the male fertility restoration of the cytoplasmic-nuclear male-sterile line NJCMS1A in soybean. The results of genetic analysis showed two pairs of dominant genes conferring the male fertility restoration of NJCMS1A, which further confirmed previous results. The F₂ population from the NJCMS1A × 'Zhongdou 5' cross was used for tagging the restorer genes for NJCMS1A with 664 pairs of simple sequence repeat primers selected randomly from the genetic linkage map of soybean published by Cregan et al. (1999) . Satt626 on linkage group M and Satt300 on linkage group A1 of the integrated linkage map by Song et al. (2004) were found to link to the two restorer genes of NJCMS1A. The maximum-likelihood estimates of the genetic distance between the two markers, Satt626 and Satt300, and the two restorer genes of 'Zhongdou 5' were 9.75 and 11.18 cM, respectively.     

Inheritance of photoperiod sensitive genic male sterility and breeding of photoperiod sensitive genic male-sterile lines in rice (Oryza sativa L.) through anther culture

The fertility segregations of F₁, F₂, BCF₁ descended from crosses between PSGMR and japonica varieties, and F₁'s anther cultured homozygous diploid pollen plant populations (H₂) were studied to reveal the genetic mechanism of photoperiod sensitive genic male sterility in PSGMR under natural daylight length at Shanghai. Rate of bagged seed-setting was used as an indicator of fertility. Fifteen F₁ showed complete fertility similar to their parents. The ratio of completely sterile plants to fertile plants in fifteen F₂ and four BCF₁ was 1:15 and 1:3, respectively. The ratio of completely sterile to fertile diploid pollen plants in nine diploid populations (H₂) was 1:3. These results demonstrated that the photoperiod sensitive genic male sterility in PSGMR was governed by two pairs of independent major recessive genes. There were no significant fertility segregations in hybrids F₁ and selfed F₂ between Nongken 58S and its derivatives 7001S, 5088S, 5047S and M105-9S, indicating that the photoperiod sensitive genic male-sterile genes in Nongken 58S were allelic to those in its derivatives. Several photoperiod sensitive genic male-sterile diploid pollen lines were bred from anther cultured homozygous diploid populations (H₂) in about a three-year period. Most of these diploid lines showed significant fertility transformation and stable complete sterility from 5 August to 5 September, excellent agronomic traits and high resistance to blast and bacterial leaf blight. This revised version was published online in July 2006 with corrections to the Cover Date.     

Molecular and biological studies on male-sterile cytoplasm in the Cruciferae. IV. Ogura-type cytoplasm found in the wild radish, Raphanus raphanistrum

The orf138 gene, which is specific to Ogura male-sterile cytoplasm, was analysed in mitochondrial DNA (mtDNA) of the wild radish, Raphanus raphanistrum, by polymerase chain reaction (PCR), Southern hybridization and sequencing. The effect of R. raphanistrum cytoplasm on the expression of male sterility was also examined in progeny with R. sativus. A PCR-aided assay and Southern hybridization revealed that three out of six strains analysed included plants with orf138. The sequence of wild type orf138 was same as that of Ogura, except for one or two nucleotide substitutions. Southern hybridization showed a novel mtDNA configuration in R. raphanistrum, in addition to the normal and Ogura types identical to those in R. sativus. Among interspecific hybrids, all the F₁ had normal pollen fertility. In the F₂ progeny between female wild plants having orf138 and the maintainer of Ogura male sterility, male-sterile plants were segregated, fitting the ratio of 3 fertile: 1 sterile plant. R. raphanistrum has cytoplasm that induces male sterility in radishes, and contains a dominant fertility restorer gene.     

A unique introgression from Moricandia arvensis confers male fertility upon two different cytoplasmic male-sterile lines of Brassica juncea

A Brassica juncea line carrying an introgression from Moricandia arvensis restored male fertility to two cytoplasmic male‐sterile (CMS) B. juncea lines carrying either M. arvensis or Diplotaxis catholica cytoplasm. Genetics of fertility restoration was studied in the F₁, F₂, F₃ and backcross generations of the cross between CMS and fertility‐restorer lines. No male‐sterile plants were found in F1‐F₃ generations of the cross between CMS [M. arvensis] B. juncea and the restorer. However, a 1: 1 segregation for male sterility and fertility was observed when the F1 was pollinated with non‐restorer pollen from a euplasmic line. These results clearly show that restoration is mono‐genic and gametophytic. In CMS lines carrying D. catholica cytoplasm, the restorer conferred male fertility to the F1 and showed 3: 1 and 1: 1 segregations for male fertility and sterility in F₂ and BC1 generations, respectively, indicating a monogenic, sporophytic mode of fertility restoration. The results were also supported by pollen stainability in the F1 which was about 65% in M. arvensis‐based CMS and >90% in D. catholica‐based CMS. The above results are discussed in the light of previous molecular studies which showed association between CMS and atpA in both systems.     

Assessment of cytoplasmic effects of cytoplasmic male-sterile lines in upland cotton

Paired A- and B-lines, cytoplasmic male-sterile (CMS)-lines and main-tainer lines, respectively, were crossed with R-lines (restorer) to produce A × R, R × B and B × R hybrids, which were used in 1993 and 1996 to predict the performance of three lypes of CMS cotton lines available in China. A significant difference in yield and yield components was revealed between paired A × R and B × R hybrids. This difference was greatly influenced by both CMS cytoplasm and the interaction between cytoplasm and nuclear genotypes. It is suggested that there are detrimental effects of CMS cytoplasm on yield and yield components. General combining ability of near-isogenic CMS lines was also affected by this negative effect. The detrimental effect was closely related to an increased number of immature seeds per boll, which might be caused by partial female sterility associated with CMS cytoplasm. The possibility of developing specific combinations of CMS Upland × Upland restorer hybrids that express enough heterosis for yield to overcome the detrimental effect of the CMS cytoplasm is discussed.     

Chromosome 1D as a possible location of a gene (s) controlling variation between wheat (Triticum aestivum L.) varieties for carbon isotope discrimination (Δ) under water-stress conditions

Cytoplasmic male-sterility (CMS) in pigeonpea has been reported when some wild relatives of pigeonpea were crossed as the female parent with cultivated types as the male parent. In this paper we report a new source of CMS developed by using the cultivated pigeonpea as the female parent and one of its wild relative Cajanus acutifolius as the pollen donor. This is the first report in pigeonpea where CMS has been developed using the cytoplasm of cultivated pigeonpea. Several pure line cultivars of pigeonpea restored pollen fertility whereas cv. HPL 24 partially maintained male-sterility. The wild species C. acutifolius used as one of the parents, maintained complete sterility. Cytological analysis revealed that both in male-sterile as well as the fertile floral buds, meiosis proceeded normally till the tetrad stage. However in the male-sterile genotypes during the formation of tetrads, the pollen mother cell (PMC) wall did not dissolve to release the tetrads unlike in the fertile genotypes and this major event was found to be responsible for male-sterility.     

Smut reaction of pearl millet hybrids affected by fertility restoration and genetic resistance of parental lines

Summary Pearl millet (Pennisetum glaucum (L.) R. Br.) hybrids based on the A₁ cytoplasmic-nuclear male-sterile (CMS) lines are more susceptible to smut (Tolyposporium penicillariae Bref.) than open-pollinated varieties. Seventy eight pairs of hybrids, made onto male-sterile (A) lines and their counterpart maintainer (B) lines, were evaluated to examine the effects of male sterility and genetic resistance of parental lines on the smut severity of hybrids. The A-line hybrids had higher smut severity and lower selfed seedset than the counterpart B-line hybrids, indicating that it is the CMS-mediated male sterility rather than the A₁ cytoplasm per se that caused greater smut severity of A-line hybrids. However, with the use of resistant parental lines even male-sterile hybrids of A-lines, in several cases, were as resistant as some of the highly resistant male-fertile hybrids of B-lines. It would be possible to produce smut resistant hybrids (< 10% severity) on A-lines, albeit in low frequency, even if only one parent of a hybrid were resistant. However, the probability of producing such hybrids would be higher when both parents were resistant to smut. Thus, improvement in smut resistance of parental lines and fertility restoration ability of pollinators would provide the most effective genetic approach to smut disease management in hybrids.Submitted as JA No 1737 by the International Crops Research Institute for the Semi-Arid Tropics (ICRISAT).     

Inheritance and allelic relationships of fertility restoration genes for seven new sources of male-sterile cytoplasm in sunflower

The inheritance of fertility restoration of six mitomycin C and streptomycin‐induced cytoplasmic male‐sterile (cms) mutants and one cms line derived from Native American cultivar PI 432513 in sunflower was evaluated. These seven new cms sources were also compared with the commercially used cms PET1 (Helianthus petiolaris Nutt.) cytoplasm, using USDA inbred lines with restoration genes (Rf₁) specific for cms PET1 and new restoration lines identified for cms PI 432513. Restoration genes for cms PI 432513 were found in ‘Armavir’, VNIIMK, P21 and male‐fertile (MF) plants of PI 432513. F₂ and F₃ segregation ratios of crosses between cms PI 432513 and these restoration sources indicated a single dominant gene controlled fertility restoration. Progenies of cms PI 432513 testcrossed with F₁’s of half‐diallel crosses among the respective four homozygous restoration lines and RHA 274 suggested that the restoration genes of RHA 274, VNIIMK, P21 and PI 432513 were at the same locus. Restoration genes from VNIIMK, P21 and PI 432513 satisfactorily restored pollen stainability in the heterozygous condition. A very weak expression of the Rf gene in ‘Armavir’ was observed in the heterozygous condition. Fertility restoration capability of these genes for the six mutant cms HA 89 and cms HA 89 (in PET1 cytoplasm) was observed. The mutant cms HA 89 lines were also restored completely by RHA 266, RHA 274, RHA 280 and RHA 296, and F₂’s segregation ratios indicated single dominant gene control, implying a common cytoplasmic male sterility in all lines. F₁’s of half‐diallel crosses among RHA 266, RHA 273, RHA 274, RHA 280 and RHA 296 were testcrossed onto the cms lines, and their all MF progenies among lines, except RHA 280, confirmed that fertility restoration was controlled by a single Rf₁ gene locus. The restoration gene in confection line RHA 280, namely Rf₃, was at a different locus than Rf₁ and was equally capable of restoring all the cms lines. Cms HA 89 mutants and cms PI 432513 are in H. annuus cytoplasm, and are agronomically equal in hybrid performance to the cms PET1 used in commercial sunflower hybrids. These new cms lines will provide immediate alternative cms sources for reducing the genetic vulnerability resulting from the exclusive use of the single cms source PET1 in sunflower hybrid production.     

Detection and characterization of two new CMS systems in faba bean (Vicia faba) *

Wide crosses were made to identify new cytoplasmic male sterility (CMS) systems in faba beans, based on the interaction of cytoplasm with restorer and maintainer alleles. A total of 330 F₁ hybrids were produced in both reciprocal forms. Male sterile segregates were observed in one reciprocal version in the F₂ generation of six crosses. Two of these crosses with female parents originating from Afghanistan and Egypt expressed stable male sterility in subsequent backcross generations. Based on the female parents of the two crosses, these two CMS systems were designated CMS 199 and CMS 297. CMS 199 was more stable than CMS 297 during backcross generations and across different environments. Maintainer and restorer lines for both CMS systems were identified. Lower expression of male sterility occurred in CMS 297 in the greenhouse during the winter generations than in isolation cages during the summer generations, which may be utilized to maintain male sterile lines by selfing. Regarding practical applications, the CMS 199 shows great promise for hybrid breeding in faba beans.     

A new cytoplasmic-nuclear male sterility system in pearl millet

Among the cytoplasmic-nuclear male sterility (CMS) systems reported in pearl millet, Pennisetum glaucum (L.) R. Br., the A_m= A₄ system produces the highest frequency of male-sterile hybrids. A CMS source identified in a large-seeded gene pool (LSGP) was compared with the A₄ system. Seven diverse restorer lines of the A4 system produced hybrids with 81A4 that were all fertile (pollen-shedding score 4 and 68–89% selfed seedset). In contrast, all the hybrids of these inbreds made with the isonuclear line with the LSGP cytoplasm were sterile (pollen-shedding score 1 and 0–3% selfed seedset). Topcross hybrids of four diverse composites made with 81A4 had 10–35% plants that had good fertility (> 50% selfed seedset). In comparison, no plant of any topcross hybrid with the isonuclear line having LSGP cytoplasm exceeded 20% selfed seedset, and it was rare for a plant to exceed even 10% selfed seedset. These differential fertility restoration patterns of hybrids indicate that the LSGP cytoplasm represents a CMS system that is different from the A4 and, by implication, from all those reported to date. This new CMS system is designated A₅.     

大豆质核互作雄性不育系NJCMS2A及其保持系的花药蛋白质组比较研究

大豆质核互作雄性不育系NJCMS2A是以栽培大豆组合（N8855 ´ N1628）F₂不育株为母本,以N1628为父本,通过连续回交选育而成的,N1628（或NJCMS2B）为其同型保持系。对NJCMS2A和NJCMS2B的二胞花粉期花药进行蛋白质组比较分析,获得重复性好的双向电泳图谱,在分子量18.4~116.0 kD、等电点4~7线性范围内,检测到约217个蛋白点,其中差异表达蛋白点25个,包括在NJCMS2A 中出现而在NJCMS2B中缺失的蛋白点13个,在NJCMS2A中缺失而在NJCMS2B中出现的蛋白点10个,另有2个蛋白点的表达量在NJCMS2B中比在NJCMS2A中明显增强。利用基质辅助激光解吸飞行时间质谱（MALDI-TOF-MS）技术对差异表达蛋白进行分析,获得肽质量指纹图谱,用Mascot软件搜索NCBInr数据库,鉴定出14个差异表达蛋白,其中10个在NJCMS2A中出现而在NJCMS2B中缺失和4个在NJCMS2A中缺失而在NJCMS2B中出现。对热激蛋白22 kD、半胱氨酸蛋白酶、V型H+-ATP酶A亚基、MADS盒蛋白和淀粉分枝酶等主要差异蛋白进行功能分析,推测不育系NJCMS2A雄性不育性可能与能量代谢紊乱、细胞程序化死亡（PCD）、淀粉合成受抑制和花器官发育调节基因作用失控等有关。