Morphological and cytological assessments reveal pollen degradation causes pollen abortion in cotton cytoplasmic male sterility lines

Background Understanding the mechanism of male sterility is crucial for producing hybrid seeds and developing sterile germplasm resources.However,only a few cytoplasmic male sterility(CMS)lines of cotton have been produced due to several challenges,like inadequate variation of agronomic traits,incomplete sterility,weak resilience of restorer lines,and difficulty in combining strong dominance.Therefore,the morphological and cytological identification of CMS in cotton will facilitate hybrid breeding.Results Two F_(2) segregating populations of cotton were constructed from cytoplasmic male sterile lines(HaA and 01A,maternal)and restorer lines(HaR and 26R,paternal).Genetic analysis of these populations revealed a segregation ratio of 3:1 for fertile to sterile plants.Phenotypic analysis indicated no significant differences in traits of flower bud development between sterile and fertile plants.However,sterile plants exhibited smaller floral organs,shortened filament lengths,and anther atrophy on the flowering day in comparison with the fertile plants.When performed scanning electron microscopy(SEM),the two F_(2) populations revealed morphological variations in the anther epidermis.Cellular analysis showed no significant differences in pollen development before pollen maturation.Interestingly,between the pollen maturation and flowering stages,the tapetum layer of sterile plants degenerated prematurely,resulting in abnormal pollen grains and gradual pollen degradation.Conclusion The results of this study suggest that fertility-restoring genes are controlled by a single dominant gene.Sterile plants exhibit distinctive floral morphology,which is characterized by stamen atrophy and abnormal anthers.Pollen abortion occurs between pollen maturity and flowering,indicating that premature tapetum degradation may be the primary cause of pollen abortion.Overall,our study provides a theoretical basis for utilizing CMS in hybrid breeding and in-depth investigation of the dominant configuration of cotton hybrid combinations,mechanisms of sterility,and the role of sterile and restorer genes.

The Relation between Anther's Nutrient Metabolism and Pollen Abortion of Male Sterile Lines in Lycium barbarum L.

[ Objective] This study deals with the relation between anther nutrient metabolism and pollen abortion of male sterile lines in Lycium barbarum L., and provides some theoretical references for the pollen abortion mechanism of male sterile lines in Lyciurn barbarurn L.. [Method] By using semi-thin section and cytochemistry technology, the accumulation and distribution of anther nutrient of male sterile and fertile lines in Lycium barbarum L. were observed and compared. [ Result] The result showed that after meiosis, starch grains in the connective parenchyma of anther decreased sharply, and starch grains in epidermis and endothecium were also greatly decreased, while nearly no lipid accumulated in tapetal cells in male sterile lines compared with the fertile lines. The tapetal cells and tetraspore had vacuoles appear successively, and then entered the degenerate process. During the degeneration stage of tapetal cells and tetraspore, starch grains in epidermis and endothecium were still in a smell number and in the connective parenchyme as well. [ Conclusion] The decrease of polysaccharide supplying in anther vascular leads to the disorder of mechanism of glycelipid transforming in tapetal ceils, which triggers the tapetal cells degenerating ahead of time, and the latter gives rise to callus wall failing to degenerate in time. Therefore, the tetrads disintegrate and disappear ultimately due to lack of nutrition.

DIA-based proteome profiling with PRM verification reveals the involvement of ER-associated protein processing in pollen abortion in Ogura CMS cabbage

Ogura cytoplasmic male sterility(Ogura CMS)is extensively applied in hybrid seed production in cruciferous crops.However,the posttranscriptional molecular basis of Ogura CMS in cruciferous crops remains elusive.Here,a data-independent acquisition-based proteomic approach coupled with a parallel reaction monitoring-based targeted proteomic assay was used to analyze the proteome dynamics of Ogura CMS cabbage line RM and its maintainer line RF during floral bud development to obtain insights into the mechanism underlying Ogura CMS in cruciferous crops.A total of 9162 proteins corresponding to 61464 peptides were identified in RM and RF floral buds.The proteomic fluctuation of RM was weaker than that of RF.Differences in protein expression between RM and RF gradually enlarged with floral bud development.Fifteen continually up-regulated and eight continually down-regulated proteins were found in RM relative to RF throughout floral bud development.Differentially expressed proteins between RM and RF during floral bud development were implicated in the endoplasmic reticulum(ER)-associated protein processing pathway,in which most of them exhibited down-regulated expression in RM.These data suggest that ER-associated protein processing may be involved in pollen abortion in Ogura CMS cabbage by inhibiting the expression of critical factors.Our findings not only deepen the understanding of the molecular mechanisms of Ogura CMS in cruciferous crops but also provide better guidance for applying Ogura CMS in the hybrid breeding of cruciferous crops.

Study on the Pollen Thermo-Sensitive and Stigma Exsertion Male Sterile Line Tomato (Lycopersicon esculentum Mill.) cv. Da107

To accelerate the breeding process, male sterile line is used to leave out the troublesome procedures of the artificial emasculation in tomato breeding. However, the fertility of the pollen thermo-sensitivity male sterile line (PTMSL) and the stigma exsertion male sterile line (SEMSL) are affected easily by the environments when used alone. The trial materials were Da107 and the control was First. This study was conducted to create a new male sterile line of tomato characterized by pollen thermo-sensitivity and long style by genic recombination through the hybridizing of the PTMSL and SEMSL. Research on the statistics of the pollen germination rate, the contamination rate in F1 and the flower organics indicated that Da107 was an ideal TS and SE male sterile line with the sterility of 95%, as well as it also could be used as fertile line at low temperature. Meanwhile, the results showed that hybrid-seed contamination risk with selfed seeds from residual fertility in Da107 was low.

Mapping of S-b Locus for F_1 Pollen Sterility in Cultivated Rice Using PCR Based Markers

In cultivated rice ( Oryza sativa L.), F-1 pollen sterility is controlled by at least 6 loci of the F, pollen sterility genes. To map S-b, one of loci, rice variety Taichung 65 (T65) carrying S-b(j)/S-b(j) and its near-isogenic line TIST2 carrying S-b(i)/S-b(i) were used to develop the mapping population. One hundred and fifty-eight microsatellite markers were selected to survey T65 and TISL2. RM13 on chromosome 5 was found to be polymorphic between them. Cosegregation indicated that RM13 was closely linked with locus S-b. Eleven RFLP markers were selected on the corresponding region from the genetic map of Rice Genome Research Program (RGP) of Japan to convert into sequence-tagged site (STS) markers. Amplicon length polymorphism (ALP) was carried out, but none of them was found to be polymorphic between T65 and TISL2. Then PCR-based RFLP (PBR) was done using six 4-nucleotide recognizing restriction endonucleases. Polymorphism was detected when PCR products of R830STS and R2213SSTS were digested with Taq I. Genetic analysis indicated that the distance between locus S-b and markers, R830STS, RM13 and R2213SSTS were 3.3 cM (centi-Morgan), 5.2 cM and 5.5 cM, respectively. These PCR-based markers could be directly used in marker-assisted selection. The technical system combining genetic mapping and PCR-based marker-assisted selection will facilitate the development of molecular breeding.

Analysis of Introgressed Segments in Near-isogenic Lines for F_1 Pollen Sterility in Rice (Oryza sativa)

One hundred and fifty-eight microsatellite markers showing polymorphism among parents were used to survey the introgressed segments in the 50 near-isogenic lines of F_1 pollen sterility. Two hundred and sixty introgressed segments were detected in 50 near-isogenic lines, each carrying 5.2 introgressed segments on an average. Among the 260 segments, one hundred carrying F_1 pollen sterility loci concentrated on the region of F_1 pollen sterility genes, and the remaining one hundred and sixty without F_1 pollen sterility loci distributed randomly over 12 chromosomes. Both the average number and length of the introgressed segments decreased along with the increase of backcross generations. The number of introgressed segments was less than four and the length was less than 20 cM in the near-isogenic lines after backcrossing for four or more times.

Introgression of Gene for Non-Pollen Type Thermo-Sensitive Genic Male Sterility to Thai Rice Cultivars

For the two-line hybrid rice system, pol en sterility is regulated by recessive gene that responds to temperature. The recessive gene controlling thermo-sensitive genetic male sterility （TGMS） is expressed when the plants are grown in conditions with higher or lower critical temperatures. To transfer tgms gene（s） control ing TGMS to Thai rice cultivars by backcross breeding method, a male sterile line was used as a donor parent while Thai rice cultivars ChaiNat 1, PathumThani 1, and SuphanBuri 1 were used as recurrent parents. The BC2F2 lines were developed from backcrossing and selfing. Moreover, the simple sequence repeat （SSR） markers were developed for identifying tgms gene and the linked marker was used for assisting selection in backcrossing. The identification lines were confirmed by pol en observation. The results showed the success of introgression of the tgms gene into Thai rice cultivars. These lines will be tested for combining ability and used as female parent in hybrid rice production in Thailand.

外源茉莉酸甲酯对BNS366雄性育性的影响

为探究外源茉莉酸甲酯(methyl jasmonate,MeJA)对小麦温敏雄性不育系BNS366雄性育性的影响,以BNS366及其近等基因系郑麦366为试验材料,在正常秋季播种(2020年10月12日)和晚播(2020年12月2日)条件下,分别于2021年3月22日和3月31日开始至开花期前,设置0(清水,对照)、50、100、200、300、400和500μmol·L^(-1) MeJA(水溶液,喷施)7个处理,比较分析了不同处理间花粉可育率和自交结实率的差异。结果表明:在正常秋季播种条件下,郑麦366花粉可育率、国内法自交结实率和国际法自交结实率分别为86.31%、70.36%和112.22%,在晚播条件下分别为82.53%、92.53%和166.18%,均正常可育;在正常秋季播种条件下,200μmol·L^(-1) MeJA处理的国际法自交结实率为70.15%,比对照显著降低了42.07个百分点;在晚播条件下,200、300和500μmol·L^(-1) MeJA处理的国内法自交结实率分别为74.71%、74.01%和73.45%,比对照显著降低了17.82、18.52和19.08个百分点;在两个播期下,郑麦366其他浓度MeJA处理的上述3个指标与对照差异均不显著。在正常秋季播种条件下,BNS366花粉可育率为零,达到全不育水平,国内法自交结实率和国际法自交结实率均为0.24%,100μmol·L^(-1) MeJA处理的花粉可育率为88.25%,达到正常可育水平,国内法自交结实率和国际法自交结实率分别为56.41%和94.01%,能正常结实,与对照差异达到显著水平;在晚播条件下,BNS366的上述3个指标分别为51.72%、41.23%和93.08%,正常可育,100μmol·L^(-1) MeJA处理的国际法自交结实率为39.72%,比对照显著降低了53.36个百分点;在两个播期下,BNS366其他浓度MeJA处理的上述3个指标与对照差异均不显著。由此说明,在2020-2021年,外源MeJA对郑麦366和BNS366可育植株的雄性育性可能具有降低效应,对BNS366不育植株的雄性不育性具有较强恢复效应。

大花紫薇和‘丹红紫叶’紫薇杂交F_(1)代不育细胞学分析

【目的】大花紫薇和‘丹红紫叶’紫薇子代高度不育,为了解析其子代不育的机理。【方法】本试验以大花紫薇作母本和‘丹红紫叶’紫薇作父本的杂交F_(1)代‘潇湘华秀’为材料,通过石蜡切片显微技术观察其雌雄蕊的生长发育过程及成熟花粉粒中的可溶性糖、淀粉、脂类物质的积累情况;并对3种紫薇花蕾不同生长发育阶段的可溶性糖含量、淀粉含量、游离脯氨酸含量进行分析测定。【结果】1)‘潇湘华秀’不育是雄性不育和雌性不育共同作用形成的,其花粉存在干瘪、畸形、大小不均等异常现象,绝大部分花粉不能萌发。2)与大花紫薇和‘丹红紫叶’紫薇相比,F_(1)代在减数分裂时期发生异常,具体表现为减数分裂时,有部分染色体无法正常联会并排布到赤道板中央,染色体不均匀分离,发育成异常的二分体、带微核二分体、带微核四分体、五分体、六分体,且大部分花粉细胞核在二核期消解,成熟花粉粒大部分畸形,无内含物且不能萌发,可萌发的花粉粒为2n花粉粒。3)大孢子在四分体时期萎缩消解,后期形成有少量胚囊痕迹的空洞。4)F_(1)代花蕾的可溶性糖、淀粉、游离脯氨酸含量都低于同等时期的亲本花蕾,且大部分花粉中未观测到脂类、可溶性糖和淀粉积淀。【结论】染色体行为异常导致异常四分体的出现和二核花粉粒时期细胞核的解体是花粉败育的主要原因;四分体时期大孢子萎缩消解是雌性不育的主要原因。

OsMYB80下游基因鉴定及其在调控花粉育性中的作用分析

OsMYB80是水稻花药和花粉发育过程中的重要转录因子,其下游靶标基因的相关研究仍有待补充。该研究从可能受OsMYB80直接调控的基因中筛选出24个可能参与信号转导、泛素化修饰、囊泡运输和未知功能的候选基因,利用qRT-PCR验证其表达模式,并通过CRISPR/Cas9基因编辑技术对其中7个基因(LOC_Os06g11930、LOC_Os09g26470、LOC_Os01g04409、LOC_Os06g35160、LOC_Os06g11135、LOC_Os05g13650、LOC_Os01g14880)加以敲除。经I2-KI花粉染色分析和结实情况考察发现,上述7个基因敲除后对植株育性影响都不显著,说明上述7个基因并非OsMYB80下游调控花粉育性的关键基因。这些结果也暗示某些受OsMYB80调控的下游基因及其参与的生物化学反应可能在花药花粉发育过程中功能冗余或者只发挥微效作用。

大豆雄蕊优势表达基因GmARFA1a通过调控花粉萌发影响结实率

大豆(Glycine max (L.) Merr.)是自花授粉作物,通过人工去雄的办法生产杂交种,不仅繁琐且成本高。雄性不育基因功能的研究是大豆杂种优势利用的前提之一,大豆雄性不育位点报道较少,定位及功能研究进展缓慢。随着大豆转基因体系的成熟及生物技术的发展,利用反向遗传学研究大豆雄性不育基因的功能变得相对容易。本研究通过转录组数据分析发现大豆中编码小G蛋白的GmARFA1a受到大豆雄性育性控制基因MS1(Male Sterile 1)和MS2的调控,公共数据库数据表明GmARFA1a在大豆未开放的花中表达量最高,而qRT-PCR数据进一步明确GmARFA1a在大豆授粉前雄蕊中优势表达。花粉萌发实验及结实率统计发现Gmarfa1a突变体花粉活力下降导致结实率受到明显抑制。本研究对GmARFA1a基因功能进行了初步解析,明确其对大豆雄性育性存在一定影响。研究结果不仅丰富了对GmARFA1a乃至ARF基因家族成员功能的认识,也为后续深入研究大豆GmARFA1a功能及大豆杂种优势利用奠定了基础。

拟南芥雄性不育突变体opw(only pollen wall)候选突变基因的克隆

在T-DNA插入突变体Salk_059463株系的群体中,筛选到两株雄性不育突变体,对TDNA序列上的一对引物进行PCR鉴定,结果表明:其基因组中没有T-DNA插入.遗传分析表明这两株雄性不育突变体由同一单个隐性基因控制,引起不育的主要原因是从花药发育的第8期开始,小孢子细胞质内容物逐渐减少直至消失,到花药发育的第12期,药室内的小孢子只剩下一个花粉壁空壳,故该突变体命名为opw(only pollen wall).利用图位克隆的方法对OPW基因进行了定位,结果表明OPW基因位于第二条染色体上分子标记T28M21和T3G21之间的12 kb区间内,该区间内一共有21个基因注释.通过克隆区间内的基因并测序发现opw-1突变体基因组中At2g40140基因编码序列的外显子在第289和第290个碱基之间插入了一个A碱基,而opw-2突变体基因组中At2g40140基因编码序列的外显子在第412和第413个碱基之间插入了一个T碱基,造成的编码序列移码使第424至第426碱基成为终止密码子,故At2g40140是编码OPW的候选基因.

The essential roles of sugar metabolism for pollen development and male fertility in plants

Sugar metabolism plays an essential role in plant male reproduction. Defects in sugar metabolism during anther and pollen development often result in genic male sterility(GMS). In this review, we summarize the recent progresses of the sugar metabolism-related GMS genes and their roles during plant anther and pollen development, including callose wall and primexine formation, intine development, pollen maturation and starch accumulation, anther dehiscence, and pollen germination and tube growth. We predict 112 putative sugar metabolic GMS genes in maize based on bioinformatics and RNA-seq analyses, and most of them have peak expression patterns during middle or late anther developmental stages.Finally, we outline the potential applications of sugar metabolic GMS genes in crop hybrid breeding and seed production. This review will deepen our understanding on sugar metabolic pathways in controlling pollen development and male fertility in plants.

Detection of Distorted Segregation in Genotype of Pollen Calli Derived from Hybrid F_1 of Cultivated Rice (Oryza sativa L.) Using SSR Markers

S-a, S-b and S-c are three loci for F1 pollen sterility in cultivated rice （Oryza sativa L.）. Taichung 65 （T65） is all Sj/Sj at these three loci, while its F1 pollen sterile near-isogenic lines, TISL2 （S-b）, TISL4 （S-a） and TISL5 （S-c） is Sj/Sj according to their respective sterility locus. Using SSR molecular marker to detect the segregation of the allele Si and Sj in pollen calli population induced from different hybrid F1, which have different pollen sterility locus, showed that the segregation of allele Si and Sj was distorted. The distorted direction of pollen calli population in vitro was not the same as F2 population in vivo. The quantities of pollen callus carrying Sj were much more than that of carrying Siat S-a and S-c locus, the ratio of Si and Sj were 1：4.81 and 1：1.96 respectively. But the opposite tendency was observed at S-b locus, the ratio of Si and Sj being 1：0.35. At the same time, all these results were undisturbed by either culture medium or culture period.

Identification of no pollen 1 provides a candidate gene for heterosis utilization in foxtail millet(Setaria italica L.)

Male sterility is a common biological phenomenon in plant kingdom and has been used to generate male-sterile lines, which are important genetic resources for commercial hybrid seed production. Although increasing numbers of male-sterility genes have been identified in rice(Oryza sativa) and Arabidopsis(Arabidopsis thaliana), few male-sterility-related genes have been characterized in foxtail millet(Setaria italica). In this study, we isolated a male-sterile ethyl methanesulfonate-generated mutant in foxtail millet, no pollen 1(sinp1), which displayed abnormal Ubisch bodies, defective pollen exine and complete male sterility. Using bulk segregation analysis, we cloned SiNP1 and confirmed its function with CRISPR/Cas9 genome editing. SiNP1 encoded a putative glucose-methanol-choline oxidoreductase.Subcellular localization showed that the SiNP1 protein was preferentially localized to the endoplasmic reticulum and was predominantly expressed in panicle. Transcriptome analysis revealed that many genes were differentially expressed in the sinp1 mutant, some of which encoded proteins putatively involved in carbohydrate metabolism, fatty acid biosynthesis, and lipid transport and metabolism, which were closely associated with pollen wall development. Metabolome analysis revealed the disturbance of flavonoids metabolism and fatty acid biosynthesis in the mutant. In conclusion, identification of SiNP1 provides a candidate male-sterility gene for heterosis utilization in foxtail millet and gives further insight into the mechanism of pollen reproduction in plants.

荔枝雄性不育株系MS1的发现和鉴定

【目的】对新发现的荔枝雄性不育株系MS1进行鉴定,为后续研究利用奠定基础。【方法】以荔枝雄性不育株系MS1为研究材料,以雄性可育株系D13为对照,通过外观比较、扫描电镜观察、研磨花药镜检、花药石蜡切片等方法对MS1株系雄性不育进行鉴定。【结果】荔枝雄性不育株系MS1雄花数量少、个头小、花药瘦小、表面多凹陷、成熟后多不开裂、药室内无花粉粒且自交无坐果。【结论】荔枝雄性不育株系MS1为无花粉型雄性不育。

The miR159a-DUO1 module regulates pollen development by modulating auxin biosynthesis and starch metabolism in citrus

Achieving seedlessness in citrus varieties is one of the important objectives of citrus breeding.Male sterility associated with abnormal pollen development is an important factor in seedlessness.However,our understanding of the regulatory mechanism underlying the seedlessness phenotype in citrus is still limited.Here,we determined that the miR159a-DUO1 module played an important role in regulating pollen development in citrus,which further indirectly modulated seed development and fruit size.Both the overexpression of csi-miR159a and the knocking out of DUO1 in Hong Kong kumquat(Fortunella hindsii)resulted in small and seedless fruit phenotypes.Moreover,pollen was severely aborted in both transgenic lines,with arrested pollen mitotic I and abnormal pollen starch metabolism.Through additional cross-pollination experiments,DUO1 was proven to be the key target gene for miR159a to regulate male sterility in citrus.Based on DNA affinity purification sequencing(DAP-seq),RNA-seq,and verified interaction assays,YUC2/YUC6,SS4 and STP8 were identified as downstream target genes of DUO1,those were all positively regulated by DUO1.In transgenic F.hindsii lines,the miR159a-DUO1 module down-regulated the expression of YUC2/YUC6,which decreased indoleacetic acid(IAA)levels and modulated auxin signaling to repress pollen mitotic I.The miR159a-DUO1 module reduced the expression of the starch synthesis gene SS4 and sugar transport gene STP8 to disrupt starch metabolism in pollen.Overall,this work reveals a new mechanism by which the miR159a-DUO1 module regulates pollen development and elucidates the molecular regulatory network underlying male sterility in citrus.

ZmMS39 encodes a callose synthase essential for male fertility in maize(Zea mays L.)

Callose contributes to many biological processes of higher plants including pollen development,cell plate and vascular tissue formation,as well as regulating the transport function of plasmodesmata.The functions of callose synthase genes in maize have been little studied.We describe a maize male-sterile mutant 39(ms39)characterized by reduced plant height.In this study,we confirmed using CRISPR/Cas9 technology that a mutation in Zm00001d043909(ZmCals12),encoding a callose synthase,is responsible for the male sterility of the ms39 mutant.Compared with male-fertile plants,callose deposition around the dyads and tetrads in ms39 anthers was significantly reduced.Increased cell autophagy observed in ms39 anthers may have been due to the premature programmed cell death of tapetal cells,leading to collapse of the anther wall structure.Disordered glucose metabolism in ms39 may have intensified autophagy in anthers.Evaluation of the ms39 gene on maize heterosis by paired-crossed experiment with 11 maize inbred lines indicated that ms39 can be used for maize hybrid seed production.

新白凤桃花粉的发生和发育

新白凤桃为雄性败育品种的主要授粉品种之一，其大部分花粉能育，败育花粉占８％～３７．７％。花粉败育与药壁绒毡层无关。导致花粉败育的主要因素是由于花粉母细胞的不正常减数分裂，致使在减Ⅱ末期出现多于４核的大小不一的多核现象。在四分体时期，这些核被分配到４个子细胞中，因此部分子细胞中具２～３核现象。由异常减数分裂所产生的花粉粒，其细胞质和细胞核解体消失，而呈现空囊状的孢壁，或具细胞质和核的异形花粉。

水稻花期高温胁迫研究进展与展望

水稻花期高温引起的不育危害,具有发生可预测性低、作用局限于特定部位、致害程度严重等特点.本文就水稻花期高温不育问题,在发生时间、致害温度、品种反应差异、作用机制、鉴定方法以及抗性性状遗传等方面作了综述.并结合在日本的相关研究及对中国江汉平原杂交中稻花期高温危害发生的气候条件、品种差异等的初步分析,提出了该领域研究目前存在的关键问题和主要解决途径.