Chen Jianhua, Xu Hao, Zhang Jian, Dong Shengjun, Liu Quangang, Wang Ruoxi
College of Forestry, Shenyang Agricultural University, Shenyang, Liaoning, China.
PeerJ. 2021 Oct 20;9:e12349. doi: 10.7717/peerj.12349. eCollection 2021.
The phenomenon of male sterility widely occurs in and has a serious negative impact on yield. We identified the key stage and cause of male sterility and found differentially expressed genes related to male sterility in , and we analyzed the expression pattern of these genes. This work aimed to provide valuable reference and theoretical basis for the study of reproductive development and the mechanisms of male sterility in
The microstructures of male sterile flower buds and male fertile flower buds were observed by paraffin section. Transcriptome sequencing was used to screen genes related to male sterility in Quantitative real-time PCR analysis was performed to verify the transcriptome data.
Anther development was divided into the sporogenous cell stage, tetrad stage, microspore stage, and pollen maturity stage. Compared with male fertile flower buds, in the microspore stage, the pollen sac wall tissue in the male sterile flower buds showed no signs of degeneration. In the pollen maturity stage, the tapetum and middle layer were not fully degraded, and anther development stopped. Therefore, the microspore stage was the key stage for anther abortion , and the pollen maturity stage was the post stage for anther abortion. A total of 4,108 differentially expressed genes were identified by transcriptome analysis. Among them, 1,899 were up-regulated, and 2,209 were down-regulated in the transcriptome of male sterile flower buds. We found that "protein kinase activity", "apoptosis process", "calcium binding", "cell death", "cytochrome c oxidase activity", "aspartate peptidase activity", "cysteine peptidase activity" and other biological pathways such as "starch and sucrose metabolism" and "proteasome" were closely related to male sterility in . A total of 331 key genes were preliminarily screened.
The occurrence of male sterility in involved many biological processes and metabolic pathways. According to the results of microstructure observations, related physiological indexes determination and transcriptome analysis, we reveal that the occurrence of male sterility in may be caused by abnormal metabolic processes such as the release of cytochrome c in the male sterile flower buds, the imbalance of the antioxidant system being destroyed, and the inability of macromolecular substances such as starch to be converted into soluble small molecules at the correct stage of reproductive development, resulting in energy loss. As a result, the tapetum cannot be fully degraded, thereby blocking anther development, which eventually led to the formation of male sterility.
雄性不育现象在[具体物种]中广泛存在,对产量产生严重负面影响。我们确定了雄性不育的关键阶段和原因,发现了与[具体物种]雄性不育相关的差异表达基因,并分析了这些基因的表达模式。这项工作旨在为[具体物种]生殖发育及雄性不育机制的研究提供有价值的参考和理论依据。
通过石蜡切片观察雄性不育花芽和可育花芽的微观结构。利用转录组测序筛选[具体物种]中与雄性不育相关的基因。进行定量实时PCR分析以验证转录组数据。
花药发育分为造孢细胞期、四分体期、小孢子期和花粉成熟期。与可育花芽相比,在小孢子期,雄性不育花芽的花粉囊壁组织没有退化迹象。在花粉成熟期,绒毡层和中层没有完全降解,花药发育停止。因此,小孢子期是花药败育的关键阶段,花粉成熟期是花药败育的后期阶段。通过转录组分析共鉴定出4108个差异表达基因。其中,在雄性不育花芽转录组中,1899个基因上调,2209个基因下调。我们发现“蛋白激酶活性”“凋亡过程”“钙结合”“细胞死亡”“细胞色素c氧化酶活性”“天冬氨酸肽酶活性”“半胱氨酸肽酶活性”等生物途径以及“淀粉和蔗糖代谢”“蛋白酶体”等与[具体物种]的雄性不育密切相关。初步筛选出331个关键基因。
[具体物种]中雄性不育的发生涉及许多生物学过程和代谢途径。根据微观结构观察、相关生理指标测定和转录组分析结果,我们揭示[具体物种]中雄性不育的发生可能是由于雄性不育花芽中细胞色素c释放、抗氧化系统失衡被破坏以及淀粉等大分子物质在生殖发育的正确阶段无法转化为可溶性小分子等异常代谢过程导致能量损失。结果,绒毡层不能完全降解,从而阻碍花药发育,最终导致雄性不育的形成。