首页> 外文期刊>International Journal of Molecular Sciences >Complementary Transcriptomic and Proteomic Analysis Reveals a Complex Network Regulating Pollen Abortion in GMS ( msc-1 ) Pepper ( Capsicum annuum L.)
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Complementary Transcriptomic and Proteomic Analysis Reveals a Complex Network Regulating Pollen Abortion in GMS ( msc-1 ) Pepper ( Capsicum annuum L.)

机译:互补的转录组学和蛋白质组学分析揭示了调控GMS(msc-1)辣椒(Capsicum annuum L.)花粉败育的复杂网络。

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Pepper ( Capsicum annuum L.) is a globally important horticultural crop. Use of the genic male-sterile (GMS) line enables efficient commercial hybrid pepper seed production. However, the mechanisms of pepper GMS functioning remain unclear. In this study, we used proteomic and transcriptomic analysis to identify proteins and genes related to genic male sterility. A total of 764 differentially expressed proteins (DEPs) and 1069 differentially expressed genes (DEGs) were identified in the proteomic and transcriptomic level respectively, and 52 genes (hereafter “cor-DEGs-DEPs” genes) were detected at both levels. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis identified 13 DEPs and 14 DEGs involved in tapetum and pollen development. Among the 13 DEPs identified, eight were involved in pollen exine formation, and they were all up-regulated in the fertile line 16C1369B. For the 14 DEGs identified, ABORTED MICROSPORES ( AMS ) and DEFECTIVE IN TAPETAL DEVELOPMENT AND FUNCTION1 ( TDF1 ) were involved in tapetum development, and both are possibly regulated by Msc-1 . All of these genes were detected and confirmed by qRT-PCR. The presence of these genes suggests their possible role in tapetum and pollen exine formation in GMS pepper. Most key genes and transcription factors involved in these processes were down-regulated in the sterile line 16C1369A. This study provides a better understanding of GMS ( msc-1 ) molecular functioning in pepper.
机译:胡椒(Capsicum annuum L.)是一种全球重要的园艺作物。使用基因雄性不育(GMS)品系可实现高效的商业化杂交胡椒种子生产。但是,辣椒GMS功能的机制尚不清楚。在这项研究中,我们使用蛋白质组学和转录组学分析来鉴定与男性不育相关的蛋白质和基因。分别在蛋白质组学和转录组学水平上共鉴定了764个差异表达蛋白(DEPs)和1069个差异表达基因(DEGs),并且在这两个水平上共检测到52个基因(此后称为“ cor-DEGs-DEPs”基因)。基因本体论(GO)和《京都议定书》的基因与基因组百科全书(KEGG)分析确定了13种DEP和14种DEG参与绒毡层和花粉发育。在鉴定出的13个DEP中,有8个参与了花粉外壁的形成,它们在可育系16C1369B中均被上调。对于鉴定出的14个DEG,在胎盘发育和功能中的异常微孢子(AMS)和缺陷型(TDF1)参与绒毡层的发育,并且都可能受Msc-1调控。通过qRT-PCR检测并确认所有这些基因。这些基因的存在表明它们可能在GMS胡椒的绒毡层和花粉外壁形成中起作用。这些过程中涉及的大多数关键基因和转录因子在无菌株系16C1369A中均被下调。这项研究可以更好地了解辣椒中的GMS(msc-1)分子功能。

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