首页> 外文期刊>Journal of proteomics >iTRAQ-based proteomic analysis of fertile and sterile flower buds from a genetic male sterile line 'AB01' in Chinese cabbage (Brassica campestris L. ssp. pekinensis)
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iTRAQ-based proteomic analysis of fertile and sterile flower buds from a genetic male sterile line 'AB01' in Chinese cabbage (Brassica campestris L. ssp. pekinensis)

机译:大白菜遗传性雄性不育线'AB01'植物育种花蕾的基于ITRAQ的蛋白质组学分析(Brassica Campestris L. SSP。Pekinensis)

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摘要

To investigate the molecular basis of multiple-allele-inherited male sterility in Chinese cabbage (Brassica campestris L. ssp. pekinensis), we performed differential proteomic analysis using iTRAQ to identify differentially abundant proteins between fertile and sterile flower buds from the genetic male sterile line 'AB01'. We identified 5932 high-confidence proteins; 1494 were differentially abundant between the two samples, including 749 up-and 745 down-regulated proteins. The up- and down-regulated proteins that could be essential for anther development and male sterility in sterile buds were mainly involved in (1) carbohydrate and energy metabolism (pyruvate dehydrogenase, glycolysis/gluconeogenesis, TCA cycle, starch and sucrose metabolism), (2) pollen wall synthesis and regulation (pectinesterase, polygalacturonase, pectate lyase, beta-galactosidase, glycosyl hydrolase), (3) protein synthesis and degradation (proteasome subunits, ribosome proteins, ABC transporters, RNA transport, protein processing in endoplasmic reticulum), (4) flavonoid biosynthesis, and (5) plant hormone signal transduction. We identified 10 genes/proteins that were both up-regulated and 122 that were both down-regulated in a conjoint analysis. Multiple reaction monitoring and qRT-PCR validation showed that the iTRAQ results were accurate and reliable. These findings will provide valuable information on proteins involved in anther development, and will contribute to the understanding of the molecular mechanism(s) that underlie male sterility in Chinese cabbage.
机译:探讨大白菜(Brassica Campestris L. SSP)中多等位基因遗传性雄性不育的分子基础'ab01'。我们确定了5932个高信心蛋白;在两个样品之间差异丰富,包括749升至745个下调蛋白质。对花药发育和雄性不育的血液无菌在无菌芽中的上调蛋白质主要涉及(1)碳水化合物和能量代谢(丙酮酸脱氢酶,糖酵解/葡糖生成,TCA循环,淀粉和蔗糖代谢),( 2)花粉壁合成和调节(果白酶,多肢乳糖酶,果胶酶,β-半乳糖苷酶,糖基水解酶),(3)蛋白质合成和降解(蛋白酶体亚基,核糖体蛋白,ABC转运蛋白,RNA输送,蛋白质加工在内质网中), (4)黄酮类生物合成,(5)植物激素信号转导。我们鉴定了既上调的10个基因/蛋白质,也可以在联合分析中下调122个。多重反应监测和QRT-PCR验证表明ITRAQ结果准确可靠。这些发现将提供有关涉及花药开发的蛋白质的有价值的信息,并有助于了解大白菜中雄性不育的分子机制。

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