Suppr超能文献

栽培花生(Arachis hypogaea)中的表达序列标签:种子发育和对青枯病病原菌侵染响应相关基因的发现。

Expressed sequence tags in cultivated peanut (Arachis hypogaea): discovery of genes in seed development and response to Ralstonia solanacearum challenge.

机构信息

Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture, Oil Crops Research Institute of the Chinese Academy of Agricultural Sciences, Wuhan, People's Republic of China.

出版信息

J Plant Res. 2012 Nov;125(6):755-69. doi: 10.1007/s10265-012-0491-9. Epub 2012 May 31.

Abstract

Although an important oil crop, peanut has only 162,030 expressed sequence tags (ESTs) publicly available, 86,943 of which are from cultivated plants. More ESTs from cultivated peanuts are needed for isolation of stress-resistant, tissue-specific and developmentally important genes. Here, we generated 63,234 ESTs from our 5 constructed peanut cDNA libraries of Ralstonia solanacearum challenged roots, R. solanacearum challenged leaves, and unchallenged cultured peanut roots, leaves and developing seeds. Among these ESTs, there were 14,547 unique sequences with 7,961 tentative consensus sequences and 6,586 singletons. Putative functions for 47.8 % of the sequences were identified, including transcription factors, tissue-specific genes, genes involved in fatty acid biosynthesis and oil formation regulation, and resistance gene analogue genes. Additionally, differentially expressed genes, including those involved in ethylene and jasmonic acid signal transduction pathways, from both peanut leaves and roots, were identified in R. solanacearum challenged samples. This large expression dataset from different peanut tissues will be a valuable source for marker development and gene expression analysis. It will also be helpful for finding candidate genes for fatty acid synthesis and oil formation regulation as well as for studying mechanisms of interactions between the peanut host and R. solanacearum pathogen.

摘要

虽然花生是一种重要的油料作物,但仅有 162030 条公开的花生表达序列标签(EST),其中 86943 条来自栽培植物。为了分离出具有抗逆性、组织特异性和发育重要性的基因,需要更多来自栽培花生的 EST。在此,我们从接种青枯菌的花生根、叶片以及未接种的培养花生根、叶片和发育种子的 5 个 cDNA 文库中生成了 63234 条 EST。这些 EST 中,有 14547 条独特序列,7961 条推测的一致序列和 6586 条单序列。47.8%的序列具有推测的功能,包括转录因子、组织特异性基因、参与脂肪酸生物合成和油脂形成调控的基因以及抗病基因类似物基因。此外,在接种青枯菌的花生叶片和根部样本中,还鉴定到了包括乙烯和茉莉酸信号转导途径相关基因在内的差异表达基因。该研究从不同的花生组织中获得了大量的表达数据集,这将成为标记开发和基因表达分析的宝贵资源。它还有助于发现脂肪酸合成和油脂形成调控的候选基因,并研究花生宿主与青枯菌病原体相互作用的机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验