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对普通豆两个在共生固氮方面具有差异的重组自交系进行转录组分析。

Transcriptome analysis of two recombinant inbred lines of common bean contrasting for symbiotic nitrogen fixation.

作者信息

Kamfwa Kelvin, Zhao Dongyan, Kelly James D, Cichy Karen A

机构信息

Department of Plant Sciences, University of Zambia, Lusaka, Zambia.

Department of Plant Soil and Microbial Sciences, Michigan State University, East Lansing, Michigan, United States of America.

出版信息

PLoS One. 2017 Feb 13;12(2):e0172141. doi: 10.1371/journal.pone.0172141. eCollection 2017.

Abstract

Common bean (Phaseolus vulgaris L.) fixes atmospheric nitrogen (N2) through symbiotic nitrogen fixation (SNF) at levels lower than other grain legume crops. An understanding of the genes and molecular mechanisms underlying SNF will enable more effective strategies for the genetic improvement of SNF traits in common bean. In this study, transcriptome profiling was used to identify genes and molecular mechanisms underlying SNF differences between two common bean recombinant inbred lines that differed in their N-fixing abilities. Differential gene expression and functional enrichment analyses were performed on leaves, nodules and roots of the two lines when grown under N-fixing and non-fixing conditions. Receptor kinases, transmembrane transporters, and transcription factors were among the differentially expressed genes identified under N-fixing conditions, but not under non-fixing conditions. Genes up-regulated in the stronger nitrogen fixer, SA36, included those involved in molecular functions such as purine nucleoside binding, oxidoreductase and transmembrane receptor activities in nodules, and transport activity in roots. Transcription factors identified in this study are candidates for future work aimed at understanding the functional role of these genes in SNF. Information generated in this study will support the development of gene-based markers to accelerate genetic improvement of SNF in common bean.

摘要

普通菜豆(Phaseolus vulgaris L.)通过共生固氮作用(SNF)固定大气中的氮(N2),但其固氮水平低于其他豆类作物。了解SNF背后的基因和分子机制将有助于制定更有效的策略,对普通菜豆的SNF性状进行遗传改良。在本研究中,利用转录组分析来鉴定两个固氮能力不同的普通菜豆重组自交系之间SNF差异背后的基因和分子机制。对这两个品系在固氮和非固氮条件下生长时的叶片、根瘤和根系进行了差异基因表达和功能富集分析。受体激酶、跨膜转运蛋白和转录因子是在固氮条件下而非非固氮条件下鉴定出的差异表达基因。在固氮能力较强的SA36中上调的基因包括那些参与分子功能的基因,如在根瘤中的嘌呤核苷结合、氧化还原酶和跨膜受体活性,以及在根系中的转运活性。本研究中鉴定出的转录因子是未来旨在了解这些基因在SNF中功能作用的研究的候选对象。本研究产生的信息将支持基于基因的标记的开发,以加速普通菜豆SNF的遗传改良。

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