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Transcriptomic Analysis Identifies New Non-Target Site Glyphosate-Resistance Genes in Conyza bonariensis

机译:转录组学分析确定了新的非目标站点草甘蓝抗草甘膦抗性基因。

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摘要

Conyza bonariensis (hairy fleabane) is one of the most problematic and widespread glyphosate-resistant weeds in the world. This highly competitive weed species significantly interferes with crop growth and substantially decreases crop yield. Despite its agricultural importance, the molecular mechanisms of glyphosate resistance are still unknown. The present RNA-Seq study was performed with the goal of identifying differentially expressed candidate transcripts (genes) related to metabolism-based non-target site glyphosate resistance in C. bonariensis. The whole-transcriptome was de novo assembled from glyphosate-resistant and -sensitive biotypes of C. bonariensis from Southern Brazil. The RNA was extracted from untreated and glyphosate-treated plants at several timepoints up to 288 h after treatment in both biotypes. The transcriptome assembly produced 90,124 contigs with an average length of 777 bp and N50 of 1118 bp. In response to glyphosate treatment, differential gene expression analysis was performed on glyphosate-resistant and -sensitive biotypes. A total of 9622 genes were differentially expressed as a response to glyphosate treatment in both biotypes, 4297 (44.6%) being up- and 5325 (55.4%) down-regulated. The resistant biotype presented 1770 up- and 2333 down-regulated genes while the sensitive biotype had 2335 and 2800 up- and down-regulated genes, respectively. Among them, 974 up- and 1290 down-regulated genes were co-expressed in both biotypes. In the present work, we identified 41 new candidate target genes from five families related to herbicide transport and metabolism: 19 ABC transporters, 10 CYP450s, one glutathione S-transferase (GST), five glycosyltransferases (GT), and six genes related to antioxidant enzyme catalase (CAT), peroxidase (POD), and superoxide dismutase (SOD). The candidate genes may participate in metabolic-based glyphosate resistance via oxidation, conjugation, transport, and degradation, plus antioxidation. One or more of these genes might ‘rescue’ resistant plants from irreversible damage after glyphosate treatment. The 41 target genes we report in the present study may inform further functional genomics studies, including gene editing approaches to elucidate glyphosate-resistance mechanisms in C. bonariensis.
机译:Conyza bonariensis(有毛的fleabane)是世界上最成问题且分布最广的抗草甘膦杂草之一。这种竞争激烈的杂草物种极大地干扰了作物的生长,并大大降低了作物的产量。尽管其具有农业重要性,但抗草甘膦的分子机制仍然未知。进行本RNA-Seq研究的目的是鉴定与Bonariensis C.中基于代谢的非靶位点草甘膦抗性相关的差异表达候选转录本(基因)。整个转录组是从巴西南部的抗草甘膦和敏感的C. bonariensis生物型组装而成的。在两种生物型中,在处理后直至288小时的几个时间点都从未经处理和草甘膦处理过的植物中提取RNA。转录组装配产生90,124个重叠群,平均长度为777 bp,N50为1118 bp。响应于草甘膦处理,对草甘膦抗性和敏感性生物型进行了差异基因表达分析。在两种生物型中,总共有9622个基因被差异表达为对草甘膦处理的响应,其中4297个(44.6%)被上调,而5325个(55.4%)被下调。抗性生物型呈现1770个上调和2333个下调的基因,而敏感生物型分别具有2335和2800个上调和下调的基因。其中,在两种生物型中共表达974个上调基因和1290个下调基因。在目前的工作中,我们从五个与除草剂运输和代谢相关的家族中鉴定了41个新的候选目标基因:19个ABC转运蛋白,10个CYP450,一个谷胱甘肽S-转移酶(GST),五个糖基转移酶(GT)和六个与抗氧化剂相关的基因酶过氧化氢酶(CAT),过氧化物酶(POD)和超氧化物歧化酶(SOD)。候选基因可以通过氧化,结合,转运和降解以及抗氧化作用参与基于代谢的草甘膦抗性。这些基因中的一个或多个可能会在草甘膦处理后“挽救”抗性植物免受不可逆转的伤害。我们在本研究中报告的41个靶基因可能会为进一步的功能基因组学研究提供信息,包括阐明bonariensis的草甘膦抗性机制的基因编辑方法。

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