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作 者:鲁琳[1] 杨尚谕 刘维东[1] 鲁黎明[2] LU Lin;YANG Shang-yu;LIU Wei-dong;LU Li-ming(College of Landscape Architecture,Sichuan Agricultural University,Chengdu 611130;College of Agronomy,Sichuan Agricultural University,Chengdu 611130)
机构地区:[1]四川农业大学风景园林学院,成都611130 [2]四川农业大学农学院,成都611130
出 处:《生物技术通报》2020年第12期42-53,共12页Biotechnology Bulletin
基 金:四川省教育厅科技项目(12ZA272)。
摘 要:为了鉴定参与花烟草盐胁迫响应的活性氧清除相关基因,用200 mmol/L NaCl处理花烟草幼苗,并在处理后12 h采集其幼苗样本,提取总RNA,采用高通量测序技术,进行转录组测序。基于差异表达基因GO及KEGG分析的基础上,对参与其中的活性氧清除基因进行挖掘,利用qRT-PCR的方法验证转录组测序结果。结果表明,盐处理后,花烟草基因表达量变化在2倍以上的基因有7239个(P<0.01),其中,上调表达基因4037个,下调表达基因3162个,将其功能归类于生物过程、细胞组分及分子功能三大类159个GO条目,并显著富集在12条KEGG代谢通路中。同时,在盐胁迫下,花烟草有45个活性氧清除相关基因的表达发生了显著改变,其中,上调表达基因28个,下调表达基因17个。此结果说明,活性氧的清除是花烟草抵御盐胁迫的重要机制之一。In order to identify the genes related to reactive oxygen species(ROS)scavenging involved in salt stress response of Nicotiana tabacum seedlings,tobacco plants were treated with 200 mmol/L NaCl,and the samples of the seedlings were collected at 12 h after the treatment.After total RNA was extracted,high-throughput sequencing technology was carried out to sequence the transcriptome.On the basis of GO and KEGG analysis of the differentially expressed genes,ROS scavenging genes involved were mined,and the results of transcriptome sequencing were verified by qRT-PCR.The results showed that there were 7239 genes(P<0.01)with more than two-fold in the expression of tobacco genes after high salt treatment,among which 4037 genes were up-regulated and 3162 genes were down-regulated.The functions of these differentially expressed genes were classified into 159 GO items in three categories:biological process,cell components and molecular functions,and were significantly enriched in 12 KEGG metabolic pathways.Meanwhile,the expressions of 45 genes related to ROS scavenging processes changed significantly in tobacco plants under high salt stress,among which 28 genes were up-regulated and 17 genes were down-regulated.The results of this study suggest that the enhanced ROS scavenging ability could be one of the essential mechanisms of N.alata plants in response to salt stress.
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