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通过对7653R进行比较分析对基因间小RNA进行全基因组预测与鉴定

A Genome-Wide Prediction and Identification of Intergenic Small RNAs by Comparative Analysis in 7653R.

作者信息

Fuli Xie, Wenlong Zhao, Xiao Wang, Jing Zhang, Baohai Hao, Zhengzheng Zou, Bin-Guang Ma, Youguo Li

机构信息

State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural UniversityWuhan, China.

出版信息

Front Microbiol. 2017 Sep 8;8:1730. doi: 10.3389/fmicb.2017.01730. eCollection 2017.

Abstract

In bacteria, small non-coding RNAs (sRNAs) are critical regulators of cellular adaptation to changes in metabolism, physiology, or the external environment. In the last decade, more than 2000 of sRNA families have been reported in the Rfam database and have been shown to exert various regulatory functions in bacterial transcription and translation. However, little is known about sRNAs and their functions in . Here, we predicted putative sRNAs in the intergenic regions (IGRs) of 7653R by genome-wide comparisons with four related Mesorhizobial strains. The expression and transcribed regions of candidate sRNAs were analyzed using a set of high-throughput RNA deep sequencing data. In all, 39 candidate sRNAs were found, with 5 located in the symbiotic megaplasmids and 34 in the chromosome of 7653R. Of these, 24 were annotated as functional sRNAs in the Rfam database and 15 were recognized as putative novel sRNAs. The expression of nine selected sRNAs was confirmed by Northern blotting, and most of the nine selected sRNAs were highly expressed in 28 dpi nodules and under symbiosis-mimicking conditions. For those putative novel sRNAs, functional categorizations of their target genes were performed by analyzing the enriched GO terms. In addition, MH_s15 was shown to be an abundant and conserved sRNA.

摘要

在细菌中,小非编码RNA(sRNA)是细胞适应代谢、生理或外部环境变化的关键调节因子。在过去十年中,Rfam数据库已报道了2000多个sRNA家族,并已证明它们在细菌转录和翻译中发挥各种调节功能。然而,关于sRNA及其在[此处原文缺失相关内容]中的功能却知之甚少。在这里,我们通过与四种相关的中生根瘤菌菌株进行全基因组比较,预测了7653R基因间区域(IGR)中的假定sRNA。使用一组高通量RNA深度测序数据分析了候选sRNA的表达和转录区域。总共发现了39个候选sRNA,其中5个位于共生大质粒中,34个位于7653R的染色体中。其中,24个在Rfam数据库中被注释为功能性sRNA,15个被认为是假定的新型sRNA。通过Northern印迹法证实了9个选定sRNA的表达,并且这9个选定sRNA中的大多数在接种后28天的根瘤中和在模拟共生条件下高表达。对于那些假定的新型sRNA,通过分析富集的GO术语对其靶基因进行功能分类。此外,MH_s15被证明是一种丰富且保守的sRNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c1d/5596092/90c232deb038/fmicb-08-01730-g0001.jpg

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