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利用 RNA 测序数据分析盐胁迫下孢子生长中 tRNA 的加工。

Analysis of tRNA processing under salt stress in spore outgrowth using RNA sequencing data.

机构信息

Facultad de Química, Universidad Autónoma de Querétaro, Cerro de las Campanas S/N, Querétaro, Qro., 76010, Mexico.

Laboratorio de Bioseguridad y Análisis de Riesgo, Departamento de Ingeniería Genética, Centro de Investigación y de Estudios Avanzados del IPN, Irapuato, Guanajuato, 36824, Mexico.

出版信息

F1000Res. 2020 Jun 3;9:501. doi: 10.12688/f1000research.23780.1. eCollection 2020.

Abstract

In spore-forming bacteria, the molecular mechanisms of accumulation of transfer RNA (tRNA) during sporulation must be a priority as tRNAs play an essential role in protein synthesis during spore germination and outgrowth. However, tRNA processing has not been extensively studied in these conditions, and knowledge of these mechanisms is important to understand long-term stress survival.    To gain further insight into tRNA processing during spore germination and outgrowth, the expression of the single copy tRNA gene was analyzed in the presence and absence of 1.2 M NaCl in using RNA-Seq data obtained from the Gene Expression Omnibus (GEO) database. The CLC Genomics work bench 12.0.2 (CLC Bio, Aarhus, Denmark, https://www.qiagenbioinformatics.com/) was used to analyze reads from the tRNA gene.  The results show that spores store different populations of tRNA -related molecules.  One such population, representing 60% of total tRNA , was composed of tRNA fragments.  Half of these fragments (3´-tRF) possessed CC, CCA or incorrect additions at the 3´end. tRNA with correct CCA addition at the 3´end represented 23% of total tRNA , while with CC addition represented 9% of the total and with incorrect addition represented 7%. While an accumulation of tRNA precursors was induced by upregulation of the operon under the control of  σ -dependent promoters under both conditions investigated, salt stress produced only a modest effect on tRNA expression and the accumulation of tRNA related species. :The results demonstrate that tRNA molecules resident in spores undergo dynamic processing to produce functional molecules that may play an essential role during protein synthesis.

摘要

在产芽孢细菌中,积累转移 RNA(tRNA)的分子机制在芽孢形成期间必须是优先考虑的,因为 tRNA 在芽孢萌发和生长过程中的蛋白质合成中发挥着至关重要的作用。然而,在这些条件下,tRNA 的加工尚未得到广泛研究,而了解这些机制对于理解长期应激生存是很重要的。为了更深入地了解 tRNA 在芽孢萌发和生长过程中的加工,分析了在存在和不存在 1.2 M NaCl 的情况下,单个拷贝 tRNA 基因的表达,使用了来自基因表达综合数据库(GEO)的 RNA-Seq 数据。CLC Genomics 工作平台 12.0.2(CLC Bio,丹麦奥胡斯,https://www.qiagenbioinformatics.com/)用于分析来自 tRNA 基因的读段。结果表明,芽孢储存了不同的 tRNA 相关分子群体。其中一个群体代表总 tRNA 的 60%,由 tRNA 片段组成。这些片段的一半(3´-tRF)在 3´末端具有 CC、CCA 或不正确的添加。具有正确的 3´末端 CCA 添加的 tRNA 占总 tRNA 的 23%,而具有 CC 添加的占总 tRNA 的 9%,具有不正确添加的占总 tRNA 的 7%。在两种研究条件下,在 σ 依赖启动子的控制下,操纵子的上调诱导了 tRNA 前体的积累,而盐胁迫对 tRNA 的表达和 tRNA 相关物种的积累只有适度的影响。结果表明,驻留在芽孢中的 tRNA 分子经历动态加工,产生可能在蛋白质合成中发挥重要作用的功能分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d2a/8097732/ba5bf2b7de45/f1000research-9-26240-g0000.jpg

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