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在苜蓿中华根瘤菌2011中,小调控RNA基因mmgR的表达受到AniA的负调控和NtrC的正调控。

Expression of the small regulatory RNA gene mmgR is regulated negatively by AniA and positively by NtrC in Sinorhizobium meliloti 2011.

作者信息

Ceizel Borella Germán, Lagares Antonio, Valverde Claudio

机构信息

Laboratorio de Bioquímica, Microbiología e Interacciones Biológicas en el Suelo, Departamento de Ciencia y Tecnología, Universidad Nacional de Quilmes - CONICET, Roque Sáenz Peña 352 - Bernal B1876BXD - Buenos Aires, Argentina.

出版信息

Microbiology (Reading). 2018 Jan;164(1):88-98. doi: 10.1099/mic.0.000586. Epub 2017 Dec 7.

Abstract

In the N2-fixing symbiont of alfalfa root nodules, Sinorhizobium meliloti 2011, the mmgR gene encodes a 77 nt small untranslated RNA (sRNA) that negatively regulates the accumulation of polyhydroxybutyrate (PHB) when the bacterium is grown under conditions of surplus carbon (C) in relation to nitrogen (N). We previously showed that the expression of mmgR is primarily controlled at the transcriptional level and that it depends on the cellular N status, although the regulatory mechanism and the factors involved were unknown. In this study, we provide experimental data supporting that: (a) mmgR is induced upon N limitation with the maximum expression found at the highest tested C/N molar ratio in the growth medium; (b) a conserved heptamer TTGTGCA located between the -35 and -10 mmgR promoter elements is necessary and sufficient for induction by N limitation; (c) induction of mmgR requires the N-status regulator NtrC; (d) under C limitation, mmgR transcription is repressed by AniA, a global regulator of C flow; (e) the mmgR promoter contains a conserved dyadic motif (TGC[N3]GCA) partially overlapping the heptamer TTGTGCA, which was also found in the promoters of the PHB-related genes phaP1, phaP2, phaZ and phaR (aniA) of S. meliloti and other alpha-proteobacteria. Taken together, these results suggest that the mmgR promoter would integrate signals from the metabolism of C and N through - at least - the global regulators NtrC and AniA, to provide an optimal level of the MmgR sRNA to fine-tune gene expression post-transcriptionally according to varying C and N availability.

摘要

在紫花苜蓿根瘤的固氮共生菌苜蓿中华根瘤菌2011中,mmgR基因编码一种77个核苷酸的小非编码RNA(sRNA),当细菌在碳(C)相对于氮(N)过剩的条件下生长时,该RNA负向调节聚羟基丁酸酯(PHB)的积累。我们之前表明,mmgR的表达主要在转录水平受到控制,并且它取决于细胞的氮状态,尽管其调控机制和涉及的因子尚不清楚。在本研究中,我们提供的实验数据支持以下几点:(a)mmgR在氮限制时被诱导,在生长培养基中测试的最高碳/氮摩尔比下表达量最高;(b)位于mmgR启动子元件的-35和-10之间的保守七聚体TTGTGCA对于氮限制诱导是必需且充分的;(c)mmgR的诱导需要氮状态调节因子NtrC;(d)在碳限制下,mmgR转录受到碳流全局调节因子AniA的抑制;(e)mmgR启动子包含一个保守的二元基序(TGC[N3]GCA),部分与七聚体TTGTGCA重叠,该基序也存在于苜蓿中华根瘤菌和其他α-变形菌的PHB相关基因phaP1、phaP2、phaZ和phaR(aniA)的启动子中。综上所述,这些结果表明,mmgR启动子将通过至少全局调节因子NtrC和AniA整合来自碳和氮代谢的信号,以提供最佳水平的MmgR sRNA,从而根据碳和氮的可用性在转录后微调基因表达。

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