...
首页> 外文期刊>Nucleic Acids Research >Interplay between the catabolite repression control protein Crc, Hfq and RNA in Hfq-dependent translational regulation in Pseudomonas aeruginosa
【24h】

Interplay between the catabolite repression control protein Crc, Hfq and RNA in Hfq-dependent translational regulation in Pseudomonas aeruginosa

机译:在Pseudomonas Aeruginosa的HFQ依赖性转化调节中相互作用。

获取原文
获取原文并翻译 | 示例
           

摘要

In Pseudomonas aeruginosa the RNA chaperone Hfq and the catabolite repression control protein (Crc) act as post-transcriptional regulators during carbon catabolite repression (CCR). In this regard Crc is required for full-fledged Hfq-mediated translational repression of catabolic genes. RNAseq based transcriptome analyses revealed a significant overlap between the Crc and Hfq regulons, which in conjunction with genetic data supported a concerted action of both proteins. Biochemical and biophysical approaches further suggest that Crc and Hfq form an assembly in the presence of RNAs containing A-rich motifs, and that Crc interacts with both, Hfq and RNA. Through these interactions, Crc enhances the stability of Hfq/Crc/RNA complexes, which can explain its facilitating role in Hfq-mediated translational repression. Hence, these studies revealed for the first time insights into how an interacting protein can modulate Hfq function. Moreover, Crc is shown to interfere with binding of a regulatory RNA to Hfq, which bears implications for riboregulation. These results are discussed in terms of a working model, wherein Crc prioritizes the function of Hfq toward utilization of favored carbon sources.
机译:在假单胞菌铜绿假单胞菌中,RNA伴侣HFQ和分解代谢抑制控制蛋白(CRC)在碳分子抑制期间作为转录后调节剂(CCR)。在这方面,CRC是针对分解代谢基因的全替代HFQ介导的翻译抑制所必需的。基于RNASEQ的转录组分析显示CRC和HFQ调节件之间的显着重叠,其与遗传数据结合支持两种蛋白质的一致作用。生物化学和生物物理方法进一步表明CRC和HFQ在含有富含族基序的RNA存在下形成组件,并且CRC与两者,HFQ和RNA相互作用。通过这些相互作用,CRC增强了HFQ / CRC / RNA配合物的稳定性,其可以解释其在HFQ介导的翻译抑制中的作用。因此,这些研究表明,第一次见解互动蛋白质如何调节HFQ功能。此外,CRC被示出干扰调节RNA对HFQ的结合,这对核来调节有影响。这些结果是根据工作模型讨论的,其中CRC优先考虑HFQ对有利碳源的利用的功能。

著录项

  • 来源
    《Nucleic Acids Research》 |2018年第3期|共16页
  • 作者单位

    Univ Vienna Dept Microbiol Immunobiol &

    Genet Max F Perutz Labs Vienna Bioctr Dr Bohrgasse 9 A-1030 Vienna Austria;

    Max Planck Inst Biophys Chem Biophys Mass Spectrometry Grp D-37077 Gottingen Germany;

    Swiss Fed Inst Technol Inst Mol Biol &

    Biophys CH-8093 Zurich Switzerland;

    Univ Vienna Inst Theoret Chem A-1090 Vienna Austria;

    Univ Vienna Dept Microbiol Immunobiol &

    Genet Max F Perutz Labs Vienna Bioctr Dr Bohrgasse 9 A-1030 Vienna Austria;

    Univ Vienna Dept Microbiol Immunobiol &

    Genet Max F Perutz Labs Vienna Bioctr Dr Bohrgasse 9 A-1030 Vienna Austria;

    Univ Lausanne Dept Fundamental Microbiol CH-1015 Lausanne Switzerland;

    Univ Vienna Dept Microbiol Immunobiol &

    Genet Max F Perutz Labs Vienna Bioctr Dr Bohrgasse 9 A-1030 Vienna Austria;

    Swiss Fed Inst Technol Inst Mol Biol &

    Biophys CH-8093 Zurich Switzerland;

    Univ Cambridge Dept Biochem Cambridge CB2 1GA England;

    Max Planck Inst Biophys Chem Biophys Mass Spectrometry Grp D-37077 Gottingen Germany;

    Univ Vienna Dept Microbiol Immunobiol &

    Genet Max F Perutz Labs Vienna Bioctr Dr Bohrgasse 9 A-1030 Vienna Austria;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号