Literature DB >> 19161845

Preparation of the Escherichia coli RNase E protein and reconstitution of the RNA degradosome.

George A Mackie1, Glen A Coburn, Xin Miao, Douglas J Briant, Annie Prud'homme-Généreux, Leigh M Stickney, Janet S Hankins.   

Abstract

The RNA degradosome is a multienzyme complex that plays a key role in the processing of stable RNAs, the degradation of mRNAs, and the action of small regulatory RNAs. Initially discovered in Escherichia coli, similar or related complexes are found in other bacteria. The core of the RNA degradosome is the essential endoribonuclease, RNase E. The C-terminus of this enzyme serves as a scaffold to which other components of the RNA degradosome bind. These ligands include the phosphorolytic 3'-exonuclease, polynucleotide phosphorylase, the DEAD-box RNA helicase, RhlB, and the glycolytic enzyme, enolase. In addition, the DEAD-box RNA helicases CsdA and RhlE and the RNA binding protein, Hfq, may bind to RNase E in place of one or more of the prototypical components. This chapter describes purification of RNase E (the Rne protein), reconstitution of a minimal degradosome that recapitulates the activity of authentic degradosomes, and methods for the assay of the reconstituted complex.

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Year:  2008        PMID: 19161845     DOI: 10.1016/S0076-6879(08)02211-8

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  2 in total

1.  The important conformational plasticity of DsrA sRNA for adapting multiple target regulation.

Authors:  Pengzhi Wu; Xiaodan Liu; Lingna Yang; Yitong Sun; Qingguo Gong; Jihui Wu; Yunyu Shi
Journal:  Nucleic Acids Res       Date:  2017-09-19       Impact factor: 16.971

2.  Recognition of the 70S ribosome and polysome by the RNA degradosome in Escherichia coli.

Authors:  Yi-Chun Tsai; Dijun Du; Lilianha Domínguez-Malfavón; Daniela Dimastrogiovanni; Jonathan Cross; Anastasia J Callaghan; Jaime García-Mena; Ben F Luisi
Journal:  Nucleic Acids Res       Date:  2012-08-25       Impact factor: 16.971

  2 in total

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