Literature DB >> 17455763

Cold shock proteins aid coupling of transcription and translation in bacteria.

Walid M El-Sharoud1, Peter L Graumann.   

Abstract

Transcription and translation are tightly coupled in bacterial cells. However, the transcription machinery and ribosomes generally occupy different subcellular regions in bacteria such as Escherichia coli and Bacillus subtilis, indicating the need for (a) mechanism(s) coupling these processes. A prime function of this mechanism(s) would be ensuring the transfer of unfolded mRNA from the nucleoid to ribosomes, which require linear mRNA for the initiation of translation. During conditions of a sudden decrease in temperature (cold shock), secondary structures in mRNA would pose an even greater problem for the initiation process. Two conserved classes of proteins, cold shock proteins (CSPs) and cold induced RNA helicases (CSHs), appear to be major players in the prevention of secondary mRNA structures and in transcription/translation coupling. CSPs are general mRNA-binding proteins, and like CSH-type RNA helicases, the presence of at least one csp gene in the cell is essential for viability. Members of both protein families have recently been shown to interact, suggesting that a two-step process achieves the coupling process, removal of secondary mRNA structures through CSHs and prevention of reformation through CSPs.

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Year:  2007        PMID: 17455763     DOI: 10.3184/003685007780440549

Source DB:  PubMed          Journal:  Sci Prog        ISSN: 0036-8504            Impact factor:   2.774


  13 in total

1.  Bacterial RNA chaperones confer abiotic stress tolerance in plants and improved grain yield in maize under water-limited conditions.

Authors:  Paolo Castiglioni; Dave Warner; Robert J Bensen; Don C Anstrom; Jay Harrison; Martin Stoecker; Mark Abad; Ganesh Kumar; Sara Salvador; Robert D'Ordine; Santiago Navarro; Stephanie Back; Mary Fernandes; Jayaprakash Targolli; Santanu Dasgupta; Christopher Bonin; Michael H Luethy; Jacqueline E Heard
Journal:  Plant Physiol       Date:  2008-06       Impact factor: 8.340

Review 2.  Microbial thermosensors.

Authors:  Birgit Klinkert; Franz Narberhaus
Journal:  Cell Mol Life Sci       Date:  2009-05-12       Impact factor: 9.261

3.  Spatially segregated transcription and translation in cells of the endomembrane-containing bacterium Gemmata obscuriglobus.

Authors:  Ekaterina Y Gottshall; Corrine Seebart; Jesse C Gatlin; Naomi L Ward
Journal:  Proc Natl Acad Sci U S A       Date:  2014-07-14       Impact factor: 11.205

4.  Superresolution imaging of ribosomes and RNA polymerase in live Escherichia coli cells.

Authors:  Somenath Bakshi; Albert Siryaporn; Mark Goulian; James C Weisshaar
Journal:  Mol Microbiol       Date:  2012-05-24       Impact factor: 3.501

5.  Sequence features of E. coli mRNAs affect their degradation.

Authors:  Gal Lenz; Adi Doron-Faigenboim; Eliora Z Ron; Tamir Tuller; Uri Gophna
Journal:  PLoS One       Date:  2011-12-07       Impact factor: 3.240

6.  "Genes".

Authors:  Sonja J Prohaska; Peter F Stadler
Journal:  Theory Biosci       Date:  2008-03-05       Impact factor: 1.919

Review 7.  Bacterial stressors in minimally processed food.

Authors:  Vittorio Capozzi; Daniela Fiocco; Maria Luisa Amodio; Anna Gallone; Giuseppe Spano
Journal:  Int J Mol Sci       Date:  2009-07-08       Impact factor: 6.208

8.  Transcriptome and proteome exploration to model translation efficiency and protein stability in Lactococcus lactis.

Authors:  Clémentine Dressaire; Christophe Gitton; Pascal Loubière; Véronique Monnet; Isabelle Queinnec; Muriel Cocaign-Bousquet
Journal:  PLoS Comput Biol       Date:  2009-12-18       Impact factor: 4.475

Review 9.  RNA helicases: diverse roles in prokaryotic response to abiotic stress.

Authors:  George W Owttrim
Journal:  RNA Biol       Date:  2012-10-23       Impact factor: 4.652

Review 10.  Initiation of mRNA decay in bacteria.

Authors:  Soumaya Laalami; Léna Zig; Harald Putzer
Journal:  Cell Mol Life Sci       Date:  2013-09-25       Impact factor: 9.261

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