Literature DB >> 27215789

Cyanobacterial RNA Helicase CrhR Localizes to the Thylakoid Membrane Region and Cosediments with Degradosome and Polysome Complexes in Synechocystis sp. Strain PCC 6803.

Albert Remus R Rosana1, Denise S Whitford1, Richard P Fahlman2, George W Owttrim3.   

Abstract

UNLABELLED: The cyanobacterium Synechocystis sp. strain PCC 6803 encodes a single DEAD box RNA helicase, CrhR, whose expression is tightly autoregulated in response to cold stress. Subcellular localization and proteomic analysis results indicate that CrhR localizes to both the cytoplasmic and thylakoid membrane regions and cosediments with polysome and RNA degradosome components. Evidence is presented that either functional RNA helicase activity or a C-terminal localization signal was required for polysome but not thylakoid membrane localization. Polysome fractionation and runoff translation analysis results indicate that CrhR associates with actively translating polysomes. The data implicate a role for CrhR in translation or RNA degradation in the thylakoid region related to thylakoid biogenesis or stability, a role that is enhanced at low temperature. Furthermore, CrhR cosedimentation with polysome and RNA degradosome complexes links alteration of RNA secondary structure with a potential translation-RNA degradation complex in Synechocystis IMPORTANCE: The interaction between mRNA translation and degradation is a major determinant controlling gene expression. Regulation of RNA function by alteration of secondary structure by RNA helicases performs crucial roles, not only in both of these processes but also in all aspects of RNA metabolism. Here, we provide evidence that the cyanobacterial RNA helicase CrhR localizes to both the cytoplasmic and thylakoid membrane regions and cosediments with actively translating polysomes and RNA degradosome components. These findings link RNA helicase alteration of RNA secondary structure with translation and RNA degradation in prokaryotic systems and contribute to the data supporting the idea of the existence of a macromolecular machine catalyzing these reactions in prokaryotic systems, an association hitherto recognized only in archaea and eukarya.
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

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Year:  2016        PMID: 27215789      PMCID: PMC4944217          DOI: 10.1128/JB.00267-16

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  58 in total

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2.  A cold shock-induced cyanobacterial RNA helicase.

Authors:  D Chamot; W C Magee; E Yu; G W Owttrim
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3.  Polar-biased localization of the cold stress-induced RNA helicase, CrhC, in the Cyanobacterium Anabaena sp. strain PCC 7120.

Authors:  Bassam El-Fahmawi; George W Owttrim
Journal:  Mol Microbiol       Date:  2003-11       Impact factor: 3.501

4.  Post-transcriptional regulation of the psbA gene family in the cyanobacterium Synechococcus sp. PCC 7942.

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5.  Differential involvement of the five RNA helicases in adaptation of Bacillus cereus ATCC 14579 to low growth temperatures.

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6.  Magnetosomes are cell membrane invaginations organized by the actin-like protein MamK.

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7.  The small regulatory RNA SyR1/PsrR1 controls photosynthetic functions in cyanobacteria.

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8.  CsdA, a cold-shock RNA helicase from Escherichia coli, is involved in the biogenesis of 50S ribosomal subunit.

Authors:  Julie Charollais; Marc Dreyfus; Isabelle Iost
Journal:  Nucleic Acids Res       Date:  2004-05-17       Impact factor: 16.971

Review 9.  Cellular organization of the transfer of genetic information.

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10.  A minimal bacterial RNase J-based degradosome is associated with translating ribosomes.

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  6 in total

1.  RNA helicase-regulated processing of the Synechocystis rimO-crhR operon results in differential cistron expression and accumulation of two sRNAs.

Authors:  Albert Remus R Rosana; Denise S Whitford; Anzhela Migur; Claudia Steglich; Sonya L Kujat-Choy; Wolfgang R Hess; George W Owttrim
Journal:  J Biol Chem       Date:  2020-03-24       Impact factor: 5.157

Review 2.  Phase-separated bacterial ribonucleoprotein bodies organize mRNA decay.

Authors:  Nisansala S Muthunayake; Dylan T Tomares; W Seth Childers; Jared M Schrader
Journal:  Wiley Interdiscip Rev RNA       Date:  2020-05-23       Impact factor: 9.957

3.  Both Enolase and the DEAD-Box RNA Helicase CrhB Can Form Complexes with RNase E in Anabaena sp. Strain PCC 7120.

Authors:  Huaduo Yan; Xiuxiu Qin; Li Wang; Wenli Chen
Journal:  Appl Environ Microbiol       Date:  2020-06-17       Impact factor: 4.792

Review 4.  Bacterial RNA Degradosomes: Molecular Machines under Tight Control.

Authors:  Alejandro Tejada-Arranz; Valérie de Crécy-Lagard; Hilde de Reuse
Journal:  Trends Biochem Sci       Date:  2019-11-01       Impact factor: 13.807

Review 5.  RNA helicases in RNA decay.

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Journal:  Biochem Soc Trans       Date:  2018-01-19       Impact factor: 5.407

6.  Degron-mediated proteolysis of CrhR-like DEAD-box RNA helicases in cyanobacteria.

Authors:  Brendan T Whitman; Cameron R A Murray; Denise S Whitford; Simanta S Paul; Richard P Fahlman; Mark J N Glover; George W Owttrim
Journal:  J Biol Chem       Date:  2022-04-10       Impact factor: 5.486

  6 in total

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