iRAPs curb antisense transcription in E. coli.


Journal

Nucleic acids research
ISSN: 1362-4962
Titre abrégé: Nucleic Acids Res
Pays: England
ID NLM: 0411011

Informations de publication

Date de publication:
18 11 2019
Historique:
accepted: 09 09 2019
revised: 03 09 2019
received: 09 05 2019
pubmed: 20 9 2019
medline: 13 5 2020
entrez: 20 9 2019
Statut: ppublish

Résumé

RNA polymerase-binding RNA aptamers (RAPs) are natural RNA elements that control transcription in cis by directly contacting RNA polymerase. Many RAPs inhibit transcription by inducing Rho-dependent termination in Escherichia coli. Here, we studied the role of inhibitory RAPs (iRAPs) in modulation of antisense transcription (AT) using in silico and in vivo approaches. We revisited the antisense transcriptome in cells with impaired AT regulators (Rho, H-NS and RNaseIII) and searched for the presence of RAPs within antisense RNAs. Many of these RAPs were found at key genomic positions where they terminate AT. By exploring the activity of several RAPs both in a reporter system and in their natural genomic context, we confirmed their significant role in AT regulation. RAPs coordinate Rho activity at the antisense strand and terminate antisense transcripts. In some cases, they stimulated sense expression by alleviating ongoing transcriptional interference. Essentially, our data postulate RAPs as key determinants of Rho-mediated AT regulation in E. coli.

Identifiants

pubmed: 31535128
pii: 5571581
doi: 10.1093/nar/gkz791
pmc: PMC6847712
doi:

Substances chimiques

Aptamers, Nucleotide 0
RNA, Antisense 0
DNA-Directed RNA Polymerases EC 2.7.7.6

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

10894-10905

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM126891
Pays : United States

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research.

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Auteurs

Andrés Magán (A)

Department of Biochemistry and Cell biology, Max F. Perutz Laboratories, University of Vienna, Vienna 1030, Austria.

Fabian Amman (F)

Department of Biochemistry and Cell biology, Max F. Perutz Laboratories, University of Vienna, Vienna 1030, Austria.
Institute for Theoretical Chemistry, University of Vienna, Vienna 1090, Austria.
Department of Cell and Developmental Biology, Center for Anatomy and Cell Biology, Medical University of Vienna, Vienna 1090, Austria.

Fatinah El-Isa (F)

Department of Biochemistry and Cell biology, Max F. Perutz Laboratories, University of Vienna, Vienna 1030, Austria.

Natascha Hartl (N)

Department of Biochemistry and Cell biology, Max F. Perutz Laboratories, University of Vienna, Vienna 1030, Austria.

Ilya Shamovsky (I)

Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA.

Evgeny Nudler (E)

Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA.
Howard Hughes Medical Institute, New York University School of Medicine, New York, NY 10016, USA.

Renée Schroeder (R)

Department of Biochemistry and Cell biology, Max F. Perutz Laboratories, University of Vienna, Vienna 1030, Austria.

Nadezda Sedlyarova (N)

Department of Biochemistry and Cell biology, Max F. Perutz Laboratories, University of Vienna, Vienna 1030, Austria.

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