RNA extension drives a stepwise displacement of an initiation-factor structural module in initial transcription.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
17 03 2020
Historique:
pubmed: 5 3 2020
medline: 4 7 2020
entrez: 5 3 2020
Statut: ppublish

Résumé

All organisms-bacteria, archaea, and eukaryotes-have a transcription initiation factor that contains a structural module that binds within the RNA polymerase (RNAP) active-center cleft and interacts with template-strand single-stranded DNA (ssDNA) in the immediate vicinity of the RNAP active center. This transcription initiation-factor structural module preorganizes template-strand ssDNA to engage the RNAP active center, thereby facilitating binding of initiating nucleotides and enabling transcription initiation from initiating mononucleotides. However, this transcription initiation-factor structural module occupies the path of nascent RNA and thus presumably must be displaced before or during initial transcription. Here, we report four sets of crystal structures of bacterial initially transcribing complexes that demonstrate and define details of stepwise, RNA-extension-driven displacement of the "σ-finger" of the bacterial transcription initiation factor σ. The structures reveal that-for both the primary σ-factor and extracytoplasmic (ECF) σ-factors, and for both 5'-triphosphate RNA and 5'-hydroxy RNA-the "σ-finger" is displaced in stepwise fashion, progressively folding back upon itself, driven by collision with the RNA 5'-end, upon extension of nascent RNA from ∼5 nt to ∼10 nt.

Identifiants

pubmed: 32127479
pii: 1920747117
doi: 10.1073/pnas.1920747117
pmc: PMC7084136
doi:

Substances chimiques

DNA, Single-Stranded 0
Escherichia coli Proteins 0
Sigma Factor 0
RNA 63231-63-0
DNA-Directed RNA Polymerases EC 2.7.7.6

Banques de données

PDB
['6LTS', '6KQD', '6KQE', '6KQF', '6KQG', '6KQH', '6L74', '6KQL', '6KQM', '6KQN', '6KON', '6KOO', '6KOP', '6KOQ', '6TYE', '6TYF', '6TYG']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5801-5809

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM041376
Pays : United States
Organisme : NIGMS NIH HHS
ID : R37 GM041376
Pays : United States

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Lingting Li (L)

Key Laboratory of Synthetic Biology, Chinese Academy of Sciences Center for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, 200032 Shanghai, China.
University of Chinese Academy of Sciences, 100049 Beijing, China.

Vadim Molodtsov (V)

Waksman Institute of Microbiology, Rutgers University, Piscataway, NJ 08854.
Department of Chemistry, Rutgers University, Piscataway, NJ 08854.

Wei Lin (W)

Waksman Institute of Microbiology, Rutgers University, Piscataway, NJ 08854.

Richard H Ebright (RH)

Waksman Institute of Microbiology, Rutgers University, Piscataway, NJ 08854; ebright@waksman.rutgers.edu yzhang@sippe.ac.cn.
Department of Chemistry, Rutgers University, Piscataway, NJ 08854.

Yu Zhang (Y)

Key Laboratory of Synthetic Biology, Chinese Academy of Sciences Center for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, 200032 Shanghai, China; ebright@waksman.rutgers.edu yzhang@sippe.ac.cn.
Waksman Institute of Microbiology, Rutgers University, Piscataway, NJ 08854.
Department of Chemistry, Rutgers University, Piscataway, NJ 08854.

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