RIP-seq reveals RNAs that interact with RNA polymerase and primary sigma factors in bacteria.
Journal
Nucleic acids research
ISSN: 1362-4962
Titre abrégé: Nucleic Acids Res
Pays: England
ID NLM: 0411011
Informations de publication
Date de publication:
13 Feb 2024
13 Feb 2024
Historique:
accepted:
29
01
2024
revised:
24
01
2024
received:
21
07
2023
medline:
13
2
2024
pubmed:
13
2
2024
entrez:
13
2
2024
Statut:
aheadofprint
Résumé
Bacteria have evolved structured RNAs that can associate with RNA polymerase (RNAP). Two of them have been known so far-6S RNA and Ms1 RNA but it is unclear if any other types of RNAs binding to RNAP exist in bacteria. To identify all RNAs interacting with RNAP and the primary σ factors, we have established and performed native RIP-seq in Bacillus subtilis, Corynebacterium glutamicum, Streptomyces coelicolor, Mycobacterium smegmatis and the pathogenic Mycobacterium tuberculosis. Besides known 6S RNAs in B. subtilis and Ms1 in M. smegmatis, we detected MTS2823, a homologue of Ms1, on RNAP in M. tuberculosis. In C. glutamicum, we discovered novel types of structured RNAs that associate with RNAP. Furthermore, we identified other species-specific RNAs including full-length mRNAs, revealing a previously unknown landscape of RNAs interacting with the bacterial transcription machinery.
Identifiants
pubmed: 38348908
pii: 7606967
doi: 10.1093/nar/gkae081
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Czech Science Foundation
ID : 20-07473S
Organisme : Charles University
ID : 275823
Organisme : European Union - Next Generation EU, National Institute of Virology and Bacteriology
ID : EXCELES LX22NPO5103
Organisme : Ministry of Education
ID : LM2023055
Organisme : European Regional Development Fund
ID : CZ.02.1.01/0.0/0.0/18_046/0015974
Organisme : Ministry of Defense
ID : 907930101413
Organisme : Charles University
ID : SVV 260679
Organisme : Czech Academy of Sciences
Informations de copyright
© The Author(s) 2024. Published by Oxford University Press on behalf of Nucleic Acids Research.