The C-terminal tail of the yeast mitochondrial transcription factor Mtf1 coordinates template strand alignment, DNA scrunching and timely transition into elongation.


Journal

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

Informations de publication

Date de publication:
18 03 2020
Historique:
accepted: 13 01 2020
revised: 20 12 2019
received: 27 11 2019
pubmed: 26 1 2020
medline: 19 5 2020
entrez: 26 1 2020
Statut: ppublish

Résumé

Mitochondrial RNA polymerases depend on initiation factors, such as TFB2M in humans and Mtf1 in yeast Saccharomyces cerevisiae, for promoter-specific transcription. These factors drive the melting of promoter DNA, but how they support RNA priming and growth was not understood. We show that the flexible C-terminal tails of Mtf1 and TFB2M play a crucial role in RNA priming by aiding template strand alignment in the active site for high-affinity binding of the initiating nucleotides. Using single-molecule fluorescence approaches, we show that the Mtf1 C-tail promotes RNA growth during initiation by stabilizing the scrunched DNA conformation. Additionally, due to its location in the path of the nascent RNA, the C-tail of Mtf1 serves as a sensor of the RNA-DNA hybrid length. Initially, steric clashes of the Mtf1 C-tail with short RNA-DNA hybrids cause abortive synthesis but clashes with longer RNA-DNA trigger conformational changes for the timely release of the promoter DNA to commence the transition into elongation. The remarkable similarities in the functions of the C-tail and σ3.2 finger of the bacterial factor suggest mechanistic convergence of a flexible element in the transcription initiation factor that engages the DNA template for RNA priming and growth and disengages when needed to generate the elongation complex.

Identifiants

pubmed: 31980825
pii: 5715817
doi: 10.1093/nar/gkaa040
pmc: PMC7049685
doi:

Substances chimiques

DNA, Fungal 0
MTF1 protein, S cerevisiae 0
Mitochondrial Proteins 0
Nucleotides 0
RNA, Fungal 0
Saccharomyces cerevisiae Proteins 0
Transcription Factors 0
Methyltransferases EC 2.1.1.-
TFB2M protein, human EC 2.1.1.-

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

2604-2620

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM118086
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.

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Auteurs

Urmimala Basu (U)

Department of Biochemistry and Molecular Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
Graduate School of Biomedical Sciences at Robert Wood Johnson Medical School of the Rutgers University, USA.

Seung-Won Lee (SW)

School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.

Aishwarya Deshpande (A)

Department of Biochemistry and Molecular Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.

Jiayu Shen (J)

Department of Biochemistry and Molecular Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
Graduate School of Biomedical Sciences at Robert Wood Johnson Medical School of the Rutgers University, USA.

Byeong-Kwon Sohn (BK)

School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.

Hayoon Cho (H)

School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.

Hajin Kim (H)

School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
Center for Genomic Integrity, Institute for Basic Science, Ulsan, Republic of Korea.

Smita S Patel (SS)

Department of Biochemistry and Molecular Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.

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