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The C-terminal tail of the yeast mitochondrial transcription factor Mtf1 coordinates template strand alignment, DNA scrunching and timely transition into elongation.
Basu, Urmimala; Lee, Seung-Won; Deshpande, Aishwarya; Shen, Jiayu; Sohn, Byeong-Kwon; Cho, Hayoon; Kim, Hajin; Patel, Smita S.
Afiliação
  • Basu U; Department of Biochemistry and Molecular Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
  • Lee SW; Graduate School of Biomedical Sciences at Robert Wood Johnson Medical School of the Rutgers University, USA.
  • Deshpande A; School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
  • Shen J; Department of Biochemistry and Molecular Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
  • Sohn BK; Department of Biochemistry and Molecular Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
  • Cho H; Graduate School of Biomedical Sciences at Robert Wood Johnson Medical School of the Rutgers University, USA.
  • Kim H; School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
  • Patel SS; School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
Nucleic Acids Res ; 48(5): 2604-2620, 2020 03 18.
Article em En | MEDLINE | ID: mdl-31980825
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Moldes Genéticos / Fatores de Transcrição / DNA Fúngico / Proteínas de Saccharomyces cerevisiae / Proteínas Mitocondriais / Elongação da Transcrição Genética Tipo de estudo: Health_economic_evaluation Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Moldes Genéticos / Fatores de Transcrição / DNA Fúngico / Proteínas de Saccharomyces cerevisiae / Proteínas Mitocondriais / Elongação da Transcrição Genética Tipo de estudo: Health_economic_evaluation Idioma: En Ano de publicação: 2020 Tipo de documento: Article