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Structural insights into transcriptional regulation of human RNA polymerase III.
Wang, Qianmin; Li, Shaobai; Wan, Futang; Xu, Youwei; Wu, Zhenfang; Cao, Mi; Lan, Pengfei; Lei, Ming; Wu, Jian.
Afiliação
  • Wang Q; State Key Laboratory of Oncogenes and Related Genes, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Li S; Shanghai Institute of Precision Medicine, Shanghai, China.
  • Wan F; State Key Laboratory of Oncogenes and Related Genes, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Xu Y; Shanghai Institute of Precision Medicine, Shanghai, China.
  • Wu Z; State Key Laboratory of Oncogenes and Related Genes, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Cao M; Shanghai Institute of Precision Medicine, Shanghai, China.
  • Lan P; Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
  • Lei M; State Key Laboratory of Oncogenes and Related Genes, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Wu J; Shanghai Institute of Precision Medicine, Shanghai, China.
Nat Struct Mol Biol ; 28(2): 220-227, 2021 02.
Article em En | MEDLINE | ID: mdl-33558766
RNA polymerase III (Pol III) synthesizes structured, essential small RNAs, such as transfer RNA, 5S ribosomal RNA and U6 small nuclear RNA. Pol III, the largest nuclear RNA polymerase, is composed of a conserved core region and eight constitutive regulatory subunits, but how these factors jointly regulate Pol III transcription remains unclear. Here, we present cryo-EM structures of human Pol III in both apo and elongating states, which unveil both an orchestrated movement during the apo-to-elongating transition and an unexpected apo state in which the RPC7 subunit tail occupies the DNA-RNA-binding cleft of Pol III, suggesting that RPC7 plays important roles in both autoinhibition and transcription initiation. The structures also reveal a proofreading mechanism for the TFIIS-like subunit RPC10, which stably retains its catalytic position in the secondary channel, explaining the high fidelity of Pol III transcription. Our work provides an integrated picture of the mechanism of Pol III transcription regulation.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: RNA Polimerase III / Modelos Moleculares Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nat Struct Mol Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: RNA Polimerase III / Modelos Moleculares Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nat Struct Mol Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China