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Structure paper

TitleStructural basis of exoribonuclease-mediated mRNA transcription termination.
Journal, issue, pagesNature, Year 2024
Publish dateMar 27, 2024
AuthorsYuan Zeng / Hong-Wei Zhang / Xiao-Xian Wu / Yu Zhang /
PubMed AbstractEfficient termination is required for robust gene transcription. Eukaryotic organisms use a conserved exoribonuclease-mediated mechanism to terminate the mRNA transcription by RNA polymerase II ...Efficient termination is required for robust gene transcription. Eukaryotic organisms use a conserved exoribonuclease-mediated mechanism to terminate the mRNA transcription by RNA polymerase II (Pol II). Here we report two cryogenic electron microscopy structures of Saccharomyces cerevisiae Pol II pre-termination transcription complexes bound to the 5'-to-3' exoribonuclease Rat1 and its partner Rai1. Our structures show that Rat1 displaces the elongation factor Spt5 to dock at the Pol II stalk domain. Rat1 shields the RNA exit channel of Pol II, guides the nascent RNA towards its active centre and stacks three nucleotides at the 5' terminus of the nascent RNA. The structures further show that Rat1 rotates towards Pol II as it shortens RNA. Our results provide the structural mechanism for the Rat1-mediated termination of mRNA transcription by Pol II in yeast and the exoribonuclease-mediated termination of mRNA transcription in other eukaryotes.
External linksNature / PubMed:38538796
MethodsEM (single particle)
Resolution2.7 - 2.8 Å
Structure data

EMDB-36162, PDB-8jch:
Cryo-EM structure of yeast Rat1-bound Pol II pre-termination transcription complex 1 (Pol II Rat1-PTTC1)
Method: EM (single particle) / Resolution: 2.7 Å

EMDB-36908, PDB-8k5p:
Cryo-EM structure of yeast Rat1-bound Pol II pre-termination transcription complex 2 (Pol II Rat1-PTTC2)
Method: EM (single particle) / Resolution: 2.8 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-MG:
Unknown entry

Source
  • saccharomyces cerevisiae s288c (yeast)
  • synthetic construct (others)
KeywordsTRANSCRIPTION / Transcription termination / Pol II / Rat1/Rai1 / Spt5 / Rat1/Rai1 Spt5

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