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Structural Basis of RNA Polymerase I Transcription Initiation
Author(s) -
Christoph Engel,
T. Gubbey,
Simon Neyer,
Sarah Sainsbury,
Christiane Oberthuer,
Carlo Baejen,
Carrie Bernecky,
Patrick Cramer
Publication year - 2017
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2017.03.003
Subject(s) - biology , rna polymerase ii , rna polymerase i , abortive initiation , transcription factor ii e , transcription bubble , transcription factor ii d , transcription (linguistics) , microbiology and biotechnology , polymerase , general transcription factor , rna polymerase , rna polymerase iii , transcription factor ii f , processivity , dna , promoter , rna , genetics , rna dependent rna polymerase , gene expression , gene , linguistics , philosophy
Transcription initiation at the ribosomal RNA promoter requires RNA polymerase (Pol) I and the initiation factors Rrn3 and core factor (CF). Here, we combine X-ray crystallography and cryo-electron microscopy (cryo-EM) to obtain a molecular model for basal Pol I initiation. The three-subunit CF binds upstream promoter DNA, docks to the Pol I-Rrn3 complex, and loads DNA into the expanded active center cleft of the polymerase. DNA unwinding between the Pol I protrusion and clamp domains enables cleft contraction, resulting in an active Pol I conformation and RNA synthesis. Comparison with the Pol II system suggests that promoter specificity relies on a distinct "bendability" and "meltability" of the promoter sequence that enables contacts between initiation factors, DNA, and polymerase.

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