Structural Basis of RNA Polymerase I Transcription Initiation

被引:80
|
作者
Engel, Christoph [1 ]
Gubbey, Tobias [1 ]
Neyer, Simon [1 ]
Sainsbury, Sarah [1 ]
Oberthuer, Christiane [1 ]
Baejen, Carlo [1 ]
Bernecky, Carrie [1 ]
Cramer, Patrick [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Mol Biol, Fassberg 11, D-37077 Gottingen, Germany
基金
欧洲研究理事会;
关键词
TATA-BINDING PROTEIN; UPSTREAM ACTIVATION FACTOR; RIBOSOMAL DNA; FACTOR UAF; RDNA TRANSCRIPTION; PREINITIATION COMPLEX; MOLECULAR-STRUCTURES; CRYSTAL-STRUCTURE; FACTOR-TFIIB; PROMOTER;
D O I
10.1016/j.cell.2017.03.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-Rrn(3) 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.
引用
收藏
页码:120 / +
页数:34
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