Structural insights into transcription initiation by yeast RNA polymerase I

被引:41
|
作者
Sadian, Yashar [1 ]
Tafur, Lucas [1 ]
Kosinski, Jan [1 ]
Jakobi, Arjen J. [1 ,2 ,3 ]
Wetzel, Rene [1 ]
Buczak, Katarzyna [1 ]
Hagen, Wim J. H. [1 ]
Beck, Martin [1 ]
Sachse, Carsten [1 ]
Mueller, Christoph W. [1 ]
机构
[1] European Mol Biol Lab, Struct & Computat Biol Unit, Heidelberg, Germany
[2] European Mol Biol Lab, Hamburg Unit, Hamburg, Germany
[3] Hamburg Ctr Ultrafast Imaging CUI, Hamburg, Germany
来源
EMBO JOURNAL | 2017年 / 36卷 / 18期
关键词
Core Factor; electron cryo-microscopy; Pol I pre-initiation complex; ribosomal RNA; transcription; CRYSTAL-STRUCTURE; COMPLEX; PROTEIN; ARCHITECTURE; CLASSIFICATION; VISUALIZATION; CONSERVATION; RECRUITMENT; PREDICTION; RESOLUTION;
D O I
10.15252/embj.201796958
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
In eukaryotic cells, RNA polymerase I (Pol I) synthesizes precursor ribosomal RNA (pre-rRNA) that is subsequently processed into mature rRNA. To initiate transcription, Pol I requires the assembly of a multi-subunit pre-initiation complex (PIC) at the ribosomal RNA promoter. In yeast, the minimal PIC includes Pol I, the transcription factor Rrn3, and Core Factor (CF) composed of subunits Rrn6, Rrn7, and Rrn11. Here, we present the cryo-EM structure of the 18-subunit yeast Pol I PIC bound to a transcription scaffold. The cryo-EM map reveals an unexpected arrangement of the DNA and CF subunits relative to Pol I. The upstream DNA is positioned differently than in any previous structures of the Pol II PIC. Furthermore, the TFIIB-related subunit Rrn7 also occupies a different location compared to the Pol II PIC although it uses similar interfaces as TFIIB to contact DNA. Our results show that although general features of eukaryotic transcription initiation are conserved, Pol I and Pol II use them differently in their respective transcription initiation complexes.
引用
收藏
页码:2698 / 2709
页数:12
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