Mechanism of 5′ splice site transfer for human spliceosome activation

被引:119
作者
Charenton, Clement [1 ]
Wilkinson, Max E. [1 ]
Nagai, Kiyoshi [1 ]
机构
[1] MRC Lab Mol Biol, Cambridge CB2 0QH, England
基金
英国医学研究理事会; 欧洲研究理事会;
关键词
U4/U6.U5; TRI-SNRNP; CRYO-EM STRUCTURE; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; REQUIRES ATP; RNA; PROTEIN; ARCHITECTURE; RESOLUTION; NUCLEAR;
D O I
10.1126/science.aax3289
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The prespliceosome, comprising U1 and U2 small nuclear ribonucleoproteins (snRNPs) bound to the precursor messenger RNA 5'splice site (5'SS) and branch point sequence, associates with the U4/U6. U5 tri-snRNP to form the fully assembled precatalytic pre-B spliceosome. Here, we report cryo-electron microscopy structures of the human pre-B complex captured before U1 snRNP dissociation at 3.3-angstrom core resolution and the human tri-snRNP at 2.9-angstrom resolution. U1 snRNP inserts the 5'SS-U1 snRNA helix between the two RecA domains of the Prp28 DEAD-box helicase. Adenosine 5'-triphosphate-dependent closure of the Prp28 RecA domains releases the 5'SS to pair with the nearby U6 ACAGAGA-box sequence presented as a mobile loop. The structures suggest that formation of the 5'SS-ACAGAGA helix triggers remodeling of an intricate protein-RNA network to induce Brr2 helicase relocation to its loading sequence in U4 snRNA, enabling Brr2 to unwind the U4/U6 snRNA duplex to allow U6 snRNA to form the catalytic center of the spliceosome.
引用
收藏
页码:362 / +
页数:34
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