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PMID: 26292707 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Structure of a yeast spliceosome at 3.6-angstrom resolution.

Science (New York, N.Y.) ·Vol. 349 ·No. 6253 ·2015-09-11 ·Pages 1182-91

Yan C, Hang J, Wan R, Huang M, Wong CC, Shi Y

Abstract

Splicing of precursor messenger RNA (pre-mRNA) in yeast is executed by the spliceosome, which consists of five small nuclear ribonucleoproteins (snRNPs), NTC (nineteen complex), NTC-related proteins (NTR), and a number of associated enzymes and cofactors. Here, we report the three-dimensional structure of a Schizosaccharomyces pombe spliceosome at 3.6-angstrom resolution, revealed by means of single-particle cryogenic electron microscopy. This spliceosome contains U2 and U5 snRNPs, NTC, NTR, U6 small nuclear RNA, and an RNA intron lariat. The atomic model includes 10,574 amino acids from 37 proteins and four RNA molecules, with a combined molecular mass of approximately 1.3 megadaltons. Spp42 (Prp8 in Saccharomyces cerevisiae), the key protein component of the U5 snRNP, forms a central scaffold and anchors the catalytic center. Both the morphology and the placement of protein components appear to have evolved to facilitate the dynamic process of pre-mRNA splicing. Our near-atomic-resolution structure of a central spliceosome provides a molecular framework for mechanistic understanding of pre-mRNA splicing.

MeSH Terms
Catalytic Domain Cryoelectron Microscopy Models, Molecular Protein Structure, Secondary RNA, Small Nuclear/chemistry Repressor Proteins/chemistry Ribonucleoprotein, U5 Small Nuclear/chemistry Schizosaccharomyces/ultrastructure Schizosaccharomyces pombe Proteins/chemistry Spliceosomes/chemistry,ultrastructure
Chemicals
RNA, Small Nuclear Repressor Proteins Ribonucleoprotein, U5 Small Nuclear Schizosaccharomyces pombe Proteins Spp42 protein, S pombe U6 small nuclear RNA
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Yan Chuangye
Ministry of Education Key Laboratory of Protein Science, Tsinghua-Peking Joint Center for Life Sciences, Center for Structural Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Hang Jing
Ministry of Education Key Laboratory of Protein Science, Tsinghua-Peking Joint Center for Life Sciences, Center for Structural Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Wan Ruixue
Ministry of Education Key Laboratory of Protein Science, Tsinghua-Peking Joint Center for Life Sciences, Center for Structural Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Huang Min
National Center for Protein Science Shanghai, Institute of Biochemistry and Cell Biology, Shanghai Institutes of Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Wong Catherine C L
National Center for Protein Science Shanghai, Institute of Biochemistry and Cell Biology, Shanghai Institutes of Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Shi Yigong
Ministry of Education Key Laboratory of Protein Science, Tsinghua-Peking Joint Center for Life Sciences, Center for Structural Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2015-09-11
Epub
2015-00-20
Pages
1182-91
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Databases
PDB
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