剪接体
RNA剪接
埃
核糖核酸
分辨率(逻辑)
生物
计算生物学
遗传学
物理
化学
生物物理学
结晶学
酵母
计算机科学
基因
人工智能
作者
Chuangye Yan,Jing Hang,Ruixue Wan,Min Huang,Catherine C. L. Wong,Yigong Shi
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2015-08-21
卷期号:349 (6253): 1182-1191
被引量:341
标识
DOI:10.1126/science.aac7629
摘要
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.
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