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Spliceosome structure: Piece by piece
被引:29
|作者:
Ritchie, Dustin B.
[1
]
Schellenberg, Matthew J.
[1
]
MacMillan, Andrew M.
[1
]
机构:
[1] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
来源:
基金:
加拿大健康研究院;
加拿大自然科学与工程研究理事会;
关键词:
Spliceosome;
Structure;
X-ray;
NMR;
EM;
PRE-MESSENGER-RNA;
GROUP-II INTRON;
CRYSTAL-STRUCTURE;
BRANCH-SITE;
ANGSTROM RESOLUTION;
RECOGNITION MOTIF;
ELECTRON CRYOMICROSCOPY;
3-DIMENSIONAL STRUCTURE;
POLYPYRIMIDINE TRACT;
SPLICING REGULATION;
D O I:
10.1016/j.bbagrm.2009.08.010
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:
Processing of pre-mRNAs by RNA splicing is an essential step in the maturation of protein coding RNAs in eukaryotes. Structural studies of the cellular splicing machinery, the spliceosome, are a major challenge in structural biology due to the size and complexity of the splicing ensemble. Specifically, the structural details of splice site recognition and the architecture of the spliceosome active site are poorly understood. X-ray and NMR techniques have been successfully used to address these questions defining the structure of individual domains, isolated splicing proteins, spliceosomal RNA fragments and recently the U1 snRNP multiprotein.RNA complex. These results combined with extant biochemical and genetic data have yielded important insights as well as posing fresh questions with respect to the regulation and mechanism of this critical gene regulatory process. (C) 2009 Elsevier B.V. All rights reserved.
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页码:624 / 633
页数:10
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