'Cap-tabolism'

被引:88
作者
Cougot, N [1 ]
van Dijk, E [1 ]
Babajko, S [1 ]
Séraphin, B [1 ]
机构
[1] Univ Paris 06, CNRS UPR2167, Equpe Labellisee La Ligue, Ctr Mol Genet, F-91198 Gif Sur Yvette, France
关键词
D O I
10.1016/j.tibs.2004.06.008
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
A distinctive feature of eukaryotic mRNA and small nuclear RNA (snRNA) that are transcribed by RNA polymerase II (Pol II) is the presence of a cap structure at their 5' end. This essential modification serves as an inviting 'landing pad' for factors that are involved in various cellular processes such as pre-mRNA splicing, nucleocytoplasmic RNA export and localization, and translation initiation. Because of the important functions mediated by the mRNA cap, this structure needs to be modified and/or degraded in a tightly controlled manner. Several cellular and viral systems implicated in cap metabolism have been uncovered recently; their analyses provide interesting new information on cell structure and function.
引用
收藏
页码:436 / 444
页数:9
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