Hypermethylation of the cap structure of both yeast snRNAs and snoRNAs requires a conserved methyltransferase that is localized to the nucleolus

被引:190
作者
Mouaikel, J [1 ]
Verheggen, C [1 ]
Bertrand, E [1 ]
Tazi, J [1 ]
Bordonné, R [1 ]
机构
[1] Inst Mol Genet, IFR 24, CNRS, UMR 5535, F-34000 Montpellier, France
基金
澳大利亚研究理事会;
关键词
D O I
10.1016/S1097-2765(02)00484-7
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
The m(7)G caps of most spliceosomal snRNAs and certain snoRNAs are converted posttranscriptionally to 2,2,7-trimethylguanosine (m(3)G) cap structures. Here, we show that yeast Tgs1p, an evolutionarily conserved protein carrying a signature of S-AdoMet methyltransferase, is essential for hypermethylation of the m(7)G caps of both snRNAs and snoRNAs. Deletion of the yeast TGS1 gene abolishes the conversion of the m(7)G to m(3)G caps and produces a cold-sensitive splicing defect that correlates with the retention of U1 snRNA in the nucleolus. Consistently, Tgs1p is also localized in the nucleolus. Our results suggest a trafficking pathway in which yeast snRNAs and snoRNAs cycle through the nucleolus to undergo m(7)G cap hypermethylation.
引用
收藏
页码:891 / 901
页数:11
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