An RNA-dependent ATPase associated with U2/U6 snRNAs in pre-mRNA splicing

被引:70
|
作者
Xu, DM
Nouraini, S
Field, D
Tang, SJ
Friesen, JD
机构
[1] HOSP SICK CHILDREN, RES INST, DEPT GENET, TORONTO, ON M5G 1X8, CANADA
[2] UNIV TORONTO, DEPT MOLEC & MED GENET, TORONTO, ON M5G 1X8, CANADA
关键词
D O I
10.1038/381709a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
THE hydrolysis of ATP by a group of RNA dependent ATPases (DEAD/H proteins(1)) is required for spliceosome assembly, but not for the subsequent transesterification reactions(2). Little is known about the function of these ATPases in relation to the RNA conformational changes that occur in formation of active structures, in which U2/U6 small nuclear RNA (snRNA) interactions(3,4) are essential for splicing to take place, Using a synthetic lethal genetic screen, we have isolated four yeast splicing factors involved in U2/U6 snRNA interactions (D.X. et al., manuscript in preparation). The RNA-dependent ATPase activity associated with one such factor, the Slt22 protein, is stimulated preferentially by annealed U2/U6 snRNAs. Both mutant slt22-1 and U2 snRNA cause a reduction in stimulation, The slt22-1 mutation blocks splicing at or before the first step, resulting in the accumulation of an unusual complex which lacks U5 snRNA. Our results indicate that the U2/U6 snRNA interactions facilitated by Slt22 are also Involved in the interaction of U5 snRNA with tire spliceosome.
引用
收藏
页码:709 / 713
页数:5
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