U2 and U6 snRNA genes in the microsporidian Nosema locustae:: evidence for a functional spliceosome

被引:29
作者
Fast, NM [1 ]
Roger, AJ
Richardson, CA
Doolittle, WF
机构
[1] Dalhousie Univ, Dept Biochem, Halifax, NS B3H 4H7, Canada
[2] Marine Biol Lab, Woods Hole, MA 02543 USA
基金
加拿大自然科学与工程研究理事会; 英国医学研究理事会;
关键词
D O I
10.1093/nar/26.13.3202
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 removal of introns from pre-messenger RNA is mediated by the spliceosome, a large complex composed of many proteins and five small nuclear RNAs (snRNAs), Of the snRNAs, the U6 and U2 snRNAs are the most conserved in sequence, as they interact extensively with each other and also with the intron, in several base pairings that are necessary for splicing. We have isolated and sequenced the genes encoding both U6 and U2 snRNAs from the intracellularly parasitic microsporidian Nosema locustae, Both genes are expressed. Both RNAs can be folded into secondary structures typical of other known U6 and U2 snRNAs. In addition, the N.locustae U6 and U2 snRNAs have the potential to base pair in the functional intermolecular interactions that have been characterized by extensive analyses in yeast and mammalian systems. These results indicate that the N.locustae U6 and U2 snRNAs may be functional components of an active spliceosome, even though introns have not yet been found in microsporidian genes.
引用
收藏
页码:3202 / 3207
页数:6
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