SACCHAROMYCES-CEREVISIAE U1 SMALL NUCLEAR-RNA SECONDARY STRUCTURE CONTAINS BOTH UNIVERSAL AND YEAST-SPECIFIC DOMAINS

被引:46
作者
KRETZNER, L
KROL, A
ROSBASH, M
机构
[1] BRANDEIS UNIV,HOWARD HUGHES MED INST,WALTHAM,MA 02254
[2] CNRS,BIOCHIM LAB,INST BIOL MOLEC & CELLULAIRE,F-67084 STRASBOURG,FRANCE
[3] BRANDEIS UNIV,DEPT BIOL,WALTHAM,MA 02254
关键词
phylogenetic studies; splicing;
D O I
10.1073/pnas.87.2.851
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 five small nuclear RNAs (snRNAs) involved in mammalian pre-mRNA splicing (U1, U2, U4, U5, and U6) are well conserved in length, sequence, and especially secondary structure. These five snRNAs from Saccharomyces cerevisiae show notable size and sequence differences from their metazoan counterparts. This is most striking for the large S. cerevisiae U1 and U2 snRNAs, for which no secondary structure models currently exist. Because of the importance of U1 snRNA in the early steps of 'spliceosome' assembly, we wanted to compare the highly conserved secondary structure of metazoan U1 snRNA (~165 nucleotides) with that of S. cerevisiae U1 snRNA (568 nucleotides). To this end, we have cloned and sequenced the U1 gene from two other yeast species possessing large U1 RNAs. Using computer-derived structure predictions, phylogenetic comparisons, and structure probing, we have arrived at a secondary structure model for S. cerevisiae U1 snRNA. The results show that most elements of higher eukaryotic U1 snRNA secondary structure are conserved in S. cerevisiae. The hundreds of 'extra' nucleotides of yeast U1 RNA, also highly structured, suggest that large insertions and/or deletions have occurred during the evolution of the U1 gene.
引用
收藏
页码:851 / 855
页数:5
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