作者: B. Séraphin , L. Kretzner , M. Rosbash
DOI: 10.1002/J.1460-2075.1988.TB03101.X
关键词: Prp24 、 snRNP 、 Biology 、 Intron 、 Small nuclear RNA 、 Cell biology 、 Precursor mRNA 、 RNA splicing 、 Spliceosome 、 Commitment complex 、 Genetics
摘要: Abstract We analyzed the effects of suppressor mutations in U1 snRNA (SNR19) gene from Saccharomyces cerevisiae on splicing mutant pre-mRNA substrates. The results indicate that pairing between and highly conserved position 5 (GTATGT) intron occurs early spliceosome assembly vitro. This is important for efficient both vitro vivo. However, at does not appear to influence 5' splice site selection vivo, indicating previously described snRNA:5' junction base interaction sufficient define cleavage site.