A PROTEIN FACTOR, ASF, CONTROLS CELL-SPECIFIC ALTERNATIVE SPLICING OF SV40 EARLY PRE-MESSENGER-RNA INVITRO

被引:429
|
作者
GE, H
MANLEY, JL
机构
[1] Department of Biological Sciences Columbia University New York
关键词
D O I
10.1016/0092-8674(90)90236-8
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
SV40 early pre-mRNA is alternatively spliced by utilization of two different 5′ splice sites and a shared 3′ splice site to produce large T and small t mRNAs. The ratio of small t to large T mRNAs produced in human embryonic kidney 293 cells is 10- to 20-fold greater than in other mammalian cells, suggesting the existence of a 293 cell-specific factor that modulates alternative splicing. Here we show that nuclear extracts from 293 cells give rise to significantly more small t splicing than do extracts from HeLa cells. Using an in vitro complementation assay, we have characterized and extensively purified a factor from 293 extracts that brings about striking increases in small t splicing with concomitant decreases in large T splicing. The factor is heat sensitive and micrococcal nuclease resistant, suggesting that it is a protein lacking an accessible RNA component. Purification of the alternative splicing factor indicates that the activity is contained in one of several possibly related polypeptides of 30-35 kd. © 1990.
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页码:25 / 34
页数:10
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