PRP38 ENCODES A YEAST PROTEIN REQUIRED FOR PRE-MESSENGER-RNA SPLICING AND MAINTENANCE OF STABLE U6 SMALL NUCLEAR-RNA LEVELS

被引:73
作者
BLANTON, S [1 ]
SRINIVASAN, A [1 ]
RYMOND, BC [1 ]
机构
[1] UNIV KENTUCKY,TH MORGAN SCH BIOL SCI,LEXINGTON,KY 40506
关键词
D O I
10.1128/MCB.12.9.3939
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
An essential pre-mRNA splicing factor, the product of the PRP38 gene, has been genetically identified in a screen of temperature-sensitive mutants of Saccharomyces cerevisiae. Shifting temperature-sensitive prp38 cultures from 23 to 37-degrees-C prevents the first cleavage-ligation event in the excision of introns from mRNA precursors. In vitro splicing inactivation and complementation studies suggest that the PRP38-encoded factor functions, at least in part, after stable splicing complex formation. The PRP38 locus contains a 726-bp open reading frame coding for an acidic 28-kDa polypeptide (PRP38). While PRP38 lacks obvious structural similarity to previously defined splicing factors, heat inactivation of PRP38, PRP19, or any of the known U6 (or U4/U6) small nuclear ribonucleoprotein-associating proteins (i.e., PRP3, PRP4, PRP6, and PRP24) leads to a common, unexpected consequence: intracellular U6 small nuclear RNA (snRNA) levels decrease as splicing activity is lost. Curiously, U4 snRNA, normally extensively base paired with U6 snRNA, persists in the virtual absence of U6 snRNA.
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页码:3939 / 3947
页数:9
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