AN ATP-INDEPENDENT U2 SMALL NUCLEAR RIBONUCLEOPROTEIN PARTICLE PRECURSOR MESSENGER-RNA COMPLEX REQUIRES BOTH SPLICE SITES AND THE POLYPYRIMIDINE TRACT

被引:34
作者
JAMISON, SF
GARCIABLANCO, MA
机构
[1] DUKE UNIV,MED CTR,CELL GROWTH REGULAT & ONCOGENESIS SECT,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT MICROBIOL & IMMUNOL,DURHAM,NC 27710
[3] DUKE UNIV,MED CTR,DEPT MED,DURHAM,NC 27710
关键词
PRECURSOR MESSENGER RNA SPLICING; SPLICEOSOME; PRESPLICEOSOME;
D O I
10.1073/pnas.89.12.5482
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
A complex is formed upon incubation of a precursor mRNA (pre-mRNA) with HeLa cell nuclear extract in the absence of added ATP (-ATP complex). Pre-mRNAs with mutations in the 5' splice site, the 3' splice site, or the polypyrimidine tract did not form this complex. Once formed, the -ATP complex was stable to competition by excess premRNA. The complex was shown to contain the U2 small nuclear ribonucleoprotein particle (snRNP) and was distinct from the previously described U2 snRNP/pre-mRNA complex, the prespliceosome. These complexes have different electrophoretic mobilities, ATP requirements, and sensitivities to mutations of the 5' splice site. Although U1 snRNP was not found in the -ATP complex, a requirement for the U1 snRNP was suggested by immunodepletion experiments. The possible implications for the study of spliceosome formation are discussed.
引用
收藏
页码:5482 / 5486
页数:5
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