Concurrent splicing and transcription are not sufficient to enhance splicing efficiency

被引:27
作者
Lazarev, Denis [1 ]
Manley, James L. [1 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
关键词
transcription-splicing in vitro; coupled transcription-splicing system; RNA-POLYMERASE-II; PRE-MESSENGER-RNAS; MAMMALIAN NUCLEI; GENE-EXPRESSION; SPLICEOSOME; CLEAVAGE; POLYADENYLATION; RECRUITMENT; COMPLEXES; MECHANISM;
D O I
10.1261/rna.595907
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
The concept of a tight integration of transcription and splicing of mRNA precursors has been supported with increasing evidence in recent years. However, the mechanism and functional consequences of this integration remain largely unknown. We have examined how these processes impact upon one another when they occur together in HeLa nuclear extract. While both processes do in fact occur in parallel reactions in the extracts, we found no evidence that one process affects the other, under a variety of conditions tested. For example, neither the kinetics nor efficiency of splicing is significantly enhanced by de novo RNA polymerase II-mediated transcription, relative to that of presynthesized RNA added exogenously to the extract. Our results indicate that the act of transcription by RNA polymerase II in vitro is not sufficient to enhance splicing of the newly made RNA.
引用
收藏
页码:1546 / 1557
页数:12
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