A CDNA-ENCODING RAP74, A GENERAL INITIATION-FACTOR FOR TRANSCRIPTION BY RNA POLYMERASE-II

被引:91
作者
FINKELSTEIN, A
KOSTRUB, CF
LI, J
CHAVEZ, DP
WANG, BQ
FANG, SM
GREENBLATT, J
BURTON, ZF
机构
[1] MICHIGAN STATE UNIV,DEPT BIOCHEM,E LANSING,MI 48824
[2] MICHIGAN STATE UNIV,AGR EXPT STN,E LANSING,MI 48824
[3] UNIV TORONTO,BANTING & BEST DEPT MED RES,TORONTO M5G 1L6,ONTARIO,CANADA
[4] UNIV TORONTO,DEPT MOLEC & MED GENET,TORONTO M5G 1L6,ONTARIO,CANADA
关键词
D O I
10.1038/355464a0
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
RAP30/74 (also known as TFIIF (refs 1, 2), beta-gamma (ref. 3) and FC (ref. 4)) is one of several general factors required for initiation by RNA polymerase II (reviewed in refs 5-7). The small RAP30 subunit of RAP30/74 binds directly to polymerase and appears structurally and functionally homologous to bacterial sigma factors in their RNA polymerase-binding region 8-10. RAP30/74 or recombinant RAP30 suppresses nonspecific binding of RNA polymerase II to DNA (refs 10, 11) and is required for RNA polymerase II to assemble stably into a preinitiation complex containing promoter DNA and the general factors TFIID, TFIIA and TFIIB (refs 2, 12, 13); both RAP30 and RAP74 are physical components of the preinitiation complex 2. A complementary DNA encoding human RAP30 has been isolated 8, and here we report the isolation of a cDNA encoding human RAP74. RAP30 and RAP74 produced in Escherichia coli can be used in place of natural human RAP30/74 to direct accurate transcription initiation by RNA polymerase II in vitro.
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页码:464 / 467
页数:4
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