SEQUENCE-SPECIFIC TRANSACTIVATORS COUNTERACT TOPOISOMERASE-II-MEDIATED INHIBITION OF IN-VITRO TRANSCRIPTION BY RNA POLYMERASE-I AND POLYMERASE-II

被引:35
作者
BROU, C
KUHN, A
STAUB, A
CHAUDHARY, S
GRUMMT, I
DAVIDSON, I
TORA, L
机构
[1] FAC MED STRASBOURG,INST CHIM BIOL,CNRS,GENET MOLEC EUCARYOTES LAB,INSERM,U184,11 RUE HUMANN,F-67085 STRASBOURG,FRANCE
[2] GERMAN CANC RES CTR,INST CELL & TUMOR BIOL,D-69000 HEIDELBERG 1,GERMANY
关键词
D O I
10.1093/nar/21.17.4011
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 inhibitor of RNA polymerase II transcription in vitro has been purified from HeLa cell nuclear extracts. Partial amino acid sequences derived from the purified protein revealed that the inhibitor of transcription corresponded to human topoisomerase II. Order of addition experiments provided evidence indicating that topoisomerase II inhibited transcription by binding over the core promoter and blocking preinitiation complex formation. Topoisomerase II-mediated repression could be relieved by sequence-specific transcriptional activators, having different activating and/or DNA binding domains, but antirepression required a transcriptional activation function in addition to a DNA binding domain. Moreover, transcription by RNA polymerase I was also inhibited by topoisomerase II and this inhibition could be relieved by the RNA polymerase I transactivator UBF. These observations suggest that topoisomerase II may participate in a general repression of transcription which can be counteracted by transcriptional activators.
引用
收藏
页码:4011 / 4018
页数:8
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