共 59 条
TTF-I determines the chromatin architecture of the active rDNA promoter
被引:75
作者:
Längst, G
Becker, PB
Grummt, I
机构:
[1] Deutsch Krebsforschungszentrum, Div Mol Biol Cell 2, D-69120 Heidelberg, Germany
[2] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词:
chromatin;
nucleosome remodeling;
RNA polymerase I;
transcription activation;
TTF-I;
D O I:
10.1093/emboj/17.11.3135
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:
Transcription of ribosomal genes assembled into chromatin requires binding of the transcription termination factor TTF-I to the promoter-proximal terminator To, To analyze the mechanism of TTF-I-mediated transcriptional activation, we have used mutant templates with altered sequence, polarity and distance of To with respect to the transcription start site, Transcription activation by TTF-I is chromatin specific and requires the precise positioning of the terminator relative to the promoter, Whereas termination by TTF-I depends on the correct orientation of a terminator, TTF-I-mediated transcriptional activation is orientation independent. TTF-I can bind to nucleosomal DNA in the absence of enzymatic activities that destabilize nucleosome structure. Chromatin-bound TTF-I synergizes with ATP-dependent cofactors present in extracts of Drosophila embryos and mouse cells to position a nucleosome over the rDNA promoter and the transcription start site. Nucleosome positioning correlates tightly with the activation of rDNA transcription. We suggest that transcriptional activation by TTF-I is a stepwise process involving the creation of a defined promoter architecture and that the positioning of a nucleosome is compatible with, if not a prerequisite for, transcription initiation from rDNA chromatin.
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页码:3135 / 3145
页数:11
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