Single-molecule analysis of transcription factor binding at transcription sites in live cells

被引:126
作者
Morisaki, Tatsuya [1 ]
Mueller, Waltraud G. [1 ]
Golob, Nicole [2 ]
Mazza, Davide [3 ,4 ]
McNally, James G. [1 ]
机构
[1] NCI, Fluorescence Imaging Grp, NIH, Bethesda, MD 20892 USA
[2] Inst Pathol, A-8036 Graz, Austria
[3] Univ Vita Salute San Raffaele, I-20132 Milan, Italy
[4] IRCCS Osped San Raffaele, I-20132 Milan, Italy
基金
日本学术振兴会; 美国国家卫生研究院;
关键词
GLUCOCORTICOID-RECEPTOR; NATURAL PROMOTER; LIVING CELLS; IN-VIVO; CHROMATIN; DYNAMICS; EXCHANGE; MECHANISMS; SCALE; LINE;
D O I
10.1038/ncomms5456
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
Although numerous live-cell measurements have shown that transcription factors (TFs) bind chromatin transiently, no measurements of transient binding have been reported at the endogenous response elements (REs) where transcription is normally induced. Here we show that at endogenous REs the transcriptionally productive specific binding of two TFs, p53 and the glucocorticoid receptor (GR), is transient. We also find that the transient residence times of GR at endogenous REs are roughly comparable to those at an artificial, multi-copy array of gene regulatory sites, supporting the use of multi-copy arrays for live-cell analysis of transcription. Finally, we find that at any moment only a small fraction of TF molecules are engaged in transcriptionally productive binding at endogenous REs. The small fraction of bound factors provides one explanation for gene bursting and it also indicates that REs may often be unoccupied, resulting in partial responses to transcriptional signals.
引用
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页数:8
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