Repetitive switching between DNA-binding modes enables target finding by the glucocorticoid receptor

被引:9
|
作者
Keizer, Veer I. P. [1 ]
Coppola, Stefano [2 ]
Houtsmuller, Adriaan B. [3 ,4 ]
Geverts, Bart [3 ,4 ]
van Royen, Martin E. [3 ,4 ]
Schmidt, Thomas [2 ]
Schaaf, Marcel J. M. [1 ]
机构
[1] Leiden Univ, Inst Biol, Anim Sci & Hlth, NL-2333 CC Leiden, Netherlands
[2] Leiden Univ, Biol Matter Living Syst, Inst Phys, NL-2333 CC Leiden, Netherlands
[3] Erasmus MC, Dept Pathol, NL-3000 CA Rotterdam, Netherlands
[4] Erasmus MC, Erasmus Opt Imaging Ctr, NL-3000 CA Rotterdam, Netherlands
关键词
Fluorescence recovery after photobleaching; Single-molecule; microscopy; Glucocorticoid receptor; Transcription factor; TRANSCRIPTION FACTORS; FLUORESCENCE RECOVERY; PHOTOBLEACHING FRAP; STRUCTURAL BASIS; LIVING CELLS; DYNAMICS; MOBILITY; SITES; DETERMINANTS; MECHANISMS;
D O I
10.1242/jcs.217455
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transcription factor mobility is a determining factor in the regulation of gene expression. Here, we have studied the intranuclear dynamics of the glucocorticoid receptor (GR) by using fluorescence recovery after photobleaching and single-molecule microscopy. First, we have described the dynamic states in which the GR occurs. Second, we have analyzed the transitions between these states by using a continuous-time Markov chain model and functionally investigated these states by making specific mutations in the DNA-binding domain. This analysis revealed that the GR diffuses freely through the nucleus and, once it leaves this free diffusion state, most often enters a repetitive switching mode. In this mode it alternates between slow diffusion as a result of brief nonspecific DNA-binding events, and a state of stable binding to specific DNA target sites. This repetitive switching mechanism results in a compact search strategy that facilitates finding of DNA target sites by the GR. This article has an associated First Person interview with the first author of the paper.
引用
收藏
页数:12
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