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
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页数:12
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