Transcription factor localization dynamics and DNA binding drive distinct promoter interpretations

被引:10
|
作者
Sweeney, Kieran [1 ]
McClean, Megan N. [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Biomed Engn, Madison, WI 53706 USA
[2] Univ Wisconsin, Carbone Canc Ctr, Sch Med & Publ Hlth, Madison, WI 53706 USA
来源
CELL REPORTS | 2023年 / 42卷 / 05期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
NUCLEAR-LOCALIZATION; STIMULUS SPECIFICITY; EXPRESSION PROGRAMS; PROTEIN; ACETYLATION; ACTIVATION; STRESS; THRESHOLD; KINASE; MSN2P;
D O I
10.1016/j.celrep.2023.112426
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Environmental information may be encoded in the temporal dynamics of transcription factor (TF) activation and subsequently decoded by gene promoters to enact stimulus-specific gene expression programs. Previ-ous studies of this behavior focused on the encoding and decoding of information in TF nuclear localization dynamics, yet cells control the activity of TFs in myriad ways, including by regulating their ability to bind DNA. Here, we use light-controlled mutants of the yeast TF Msn2 as a model system to investigate how promoter decoding of TF localization dynamics is affected by changes in the ability of the TF to bind DNA. We find that yeast promoters directly decode the light-controlled localization dynamics of Msn2 and that the effects of changing Msn2 affinity on that decoding behavior are highly promoter dependent, illustrating how cells could regulate TF localization dynamics and DNA binding in concert for improved control of gene expression.
引用
收藏
页数:20
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