Sfp1 regulates transcriptional networks driving cell growth and division through multiple promoter-binding modes

被引:33
作者
Albert, Benjamin
Tomassetti, Susanna
Gloor, Yvonne
Dilg, Daniel
Mattarocci, Stefano [2 ]
Kubik, Slawomir
Hafner, Lukas
Shore, David [1 ]
机构
[1] Dept Mol Biol, CH-1211 Geneva 4, Switzerland
[2] Sorbonne Univ, Paris Sci & Lettres Res Univ, UMR8226,CNRS, Lab Biol Mol & Cellulaire Eucaryotes,Inst Biol Ph, F-75005 Paris, France
基金
瑞士国家科学基金会;
关键词
G1/S regulon; START; Sfp1; cell cycle; cell growth; chromatin endogenous cleavage (ChEC); ribosomal protein gene; ribosome biogenesis; transcription; PROTEIN; GENES; SIZE; IDENTIFICATION; ARCHITECTURES; BIOGENESIS; EXPRESSION; SEQUENCE; TORC1; DOT6;
D O I
10.1101/gad.322040.118
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The yeast Sfp1 protein regulates both cell division and growth but how it coordinates these processes is poorly understood. We demonstrate that Sfp1 directly controls genes required for ribosome production and many other growth-promoting processes. Remarkably, the complete set of Sfp1 target genes is revealed only by a combination of ChIP (chromatin immunoprecipitation) and ChEC (chromatin endogenous cleavage) methods, which uncover two promoter binding modes, one requiring a cofactor and the other a DNA-recognition motif. Glucose-regulated Sfp1 binding at cell cycle "START" genes suggests that Sfp1 controls cell size by coordinating expression of genes implicated in mass accumulation and cell division.
引用
收藏
页码:288 / 293
页数:6
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