The Forkhead Transcription Factor FOXM1 Controls Cell Cycle-Dependent Gene Expression through an Atypical Chromatin Binding Mechanism

被引:186
|
作者
Chen, Xi [1 ]
Mueller, Gerd A. [2 ]
Quaas, Marianne [2 ]
Fischer, Martin [2 ]
Han, Namshik [1 ]
Stutchbury, Benjamin [1 ]
Sharrocks, Andrew D. [1 ]
Engeland, Kurt [2 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester, Lancs, England
[2] Univ Leipzig, Sch Med, D-04109 Leipzig, Germany
基金
英国惠康基金;
关键词
MITOTIC PROGRESSION; FACTOR FOXK2; CHIP-SEQ; B-MYB; PROMOTER; COMPLEXES; PROTEIN; ELEMENTS; PROGRAM; PHOSPHORYLATION;
D O I
10.1128/MCB.00881-12
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There are nearly 50 forkhead (FOX) transcription factors encoded in the human genome and, due to sharing a common DNA binding domain, they are all thought to bind to similar DNA sequences. It is therefore unclear how these transcription factors are targeted to specific chromatin regions to elicit specific biological effects. Here, we used chromatin immunoprecipitation followed by sequencing (ChIP-seq) to investigate the genome-wide chromatin binding mechanisms used by the forkhead transcription factor FOXM1. In keeping with its previous association with cell cycle control, we demonstrate that FOXM1 binds and regulates a group of genes which are mainly involved in controlling late cell cycle events in the G(2) and M phases. However, rather than being recruited through canonical RYAAAYA forkhead binding motifs, FOXM1 binding is directed via CHR (cell cycle genes homology region) elements. FOXM1 binds these elements through protein-protein interactions with the MMB transcriptional activator complex. Thus, we have uncovered a novel and unexpected mode of chromatin binding of a FOX transcription factor that allows it to specifically control cell cycle-dependent gene expression.
引用
收藏
页码:227 / 236
页数:10
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