A Vertebrate Polycomb Response Element Governs Segmentation of the Posterior Hindbrain

被引:185
作者
Sing, Angela [1 ,3 ]
Pannell, Dylan [2 ,3 ]
Karaiskakis, Angelo [2 ,3 ]
Sturgeon, Kendra [1 ,3 ]
Djabali, Malek [4 ]
Ellis, James [2 ,3 ]
Lipshitz, Howard D. [2 ,3 ]
Cordes, Sabine P. [1 ,3 ]
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[2] Hosp Sick Children, Res Inst, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A1, Canada
[4] CNRS, INSERM, Ctr Immunol, F-13288 Marseille 9, France
关键词
EMBRYONIC STEM-CELLS; H3; LYSINE-27; METHYLATION; DNA-BINDING PROTEIN; DROSOPHILA-MELANOGASTER; TARGET GENES; METHYLTRANSFERASE ACTIVITY; DEVELOPMENTAL REGULATORS; TRANSCRIPTION FACTOR; BITHORAX COMPLEX; UBX GENE;
D O I
10.1016/j.cell.2009.08.020
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
Chromatin remodeling by Polycomb group (PcG) and trithorax group (trxG) proteins regulates gene expression in all metazoans. Two major complexes, Polycomb repressive complexes 1 and 2 (PRC1 and PRC2), are thought to mediate PcG-dependent repression in flies and mammals. In Drosophila, PcG/trxG protein complexes are recruited by PcG/trxG response elements (PREs). However, it has been unclear how PcG/trxG are recuited in vertebrates. Here we have identified a vertebrate PRE, PRE-kr, that regulates expression of the mouse MafB/Kreisler gene. PRE-kr recruits PcG proteins in flies and mouse F9 cells and represses gene expression in a PcG/trxG-dependent manner. PRC1 and 2 bind to a minimal PRE-kr region, which can recruit stable PRC1 binding but only weak PRC2 binding when introduced ectopically, suggesting that PRC1 and 2 have different binding requirements. Thus, we provide evidence that similar to invertebrates, PREs act as entry sites for PcG/trxG chromatin remodeling in vertebrates.
引用
收藏
页码:885 / 897
页数:13
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