Cohesin mediates transcriptional insulation by CCCTC-binding factor

被引:0
|
作者
Kerstin S. Wendt
Keisuke Yoshida
Takehiko Itoh
Masashige Bando
Birgit Koch
Erika Schirghuber
Shuichi Tsutsumi
Genta Nagae
Ko Ishihara
Tsuyoshi Mishiro
Kazuhide Yahata
Fumio Imamoto
Hiroyuki Aburatani
Mitsuyoshi Nakao
Naoko Imamoto
Kazuhiro Maeshima
Katsuhiko Shirahige
Jan-Michael Peters
机构
[1] Research Institute of Molecular Pathology (I.M.P.),Genome Science Division
[2] Dr. Bohr Gasse 7,Department of Molecular Biology
[3] 1030 Vienna,Department of Regeneration Medicine
[4] Austria ,undefined
[5] Graduate School of Bioscience and Biotechnology,undefined
[6] Tokyo Institute of Technology,undefined
[7] B2C 4259,undefined
[8] Nagatsuta,undefined
[9] Midori-ku,undefined
[10] Yokohama City,undefined
[11] Kanagawa 226-8501,undefined
[12] Japan ,undefined
[13] Research Center for Advanced Science and Technology,undefined
[14] Mitsubishi Research Institute Inc.,undefined
[15] Chiyoda-ku,undefined
[16] Tokyo 100-8141,undefined
[17] Japan ,undefined
[18] Research Center for Advanced Science and Technology (RCAST),undefined
[19] the University of Tokyo,undefined
[20] Research Institute for Microbial Diseases,undefined
[21] Osaka University,undefined
[22] Suita,undefined
[23] Osaka 565-0871,undefined
[24] Japan,undefined
[25] Institute of Molecular Embryology and Genetics Kumamoto University,undefined
[26] 2-2-1 Honjo,undefined
[27] Kumamoto 860-0811,undefined
[28] Japan,undefined
[29] Cellular Dynamics Laboratory,undefined
[30] RIKEN,undefined
[31] Wako,undefined
[32] Saitama 351-0198,undefined
[33] Japan ,undefined
来源
Nature | 2008年 / 451卷
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摘要
Cohesin complexes mediate sister-chromatid cohesion in dividing cells but may also contribute to gene regulation in postmitotic cells. How cohesin regulates gene expression is not known. Here we describe cohesin-binding sites in the human genome and show that most of these are associated with the CCCTC-binding factor (CTCF), a zinc-finger protein required for transcriptional insulation. CTCF is dispensable for cohesin loading onto DNA, but is needed to enrich cohesin at specific binding sites. Cohesin enables CTCF to insulate promoters from distant enhancers and controls transcription at the H19/IGF2 (insulin-like growth factor 2) locus. This role of cohesin seems to be independent of its role in cohesion. We propose that cohesin functions as a transcriptional insulator, and speculate that subtle deficiencies in this function contribute to ‘cohesinopathies’ such as Cornelia de Lange syndrome.
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页码:796 / 801
页数:5
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