共 65 条
Hierarchical recruitment of Polycomb complexes revisited
被引:17
作者:

Dorafshan, Eshagh
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机构:
Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden

Kahn, Tatyana G.
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机构:
Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden

Schwartz, Yuri B.
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h-index: 0
机构:
Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden
机构:
[1] Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden
来源:
关键词:
Drosophila;
epigenetics;
Polycomb;
Polycomb targeting;
Polycomb Response Elements;
HISTONE METHYLTRANSFERASE ACTIVITY;
GROUP RESPONSE ELEMENT;
REPRESSIVE COMPLEX;
H2A UBIQUITYLATION;
BITHORAX COMPLEX;
DROSOPHILA-MELANOGASTER;
EPIGENETIC INHERITANCE;
CHROMATIN-STRUCTURE;
PRC2;
RECRUITMENT;
GENE-EXPRESSION;
D O I:
10.1080/19491034.2017.1363136
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Polycomb Group (PcG) proteins epigenetically repress key developmental genes and thereby control alternative cell fates. PcG proteins act as complexes that can modify histones and these histone modifications play a role in transmitting the memory of the repressed state as cells divide. Here we consider mainstream models that link histone modifications to hierarchical recruitment of PcG complexes and compare them to results of a direct test of interdependence between PcG complexes for recruitment to Drosophila genes. The direct test indicates that PcG complexes do not rely on histone modifications to recognize their target genes but use them to stabilize the interactions within large chromatin domains. It also shows that multiple strategies are used to coordinate the targeting of PcG complexes to different genes, which may make the repression of these genes more or less robust.
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页码:496 / 505
页数:10
相关论文
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Univ Oxford, Dept Biochem, Oxford OX1 3QU, England Univ Oxford, Dept Biochem, Oxford OX1 3QU, England

Ponting, Chris P.
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Univ Oxford, Dept Physiol Anat & Genet, MRC Funct Genom Unit, CGAT, Oxford, England Univ Oxford, Dept Biochem, Oxford OX1 3QU, England

Kessler, Benedikt M.
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Univ Oxford, Nuffield Dept Clin Med, Ctr Cellular & Mol Physiol, Cent Prote Facil,Ubiquitin Proteolysis Grp, Oxford, England Univ Oxford, Dept Biochem, Oxford OX1 3QU, England

Klose, Robert J.
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Univ Oxford, Dept Biochem, Oxford OX1 3QU, England Univ Oxford, Dept Biochem, Oxford OX1 3QU, England