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Coordinated but physically separable interaction with H3K27-demethylase and H3K4-methyltransferase activities are required for T-box protein-mediated activation of developmental gene expression.

作者信息

Miller Sara A, Huang Albert C, Miazgowicz Michael M, Brassil Margaret M, Weinmann Amy S

机构信息

Molecular and Cellular Biology Program, University of Washington, Seattle, Washington 98195, USA.

出版信息

Genes Dev. 2008 Nov 1;22(21):2980-93. doi: 10.1101/gad.1689708.


DOI:10.1101/gad.1689708
PMID:18981476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2577798/
Abstract

During cellular differentiation, both permissive and repressive epigenetic modifications must be negotiated to create cell-type-specific gene expression patterns. The T-box transcription factor family is important in numerous developmental systems ranging from embryogenesis to the differentiation of adult tissues. By analyzing point mutations in conserved sequences in the T-box DNA-binding domain, we found that two overlapping, but physically separable regions are required for the physical and functional interaction with H3K27-demethylase and H3K4-methyltransferase activities. Importantly, the ability to associate with these histone-modifying complexes is a conserved function for the T-box family. These novel mechanisms for T-box-mediated epigenetic regulation are essential, because point mutations that disrupt these interactions are found in a diverse array of human developmental genetic diseases.

摘要

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本文引用的文献

[1]
The emerging functions of histone demethylases.

Curr Opin Genet Dev. 2008-4

[2]
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Science. 2007-10-19

[3]
T-bet's ability to regulate individual target genes requires the conserved T-box domain to recruit histone methyltransferase activity and a separate family member-specific transactivation domain.

Mol Cell Biol. 2007-12

[4]
TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression.

Am J Hum Genet. 2007-10

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The histone H3 lysine-27 demethylase Jmjd3 links inflammation to inhibition of polycomb-mediated gene silencing.

Cell. 2007-9-21

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Science. 2007-10-19

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UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development.

Nature. 2007-10-11

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Am J Hum Genet. 2007-8

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J Clin Endocrinol Metab. 2007-10

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Nature. 2007-8-2

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