Authors
Chen, Poshen B.Hung, Jui-Hung
Hickman, Taylor L.
Coles, Andrew H.
Carey, James F.
Weng, Zhiping
Chu, Feixia
Fazzio, Thomas G
UMass Chan Affiliations
Program in Molecular MedicineDepartment of Biochemistry and Molecular Pharmacology
Program in Bioinformatics and Integrative Biology
Program in Gene Function and Expression
Document Type
Journal ArticlePublication Date
2013-12-03Keywords
Hdac6Kat5
Tip60
chromatin
stem cells
Biochemistry
Cellular and Molecular Physiology
Developmental Biology
Molecular Biology
Metadata
Show full item recordAbstract
In embryonic stem cells (ESCs), the Tip60 histone acetyltransferase activates genes required for proliferation and silences genes that promote differentiation. Here we show that the class II histone deacetylase Hdac6 co-purifies with Tip60-p400 complex from ESCs. Hdac6 is necessary for regulation of most Tip60-p400 target genes, particularly those repressed by the complex. Unlike differentiated cells, where Hdac6 is mainly cytoplasmic, Hdac6 is largely nuclear in ESCs, neural stem cells (NSCs), and some cancer cell lines, and interacts with Tip60-p400 in each. Hdac6 localizes to promoters bound by Tip60-p400 in ESCs, binding downstream of transcription start sites. Surprisingly, Hdac6 does not appear to deacetylate histones, but rather is required for Tip60-p400 binding to many of its target genes. Finally, we find that, like canonical subunits of Tip60-p400, Hdac6 is necessary for robust ESC differentiation. These data suggest that Hdac6 plays a major role in the modulation of Tip60-p400 function in stem cells. DOI: http://dx.doi.org/10.7554/eLife.01557.001.Source
Chen PB, Hung JH, Hickman TL, Coles AH, Carey JF, Weng Z, Chu F, Fazzio TG. Hdac6 regulates Tip60-p400 function in stem cells. Elife. 2013 Dec 3;2:e01557. doi: 10.7554/eLife.01557. Link to article on publisher's siteDOI
10.7554/eLife.01557Permanent Link to this Item
http://hdl.handle.net/20.500.14038/44493PubMed ID
24302573Related Resources
Link to Article in PubMedRights
Copyright 2013, Chen et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
ae974a485f413a2113503eed53cd6c53
10.7554/eLife.01557