Home LiteratureArticle Details
PMID: 15621527 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Formation of MacroH2A-containing senescence-associated heterochromatin foci and senescence driven by ASF1a and HIRA.

Developmental cell ·Vol. 8 ·No. 1 ·2005-01-00 ·Pages 19-30

Zhang R, Poustovoitov MV, Ye X, Santos HA, Chen W, Daganzo SM, Erzberger JP, Serebriiskii IG, Canutescu AA, Dunbrack RL, Pehrson JR, Berger JM, Kaufman PD, Adams PD

Abstract

In senescent cells, specialized domains of transcriptionally silent senescence-associated heterochromatic foci (SAHF), containing heterochromatin proteins such as HP1, are thought to repress expression of proliferation-promoting genes. We have investigated the composition and mode of assembly of SAHF and its contribution to cell cycle exit. SAHF is enriched in a transcription-silencing histone H2A variant, macroH2A. As cells approach senescence, a known chromatin regulator, HIRA, enters PML nuclear bodies, where it transiently colocalizes with HP1 proteins, prior to incorporation of HP1 proteins into SAHF. A physical complex containing HIRA and another chromatin regulator, ASF1a, is rate limiting for formation of SAHF and onset of senescence, and ASF1a is required for formation of SAHF and efficient senescence-associated cell cycle exit. These data indicate that HIRA and ASF1a drive formation of macroH2A-containing SAHF and senescence-associated cell cycle exit, via a pathway that appears to depend on flux of heterochromatic proteins through PML bodies.

MeSH Terms
Amino Acid Sequence Blotting, Western/methods Cell Count/methods Cell Cycle/physiology Cell Cycle Proteins/physiology Cell Line Cellular Senescence/physiology Chromobox Protein Homolog 5 Chromosomal Proteins, Non-Histone/metabolism Dosage Compensation, Genetic Gene Expression Regulation/physiology Heterochromatin/metabolism Histones/metabolism Immunohistochemistry/methods Immunoprecipitation/methods Indoles Molecular Chaperones Neoplasm Proteins/metabolism Nuclear Proteins/metabolism Recombinant Fusion Proteins/metabolism Repressor Proteins Time Factors Transcription Factors/metabolism Transfection/methods Tumor Suppressor Proteins ras Proteins/metabolism
Chemicals
ASF1A protein, human Cell Cycle Proteins Chromosomal Proteins, Non-Histone Heterochromatin Histones Indoles Molecular Chaperones Neoplasm Proteins Nuclear Proteins Recombinant Fusion Proteins Repressor Proteins Transcription Factors Tumor Suppressor Proteins macroH2A histone Chromobox Protein Homolog 5 DAPI ras Proteins
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Zhang Rugang
Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Poustovoitov Maxim V
Ye Xiaofen
Santos Hidelita A
Chen Wei
Daganzo Sally M
Erzberger Jan P
Serebriiskii Ilya G
Canutescu Adrian A
Dunbrack Roland L
Pehrson John R
Berger James M
Kaufman Paul D
Adams Peter D
Article Info
Journal
Developmental cell
Abbr.
Dev Cell
ISSN
1534-5807
Published
2005-01-00
Pages
19-30
Language
English
Region
United States
NLM ID
101120028
Subset
IM
Grants
NIGMS NIH HHS · GM-49351 · United States
NIGMS NIH HHS · R01 GM062281 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com