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

被引:539
作者
Zhang, RG
Poustovoitov, MV
Ye, XF
Santos, HA
Chen, W
Daganzo, SM
Erzberger, JP
Serebriiskii, IG
Canutescu, AA
Dunbrack, RL
Pehrson, JR
Berger, JM
Kaufman, PD
Adams, PD
机构
[1] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[2] Russian State Med Univ, Moscow 117869, Russia
[3] Lawrence Berkeley Lab, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[5] Univ Penn, Sch Vet Med, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/j.devcel.2004.10.019
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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, ASF1 a, 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.
引用
收藏
页码:19 / 30
页数:12
相关论文
共 50 条
[1]  
Adams PD, 1996, MOL CELL BIOL, V16, P6623
[2]   Chromatin disassembly mediated by the histone chaperone Asf1 is essential for transcriptional activation of the yeast PH05 and PH08 genes [J].
Adkins, MW ;
Howar, SR ;
Tyler, JK .
MOLECULAR CELL, 2004, 14 (05) :657-666
[3]   The histone variant macroH2A interferes with transcription factor binding and SWI/SNF nucleosome remodeling [J].
Angelov, D ;
Molla, A ;
Perche, PY ;
Hans, F ;
Côté, J ;
Khochbin, S ;
Bouvet, P ;
Dimitrov, S .
MOLECULAR CELL, 2003, 11 (04) :1033-1041
[4]   STIMULATION OF WI-38 CELL-CYCLE TRANSIT - EFFECT OF SERUM CONCENTRATION AND CELL DENSITY [J].
BARTHOLOMEW, JC ;
NEFF, NT ;
ROSS, PA .
JOURNAL OF CELLULAR PHYSIOLOGY, 1976, 89 (02) :251-257
[5]   Pondering the promyelocytic leukemia protein (PML) puzzle: Possible functions for PML nuclear bodies [J].
Borden, KLB .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (15) :5259-5269
[6]   Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals [J].
Costanzi, C ;
Pehrson, JR .
NATURE, 1998, 393 (6685) :599-601
[7]   MACROH2A2, a new member of the MACROH2A core histone family [J].
Costanzi, C ;
Pehrson, JR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (24) :21776-21784
[8]   Structure and function of the conserved core of histone deposition protein Asf1 [J].
Daganzo, SM ;
Erzberger, JP ;
Lam, WM ;
Skordalakes, E ;
Zhang, RG ;
Franco, AA ;
Brill, SJ ;
Adams, PD ;
Berger, JM ;
Kaufman, PD .
CURRENT BIOLOGY, 2003, 13 (24) :2148-2158
[9]   PML is a direct p53 target that modulates p53 effector functions [J].
de Stanchina, E ;
Querido, E ;
Narita, M ;
Davuluri, RV ;
Pandolfi, PP ;
Ferbeyre, G ;
Lowe, SW .
MOLECULAR CELL, 2004, 13 (04) :523-535
[10]   A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO [J].
DIMRI, GP ;
LEE, XH ;
BASILE, G ;
ACOSTA, M ;
SCOTT, C ;
ROSKELLEY, C ;
MEDRANO, EE ;
LINSKENS, M ;
RUBELJ, I ;
PEREIRASMITH, O ;
PEACOCKE, M ;
CAMPISI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9363-9367