BRCA1 associates with the inactive X chromosome in late S-phase, coupled with transient H2AX phosphorylation

被引:27
作者
Chadwick, BP [1 ]
Lane, TF
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Inst Genome Sci & Policy, Durham, NC 27710 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Mol Biol Inst, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Jonsson Comprehens Canc Ctr, Div Gyn Oncol, Los Angeles, CA 90095 USA
关键词
D O I
10.1007/s00412-005-0029-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The BRCA1 tumor suppressor gene encodes an E3-ubiquitin ligase that has been implicated in several distinct biochemical processes. As the cell cycle progresses, BRCA1 proteins interact transiently with nuclear foci containing DNA replication and DNA double-strand repair machinery. A hallmark of these foci is the presence of S139 phosphorylated histone H2AX. BRCA1 was recently shown to associate with facultative heterochromatin at the inactive X chromosome (Xi), where it may play a role in maintaining gene silencing. As the kinetics of this interaction has not been described, we sought to establish whether association of BRCA1 with the Xi also correlated with replication. Here we demonstrate that the interaction of BRCA1 and the Xi is transient, occurring during late S-phase. This interaction is concomitant with the presence of distinct foci of S139 phospho-H2AX and specifically corresponds with late replication of the Xi. BRCA1 and phospho-H2AX appear on the Xi immediately adjacent to CAF-1, a known marker of replication fork activity. Taken together, these data implicate BRCA1 and the H2AX kinase in replication of facultative heterochromatin on the Xi, most likely in a fashion similar to that performed at sites of DNA replication and double-strand break repair observed on somatic chromosomes.
引用
收藏
页码:432 / 439
页数:8
相关论文
共 52 条
  • [11] CLEMSON CM, 1996, J CELL BIOL, V132, P1
  • [12] Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals
    Costanzi, C
    Pehrson, JR
    [J]. NATURE, 1998, 393 (6685) : 599 - 601
  • [13] Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation
    Csankovszki, G
    Nagy, A
    Jaenisch, R
    [J]. JOURNAL OF CELL BIOLOGY, 2001, 153 (04) : 773 - 783
  • [14] Conditional deletion of Xist disrupts histone macroH2A localization but not maintenance of X inactivation
    Csankovszki, G
    Panning, B
    Bates, B
    Pehrson, JR
    Jaenisch, R
    [J]. NATURE GENETICS, 1999, 22 (04) : 323 - 324
  • [15] Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation
    de Napoles, M
    Mermoud, JE
    Wakao, R
    Tang, YA
    Endoh, M
    Appanah, R
    Nesterova, TB
    Silva, J
    Otte, AP
    Vidal, M
    Koseki, H
    Brockdorff, N
    [J]. DEVELOPMENTAL CELL, 2004, 7 (05) : 663 - 676
  • [16] The human decatenation checkpoint
    Deming, PB
    Cistulli, CA
    Zhao, H
    Graves, PR
    Piwnica-Worms, H
    Paules, RS
    Downes, CS
    Kaufmann, WK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) : 12044 - 12049
  • [17] Chromatin dynamics at DNA replication, transcription and repair
    Ehrenhofer-Murray, AE
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 2004, 271 (12): : 2335 - 2349
  • [18] Ring1b-mediated H2A ubiquitination associates with inactive X chromosomes and is involved in initiation of X inactivation
    Fang, J
    Chen, TP
    Chadwick, B
    Li, E
    Zhang, Y
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (51) : 52812 - 52815
  • [19] H2AX is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis
    Fernandez-Capetillo, O
    Mahadevaiah, SK
    Celeste, A
    Romanienko, PJ
    Camerini-Otero, RD
    Bonner, WM
    Manova, K
    Burgoyne, P
    Nussenzweig, A
    [J]. DEVELOPMENTAL CELL, 2003, 4 (04) : 497 - 508
  • [20] H2AX: the histone guardian of the genome
    Fernandez-Capetillo, O
    Lee, A
    Nussenzweig, M
    Nussenzweig, A
    [J]. DNA REPAIR, 2004, 3 (8-9) : 959 - 967