Histone modifications and mitosis: countermarks, landmarks, and bookmarks

被引:134
作者
Wang, Fangwei [1 ]
Higgins, Jonathan M. G. [2 ]
机构
[1] Zhejiang Univ, Inst Life Sci, Hangzhou 310058, Zhejiang, Peoples R China
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
关键词
histone; phosphorylation; acetylation; methylation; mitosis; centromere; CELL-CYCLE PROGRESSION; CHROMOSOME BI-ORIENTATION; KINASE AURORA B; CENP-A; MITOTIC CHROMOSOMES; CENTROMERIC CHROMATIN; H3; PHOSPHORYLATION; IN-VIVO; THR-3; TRANSCRIPTION FACTORS;
D O I
10.1016/j.tcb.2012.11.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The roles of post-translational histone modifications in regulating transcription and DNA damage have been widely studied and discussed. Although mitotic histone marks, particularly phosphorylation, were discovered four decades ago, their roles in mitosis have been outlined only in the past few years. Here we aim to provide an integrated view of how histone modifications act as 'countermarks', 'landmarks', and 'bookmarks' to displace, recruit, and 'remember' the location of regulatory proteins during and shortly after mitosis. These capabilities allow histone marks to help downregulate interphase functions such as transcription during mitosis, to facilitate chromatin events required to accomplish chromosome segregation, and to contribute to the maintenance of epigenetic states through mitosis.
引用
收藏
页码:175 / 184
页数:10
相关论文
共 116 条
[1]   INCENP centromere and spindle targeting: Identification of essential conserved motifs and involvement of heterochromatin protein HP1 [J].
Ainsztein, AM ;
Kandels-Lewis, SE ;
Mackay, AM ;
Earnshaw, WC .
JOURNAL OF CELL BIOLOGY, 1998, 143 (07) :1763-1774
[2]   A paucity of heterochromatin at functional human neocentromeres [J].
Alonso, Alicia ;
Hasson, Dan ;
Cheung, Fanny ;
Warburton, Peter E. .
EPIGENETICS & CHROMATIN, 2010, 3
[3]   Epigenetic engineering shows H3K4me2 is required for HJURP targeting and CENP-A assembly on a synthetic human kinetochore [J].
Bergmann, Jan H. ;
Rodriguez, Mariluz Gomez ;
Martins, Nuno M. C. ;
Kimura, Hiroshi ;
Kelly, David A. ;
Masumoto, Hiroshi ;
Larionov, Vladimir ;
Jansen, Lars E. T. ;
Earnshaw, William C. .
EMBO JOURNAL, 2011, 30 (02) :328-340
[4]   Cell-Cycle-Dependent Structural Transitions in the Human CENP-A Nucleosome In Vivo [J].
Bui, Minh ;
Dimitriadis, Emilios K. ;
Hoischen, Christian ;
An, Eunkyung ;
Quenet, Delphine ;
Giebe, Sindy ;
Nita-Lazar, Aleksandra ;
Diekmann, Stephan ;
Dalal, Yamini .
CELL, 2012, 150 (02) :317-326
[5]   Active transcription and essential role of RNA polymerase II at the centromere during mitosis [J].
Chan, F. Lyn ;
Marshall, Owen J. ;
Saffery, Richard ;
Kim, Bo Won ;
Earle, Elizabeth ;
Choo, K. H. Andy ;
Wong, Lee H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (06) :1979-1984
[6]   TBP dynamics in living human cells: Constitutive association of TBP with mitotic chromosomes [J].
Chen, DY ;
Hinkley, CS ;
Henry, RW ;
Huang, S .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (01) :276-284
[7]   Cell cycle control of centromeric repeat transcription and heterochromatin assembly [J].
Chen, Ee Sin ;
Zhang, Ke ;
Nicolas, Estelle ;
Cam, Hugh P. ;
Zofall, Martin ;
Grewal, Shiv I. S. .
NATURE, 2008, 451 (7179) :734-737
[8]   The solution structure of the first PHD finger of autoimmune regulator in complex with non-modified histone H3 tail reveals the antagonistic role of H3R2 methylation [J].
Chignola, Francesca ;
Gaetani, Massimiliano ;
Rebane, Ana ;
Org, Tonis ;
Mollica, Luca ;
Zucchelli, Chiara ;
Spitaleri, Andrea ;
Mannella, Valeria ;
Peterson, Paert ;
Musco, Giovanna .
NUCLEIC ACIDS RESEARCH, 2009, 37 (09) :2951-2961
[9]   Association of human TFIID-promoter complexes with silenced mitotic chromatin in vivo [J].
Christova, R ;
Oelgeschläger, T .
NATURE CELL BIOLOGY, 2002, 4 (01) :79-82
[10]   Molecular recognition of histone H3 by the WD40 protein WDR5 [J].
Couture, Jean-Francois ;
Collazo, Evys ;
Trievel, Raymond C. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (08) :698-703