Histone H3 Variants and Their Chaperones During Development and Disease: Contributing to Epigenetic Control

被引:85
作者
Filipescu, Dan [1 ]
Mueller, Sebastian
Almouzni, Genevieve
机构
[1] Inst Curie, Ctr Rech, F-75248 Paris, France
来源
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 30 | 2014年 / 30卷
关键词
chromatin; histone; H3; variants; chaperones; epigenetics; development; cancer; CENTROMERE PROTEIN-A; ASSEMBLY FACTOR-I; DOMAIN-ASSOCIATED PROTEIN; CENP-A; CHROMATIN-STRUCTURE; TELOMERES PHENOTYPE; INTERACTING PROTEIN; DRIVER MUTATIONS; PROGNOSTIC VALUE; DNA-REPLICATION;
D O I
10.1146/annurev-cellbio-100913-013311
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Within the nucleus, the interplay between lineage-specific transcription factors and chromatin dynamics defines cellular identity. Control of this interplay is necessary to properly balance stability and plasticity during the development and entire life span of multicellular organisms. Here, we present our current knowledge of the contribution of histone H3 variants to chromatin dynamics during development. We review the network of histone chaperones that governs their deposition timing and sites of incorporation and highlight how their distinct distribution impacts genome organization and function. We integrate the importance of H3 variants in the context of nuclear reprogramming and cell differentiation, and, using the centromere as a paradigm, we describe a case in which the identity of a given genomic locus is propagated across different cell types. Finally, we compare development to changes in stress and disease. Both physiological and pathological settings underline the importance of H3 dynamics for genome and chromatin integrity.
引用
收藏
页码:615 / 646
页数:32
相关论文
共 205 条
[1]   Transcription Recovery after DNA Damage Requires Chromatin Priming by the H3.3 Histone Chaperone HIRA [J].
Adam, Salome ;
Polo, Sophie E. ;
Almouzni, Genevieve .
CELL, 2013, 155 (01) :94-106
[2]   The nuclear Hat1p/Hat2p complex: A molecular link between type B histone acetyltransferases and chromatin assembly [J].
Ai, X ;
Parthun, MR .
MOLECULAR CELL, 2004, 14 (02) :195-205
[3]   Accumulation of the FACT complex, as well as histone H3.3, serves as a target marker for somatic hypermutation [J].
Aida, Masatoshi ;
Hamad, Nesreen ;
Stanlie, Andre ;
Begum, Nasim A. ;
Honjo, Tasuku .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (19) :7784-7789
[4]   H3F3A K27M mutations in thalamic gliomas from young adult patients [J].
Aihara, Koki ;
Mukasa, Akitake ;
Gotoh, Kengo ;
Saito, Kuniaki ;
Nagae, Genta ;
Tsuji, Shingo ;
Tatsuno, Kenji ;
Yamamoto, Shogo ;
Takayanagi, Shunsaku ;
Narita, Yoshitaka ;
Shibui, Soichiro ;
Aburatani, Hiroyuki ;
Saito, Nobuhito .
NEURO-ONCOLOGY, 2014, 16 (01) :140-146
[5]   Dynamic Replacement of Histone H3 Variants Reprograms Epigenetic Marks in Early Mouse Embryos [J].
Akiyama, Tomohiko ;
Suzuki, Osamu ;
Matsuda, Junichiro ;
Aoki, Fugaku .
PLOS GENETICS, 2011, 7 (10)
[6]  
Albig W, 1996, HUM GENET, V97, P486
[7]   An epigenetic silencing pathway controlling T helper 2 cell lineage commitment [J].
Allan, Rhys S. ;
Zueva, Elina ;
Cammas, Florence ;
Schreiber, Heidi A. ;
Masson, Vanessa ;
Belz, Gabrielle T. ;
Roche, Daniele ;
Maison, Christele ;
Quivy, Jean-Pierre ;
Almouzni, Genevieve ;
Amigorena, Sebastian .
NATURE, 2012, 487 (7406) :249-U137
[8]   CENPA overexpression promotes genome instability in pRb-depleted human cells [J].
Amato, Angela ;
Schillaci, Tiziana ;
Lentini, Laura ;
Di Leonardo, Aldo .
MOLECULAR CANCER, 2009, 8
[9]   Centromere protein A dynamics in human pluripotent stem cell self-renewal, differentiation and DNA damage [J].
Ambartsumyan, Gayane ;
Gill, Rajbir K. ;
Perez, Silvia Diaz ;
Conway, Deirdre ;
Vincent, John ;
Dalal, Yamini ;
Clark, Amander T. .
HUMAN MOLECULAR GENETICS, 2010, 19 (20) :3970-3982
[10]   Nucleosome Structure(s) and Stability: Variations on a Theme [J].
Andrews, Andrew J. ;
Luger, Karolin .
ANNUAL REVIEW OF BIOPHYSICS, VOL 40, 2011, 40 :99-117