Direct assessment of histone function using histone replacement

被引:5
作者
Corcoran, Emma Tung [1 ]
Jacob, Yannick [1 ]
机构
[1] Yale Univ, Fac Arts & Sci, Dept Mol Cellular & Dev Biol, 260 Whitney Ave, New Haven, CT 06511 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
AMINO-TERMINAL TAILS; SILENT MATING LOCI; EXPRESSION IN-VIVO; GLOBAL ANALYSIS; METHYLTRANSFERASE ACTIVITY; SACCHAROMYCES-CEREVISIAE; CHROMATIN-STRUCTURE; DNA-REPLICATION; POINT MUTATIONS; CORE HISTONES;
D O I
10.1016/j.tibs.2022.06.010
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
Histones serve many purposes in eukaryotic cells in the regulation of diverse genomic processes, including transcription, replication, DNA repair, and chro-matin organization. As such, experimental systems to assess histone function are fundamental resources toward elucidating the regulation of activities occur-ring on chromatin. One set of important tools for investigating histone function are histone replacement systems, in which endogenous histone expression can be partially or completely replaced with a mutant histone. Histone replace-ment systems allow systematic screens of histone regulatory functions and the direct assessment of functions for histone residues. In this review, we describe existing histone replacement systems in model organisms, the benefits and limitations of these systems, and opportunities for future research with histone replacement strategies.
引用
收藏
页码:53 / 70
页数:18
相关论文
共 100 条
[1]   Sterile 20 kinase phosphorylates histone H2B at serine 10 during hydrogen peroxide-induced apoptosis in S. cerevisiae [J].
Ahn, SH ;
Cheung, WL ;
Hsu, JY ;
Diaz, RL ;
Smith, MM ;
Allis, CD .
CELL, 2005, 120 (01) :25-36
[2]   The dark side of histones: genomic organization and role of oncohistones in cancer [J].
Amatori, Stefano ;
Tavolaro, Simona ;
Gambardella, Stefano ;
Fanelli, Mirco .
CLINICAL EPIGENETICS, 2021, 13 (01)
[3]   Oncohistone mutations enhance chromatin remodeling and alter cell fates [J].
Bagert, John D. ;
Mitchener, Michelle M. ;
Patriotis, Agata L. ;
Dul, Barbara E. ;
Wojcik, Felix ;
Nacev, Benjamin A. ;
Feng, Lijuan ;
Allis, C. David ;
Muir, Tom W. .
NATURE CHEMICAL BIOLOGY, 2021, 17 (04) :403-+
[4]   What makes a histone variant a variant: Changing H2A to become H2A.Z [J].
Brewis, Hilary T. ;
Wang, Alice Y. ;
Gaub, Aline ;
Lau, Justine J. ;
Stirling, Peter C. ;
Kobor, Michael S. .
PLOS GENETICS, 2021, 17 (12)
[5]   Cse4 Is Part of an Octameric Nucleosome in Budding Yeast [J].
Camahort, Raymond ;
Shivaraju, Manjunatha ;
Mattingly, Mark ;
Li, Bing ;
Nakanishi, Shima ;
Zhu, Dongxiao ;
Shilatifard, Ali ;
Workman, Jerry L. ;
Gerton, Jennifer L. .
MOLECULAR CELL, 2009, 35 (06) :794-805
[6]   Role of histone H3 lysine 27 methylation in polycomb-group silencing [J].
Cao, R ;
Wang, LJ ;
Wang, HB ;
Xia, L ;
Erdjument-Bromage, H ;
Tempst, P ;
Jones, RS ;
Zhang, Y .
SCIENCE, 2002, 298 (5595) :1039-1043
[7]   A Role for Histone H4K 16 Hypoacetylation in Saccharomyces cerevisiae Kinetochore Function [J].
Choy, John S. ;
Acuna, Rachel ;
Au, Wei-Chun ;
Basrai, Munira A. .
GENETICS, 2011, 189 (01) :11-U595
[8]  
Corcoran E.T, 2022, BIORXIV, DOI [10.1101/2022.01.17.476649, DOI 10.1101/2022.01.17.476649]
[9]   Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal polycomb sites [J].
Czermin, B ;
Melfi, R ;
McCabe, D ;
Seitz, V ;
Imhof, A ;
Pirrotta, V .
CELL, 2002, 111 (02) :185-196
[10]   Probing nucleosome function: A highly versatile library of synthetic histone H3 and H4 mutants [J].
Dai, Junbiao ;
Hyland, Edel M. ;
Yuan, Daniel S. ;
Huang, Hailiang ;
Bader, Joel S. ;
Boeke, Jef D. .
CELL, 2008, 134 (06) :1066-1078