The bromodomain: A chromatin browser?

被引:29
作者
Filetici, P [1 ]
Ornaghi, P [1 ]
Ballario, P [1 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Genet & Biol Mol 2, CNR, Ctr Acidi Nucl, I-00185 Rome, Italy
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2001年 / 6卷
关键词
gene expression; chromatin; yeast; histone acetyltransferase; review;
D O I
10.2741/Filetici
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
Reversible modification of histone tails is a regulatory step in chromatin remodeling. The N-terminal tails of histones are signaling platforms that carry amino acid residues for post-translational modification and contribute to chromosomal higher order structure. These modifications are performed by a number of chromatin modulators such as histone (h) acetyltransferase, h-deacetylase, h-methyltransferase and h-kinase. Large numbers of these enzymes as well as other chromatin-associated proteins share the bromodomain, a signature protein motif. Structural studies reveal not only wide structural conservation of bromodomains but also envision a possible role of this domain in the recognition of specific modified residues in the histone tails. The widespread presence of bromodomains in leukemogenic and cancer genes has provided a fundamental tool for studies of the role of epigenetic and chromatin remodeling in malignant diseases.
引用
收藏
页码:D866 / D876
页数:11
相关论文
共 92 条
[1]   The CBP co-activator is a histone acetyltransferase [J].
Bannister, AJ ;
Kouzarides, T .
NATURE, 1996, 384 (6610) :641-643
[2]   Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain [J].
Bannister, AJ ;
Zegerman, P ;
Partridge, JF ;
Miska, EA ;
Thomas, JO ;
Allshire, RC ;
Kouzarides, T .
NATURE, 2001, 410 (6824) :120-124
[3]   Repression of GCN5 histone acetyltransferase activity via bromodomain-mediated binding and phosphorylation by the Ku-DNA-dependent protein kinase complex [J].
Barlev, NA ;
Poltoratsky, V ;
Owen-Hughes, T ;
Ying, C ;
Liu, L ;
Workman, JL ;
Berger, SL .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (03) :1349-1358
[4]   MOLECULAR-BASIS OF 11Q23 REARRANGEMENTS IN HEMATOPOIETIC MALIGNANT PROLIFERATIONS [J].
BERNARD, OA ;
BERGER, R .
GENES CHROMOSOMES & CANCER, 1995, 13 (02) :75-85
[5]   The human brm protein is cleaved during apoptosis: The role of cathepsin G [J].
Biggs, JR ;
Yang, J ;
Gullberg, U ;
Muchardt, C ;
Yaniv, M ;
Kraft, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (07) :3814-3819
[6]   BRCA1 is associated with a human SWI/SNF-related complex: Linking chromatin remodeling to breast cancer [J].
Bochar, DA ;
Wang, L ;
Beniya, H ;
Kinev, A ;
Xue, YT ;
Lane, WS ;
Wang, WD ;
Kashanchi, F ;
Shiekhattar, R .
CELL, 2000, 102 (02) :257-265
[7]   The translocation t(8;l6)(p11, p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB binding protein [J].
Borrow, J ;
Stanton, VP ;
Andresen, JM ;
Becher, R ;
Behm, FG ;
Chaganti, RSK ;
Civin, CI ;
Disteche, C ;
Dube, I ;
Frischauf, AM ;
Horsman, D ;
Mitelman, F ;
Volinia, S ;
Watmore, AE ;
Housman, DE .
NATURE GENETICS, 1996, 14 (01) :33-41
[8]   Tetrahymena histone acetyltransferase A: A homolog to yeast Gcn5p linking histone acetylation to gene activation [J].
Brownell, JE ;
Zhou, JX ;
Ranalli, T ;
Kobayashi, R ;
Edmondson, DG ;
Roth, SY ;
Allis, CD .
CELL, 1996, 84 (06) :843-851
[9]   Two functionally distinct forms of the RSC nucleosome-remodeling complex, containing essential AT hook, BAH, and bromodomains [J].
Cairns, BR ;
Schlichter, A ;
Erdjument-Bromage, H ;
Tempst, P ;
Kornberg, RD ;
Winston, F .
MOLECULAR CELL, 1999, 4 (05) :715-723
[10]   Histone acetyltransferase activity and interaction with ADA2 are critical for GCN5 function in vivo [J].
Candau, R ;
Zhou, JX ;
Allis, CD ;
Berger, SL .
EMBO JOURNAL, 1997, 16 (03) :555-565