Dietary manipulation of histone structure and function

被引:85
作者
Delage, Barbara [1 ]
Dashwood, Roderick H. [1 ]
机构
[1] Oregon State Univ, Linus Pauling Inst Sci & Med, Corvallis, OR 97331 USA
关键词
epigenetics; histone code; diet; fetal development; cancer; HDAC; HAT;
D O I
10.1146/annurev.nutr.28.061807.155354
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Post-translational modifications of histones are the subject of intensive investigations with the aim of decoding how they regulate, alone or in combination, chromatin structure, genomic stability, and gene expression. Major epigenetic programming events take place during gametogenesis and fetal development and are thought to have long-lasting consequences on adult health. Epidemiological and experimental studies have pointed toward maternal nutrition as a major player during prenatal development in influencing disease susceptibility later in life. Although the mechanisms underlying such observations are not well elucidated, epigenetic alterations of histones by particular maternal diets might be of central importance. Moreover, as much as dietary sources can influence epigenetic programming during pregnancy, they have started to be implicated in cancer chemoprevention, via the targeting of reversible epigenetic deregulations at the level of the histones.
引用
收藏
页码:347 / MC4
页数:24
相关论文
共 139 条
[1]  
Adenot PG, 1997, DEVELOPMENT, V124, P4615
[2]   MeCP2 interacts with HP1 and modulates its heterochromatin association during myogenic differentiation [J].
Agarwal, Noopur ;
Hardt, Tanja ;
Brero, Alessandro ;
Nowak, Danny ;
Rothbauer, Ulrich ;
Becker, Annette ;
Leonhardt, Heinrich ;
Cardoso, M. Cristina .
NUCLEIC ACIDS RESEARCH, 2007, 35 (16) :5402-5408
[3]   Inadequate histone deacetylation during oocyte meiosis causes aneuploidy and embryo death in mice [J].
Akiyama, Tomohiko ;
Nagata, Masao ;
Aoki, Fugaku .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (19) :7339-7344
[4]   Regulation of transcriptional activity during the first and second cell cycles in the preimplantation mouse embryo [J].
Aoki, F ;
Worrad, DM ;
Schultz, RM .
DEVELOPMENTAL BIOLOGY, 1997, 181 (02) :296-307
[5]   Histone deacetylase 3 (HDAC3) is recruited to target promoters by PML-RARα as a component of the N-CoR co-repressor complex to repress transcription in vivo [J].
Atsumi, Akihide ;
Tomita, Akihiro ;
Kiyoi, Hitoshi ;
Naoe, Tomoki .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 345 (04) :1471-1480
[6]   Epigenetic characterization of hematopoietic stem cell differentiation using miniChIP and bisulfite sequencing analysis [J].
Attema, Joanne L. ;
Papathanasiou, Peter ;
Forsberg, E. Camilla ;
Xu, Jian ;
Smale, Stephen T. ;
Weissman, Irving L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (30) :12371-12376
[7]   Chromatin signatures of pluripotent cell lines [J].
Azuara, V ;
Perry, P ;
Sauer, S ;
Spivakov, M ;
Jorgensen, HF ;
John, RM ;
Gouti, M ;
Casanova, M ;
Warnes, G ;
Merkenschlager, M ;
Fisher, AG .
NATURE CELL BIOLOGY, 2006, 8 (05) :532-U189
[8]  
Bachvarova R, 1985, Dev Biol (N Y 1985), V1, P453
[9]   Curcumin, a novel p300/CREB-binding protein-specific inhibitor of acetyltransferase, represses the acetylation of histone/nonhistone proteins and histone acetyltransferase-dependent chromatin transcription [J].
Balasubramanyam, K ;
Varier, RA ;
Altaf, M ;
Swaminathan, V ;
Siddappa, NB ;
Ranga, U ;
Kundu, TK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (49) :51163-51171
[10]   Polyisoprenylated benzophenone, garcinol, a natural histone acetyltransferase inhibitor, represses chromatin transcription and alters global gene expression [J].
Balasubramanyam, K ;
Altaf, M ;
Varier, RA ;
Swaminathan, V ;
Ravindran, A ;
Sadhale, PP ;
Kundu, TK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (32) :33716-33726