Histone lysine methylation in genomic imprinting

被引:14
作者
Ciccone, David N. [1 ]
Chen, Taiping [1 ]
机构
[1] Novartis Inst Biomed Res, Cambridge, MA 02139 USA
关键词
genomic imprinting; DNA methylation; lysine methylation; chromatin; Dnmt; Zfp57; ZINC-FINGER PROTEINS; EMBRYONIC STEM-CELLS; DE-NOVO METHYLATION; DNA METHYLATION; H3; METHYLTRANSFERASE; EARLY EMBRYOGENESIS; EFFECT GENE; DNMT3L; ESTABLISHMENT; DOMAIN;
D O I
10.4161/epi.8974
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
Genomic imprinting is an epigenetic phenomenon that causes parent-of-origin-specific expression of a small subset of genes in mammals. DNA methylation is believed to be the primary epigenetic signal that controls genomic imprinting. These methylation imprints are established during gametogenesis in male and female germ cells and maintained and interpreted during embryogenesis and in somatic tissues. Based on recent studies, histone lysine methylation plays an important role in the regulation of imprinted gene expression and, more intriguingly, may also be involved in the establishment and maintenance of DNA methylation imprints. In this point of view, we discuss these studies and their implications.
引用
收藏
页码:216 / 220
页数:5
相关论文
共 38 条
[1]   New nomenclature for chromatin-modifying enzymes [J].
Allis, C. David ;
Berger, Shelley L. ;
Cote, Jacques ;
Dent, Sharon ;
Jenuwien, Thomas ;
Kouzarides, Tony ;
Pillus, Lorraine ;
Reinberg, Danny ;
Shi, Yang ;
Shiekhattar, Ramin ;
Shilatifard, Ali ;
Workman, Jerry ;
Zhang, Yi .
CELL, 2007, 131 (04) :633-636
[2]   Dnmt3L and the establishment of maternal genomic imprints [J].
Bourc'his, D ;
Xu, GL ;
Lin, CS ;
Bollman, B ;
Bestor, TH .
SCIENCE, 2001, 294 (5551) :2536-2539
[3]   The DNA methyltransferase-like protein DNMT3L stimulates de novo methylation by Dnmt3a [J].
Chédin, F ;
Lieber, MR ;
Hsieh, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (26) :16916-16921
[4]   Establishment and maintenance of genomic methylation patterns in mouse embryonic stem cells by Dnmt3a and Dnmt3b [J].
Chen, TP ;
Ueda, Y ;
Dodge, JE ;
Wang, ZJ ;
Li, E .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (16) :5594-5605
[5]   Transcription is required for establishment of germline methylation marks at imprinted genes [J].
Chotalia, Mita ;
Smallwood, Sebastien A. ;
Ruf, Nico ;
Dawson, Claire ;
Lucifero, Diana ;
Frontera, Marga ;
James, Katherine ;
Dean, Wendy ;
Kelsey, Gavin .
GENES & DEVELOPMENT, 2009, 23 (01) :105-117
[6]   Phenotypic plasticity and the epigenetics of human disease [J].
Feinberg, Andrew P. .
NATURE, 2007, 447 (7143) :433-440
[7]   Epigenetics - Perceptive enzymes [J].
Ferguson-Smith, Anne C. ;
Greally, John M. .
NATURE, 2007, 449 (7159) :148-149
[8]   KAP-1, a novel corepressor for the highly conserved KRAB repression domain [J].
Friedman, JR ;
Fredericks, WJ ;
Jensen, DE ;
Speicher, DW ;
Huang, XP ;
Neilson, EG ;
Rauscher, FJ .
GENES & DEVELOPMENT, 1996, 10 (16) :2067-2078
[9]   Mechanism of stimulation of catalytic activity of Dnmt3A and Dnmt3B DNA-(cytosine-C5)-methyltransferases by Dnmt3L [J].
Gowher, H ;
Liebert, K ;
Hermann, A ;
Xu, GL ;
Jeltsch, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (14) :13341-13348
[10]  
Hata K, 2002, DEVELOPMENT, V129, P1983