Chromatin mechanisms in genomic imprinting

被引:75
作者
Kacem, Slim [1 ,2 ,3 ]
Feil, Robert [1 ,2 ]
机构
[1] CNRS, UMR 5535, Inst Mol Genet IGMM, F-34293 Montpellier 5, France
[2] Univ Montpellier 1 & 2, Montpellier, France
[3] Farhat Hached Hosp, Dept Cytogenet Mol Genet & Biol Reprod, Sousse 4000, Tunisia
关键词
REPRESSIVE HISTONE METHYLATION; DIRECT REPEAT ELEMENT; DE-NOVO METHYLATION; DNA METHYLATION; CONTROL REGION; NONCODING RNAS; EVOLUTIONARY CONSERVATION; PARENTAL ORIGIN; CPG ISLANDS; MOUSE;
D O I
10.1007/s00335-009-9223-4
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
Mammalian imprinted genes are clustered in chromosomal domains. Their mono-allelic, parent-of-origin-specific expression is regulated by imprinting control regions (ICRs), which are essential sequence elements marked by DNA methylation on one of the two parental alleles. These methylation "imprints" are established during gametogenesis and, after fertilization, are somatically maintained throughout development. Nonhistone proteins and histone modifications contribute to this epigenetic process. The way ICRs mediate imprinted gene expression differs between domains. At some domains, for instance, ICRs produce long noncoding RNAs that mediate chromatin silencing. Lysine methylation on histone H3 is involved in this developmental process and is particularly important for imprinting in the placenta and brain. Together, the newly discovered chromatin mechanisms provide further clues for addressing imprinting-related pathologies in humans.
引用
收藏
页码:544 / 556
页数:13
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