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Mammalian Genomic Imprinting
被引:327
|作者:
Bartolomei, Marisa S.
[1
]
Ferguson-Smith, Anne C.
[2
]
机构:
[1] Univ Penn, Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19063 USA
[2] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
来源:
基金:
英国生物技术与生命科学研究理事会;
英国惠康基金;
关键词:
BECKWITH-WIEDEMANN-SYNDROME;
MOUSE H19 GENE;
DNA METHYLATION;
PRADER-WILLI;
GERM-CELLS;
PREIMPLANTATION DEVELOPMENT;
PATERNAL METHYLATION;
GROWTH-RETARDATION;
MATERNAL-BEHAVIOR;
PARENTAL ORIGIN;
D O I:
10.1101/cshperspect.a002592
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Normal mammalian development requires a maternal and paternal contribution, which is attributed to imprinted genes, or genes that are expressed from a single parental allele. Approximately 100 imprinted genes have been reported in mammals thus far. Imprinted genes are controlled by cis-acting regulatory elements, termed imprinting control regions (ICRs), which have parental-specific epigenetic modifications, including DNA methylation. ICRs are methylated by de novo DNA methyltransferases during germline development; these parental-specific modifications must be maintained following fertilization when the genome is extensively reprogrammed. Many imprinted genes reside in similar to 1-megabase clusters, with two major mechanisms of imprinting regulation currently recognized, CTCF-dependent insulators and long noncoding RNAs. Unclustered imprinted genes are generally regulated by germline-derived differential promoter methylation. Here, we describe the identification and functions of imprinted genes, cis-acting control sequences, trans-acting factors, and imprinting mechanisms in clusters. Finally, we define questions that require more extensive research.
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页码:1 / 17
页数:17
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