Regulation of Imprinting in Clusters: Noncoding RNAs Versus Insulators

被引:96
作者
Wan, Le-Ben [1 ]
Bartolomei, Marisa S. [1 ]
机构
[1] Univ Penn, Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
来源
LONG-RANGE CONTROL OF GENE EXPRESSION | 2008年 / 61卷
关键词
D O I
10.1016/S0065-2660(07)00007-7
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Genomic imprinting is an epigenetic mechanism of transcriptional regulation through which expression of a subset of mammalian genes is restricted to one parental allele. An intriguing characteristic of imprinted genes is that they often cluster in megabase-sized chromosomal domains, indicating that domain-specific mechanisms regulate imprinting. Detailed study of the known imprinted domains has revealed a number of common characteristics. First, all clusters have an imprinting control region (ICR) that is typically 1-5 kb in size and differentially methylated, and that regulates imprinting across the entire domain. Second, the clusters have at least one noncoding RNA (ncRNA) that is usually expressed from the maternal allele and multiple paternally expressed protein-coding genes. Finally, the clusters are likely regulated by one of two mechanisms, transcription of a long ncRNA that silences expression of protein-coding genes bidirectionally in cis and blocking of shared enhancer elements by CCCTC binding factor (CTCF) binding insulators. More recent experiments may even suggest that both mechanisms operate at some clusters. In this chapter, we will describe what is known about imprinting at five well-studied imprinted loci and highlight some of the critical experiments that are required before a full understanding of imprinting mechanisms is achieved. (C) 2008, Elsevier Inc.
引用
收藏
页码:207 / 223
页数:17
相关论文
共 78 条
[1]
Ainscough JFX, 2000, DEVELOPMENT, V127, P3923
[2]
THE MOUSE INSULIN-LIKE GROWTH-FACTOR TYPE-2 RECEPTOR IS IMPRINTED AND CLOSELY LINKED TO THE TME LOCUS [J].
BARLOW, DP ;
STOGER, R ;
HERRMANN, BG ;
SAITO, K ;
SCHWEIFER, N .
NATURE, 1991, 349 (6304) :84-87
[3]
PARENTAL IMPRINTING OF THE MOUSE H19 GENE [J].
BARTOLOMEI, MS ;
ZEMEL, S ;
TILGHMAN, SM .
NATURE, 1991, 351 (6322) :153-155
[4]
The protein CTCF is required for the enhancer blocking activity of vertebrate insulators [J].
Bell, AC ;
West, AG ;
Felsenfeld, G .
CELL, 1999, 98 (03) :387-396
[5]
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene [J].
Bell, AC ;
Felsenfeld, G .
NATURE, 2000, 405 (6785) :482-485
[6]
THE ONTOGENY OF ALLELE-SPECIFIC METHYLATION ASSOCIATED WITH IMPRINTED GENES IN THE MOUSE [J].
BRANDEIS, M ;
KAFRI, T ;
ARIEL, M ;
CHAILLET, JR ;
MCCARREY, J ;
RAZIN, A ;
CEDAR, H .
EMBO JOURNAL, 1993, 12 (09) :3669-3677
[7]
Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region [J].
Cavaillé, J ;
Seitz, H ;
Paulsen, M ;
Ferguson-Smith, AC ;
Bachellerie, JP .
HUMAN MOLECULAR GENETICS, 2002, 11 (13) :1527-1538
[8]
The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status [J].
Charlier, C ;
Segers, K ;
Karim, L ;
Shay, T ;
Gyapay, G ;
Cockett, N ;
Georges, M .
NATURE GENETICS, 2001, 27 (04) :367-369
[9]
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts:: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8 [J].
Charlier, C ;
Segers, K ;
Wagenaar, D ;
Karim, L ;
Berghams, S ;
Jaillon, O ;
Shay, T ;
Weissenbach, J ;
Cockett, N ;
Gyapay, G ;
Georges, M .
GENOME RESEARCH, 2001, 11 (05) :850-862
[10]
Polar overdominance at the Ovine callipyge locus [J].
Cockett, NE ;
Jackson, SP ;
Shay, TL ;
Farnir, F ;
Berghmans, S ;
Snowder, GD ;
Nielsen, DM ;
Georges, M .
SCIENCE, 1996, 273 (5272) :236-238