Promoter cross-talk via a shared enhancer explains paternally biased expression of Nctc1 at the Igf2/H19/Nctc1 imprinted locus

被引:23
作者
Eun, Bokkee [1 ]
Sampley, Megan L. [1 ]
Good, Austin L. [1 ]
Gebert, Claudia M. [1 ]
Pfeifer, Karl [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Program Genom Differentiat, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
RNA-POLYMERASE-II; CONTROL REGION; H19; GENE; CHROMATIN INTERACTIONS; METHYLATED REGION; IGF2; TRANSCRIPTION; CTCF; INSULATOR; DELETION;
D O I
10.1093/nar/gks1182
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
Developmentally regulated transcription often depends on physical interactions between distal enhancers and their cognate promoters. Recent genomic analyses suggest that promoter-promoter interactions might play a similarly critical role in organizing the genome and establishing cell-type-specific gene expression. The Igf2/H19 locus has been a valuable model for clarifying the role of long-range interactions between cis-regulatory elements. Imprinted expression of the linked, reciprocally imprinted genes is explained by parent-of-origin-specific chromosomal loop structures between the paternal Igf2 or maternal H19 promoters and their shared tissue-specific enhancer elements. Here, we further analyze these loop structures for their composition and their impact on expression of the linked long non-coding RNA, Nctc1. We show that Nctc1 is co-regulated with Igf2 and H19 and physically interacts with the shared muscle enhancer. In fact, all three co-regulated genes have the potential to interact not only with the shared enhancer but also with each other via their enhancer interactions. Furthermore, developmental and genetic analyses indicate functional significance for these promoter-promoter interactions. Altogether, we present a novel mechanism to explain developmental specific imprinting of Nctc1 and provide new information about enhancer mechanisms and about the role of chromatin domains in establishing gene expression patterns.
引用
收藏
页码:817 / 826
页数:10
相关论文
共 63 条
[1]   Appropriate expression of the mouse H19 gene utilises three or more distinct enhancer regions spread over more than 130 kb [J].
Ainscough, JFX ;
Dandolo, L ;
Surani, MA .
MECHANISMS OF DEVELOPMENT, 2000, 91 (1-2) :365-368
[2]   Long Range Interactions Regulate Igf2 Gene Transcription during Skeletal Muscle Differentiation [J].
Alzhanov, Damir T. ;
McInerney, Stephanie F. ;
Rotwein, Peter .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (50) :38969-38977
[3]  
Bartolomei M.S., 2011, COLD SPRING HARB PER, V3
[4]   Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene [J].
Bell, AC ;
Felsenfeld, G .
NATURE, 2000, 405 (6785) :482-485
[5]   FKHR (FOXO1a) is required for myotube fusion of primary mouse myoblasts [J].
Bois, PRJ ;
Grosveld, GC .
EMBO JOURNAL, 2003, 22 (05) :1147-1157
[6]   ECTOPIC EXPRESSION OF THE H19 GENE IN MICE CAUSES PRENATAL LETHALITY [J].
BRUNKOW, ME ;
TILGHMAN, SM .
GENES & DEVELOPMENT, 1991, 5 (06) :1092-1101
[7]   Functional and Mechanistic Diversity of Distal Transcription Enhancers [J].
Bulger, Michael ;
Groudine, Mark .
CELL, 2011, 144 (03) :327-339
[8]   Deletion of a silencer element in lgf2 results in loss of imprinting independent of H19 [J].
Constância, M ;
Dean, W ;
Lopes, S ;
Moore, T ;
Kelsey, G ;
Reik, W .
NATURE GENETICS, 2000, 26 (02) :203-206
[9]   Long-range chromatin interactions at the mouse Igf2/H19 locus reveal a novel paternally expressed long non-coding RNA [J].
Court, Franck ;
Baniol, Marion ;
Hagege, Helene ;
Petit, Julie Sandrine ;
Lelay-Taha, Marie-Noelle ;
Carbonell, Francoise ;
Weber, Michael ;
Cathala, Guy ;
Forne, Thierry .
NUCLEIC ACIDS RESEARCH, 2011, 39 (14) :5893-5906
[10]   Elucidation of the minimal sequence required to imprint H19 transgenes [J].
Cranston, MJ ;
Spinka, TL ;
Elson, DA ;
Bartolomei, MS .
GENOMICS, 2001, 73 (01) :98-107