Genomic imprinting in the rat: Linkage of Igf2 and H19 genes and opposite parental allele-specific expression during embryogenesis

被引:27
作者
Overall, M
Bakker, M
Spencer, J
Parker, N
Smith, P
Dziadek, M
机构
[1] UNIV MELBOURNE,DEPT ANAT & CELL BIOL,PARKVILLE,VIC 3052,AUSTRALIA
[2] MONASH UNIV,DEPT OBSTET & GYNAECOL,CLAYTON,VIC 3168,AUSTRALIA
[3] ROYAL CHILDRENS HOSP,DEPT PAEDIAT,PARKVILLE,VIC 3052,AUSTRALIA
基金
英国医学研究理事会;
关键词
D O I
10.1006/geno.1997.4933
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Igf2 and H19 are closely linked imprinted genes in both mice and humans that are expressed from opposite parental alleles. In this study we demonstrate that these two genes are also closely linked in the rat, with the H19 gene mapping to within 145 kb of Igf2 on rat chromosome 1. We identified polymorphisms in H19 and Igf2 transcripts in two inbred rat strains and determined the expression of the parental alleles in F1 offspring. The H19 gene was shown to be expressed exclusively from the maternal allele in all fetal and neonatal tissues. Monoallelic expression of Igf2 from the paternal allele was found in all tissues except the leptomeninges and choroid plexus. Igf2 in the choroid plexus was monoallelic at days 13.5 and 15.5 of gestation with a switch to biallelic expression by day 18.5, demonstrating a loss of imprinting after the choroid plexus has differentiated. Biallelic expression of Igf2 was observed in the leptomeninges at all fetal and neonatal stages analyzed. These studies demonstrate conservation of imprinting of two closely linked genes transcribed from opposite parental alleles in a species other than human or mouse. A comparative approach between different species will be important in defining the mechanisms that regulate the tissue-specific expression of imprinted genes. (C) 1997 Academic Press.
引用
收藏
页码:416 / 420
页数:5
相关论文
共 46 条
[1]   PARENTAL IMPRINTING OF THE MOUSE H19 GENE [J].
BARTOLOMEI, MS ;
ZEMEL, S ;
TILGHMAN, SM .
NATURE, 1991, 351 (6322) :153-155
[2]   EPIGENETIC MECHANISMS UNDERLYING THE IMPRINTING OF THE MOUSE H19-GENE [J].
BARTOLOMEI, MS ;
WEBBER, AL ;
BRUNKOW, ME ;
TILGHMAN, SM .
GENES & DEVELOPMENT, 1993, 7 (09) :1663-1673
[3]  
CATTANACH BM, 1995, GENOMIC IMPRINTING C, P327
[4]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[5]  
COOPER DW, 1990, AUST J ZOOL, V37, P411
[6]   PARENTAL IMPRINTING OF THE MOUSE INSULIN-LIKE GROWTH FACTOR-II GENE [J].
DECHIARA, TM ;
ROBERTSON, EJ ;
EFSTRATIADIS, A .
CELL, 1991, 64 (04) :849-859
[7]   PARENTAL-ORIGIN-SPECIFIC EPIGENETIC MODIFICATION OF THE MOUSE H19 GENE [J].
FERGUSONSMITH, AC ;
SASAKI, H ;
CATTANACH, BM ;
SURANI, MA .
NATURE, 1993, 362 (6422) :751-755
[8]   PARENTAL GENOMIC IMPRINTING OF THE HUMAN IGF2 GENE [J].
GIANNOUKAKIS, N ;
DEAL, C ;
PAQUETTE, J ;
GOODYER, CG ;
POLYCHRONAKOS, C .
NATURE GENETICS, 1993, 4 (01) :98-101
[9]   GENETIC-MAP OF 12 POLYMORPHIC LOCI ON RAT CHROMOSOME-1 [J].
GOLDMUNTZ, EA ;
REMMERS, EF ;
ZHA, HB ;
CASH, JM ;
MATHERN, P ;
CROFFORD, LJ ;
WILDER, RL .
GENOMICS, 1993, 16 (03) :761-764
[10]   DIFFERENTIAL BIALLELIC ACTIVATION OF 3 INSULIN-LIKE GROWTH-FACTOR-II PROMOTERS IN THE MOUSE CENTRAL-NERVOUS-SYSTEM [J].
HU, JF ;
VU, TH ;
HOFFMAN, AR .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (05) :628-636