A NOVEL L23-RELATED GENE 40 KB DOWNSTREAM OF THE IMPRINTED H19 GENE IS BIALLELICALLY EXPRESSED IN MID-FETAL AND ADULT HUMAN TISSUES

被引:38
作者
TSANG, P
GILLES, F
YUAN, LW
KUO, YH
LUPU, F
SAMARA, G
MOOSIKASUWAN, J
GOYE, A
ZELENETZ, AD
SELLERI, L
TYCKO, B
机构
[1] COLUMBIA UNIV,COLL PHYS & SURG,DEPT PATHOL,NEW YORK,NY 10027
[2] MEM SLOAN KETTERING CANC CTR,DIV HEMATOL ONCOL,NEW YORK,NY 10021
[3] MEM SLOAN KETTERING CANC CTR,PROGRAM MOLEC BIOL,NEW YORK,NY 10021
[4] STANFORD UNIV,SCH MED,DEPT PATHOL,STANFORD,CA 94305
关键词
D O I
10.1093/hmg/4.9.1499
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
The closely linked IGF2 and H19 genes on human chromosome 11p15.5 are monoallelically expressed as a result of genomic imprinting and show altered expression in Wilms' tumors (WTs). To map regional imprinting we have sought to isolate additional human genes close to IGF2/H19 and to characterize their allelic expression patterns. Here we report a novel gene, provisionally named L23MRP [L23 (mitochondrial)-related protein], which is oriented 'tail-to-tail' with H19 and is transcribed to within 40 kb of the last H19 exon. L23MRP is expressed biallelically in many mid-fetal and adult human tissues. This gene is also expressed at normal levels in WTs which have lost expression of H19 either via loss of the maternal chromosome 11p15.5 or via an epigenetic pathway involving site-specific DNA hypermethylation. These data indicate that, at least in postembryonic stages, L23MRP is functionally insulated from the IGF2/H19 imprinted domain.
引用
收藏
页码:1499 / 1507
页数:9
相关论文
共 33 条
[1]  
ALLISON DS, 1986, P NATL ACAD SCI USA, V84, P9011
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]  
BARTOLOMEI MS, 1993, GENE DEV, V5, P1663
[4]   EXON AMPLIFICATION - A STRATEGY TO ISOLATE MAMMALIAN GENES BASED ON RNA SPLICING [J].
BUCKLER, AJ ;
CHANG, DD ;
GRAW, SL ;
BROOK, JD ;
HABER, DA ;
SHARP, PA ;
HOUSMAN, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :4005-4009
[5]   INHERITED MICRODELETIONS IN THE ANGELMAN AND PRADER-WILLI SYNDROMES DEFINE AN IMPRINTING CENTER ON HUMAN-CHROMOSOME-15 [J].
BUITING, K ;
SAITOH, S ;
GROSS, S ;
DITTRICH, B ;
SCHWARTZ, S ;
NICHOLLS, RD ;
HORSTHEMKE, B .
NATURE GENETICS, 1995, 9 (04) :395-400
[6]   ESCAPE FROM X-INACTIVATION IN HUMAN AND MOUSE [J].
DISTECHE, CM .
TRENDS IN GENETICS, 1995, 11 (01) :17-22
[7]   A DNA METHYLATION IMPRINT, DETERMINED BY THE SEX OF THE PARENT, DISTINGUISHES THE ANGELMAN AND PRADER-WILLI SYNDROMES [J].
DRISCOLL, DJ ;
WATERS, MF ;
WILLIAMS, CA ;
ZORI, RT ;
GLENN, CC ;
AVIDANO, KM ;
NICHOLLS, RD .
GENOMICS, 1992, 13 (04) :917-924
[8]  
ESTRATIADIS A, 1994, CURR OPIN GENET DEV, V4, P265
[9]  
FEARON K, 1992, J BIOL CHEM, V267, P5162
[10]   ALLELE-SPECIFIC INACTIVATION OF INSULIN-1 AND INSULIN-2, IN THE MOUSE YOLK-SAC, INDICATES IMPRINTING [J].
GIDDINGS, SJ ;
KING, CD ;
HARMAN, KW ;
FLOOD, JF ;
CARNAGHI, LR .
NATURE GENETICS, 1994, 6 (03) :310-313