A novel gene, DXS8237E. lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status

被引:24
作者
Coleman, MP
Ambrose, HJ
Carrel, L
Nemeth, AH
Willard, HF
Davies, KE
机构
[1] JOHN RADCLIFFE HOSP,INST MOLEC MED,MOLEC GENET GRP,OXFORD OX3 9LU,ENGLAND
[2] CASE WESTERN RESERVE UNIV,SCH MED,DEPT GENET,CLEVELAND,OH 44106
[3] CASE WESTERN RESERVE UNIV,SCH MED,CTR HUMAN GENET,CLEVELAND,OH 44106
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
D O I
10.1006/geno.1996.0022
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
A novel X-linked gene, DXS8237E, was isolated from human fetal brain cDNA, and its 3' end was mapped to within 20 kb upstream of UBE1 in Xp11.23. A 1.3-kb cDNA for DXS8237E detects homologous sequences in other mammals and a 3-kb mRNA that is widely expressed in human cell lines and mouse tissues. Sequence analysis indicated that the 1.3-kb cDNA contains the 3' end of the DXS8237E gene, but the sequence shows no significant homology to known genes. DXS8237E was shown to be subject to X inactivation in five somatic cell hybrids that contain an inactive human X chromosome but no active homologue. Since UBE1 escapes X inactivation, DXS8237E and UBE1 are the closest mapped genes with discordant X inactivation profiles. Sequences in the vicinity of these two genes may be important determinants of X inactivation status. (C) 1996 Academic Press, Inc.
引用
收藏
页码:135 / 138
页数:4
相关论文
共 18 条
[1]   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
[2]   A BIDIRECTIONAL YAC WALK FROM THE NORRIE DISEASE (NDP) LOCUS [J].
BLACK, GCM ;
COLEMAN, MP ;
CHEN, ZY ;
NEMETH, AH ;
DAVIES, KE ;
CRAIG, IW .
GENOMICS, 1995, 25 (03) :644-649
[3]   X-CHROMOSOME INACTIVATION OF THE HUMAN TIMP GENE [J].
BROWN, CJ ;
FLENNIKEN, AM ;
WILLIAMS, BRG ;
WILLARD, HF .
NUCLEIC ACIDS RESEARCH, 1990, 18 (14) :4191-4195
[4]  
BROWN CJ, 1990, AM J HUM GENET, V46, P273
[5]   A 1.8-MB YAC CONTIG IN XP11.23 - IDENTIFICATION OF CPG ISLANDS AND PHYSICAL MAPPING OF CA REPEATS IN A REGION OF HIGH GENE DENSITY [J].
COLEMAN, MP ;
NEMETH, AH ;
CAMPBELL, L ;
RAUT, CP ;
WEISSENBACH, J ;
DAVIES, KE .
GENOMICS, 1994, 21 (02) :337-343
[6]   ESCAPE FROM X-INACTIVATION IN HUMAN AND MOUSE [J].
DISTECHE, CM .
TRENDS IN GENETICS, 1995, 11 (01) :17-22
[7]   GENETIC-MAPPING OF A CONE AND ROD DYSFUNCTION (ALAND ISLAND EYE DISEASE) TO THE PROXIMAL SHORT ARM OF THE HUMAN X-CHROMOSOME [J].
GLASS, IA ;
GOOD, P ;
COLEMAN, MP ;
FULLWOOD, P ;
GILES, MG ;
LINDSAY, S ;
NEMETH, AH ;
DAVIES, KE ;
WILLSHAW, HA ;
FIELDER, A ;
KILPATRICK, M ;
FARNDON, PA .
JOURNAL OF MEDICAL GENETICS, 1993, 30 (12) :1044-1050
[8]  
GOODFELLOW P, 1984, AM J HUM GENET, V36, P777
[9]   A MEMBER OF THE CAUDAL FAMILY OF HOMEOBOX GENES MAPS TO THE X-INACTIVATION CENTER REGION OF THE MOUSE AND HUMAN X-CHROMOSOMES [J].
HORN, JM ;
ASHWORTH, A .
HUMAN MOLECULAR GENETICS, 1995, 4 (06) :1041-1047
[10]  
INGLE C, 1985, AM J HUM GENET, V37, P451