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
[11]  
KNIGHT JC, 1995, IN PRESS CYTOGENET C
[12]   2.6 MB YAC CONTIG OF THE HUMAN-X INACTIVATION CENTER REGION IN XQ13 - PHYSICAL LINKAGE OF THE RPS4X, PHKA1, XIST AND DXS128E GENES [J].
LAFRENIERE, RG ;
BROWN, CJ ;
RIDER, S ;
CHELLY, J ;
TAILLONMILLER, P ;
CHINAULT, AC ;
MONACO, AP ;
WILLARD, HF .
HUMAN MOLECULAR GENETICS, 1993, 2 (08) :1105-1115
[13]   DIRECT SELECTION - A METHOD FOR THE ISOLATION OF CDNAS ENCODED BY LARGE GENOMIC REGIONS [J].
LOVETT, M ;
KERE, J ;
HINTON, LM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (21) :9628-9632
[14]   GENE ACTION IN X-CHROMOSOME OF MOUSE (MUS MUSCULUS L) [J].
LYON, MF .
NATURE, 1961, 190 (477) :372-&
[15]   3 GENES THAT ESCAPE X-CHROMOSOME INACTIVATION ARE CLUSTERED WITH A 6-MB YAC-CONTIG AND STS MAP IN XP11.21-P11.22 [J].
MILLER, AP ;
GUSTASHAW, K ;
WOLFF, DJ ;
RIDER, SH ;
MONACO, AP ;
EBLE, B ;
SCHLESSINGER, D ;
GORSKI, JL ;
VANOMMEN, GJ ;
WEISSENBACH, J ;
WILLARD, HF .
HUMAN MOLECULAR GENETICS, 1995, 4 (04) :731-739
[16]   ASSIGNMENT OF THE GENE FOR COMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS (CSNB1) TO XP11.3 [J].
MUSARELLA, MA ;
WELEBER, RG ;
MURPHEY, WH ;
YOUNG, RSL ;
ANSONCARTWRIGHT, L ;
METS, M ;
KRAFT, SP ;
POLEMENO, R ;
LITT, M ;
WORTON, RG .
GENOMICS, 1989, 5 (04) :727-737
[17]   MAPPING THE GENE CAUSING X-LINKED RECESSIVE NEPHROLITHIASIS TO XP11.22 BY LINKAGE STUDIES [J].
SCHEINMAN, SJ ;
POOK, MA ;
WOODING, C ;
PANG, JT ;
FRYMOYER, PA ;
THAKKER, RV .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (06) :2351-2357
[18]   EPIGENETIC AND CHROMOSOMAL CONTROL OF GENE-EXPRESSION - MOLECULAR AND GENETIC-ANALYSIS OF X-CHROMOSOME INACTIVATION [J].
WILLARD, HF ;
BROWN, CJ ;
CARREL, L ;
HENDRICH, B ;
MILLER, AP .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1993, 58 :315-322