THE DXS423E GENE IN XP11.21 ESCAPES X-CHROMOSOME INACTIVATION

被引:40
作者
BROWN, CJ
MILLER, AP
CARREL, L
RUPERT, JL
DAVIES, KE
WILLARD, HF
机构
[1] CASE WESTERN RESERVE UNIV,SCH MED,DEPT GENET,CLEVELAND,OH 44106
[2] CASE WESTERN RESERVE UNIV,SCH MED,CTR HUMAN GENET,CLEVELAND,OH 44106
[3] UNIV CLEVELAND HOSP,CLEVELAND,OH 44106
[4] STANFORD UNIV,DEPT GENET,STANFORD,CA 94305
[5] JOHN RADCLIFFE HOSP,INST MOLEC MED,MOLEC GENET GRP,OXFORD OX3 9DU,ENGLAND
关键词
D O I
10.1093/hmg/4.2.251
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 DXS423E gene has been localized to Xp11.21 and is expressed in somatic cell hybrids retaining either the human active or inactive X chromosome, demonstrating that DXS423E escapes X chromosome inactivation. The XE169 (DXS1272E or SMCX) gene that escapes X chromosome inactivation is also located in Xp11.21-11.22 and maps within the same YAC as DXS423E. Thus the DXS423E and XE169 genes define a new region in the proximal short arm of the X chromosome that is not subject to X chromosome inactivation, supporting a regional basis for escape from inactivation.
引用
收藏
页码:251 / 255
页数:5
相关论文
共 33 条
  • [1] AGUINIK AI, 1994, HUM MOL GENET, V3, P873
  • [2] AGUINIK AI, 1994, HUM MOL GENET, V3, P879
  • [3] [Anonymous], [No title captured]
  • [4] BROWN CJ, 1989, AM J HUM GENET, V45, P592
  • [5] X-CHROMOSOME INACTIVATION OF THE HUMAN TIMP GENE
    BROWN, CJ
    FLENNIKEN, AM
    WILLIAMS, BRG
    WILLARD, HF
    [J]. NUCLEIC ACIDS RESEARCH, 1990, 18 (14) : 4191 - 4195
  • [6] DAHL H, 1990, GENOMICS, V8, P8225
  • [7] THE PSEUDOAUTOSOMAL BOUNDARY IN MAN IS DEFINED BY AN ALU REPEAT SEQUENCE INSERTED ON THE Y-CHROMOSOME
    ELLIS, NA
    GOODFELLOW, PJ
    PYM, B
    SMITH, M
    PALMER, M
    FRISCHAUF, AM
    GOODFELLOW, PN
    [J]. NATURE, 1989, 337 (6202) : 81 - 84
  • [8] DIRECTED ISOLATION OF HUMAN GENES THAT ESCAPE X-INACTIVATION
    ELLISON, J
    PASSAGE, M
    YU, LC
    YEN, P
    MOHANDAS, TK
    SHAPIRO, L
    [J]. SOMATIC CELL AND MOLECULAR GENETICS, 1992, 18 (03) : 259 - 268
  • [9] A GENE DELETED IN KALLMANNS SYNDROME SHARES HOMOLOGY WITH NEURAL CELL-ADHESION AND AXONAL PATH-FINDING MOLECULES
    FRANCO, B
    GUIOLI, S
    PRAGLIOLA, A
    INCERTI, B
    BARDONI, B
    TONLORENZI, R
    CARROZZO, R
    MAESTRINI, E
    PIERETTI, M
    TAILLONMILLER, P
    BROWN, CJ
    WILLARD, HF
    LAWRENCE, C
    PERSICO, MG
    CAMERINO, G
    BALLABIO, A
    [J]. NATURE, 1991, 353 (6344) : 529 - 536
  • [10] GOODFELLOW P, 1984, AM J HUM GENET, V36, P777