Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes

被引:30
作者
Craig, IW [1 ]
Mill, J [1 ]
Craig, GM [1 ]
Loat, C [1 ]
Schalkwyk, LC [1 ]
机构
[1] Inst Psychiat, SGDP Ctr, London SE5, England
关键词
X-inactivation; sex-differences; gene expression;
D O I
10.1038/sj.ejhg.5201212
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
Dosage compensation in mammalian females is achieved by the random inactivation of one X chromosome early in development; however, inactivation is not complete. In addition to a majority of pseudoautosomal loci, there are genes that are expressed from both the active and the inactive X chromosomes, and which are interspersed among other genes subject to regular dosage compensation. The patterns of X-linked gene expression in different tissues are of great significance for interpreting their impact on sex differences in development. We have examined the suitability and sensitivity of a microarray approach for determining the inactivation status of X-linked genes. Biotinylated cRNA from six female and six male lymphocyte samples were hybridised to Affymetrix HG-U133A microarrays. A total of 36 X-linked targets detected significantly higher levels of female transcripts, suggesting that these corresponded to sequences from loci that escaped, at least partly, from inactivation. These included genes for which previous experimental evidence, or circumstantial evidence, existed for their escape, and some novel candidates. Six of the targets were represented by more than one probe set, which gave independent support for the conclusions reached. European Journal of Human Genetics ( 2004).
引用
收藏
页码:639 / 646
页数:8
相关论文
共 44 条
  • [11] ESCAPE FROM X-INACTIVATION IN HUMAN AND MOUSE
    DISTECHE, CM
    [J]. TRENDS IN GENETICS, 1995, 11 (01) : 17 - 22
  • [12] Characterization of genes encoding translation initiation factor eIF-2γ in mouse and human:: sex chromosome localization, escape from X-inactivation and evolution
    Ehrmann, IE
    Ellis, PS
    Mazeyrat, S
    Duthie, S
    Brockdorff, N
    Mattei, MG
    Gavin, MA
    Affara, NA
    Brown, GM
    Simpson, E
    Mitchell, MJ
    Scott, DM
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (11) : 1725 - 1737
  • [13] HOMOLOGOUS RIBOSOMAL-PROTEIN GENES ON THE HUMAN X-CHROMOSOME AND Y-CHROMOSOME - ESCAPE FROM X-INACTIVATION AND POSSIBLE IMPLICATIONS FOR TURNER SYNDROME
    FISHER, EMC
    BEERROMERO, P
    BROWN, LG
    RIDLEY, A
    MCNEIL, JA
    LAWRENCE, JB
    WILLARD, HF
    BIEBER, FR
    PAGE, DC
    [J]. CELL, 1990, 63 (06) : 1205 - 1218
  • [14] AN SRY-RELATED SEQUENCE ON THE MARSUPIAL X-CHROMOSOME - IMPLICATIONS FOR THE EVOLUTION OF THE MAMMALIAN TESTISDETERMINING GENE
    FOSTER, JW
    GRAVES, JAM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (05) : 1927 - 1931
  • [15] GASPAR NJ, 1994, J BIOL CHEM, V269, P3415
  • [16] GIBBONS RJ, 1992, AM J HUM GENET, V51, P1136
  • [17] MUTATIONS IN A PUTATIVE GLOBAL TRANSCRIPTIONAL REGULATOR CAUSE X-LINKED MENTAL-RETARDATION WITH ALPHA-THALASSEMIA (ATR-X SYNDROME)
    GIBBONS, RJ
    PICKETTS, DJ
    VILLARD, L
    HIGGS, DR
    [J]. CELL, 1995, 80 (06) : 837 - 845
  • [18] An H-YDb epitope is encoded by a novel mouse Y chromosome gene
    Greenfield, A
    Scott, D
    Pennisi, D
    Ehrmann, I
    Ellis, P
    Cooper, L
    Simpson, E
    Koopman, P
    [J]. NATURE GENETICS, 1996, 14 (04) : 474 - 478
  • [19] The UTX gene escapes X inactivation in mice and humans
    Greenfield, A
    Carrel, L
    Pennisi, D
    Philippe, C
    Quaderi, N
    Siggers, P
    Steiner, K
    Tam, PPL
    Monaco, AP
    Willard, HF
    Koopman, P
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (04) : 737 - 742
  • [20] A novel human SRB/MED-containing cofactor complex, SMCC, involved in transcription regulation
    Gu, W
    Malik, S
    Ito, M
    Yuan, CX
    Fondell, JD
    Zhang, XL
    Martinez, E
    Qin, J
    Roeder, RG
    [J]. MOLECULAR CELL, 1999, 3 (01) : 97 - 108