DIFFERENTIAL METHYLATION OF THE HYPERVARIABLE LOCUS DXS255 ON ACTIVE AND INACTIVE X-CHROMOSOMES CORRELATES WITH THE EXPRESSION OF A HUMAN X-LINKED GENE

被引:79
作者
BROWN, RM
FRASER, NJ
BROWN, GK
机构
[1] ROYAL CHILDRENS HOSP,MURDOCH INST RES BIRTH DEFECTS,PARKVILLE,VIC 3052,AUSTRALIA
[2] UNIV MELBOURNE,DEPT PAEDIAT,PARKVILLE,VIC 3052,AUSTRALIA
关键词
D O I
10.1016/0888-7543(90)90543-4
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
Consistent differences in methylation of particular cytosine residues in the DNA of active and inactive X chromosomes can be used for rapid, direct analysis of X-inactivation patterns in different female tissues. We have studied methylation of the highly polymorphic DXS255 locus in tissues from patients with deficiency of the E1α subunit of the pyruvate dehydrogenase complex in whom the results can be correlated directly with total enzyme activity, levels of immunoreactive protein, and patterns of cell mosaicism. The results confirm that methylation of the DXS255 locus correlates with X-chromosome expression. In patients and normal controls, the pattern of X inactivation varied widely from tissue to tissue and often deviated markedly from a 50:50 proportion. These deviations are likely to reflect small numbers of tissue-specific stem cells at the time of random X inactivation and cannot be taken alone as evidence for selection or "nonrandom" inactivation. © 1990.
引用
收藏
页码:215 / 221
页数:7
相关论文
共 18 条
  • [1] BOYD Y, 1988, J MED GENET, V25, P645
  • [2] HYPERAMMONEMIA AND LACTIC-ACIDOSIS IN A PATIENT WITH PYRUVATE-DEHYDROGENASE DEFICIENCY
    BROWN, GK
    SCHOLEM, RD
    HUNT, SM
    HARRISON, JR
    POLLARD, AC
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1987, 10 (04) : 359 - 366
  • [3] CEREBRAL LACTIC-ACIDOSIS - DEFECTS IN PYRUVATE METABOLISM WITH PROFOUND BRAIN-DAMAGE AND MINIMAL SYSTEMIC ACIDOSIS
    BROWN, GK
    HAAN, EA
    KIRBY, DM
    SCHOLEM, RD
    WRAITH, JE
    ROGERS, JG
    DANKS, DM
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1988, 147 (01) : 10 - 14
  • [4] X-CHROMOSOME LOCALIZATION OF THE FUNCTIONAL GENE FOR THE E1-ALPHA SUBUNIT OF THE HUMAN PYRUVATE-DEHYDROGENASE COMPLEX
    BROWN, RM
    DAHL, HHM
    BROWN, GK
    [J]. GENOMICS, 1989, 4 (02) : 174 - 181
  • [5] DAHL HHM, 1987, J BIOL CHEM, V262, P7398
  • [6] CARRIER DETECTION IN X-LINKED AGAMMAGLOBULINEMIA BY ANALYSIS OF X-CHROMOSOME INACTIVATION
    FEARON, ER
    WINKELSTEIN, JA
    CIVIN, CI
    PARDOLL, DM
    VOGELSTEIN, B
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (08) : 427 - 431
  • [7] PRIMORDIAL CELL POOL SIZE AND LINEAGE RELATIONSHIPS OF 5 HUMAN CELL TYPES
    FIALKOW, PJ
    [J]. ANNALS OF HUMAN GENETICS, 1973, 37 (JUL) : 39 - 48
  • [8] WOMEN HETEROZYGOUS FOR DEFICIENCY OF (P21-]PTER) REGION OF X-CHROMOSOME ARE FERTILE
    FRACCARO, M
    MARASCHIO, P
    PASQUALI, F
    SCAPPATICCI, S
    [J]. HUMAN GENETICS, 1977, 39 (03) : 283 - 292
  • [9] ISOLATION AND CHARACTERIZATION OF A HUMAN VARIABLE COPY NUMBER TANDEM REPEAT AT XCEN-P11.22
    FRASER, NJ
    BOYD, Y
    CRAIG, I
    [J]. GENOMICS, 1989, 5 (01) : 144 - 148
  • [10] GOODSHIP J, 1988, LANCET, V1, P729