X-chromosome methylation ratios as indicators of chromosomal activity: Evidence of intraindividual divergencies among tissues of different embryonal origin

被引:14
作者
Azofeifa, J
Waldherr, R
Cremer, M
机构
[1] UNIV HEIDELBERG,INST ANTHROPOL & HUMAN GENET,D-69120 HEIDELBERG,GERMANY
[2] UNIV HEIDELBERG,INST PATHOL,D-69120 HEIDELBERG,GERMANY
关键词
D O I
10.1007/s004390050044
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To test whether the differentiation events that lead to the embryonal layers and their derived organs produce divergent X-chromosome activation ratios among the different tissues, the X-chromosome activation ratios in leucocytes and muscle (mesodermal origin), thyroid gland (endodermal origin) and medulla of the suprarenal glands (ectodermal origin) from ten deceased females were surveyed. Analysis of the degree of methylation of the polymorphic alleles recognized by the probes M27 beta and pSPT-PGK showed that the ratios for the medulla of the suprarenals correlated well with those of all other tissues except for leucocytes; the thyroid gland showed limited correlation with muscle, whereas leucocytes showed correlation only with muscle. The results of this preliminary study suggest that differentiation events result in considerable variation in the activation ratios in different tissues. As a consequence caution should be taken in extrapolating from the activation ratios observed in leucocytes or fibroblasts to tissues of endodermal or ectodermal origin.
引用
收藏
页码:330 / 333
页数:4
相关论文
共 22 条
[1]   ADDITIONAL CASE OF FEMALE MONOZYGOTIC TWINS DISCORDANT FOR THE CLINICAL MANIFESTATIONS OF DUCHENNE MUSCULAR-DYSTROPHY DUE TO OPPOSITE X-CHROMOSOME INACTIVATION [J].
ABBADI, N ;
PHILIPPE, C ;
CHERY, M ;
GILGENKRANTZ, H ;
TOME, F ;
COLLIN, H ;
THEAU, D ;
RECAN, D ;
BROUX, O ;
FARDEAU, M ;
KAPLAN, JC ;
GILGENKRANTZ, S .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 52 (02) :198-206
[2]   X-CHROMOSOME METHYLATION IN MANIFESTING AND HEALTHY CARRIERS OF DYSTROPHINOPATHIES - CONCORDANCE OF ACTIVATION RATIOS AMONG FIRST DEGREE FEMALE RELATIVES AND SKEWED INACTIVATION AS CAUSE OF THE AFFECTED PHENOTYPES [J].
AZOFEIFA, J ;
VOIT, T ;
HUBNER, C ;
CREMER, M .
HUMAN GENETICS, 1995, 96 (02) :167-176
[3]   METHYLATION PATTERNS AT THE HYPERVARIABLE X-CHROMOSOME LOCUS DXS255 (M27-BETA) - CORRELATION WITH X-INACTIVATION STATUS [J].
BOYD, Y ;
FRASER, NJ .
GENOMICS, 1990, 7 (02) :182-187
[4]   VARIABILITY IN CLINICAL, GENETIC AND PROTEIN ABNORMALITIES IN MANIFESTING CARRIERS OF DUCHENNE AND BECKER MUSCULAR-DYSTROPHY [J].
BUSHBY, KMD ;
GOODSHIP, JA ;
NICHOLSON, LVB ;
JOHNSON, MA ;
HAGGERTY, ID ;
GARDNERMEDWIN, D .
NEUROMUSCULAR DISORDERS, 1993, 3 (01) :57-64
[5]   CARRIER DETECTION IN X-LINKED AGAMMAGLOBULINEMIA BY ANALYSIS OF X-CHROMOSOME INACTIVATION [J].
FEARON, ER ;
WINKELSTEIN, JA ;
CIVIN, CI ;
PARDOLL, DM ;
VOGELSTEIN, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (08) :427-431
[6]   PRIMORDIAL CELL POOL SIZE AND LINEAGE RELATIONSHIPS OF 5 HUMAN CELL TYPES [J].
FIALKOW, PJ .
ANNALS OF HUMAN GENETICS, 1973, 37 (JUL) :39-48
[7]   INVESTIGATION OF A FEMALE MANIFESTING BECKER MUSCULAR-DYSTROPHY [J].
GLASS, IA ;
NICHOLSON, LVR ;
WATKISS, E ;
JOHNSON, MA ;
ROBERTS, RG ;
ABBS, S ;
BRITTAINJONES, S ;
BODDIE, HG .
JOURNAL OF MEDICAL GENETICS, 1992, 29 (08) :578-582
[8]  
GRANT SG, 1988, ANNU REV GENET, V22, P199, DOI 10.1146/annurev.ge.22.120188.001215
[9]   THE HYPERVARIABLE DXS255 LOCUS CONTAINS A LINE-1 REPETITIVE ELEMENT WITH A CPG ISLAND THAT IS EXTENSIVELY METHYLATED ONLY ON THE ACTIVE X-CHROMOSOME [J].
HENDRIKS, RW ;
HINDS, H ;
CHEN, ZY ;
CRAIG, IW .
GENOMICS, 1992, 14 (03) :598-603
[10]  
INGERSLEV J, 1989, CLIN GENET, V35, P41