Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: Analysis of the X-inactivation patterns

Mari Matsuo, Koji Muroya, Kenji Nanao, Yukihiro Hasegawa, Hiroshi Terasaki, Kenjiro Kosaki, Tsutomu Ogata

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

We report on a mother and daughter both with a 45,X/46,X,r(X)(p22.3q28) karyotype and mental retardation. Fluorescence in situ hybridization (FISH) and microsatellite analyses for 14 loci/region at Xp22.3 and seven loci/region at Xq28 indicated that the ring X chromosome was missing a roughly 12-Mb region from Xp22.3 with the breakpoint between DXS85 and DXS9972, and another region of less than 100 kb from Xq28 with the breakpoint distal to the region defined by the FISH probe c8.2/1. X-inactivation analysis, using the methylation status of the AR gene (exon 1) as an indicator, showed that the normal and ring X chromosomes in the X,r(X)(p22.3q28) cell lineage were randomly inactivated. The Xp22.3 deleted region partially overlaps with the regional intervals of MRX19, MRX21, MRX24, MRX37, MRX43, and MRX49 associated with heterozygote manifestation. Therefore, it is likely that one or more of these MRX genes, subject to X- inactivation, are lost from the ring X chromosome, and that reduced expression of the MRX gene(s) caused by random X-inactivation has resulted in mental retardation in the mother and daughter. (C) 2000 Wiley-Liss, Inc.

Original languageEnglish
Pages (from-to)267-272
Number of pages6
JournalAmerican Journal of Medical Genetics
Volume91
Issue number4
DOIs
Publication statusPublished - 2000 Apr 24

Fingerprint

Ring Chromosomes
X Chromosome Inactivation
X Chromosome
Intellectual Disability
Fluorescence In Situ Hybridization
Cell Lineage
Heterozygote
Karyotype
Microsatellite Repeats
Methylation
Genes
Exons
Gene Expression

Keywords

  • Familial cases
  • MRX gene
  • Random X-inactivation
  • Reduced expression
  • Ring X chromosome

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation : Analysis of the X-inactivation patterns. / Matsuo, Mari; Muroya, Koji; Nanao, Kenji; Hasegawa, Yukihiro; Terasaki, Hiroshi; Kosaki, Kenjiro; Ogata, Tsutomu.

In: American Journal of Medical Genetics, Vol. 91, No. 4, 24.04.2000, p. 267-272.

Research output: Contribution to journalArticle

Matsuo, Mari ; Muroya, Koji ; Nanao, Kenji ; Hasegawa, Yukihiro ; Terasaki, Hiroshi ; Kosaki, Kenjiro ; Ogata, Tsutomu. / Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation : Analysis of the X-inactivation patterns. In: American Journal of Medical Genetics. 2000 ; Vol. 91, No. 4. pp. 267-272.
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AU - Muroya, Koji

AU - Nanao, Kenji

AU - Hasegawa, Yukihiro

AU - Terasaki, Hiroshi

AU - Kosaki, Kenjiro

AU - Ogata, Tsutomu

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