Literature DB >> 7837250

X inactivation patterns in female monozygotic twins and their families.

E Watkiss1, T Webb, G Rysiecki, N Girdler, E Hewett, S Bundey.   

Abstract

X inactivation studies have been carried out on 22 pairs of female monozygotic twins, one set of female monozygotic triplets, and their mothers and singleton sisters, using the probe M27 beta. Forty-eight per cent of the twins, 55% of their mothers, and 42% of their singleton sisters showed skewed X inactivation. Two of the triplets and their mother had random X inactivation, while the third triplet showed skewed X inactivation. Their singleton sister was homozygous with M27 beta. Of the twins, six pairs showed skewed X inactivation in favour of the same X chromosome, one pair showed skewed X inactivation favouring opposite X chromosomes, in seven pairs one twin showed skewed X inactivation while her co-twin showed random X inactivation, and in eight pairs both twins were random. A higher frequency of skewed pattern of X inactivation was not observed in the monozygotic twins when compared to a series of non-twin females (mothers and singleton sisters) and, so, the results in this study do not lend support to the theory that skewed X inactivation predisposes to the twinning process.

Mesh:

Year:  1994        PMID: 7837250      PMCID: PMC1050120          DOI: 10.1136/jmg.31.10.754

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  26 in total

1.  The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome.

Authors:  R W Hendriks; H Hinds; Z Y Chen; I W Craig
Journal:  Genomics       Date:  1992-11       Impact factor: 5.736

2.  X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.

Authors:  A Harris; J Collins; D Vetrie; C Cole; M Bobrow
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

3.  Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27 beta): correlation with X-inactivation status.

Authors:  Y Boyd; N J Fraser
Journal:  Genomics       Date:  1990-06       Impact factor: 5.736

4.  Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency.

Authors:  A L Jørgensen; J Philip; W H Raskind; M Matsushita; B Christensen; V Dreyer; A G Motulsky
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

5.  Anomalous X chromosome inactivation: the link between female zygotes, monozygotic twinning, and neural tube defects?

Authors: 
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

6.  Do twin Lyons have larger spots?

Authors:  W E Nance
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

7.  Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.

Authors:  J R Lupski; C A Garcia; H Y Zoghbi; E P Hoffman; R G Fenwick
Journal:  Am J Med Genet       Date:  1991-09-01

8.  The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis.

Authors:  D O Robinson; Y Boyd; D Cockburn; M N Collinson; I Craig; P A Jacobs
Journal:  Genet Res       Date:  1990 Oct-Dec       Impact factor: 1.588

9.  X inactivation patterns in females with Alport's syndrome: a means of selecting against a deleterious gene?

Authors:  D Vetrie; F Flinter; M Bobrow; A Harris
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

10.  Investigation of a female manifesting Becker muscular dystrophy.

Authors:  I A Glass; L V Nicholson; E Watkiss; M A Johnson; R G Roberts; S Abbs; S Brittain-Jones; H G Boddie
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

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  4 in total

1.  Natural gene therapy in monozygotic twins with Fanconi anemia.

Authors:  Anuj Mankad; Toshiyasu Taniguchi; Barbara Cox; Yassmine Akkari; R Keaney Rathbun; Lora Lucas; Grover Bagby; Susan Olson; Alan D'Andrea; Markus Grompe
Journal:  Blood       Date:  2006-01-05       Impact factor: 22.113

2.  No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriers.

Authors:  R J Oostra; S Kemp; P A Bolhuis; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

3.  Commitment to X inactivation precedes the twinning event in monochorionic MZ twins.

Authors:  J Monteiro; C Derom; R Vlietinck; N Kohn; M Lesser; P K Gregersen
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

4.  Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair.

Authors:  Alejandro Horga; Catherine E Woodward; Alberto Mills; Isabel Pareés; Iain P Hargreaves; Ruth M Brown; Enrico Bugiardini; Tony Brooks; Andreea Manole; Elena Remzova; Shamima Rahman; Mary M Reilly; Henry Houlden; Mary G Sweeney; Garry K Brown; James M Polke; Federico Gago; Matthew J Parton; Robert D S Pitceathly; Michael G Hanna
Journal:  Hum Genet       Date:  2019-10-31       Impact factor: 4.132

  4 in total

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