Literature DB >> 8786075

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

J Azofeifa1, R Waldherr, M Cremer.   

Abstract

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 the methylation of the polymorphic alleles recognized by the probes M27beta 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.

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Year:  1996        PMID: 8786075     DOI: 10.1007/bf02185765

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  21 in total

1.  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

2.  Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase.

Authors:  D H Keith; J Singer-Sam; A D Riggs
Journal:  Mol Cell Biol       Date:  1986-11       Impact factor: 4.272

3.  Isolation of genomic DNA.

Authors:  B G Herrmann; A M Frischauf
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

4.  Primordial cell pool size and lineage relationships of five human cell types.

Authors:  P J Fialkow
Journal:  Ann Hum Genet       Date:  1973-07       Impact factor: 1.670

5.  Clonal analysis using recombinant DNA probes from the X-chromosome.

Authors:  B Vogelstein; E R Fearon; S R Hamilton; A C Preisinger; H F Willard; A M Michelson; A D Riggs; S H Orkin
Journal:  Cancer Res       Date:  1987-09-15       Impact factor: 12.701

6.  Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter.

Authors:  F Tihy; N Vogt; D Recan; B Malfoy; F Leturcq; M Coquet; F Serville; D Fontan; J M Guillard; J C Kaplan
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132

7.  Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy.

Authors:  C S Richards; S C Watkins; E P Hoffman; N R Schneider; I W Milsark; K S Katz; J D Cook; L M Kunkel; J M Cortada
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

8.  Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy.

Authors:  K M Bushby; J A Goodship; L V Nicholson; M A Johnson; I D Haggerty; D Gardner-Medwin
Journal:  Neuromuscul Disord       Date:  1993-01       Impact factor: 4.296

Review 9.  Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinning.

Authors:  B Winchester; E Young; S Geddes; S Genet; J Hurst; H Middleton-Price; N Williams; M Webb; A Habel; S Malcolm
Journal:  Am J Med Genet       Date:  1992-12-01

10.  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.

Authors:  J Azofeifa; T Voit; C Hübner; M Cremer
Journal:  Hum Genet       Date:  1995-08       Impact factor: 4.132

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  7 in total

1.  A hemizygous short tandem repeat polymorphism 3' to the human phosphoglycerate kinase gene.

Authors:  D E Riley; I R Cho; J N Krieger
Journal:  Mol Biol Rep       Date:  1999-08       Impact factor: 2.316

2.  No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans.

Authors:  Véronique Bolduc; Pierre Chagnon; Sylvie Provost; Marie-Pierre Dubé; Claude Belisle; Marianne Gingras; Luigina Mollica; Lambert Busque
Journal:  J Clin Invest       Date:  2008-01       Impact factor: 14.808

3.  Comparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome.

Authors:  Kunio Miyake; Chunshu Yang; Yohei Minakuchi; Kenta Ohori; Masaki Soutome; Takae Hirasawa; Yasuhiro Kazuki; Noboru Adachi; Seiko Suzuki; Masayuki Itoh; Yu-Ichi Goto; Tomoko Andoh; Hiroshi Kurosawa; Mitsuo Oshimura; Masayuki Sasaki; Atsushi Toyoda; Takeo Kubota
Journal:  PLoS One       Date:  2013-06-21       Impact factor: 3.240

4.  Patterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variation.

Authors:  M S Peñaherrera; R Jiang; L Avila; R K C Yuen; C J Brown; W P Robinson
Journal:  Hum Reprod       Date:  2012-03-19       Impact factor: 6.918

5.  Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases.

Authors:  Ghazi Chabchoub; Elif Uz; Abdellatif Maalej; Chigdem A Mustafa; Ahmed Rebai; Mouna Mnif; Zouheir Bahloul; Nadir R Farid; Tayfun Ozcelik; Hammadi Ayadi
Journal:  Arthritis Res Ther       Date:  2009-07-09       Impact factor: 5.156

6.  Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndrome.

Authors:  Sarah Vergult; Bart Leroy; Ilse Claerhout; Björn Menten
Journal:  Mol Vis       Date:  2013-02-06       Impact factor: 2.367

7.  X-Linked Emery-Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female Carriers.

Authors:  Emanuela Viggiano; Agnieszka Madej-Pilarczyk; Nicola Carboni; Esther Picillo; Manuela Ergoli; Stefania Del Gaudio; Michal Marchel; Gerardo Nigro; Alberto Palladino; Luisa Politano
Journal:  Genes (Basel)       Date:  2019-11-11       Impact factor: 4.096

  7 in total

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