Literature DB >> 2016093

Duplications of the X chromosome in males: evidence that most parts of the X chromosome can be active in two copies.

M Schmidt1, D Du Sart, P Kalitsis, M Leversha, S Dale, L Sheffield, D Toniolo.   

Abstract

We have analysed two duplications of the X chromosome in male patients using chromosome replication and DNA methylation patterns as determinants of the functional status of the duplicated segments. In both cases, the large duplicated regions, Xq12-q22 and Xq26.3-qter, were not inactivated. A review of previously reported male cases revealed that these duplications were also not subject to inactivation. Taken together, the examined duplications cover almost the entire X chromosome except the pericentromeric region and Xq25-26. Thus, most regions of the X chromosome can be present in two functional copies without lethal consequences.

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Year:  1991        PMID: 2016093     DOI: 10.1007/bf00194646

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


  20 in total

1.  CpG islands of the X chromosome are gene associated.

Authors:  M Alcalay; D Toniolo
Journal:  Nucleic Acids Res       Date:  1988-10-25       Impact factor: 16.971

2.  Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error.

Authors:  S Schwartz; M F Schwartz; S R Panny; C J Peterson; E Waters; M M Cohen
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

3.  Inherited tandem duplication dup(X) (q131-q212) in a male proband.

Authors:  L O Vejerslev; M Rix; B Jespersen
Journal:  Clin Genet       Date:  1985-03       Impact factor: 4.438

4.  Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation.

Authors:  P Steinbach; W Horstmann; W Scholz
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  Structural aberration of the X chromosome in a patient with gonadal dysgenesis: an approach to karyotype-phenotype correlation.

Authors:  M Varella-Garcia; E H Tajara; A R Gagliardi
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

6.  Cytogenetic and molecular studies on a recombinant human X chromosome: implications for the spreading of X chromosome inactivation.

Authors:  T Mohandas; R L Geller; P H Yen; J Rosendorff; R Bernstein; A Yoshida; L J Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1987-07       Impact factor: 11.205

7.  An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region.

Authors:  F P Cremers; R A Pfeiffer; T J van de Pol; M H Hofker; T A Kruse; B Wieringa; H H Ropers
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

8.  Inherited partial X chromosome duplication in a mentally retarded male.

Authors:  K B Nielsen; F Langkjaer
Journal:  J Med Genet       Date:  1982-06       Impact factor: 6.318

9.  Localization of the mcf.2 transforming sequence to the X chromosome.

Authors:  T Noguchi; M G Mattei; I Oberlè; J Planche; J Imbert; C Pelassy; F Birg; D Birnbaum
Journal:  EMBO J       Date:  1987-05       Impact factor: 11.598

10.  Specific methylation pattern at the 3' end of the human housekeeping gene for glucose 6-phosphate dehydrogenase.

Authors:  D Toniolo; M D'Urso; G Martini; M Persico; V Tufano; G Battistuzzi; L Luzzatto
Journal:  EMBO J       Date:  1984-09       Impact factor: 11.598

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  5 in total

1.  Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation.

Authors:  T Ogata; J R Hawkins; A Taylor; N Matsuo; J Hata; P N Goodfellow
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

2.  A familial Xp+ chromosome, dup (Xq26.3-->qter).

Authors:  A I Vasquez; H Rivera; L Bobadilla; J A Crolla
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

3.  MECP2 duplications in six patients with complex sex chromosome rearrangements.

Authors:  Amy M Breman; Melissa B Ramocki; Sung-Hae L Kang; Misti Williams; Debra Freedenberg; Ankita Patel; Patricia I Bader; Sau Wai Cheung
Journal:  Eur J Hum Genet       Date:  2010-12-01       Impact factor: 4.246

4.  Subterminal deletion/duplication event in an affected male due to maternal X chromosome pericentric inversion.

Authors:  Nadja Kokalj-Vokac; Natasa Marcun-Varda; Andreja Zagorac; Alenka Erjavec-Skerget; Boris Zagradisnik; Mirjana Todorovic; Alojz Gregoric
Journal:  Eur J Pediatr       Date:  2004-08-12       Impact factor: 3.183

5.  Trisomy Xp and partial tetrasomy Xq resulting from gain of a rearranged X chromosome in a female fetus: pathogenic or not?

Authors:  Maria Yiu; Zhongxia Qi; Anita Ki; Jingwei Yu
Journal:  Mol Cytogenet       Date:  2015-07-25       Impact factor: 2.009

  5 in total

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