Literature DB >> 1009814

A possible active segment on the inactive human X chromosome.

E Therman, G E Sarto, C Distèche, C Denniston.   

Abstract

An idic(Xp--) in which the two X chromosomes are attached short arm to short arm, and which thus has two b regions (the Q-dark segment next to the centromere on Xp) between the inactivation centers, assumed to be situated on the Q-dark region next to the centromere on Xq, showed 63.8% bipartite Barr bodies as compared with 22.2% formed by idic(Xq--). In addition, the mean distance of the two parts of the Barr bodies in the fibroblasts of a patient with idic(Xp--) is significantly greater than in the cases with one or no b region. Contrary to the other patients with abnormal X chromosomes, the buccal cells of a woman idic(Xp--) showed a number of bipartite Barr bodies. -- To explain these observations we have put forward the hypothesis that the b region on the Xp always remains active and thus, when the rest of the chromosome forms a Barr body, this segment is extended, allowing the two parts of the X chromatin to get farther apart and at the same time increasing the percentage of bipartite bodies.

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Year:  1976        PMID: 1009814     DOI: 10.1007/bf00328482

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  13 in total

1.  Reappraisal of a 46,X,i(Xp) karyotype as 46,X,del(Xg).

Authors:  A de la Chapelle; J Schröder
Journal:  Hereditas       Date:  1975       Impact factor: 3.271

2.  Increased Q fluorescence of an inactive Xq-chromosome in man.

Authors:  G E Sarto; E Therman; K Patau
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

Review 3.  Human genetics.

Authors:  V A McKusick; G A Chase
Journal:  Annu Rev Genet       Date:  1973       Impact factor: 16.830

4.  Dicentric human X chromosomes.

Authors:  A De la Chapelle; K Stenstrand
Journal:  Hereditas       Date:  1974       Impact factor: 3.271

5.  Center for Barr body condensation on the proximal part of the human Xq: a hypothesis.

Authors:  E Therman; G E Sarto; K Patau
Journal:  Chromosoma       Date:  1974-01-29       Impact factor: 4.316

6.  Fluorescence and Giemsa banding studies of the allocyclic X chromosome in embryonic and adult mouse cells.

Authors:  N Takagi; M Oshimura
Journal:  Exp Cell Res       Date:  1973-03-30       Impact factor: 3.905

7.  Abnormal X chromosomes in man: origin, behavior and effects.

Authors:  E Therman; K Patau
Journal:  Humangenetik       Date:  1974

8.  An inherited X-autosome translocation in man.

Authors:  K E Buckton; P A Jacobs; L A Rae; M S Newton; R Sanger
Journal:  Ann Hum Genet       Date:  1971-10       Impact factor: 1.670

Review 9.  Mechanisms and evolutionary origins of variable X-chromosome activity in mammals.

Authors:  M F Lyon
Journal:  Proc R Soc Lond B Biol Sci       Date:  1974-11-05

10.  Structure and Barr body formation of an Xp + chromosome with two inactivation centers.

Authors:  R F Daly; K Patau; E Therman; G E Sarto
Journal:  Am J Hum Genet       Date:  1977-01       Impact factor: 11.025

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  21 in total

1.  Clinical consequence of Xp-.

Authors:  J J Hoo
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

2.  What causes the abnormal phenotype in a 49,XXXXY male?

Authors:  G E Sarto; P G Otto; E M Kuhn; E Therman
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

3.  DNA replication and inactivation patterns in structural abnormality of sex chromosomes. I.X-A translocations, rings, fragments, isochromosomes, and pseudo-isodicentrics.

Authors:  M Camargo; J Cervenka
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocation.

Authors:  M M Cohen; J Charrow; N E Balkin; C J Harris
Journal:  Am J Hum Genet       Date:  1983-07       Impact factor: 11.025

5.  X chromosome constitution and the human female phenotype.

Authors:  E Therman; C Denniston; G E Sarto; M Ulber
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  The human inactivated X chromosome folds in early metaphase, prometaphase, and prophase.

Authors:  D L Van Dyke; M Worsham; L Weiss
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

7.  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

8.  Symmetrical replication patterns and sex chromatin bodies formation of an idic(X)(p22.3::p22.3) chromosome.

Authors:  O Mutchinik; L Casas; L Ruz; R Lisker; O Lozano
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertile.

Authors:  M Fraccaro; P Maraschio; F Pasquali; S Scappaticci
Journal:  Hum Genet       Date:  1977-12-23       Impact factor: 4.132

10.  Regional assignment of the steroid sulfatase-X-linked ichthyosis locus: implications for a noninactivated region on the short arm of human X chromosome.

Authors:  T Mohandas; L J Shapiro; R S Sparkes; M C Sparkes
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

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