Literature DB >> 6745924

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

M Camargo, J Cervenka.   

Abstract

High resolution chromosome analysis and bromodeoxyuridine (BrdUrd) incorporation have been applied to study patterns of chromosomal replication (inactivation) in two cases of unbalanced X-autosome translocations, seven cases of X and Y chromosome rings or fragments, and five cases of dicentric isochromosomes (Xq). Our results indicate the following: (1) In (X-A) translocations, detailed replicational analysis of the translocated autosomal segment is informative. Absence of "spreading effect" and partial-incomplete spreading effect are the most common observations. (2) Sex chromosome derived fragments and rings can be differentiated based on their replicational features. (3) Dicentric isochromosomes (Xq) can be classified based on intercentromeric distances, replicational asynchrony, and centromere inactivation. (4) A correlation between intercentromeric distance and degree of 45,X mosaicism was observed in dicentric "i(Xq)" chromosomes. Evidence for spreading effect based on our results and on the review of the literature has been critically analyzed and general rules in evaluating spreading effects (SE) proposed. The cytologic detection of active regions on the late replicating X chromosome and the inactivation capacity of the juxtacentromeric region of Xp is evaluated. It is proposed that centromere suppression and underreplication are related phenomena. Finally, the analysis of informative replicational stages is emphasized and the application of their analysis in basic and clinical cytogenetics demonstrated.

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Year:  1984        PMID: 6745924     DOI: 10.1007/BF00270556

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


  67 in total

1.  Replication pattern of the X chromosomes in three X/autosomal translocations.

Authors:  A Hagemeijer; J Hoovers; E M Smit; D Bootsma
Journal:  Cytogenet Cell Genet       Date:  1977

2.  Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes.

Authors:  S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1973-12       Impact factor: 11.205

3.  Different patterns of X chromosome inactivity in lymphocytes and fibroblasts of a human balanced X;autosome translocation.

Authors:  B Hellkuhl; A de la Chapelle; K H Grzeschik
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  Structural anomalies of the X chromosome and inactivation center.

Authors:  M G Mattei; J F Mattei; I Vidal; F Giraud
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  The Turner phenotype and the different types of human x isochromosome.

Authors:  P G Otto; A M Vianna-Morgante; P A Otto; A Wajntal
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  Genetic evidence for the inactivation of a human autosomal locus attached to an inactive X chromosome.

Authors:  T Mohandas; R S Sparkes; L J Shapiro
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

7.  Further observations on a 13qXp translocation associated with retinoblastoma.

Authors:  W W Nichols; R C Miller; M Sobel; E Hoffman; R S Sparkes; T Mohandas; I Veomett; J R Davis
Journal:  Am J Ophthalmol       Date:  1980-05       Impact factor: 5.258

8.  A possible active segment on the inactive human X chromosome.

Authors:  E Therman; G E Sarto; C Distèche; C Denniston
Journal:  Chromosoma       Date:  1976-12-16       Impact factor: 4.316

9.  [Familial X-autosomal translocation t (X, 2)].

Authors:  M V Mashkova; D K Verlinskaia
Journal:  Tsitologiia       Date:  1976-07

10.  Position of the human X inactivation center on Xq.

Authors:  E Therman; G E Sarto; C G Palmer; H Kallio; C Denniston
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

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  13 in total

1.  Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, southern hybridization and non-isotopic in situ hybridization.

Authors:  F Speleman; B Van der Auwera; K Mangelschots; M Vercruyssen; T Raap; J Wiegant; M Craen; J Leroy
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

2.  Study on the relationship between cytogenetics and phenotypic effect in Turner's syndrome.

Authors:  X Hu; B Zhu; H Lin; D Shu; D Tao; M Wang
Journal:  J Tongji Med Univ       Date:  1996

3.  Characterization of chromatin at structurally abnormal inactive X chromosomes reveals potential evidence of a rare hybrid active and inactive isodicentric X chromosome.

Authors:  Brian P Chadwick
Journal:  Chromosome Res       Date:  2019-11-27       Impact factor: 5.239

4.  Tentative assignment of hypomelanosis of Ito to 9q33----qter.

Authors:  R Happle
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

5.  A model for effective pairing and recombination at meiosis based on early replicating sites (R-bands) along chromosomes.

Authors:  A C Chandley
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

6.  Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG technique.

Authors:  E A Keitges; C G Palmer
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

7.  A stable dicentric chromosome: both centromeres develop kinetochores and attach to the spindle in monocentric and dicentric configuration.

Authors:  A Wandall
Journal:  Chromosoma       Date:  1994-03       Impact factor: 4.316

8.  Two cases of X/autosome translocation in females with incontinentia pigmenti.

Authors:  S V Hodgson; B Neville; R W Jones; C Fear; M Bobrow
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

9.  Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiency.

Authors:  A Pelet; A Rotig; C Bonaïti-Pellié; D Rabier; V Cormier; E Toumas; D Hentzen; J M Saudubray; A Munnich
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

Review 10.  Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.

Authors:  D J Wolff; C J Brown; S Schwartz; A M Duncan; U Surti; H F Willard
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

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