Literature DB >> 3957346

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

E A Keitges, C G Palmer.   

Abstract

Eight X autosome translocations were studied with replication banding to localize spreading of late replication into the autosomal segments. Partial spreading into the autosomal segment was seen in four translocations and no spreading of late replication was seen in four translocations. In those translocations with partial spreading of late replication into the autosomal segment, late replication did not always spread continuously from the X chromosome breakpoint throughout the autosome. Instead, it appeared to skip some bands and affect others. The data on the pattern of replication, taken to indicate also a spread of inactivation into these autosomal segments, correlated well with the clinical data in most cases and suggest that spreading of late replication is often incomplete and may be discontinuous.

Mesh:

Year:  1986        PMID: 3957346     DOI: 10.1007/bf00291884

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


  21 in total

1.  Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21).

Authors:  J Couturier; B Dutrillaux; P Garber; O Raoul; M F Croquette; J C Fourlinnie; E Maillard
Journal:  Hum Genet       Date:  1979-07-18       Impact factor: 4.132

2.  High resolution of human chromosomes.

Authors:  J J Yunis
Journal:  Science       Date:  1976-03-26       Impact factor: 47.728

3.  [Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation].

Authors:  S Carpentier; M O Rethoré; J Lejeune
Journal:  Ann Genet       Date:  1972-12

4.  Replication timing of genes and middle repetitive sequences.

Authors:  M A Goldman; G P Holmquist; M C Gray; L A Caston; A Nag
Journal:  Science       Date:  1984-05-18       Impact factor: 47.728

Review 5.  Mammalian X-chromosome inactivation.

Authors:  S M Gartler; A D Riggs
Journal:  Annu Rev Genet       Date:  1983       Impact factor: 16.830

6.  Hot spots and functional organization of human chromosomes.

Authors:  J R Korenberg; E Therman; C Denniston
Journal:  Hum Genet       Date:  1978-07-12       Impact factor: 4.132

7.  The relationship between repetitive DNA and chromosomal bands in man.

Authors:  O Sanchez; J J Yunis
Journal:  Chromosoma       Date:  1974       Impact factor: 4.316

8.  A deletion in chromosome 22 can cause DiGeorge syndrome.

Authors:  A de la Chapelle; R Herva; M Koivisto; P Aula
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Late replication in an X-autosome translocation in the mouse: correlation with genetic inactivation and evidence for selective effects during embryogenesis.

Authors:  C M Disteche; E M Eicher; S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1979-10       Impact factor: 11.205

10.  X-autosome translocations: cytogenetic characteristics and their consequences.

Authors:  M G Mattei; J F Mattei; S Ayme; F Giraud
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

View more
  7 in total

Review 1.  The critical region on the human Xq.

Authors:  E Therman; R Laxova; B Susman
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

2.  The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA.

Authors:  W M White; H F Willard; D L Van Dyke; D J Wolff
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

3.  Investigation of the "variable spreading" of X inactivation into a translocated autosome.

Authors:  S Schanz; P Steinbach
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

4.  Incorporation of 5-ethynyl-2'-deoxyuridine (EdU) as a novel strategy for identification of the skewed X inactivation pattern in balanced and unbalanced X-rearrangements.

Authors:  Luiza Sisdelli; Angela Cristina Vidi; Mariana Moysés-Oliveira; Adriana Di Battista; Adriana Bortolai; Danilo Moretti-Ferreira; Magnus R Dias da Silva; Maria Isabel Melaragno; Gianna Carvalheira
Journal:  Hum Genet       Date:  2015-12-15       Impact factor: 4.132

5.  Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation.

Authors:  A P Miller; H F Willard
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-21       Impact factor: 11.205

6.  Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation.

Authors:  P Patracchini; E Calzolari; V Aiello; P Palazzi; P Banin; G Marchetti; F Bernardi
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

7.  Spread of X-chromosome inactivation into autosomal sequences: role for DNA elements, chromatin features and chromosomal domains.

Authors:  Allison M Cotton; Chih-Yu Chen; Lucia L Lam; Wyeth W Wasserman; Michael S Kobor; Carolyn J Brown
Journal:  Hum Mol Genet       Date:  2013-10-24       Impact factor: 6.150

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.