Literature DB >> 3463206

A practical metaphase marker of the inactive X chromosome.

D L Van Dyke, W L Flejter, M J Worsham, J R Roberson, J V Higgins, H M Herr, S Knuutila, N Wang, V R Babu, L Weiss.   

Abstract

It is paradoxical that the inactivated X is the only chromosome that can be identified in the interphase nucleus, yet in metaphase, it is indistinguishable from its genetically active homolog unless special culture and staining procedures are employed. A specific inactivation-associated fold in proximal Xq resolves that paradox. We describe here how the fold in the proximal long arm can be used as a simple and reliable marker to identify the inactivated X in G-, Q-, or R-banded preparations. Several examples are given, including localization of the inactivation center to band Xq13 or q21.1, identification of nonrandom inactivation in X-chromosome rearrangements, identification of multiple active X chromosomes in tumor cell lines, analysis of X-inactivation patterns in female carriers of the fragile site at Xq27, and comparison of X-inactivation patterns among primate species.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3463206      PMCID: PMC1684029     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  24 in total

1.  Spreading of inactivation in an (X;14) translocation.

Authors:  P W Allderdice; O J Miller; D A Miller; H P Klinger
Journal:  Am J Med Genet       Date:  1978

2.  De novo paracentric inversion in an X chromosome.

Authors:  H M Herr; S J Horton; C I Scott
Journal:  J Med Genet       Date:  1985-04       Impact factor: 6.318

3.  Conference report: International Workshop on the fragile X and X-linked mental retardation.

Authors:  J M Opitz; G R Sutherland
Journal:  Am J Med Genet       Date:  1984-01

4.  A duplication within the critical fertility region of X chromosome in a mentally retarded woman with normal menarche.

Authors:  S Knuutila; K Heinonen; K Hongell; S Varonen; O Simell
Journal:  Hereditas       Date:  1984       Impact factor: 3.271

Review 5.  Significance of the Barr body in human female tumors.

Authors:  S N Ghosh; P N Shah
Journal:  Cancer Genet Cytogenet       Date:  1981-11

6.  Cytogenetic evidence for the absence of an inactivated X chromosome in a human female (XX) breast carcinoma cell line.

Authors:  M Camargo; N Wang
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center.

Authors:  W L Flejter; D L Van Dyke; L Weiss
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

8.  Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

Authors:  P A Jacobs; P A Hunt; M Mayer; R D Bart
Journal:  Am J Hum Genet       Date:  1981-07       Impact factor: 11.025

9.  The origin of inverted tandem duplications, and phenotypic effects of tandem duplication of the X chromosome long arm.

Authors:  D L Van Dyke; M J Miller; L Weiss
Journal:  Am J Med Genet       Date:  1983-07

10.  Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.

Authors:  R H Lindenbaum; G Clarke; C Patel; M Moncrieff; J T Hughes
Journal:  J Med Genet       Date:  1979-10       Impact factor: 6.318

View more
  9 in total

1.  Replication patterns of the fragile X in heterozygous carriers: analysis by a BrdUrd antibody method.

Authors:  H Ohashi; A Kuwano; M Tsukahara; T Arinami; T Kajii
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

2.  Inactivation of the mammalian X chromosome in spermatogenesis.

Authors:  T E Kelly
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

3.  Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Authors:  S E Bodrug; J R Roberson; L Weiss; P N Ray; R G Worton; D L Van Dyke
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

4.  Inactivated X chromosome fold in human leukemia and related clonal disorders.

Authors:  M R Avalos; C Léonard; F Mielot; G Tchernia
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

5.  The Barr body is a looped X chromosome formed by telomere association.

Authors:  C L Walker; C B Cargile; K M Floy; M Delannoy; B R Migeon
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-15       Impact factor: 11.205

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.  Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center.

Authors:  A L Pettigrew; E R McCabe; F F Elder; D H Ledbetter
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

8.  Location of the X inactivation center in primates and other mammals.

Authors:  W L Flejter; D L Van Dyke; L Weiss
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

9.  Neocentric X-chromosome in a girl with Turner-like syndrome.

Authors:  Morteza Hemmat; Boris T Wang; Peter E Warburton; Xiaojing Yang; Fatih Z Boyar; Mohammed El Naggar; Arturo Anguiano
Journal:  Mol Cytogenet       Date:  2012-06-09       Impact factor: 2.009

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.