Literature DB >> 2394446

Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity.

C B Sharp1, H M Bedford, H F Willard.   

Abstract

Three different long-arm X isochromosomes and an isodicentric X chromosome were examined by in situ hybridization with X-chromosome-specific alpha-satellite probes and by quantitation of Southern blots hybridized with proximal short-arm probes. Each chromosome had a unique pericentromeric structure. The isodicentric X chromosome was clearly dicentric, showing two distinct alpha-satellite hybridization signals and duplication of short-arm material. Two isochromosomes showed a larger than normal, bifid alpha-satellite signal and also had duplications of different extents of short-arm material. The third X isochromosome could not be distinguished from a classical long-arm isochromosome; it did not have a short-arm duplication and it had a single alpha-satellite signal. These data indicate that rearrangements responsible for X isochromosome formation can occur at numerous locations in the pericentromeric region and that some X isochromosomes may involve duplications of substantial portions of the short arm.

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Year:  1990        PMID: 2394446     DOI: 10.1007/bf00206757

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


  19 in total

1.  Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 [inv(2) (p15 q21)] in a patient with gonadal dysgenesis.

Authors:  M M Cohen; A Rosenmann; S Hacham-Zadeh; S Dahan
Journal:  Clin Genet       Date:  1975-07       Impact factor: 4.438

2.  A cloned sequence, p82H, of the alphoid repeated DNA family found at the centromeres of all human chromosomes.

Authors:  A R Mitchell; J R Gosden; D A Miller
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

3.  Alphoid satellite DNA is tightly associated with centromere antigens in human chromosomes throughout the cell cycle.

Authors:  H Masumoto; K Sugimoto; T Okazaki
Journal:  Exp Cell Res       Date:  1989-03       Impact factor: 3.905

4.  Cytogenetic findings in 89 cases of Turner's syndrome with abnormal karyotypes.

Authors:  W Schmid; E Naef; G Mürset; A Prader
Journal:  Humangenetik       Date:  1974

5.  Dicentric human X chromosomes.

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

6.  Molecular studies of the parental origin and nature of human X isochromosomes.

Authors:  M Harbison; T Hassold; C Kobryn; P A Jacobs
Journal:  Cytogenet Cell Genet       Date:  1988

7.  Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism.

Authors:  L Y Hsu; S Paciuc; K David; S Cristian; R Moloshok; K Hirschhorn
Journal:  J Med Genet       Date:  1978-06       Impact factor: 6.318

8.  The human neurofilament gene (NEFL) is located on the short arm of chromosome 8.

Authors:  J Hurst; D Flavell; J P Julien; D Meijer; W Mushynski; F Grosveld
Journal:  Cytogenet Cell Genet       Date:  1987

9.  Isochromosome-X in man. I.

Authors:  A De la Chapelle; J Wennström; H Hortling; C H Ockey
Journal:  Hereditas       Date:  1966       Impact factor: 3.271

10.  Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

Authors:  D Pinkel; T Straume; J W Gray
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

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  7 in total

1.  Extensive analysis of mosaicism in a case of Turner syndrome: the experience of 287 cytogenetic laboratories. College of American Pathologists/American College of Medical Genetics Cytogenetics Resource Committee.

Authors:  J P Park; A R Brothman; M G Butler; L D Cooley; G W Dewald; K F Lundquist; C G Palmer; S R Patil; K W Rao; I A Saikevych; N R Schneider; G H Vance
Journal:  Arch Pathol Lab Med       Date:  1999-05       Impact factor: 5.534

2.  Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.

Authors:  Stuart A Scott; Ninette Cohen; Tracy Brandt; Peter E Warburton; Lisa Edelmann
Journal:  Hum Mol Genet       Date:  2010-06-22       Impact factor: 6.150

3.  A molecular study of X isochromosomes: parental origin, centromeric structure, and mechanisms of formation.

Authors:  I Lorda-Sanchez; F Binkert; M Maechler; A Schinzel
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

4.  Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.

Authors:  D J Wolff; A P Miller; D L Van Dyke; S Schwartz; H F Willard
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

5.  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

6.  Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others.

Authors:  L Carrel; H F Willard
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-22       Impact factor: 11.205

7.  Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.

Authors:  F A Eggerding; S A Schonberg; F F Chehab; M E Norton; V A Cox; C J Epstein
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

  7 in total

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