Literature DB >> 3785381

Implications of fragile X expression in normal males for the nature of the mutation.

D H Ledbetter, S A Ledbetter, R L Nussbaum.   

Abstract

The fragile site at Xq27, associated with a common form of X-linked mental retardation (XLMR), is expressed in a variable proportion of the peripheral lymphocytes of affected males when the cells are cultured under thymidylate stress (Td stress) produced by folate or thymidylate deprivation. Some clinically normal males--transmitting males--are known to carry and transmit the fragile X mutation and yet show no cytogenetic expression in lymphocytes. Normal males with no family history of X-linked mental retardation express the site only rarely. When the fragile X chromosome from affected males is isolated in a rodent genetic background by somatic cell hybridization, the level of expression is similar to that seen in lymphocytes under Td stress. Here we show that X chromosomes from two transmitting males and two normal control males, all of which were fragile X negative in lymphocytes or lymphoblasts, could be made to express the fragile site in hybrids, although at levels that were below those seen in hybrids from affected males. Furthermore, transmitting males could be differentiated from normal males by their significantly higher expression rates when hybrids were exposed to caffeine before cytogenetic harvest. One male chimpanzee also showed low level expression in hybrid cells. These data suggest that the hybrid system lowers the threshold for fragile X expression, a fragile site at Xq27 may be present on all human and chimpanzee X chromosomes and constitutes a previously unrecognized common fragile site and the hybrid system with caffeine post-treatment can distinguish between the common Xq27 fragile site of control males, the occult mutant fragile site of a transmitting male, and the fully expressed fragile site of an affected male with XLMR. Thus the mutation producing XLMR may represent a multi-step alteration of a naturally occurring DNA sequence producing a continuum of cytogenetic expression and a threshold for clinical manifestation.

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Year:  1986        PMID: 3785381     DOI: 10.1038/324161a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  14 in total

1.  Estimating the stability of the proposed imprinted state of the fragile-X mutation when transmitted by females.

Authors:  P J Follette; C D Laird
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

2.  Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.

Authors:  R Sood; L M Mulligan; R Poon; B N White; J J Holden
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

Review 3.  Anticipation in hereditary disease: the history of a biomedical concept.

Authors:  Judith E Friedman
Journal:  Hum Genet       Date:  2011-06-12       Impact factor: 4.132

4.  Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa.

Authors:  D M Sosnoski; B S Emanuel; A L Hawkins; P van Tuinen; D H Ledbetter; R L Nussbaum; F T Kaos; E Schwartz; D Phillips; J S Bennett
Journal:  J Clin Invest       Date:  1988-06       Impact factor: 14.808

5.  Interpretation of the heterogeneity in the linkage relationships of DNA markers around the fragile X locus.

Authors:  R Winter; M Pembrey
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

6.  Chromosome breakage and recombination at fragile sites.

Authors:  T W Glover; C K Stein
Journal:  Am J Hum Genet       Date:  1988-09       Impact factor: 11.025

7.  Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologue.

Authors:  D Wöhrle; J P Fryns; P Steinbach
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

8.  A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

Authors:  F Rousseau; D Heitz; J Tarleton; J MacPherson; H Malmgren; N Dahl; A Barnicoat; C Mathew; E Mornet; I Tejada
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

9.  Isolation of a human DNA sequence which spans the fragile X.

Authors:  E J Kremer; S Yu; M Pritchard; R Nagaraja; D Heitz; M Lynch; E Baker; V J Hyland; R D Little; M Wada
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

10.  Induction of sister chromatid exchanges at common fragile sites.

Authors:  T W Glover; C K Stein
Journal:  Am J Hum Genet       Date:  1987-11       Impact factor: 11.025

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