Literature DB >> 1968034

New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus.

F Rousseau1, A Vincent, I Oberlé, J L Mandel.   

Abstract

The polymorphic DNA marker DXS304 detected by probe U6.2 has recently been shown to be closer to the fragile X locus than previously available markers. Its usefulness has however been limited by its relatively low heterozygosity. We have isolated, by cosmid cloning, a 67 kilobase region around probe U6.2 and have characterized a new probe (U6.2-20E) that detects BanI and BstEII restriction fragment length polymorphisms (RFLPs). The BanI RFLP has a heterozygosity of 0.49 and is in partial linkage disequilibrium with the previously described polymorphism, with a combined heterozygosity of 0.63. Furthermore, we have found that the U6.2 original probe, which probably detects an insertion-deletion polymorphism, is also informative in BanI digests. Thus, the two informative RFLPs at the DXS304 locus can be conveniently tested in a single hybridization with a single digest. An updated linkage analysis confirms that DXS304 is distal to the fragile X locus. This informative locus can now be used effectively for genetic mapping of the Xq27-q28 region, and for diagnostic applications in fragile X or Hunter syndrome families.

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Year:  1990        PMID: 1968034     DOI: 10.1007/bf00200572

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


  12 in total

1.  A 230kb cosmid walk in the Duchenne muscular dystrophy gene: detection of a conserved sequence and of a possible deletion prone region.

Authors:  R Heilig; C Lemaire; J L Mandel
Journal:  Nucleic Acids Res       Date:  1987-11-25       Impact factor: 16.971

2.  Detection of specific RNAs or specific fragments of DNA by fractionation in gels and transfer to diazobenzyloxymethyl paper.

Authors:  J C Alwine; D J Kemp; B A Parker; J Reiser; J Renart; G R Stark; G M Wahl
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

3.  A polymorphic locus at Xq27-28 detected by the probe U6.2 [DXS304].

Authors:  N Dahl; K Hammarström-Heeroma; G B van Ommen; U Pettersson
Journal:  Nucleic Acids Res       Date:  1989-04-11       Impact factor: 16.971

4.  The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.

Authors:  A Vincent; N Dahl; I Oberlé; A Hanauer; J L Mandel; H Malmgren; U Pettersson
Journal:  Genomics       Date:  1989-11       Impact factor: 5.736

Review 5.  Report of the committee on the genetic constitution of the X chromosome.

Authors:  J L Mandel; H F Willard; R L Nussbaum; G Romeo; J M Puck; K E Davies
Journal:  Cytogenet Cell Genet       Date:  1989

6.  Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci.

Authors:  J C Murray; R Shiang; L R Carlock; M Smith; K H Buetow
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

7.  Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome.

Authors:  N Dahl; K Hammarström-Heeroma; P Goonewardena; C Wadelius; K H Gustavson; G Holmgren; G J van Ommen; U Pettersson
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

8.  Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).

Authors:  N Dahl; P Goonewardena; H Malmgren; K H Gustavson; G Holmgren; E Seemanova; G Annerén; A Flood; U Pettersson
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

9.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

10.  Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: studies of the HLA class II loci.

Authors:  N Arnheim; C Strange; H Erlich
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

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  5 in total

1.  Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA).

Authors:  F Rousseau; A Vincent; S Rivella; D Heitz; C Triboli; E Maestrini; S T Warren; G K Suthers; P Goodfellow; J L Mandel
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

2.  Germline and somatic mosaicism in a female carrier of Hunter disease.

Authors:  R Froissart; I Maire; V Bonnet; T Levade; D Bozon
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

3.  Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Authors:  G K Suthers; J C Mulley; M A Voelckel; N Dahl; M L Väisänen; P Steinbach; I A Glass; C E Schwartz; B A van Oost; S N Thibodeau
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

4.  X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studies.

Authors:  D G Bichet; G N Hendy; M Lonergan; M F Arthus; S Ligier; Z Pausova; R Kluge; H Zingg; P Saenger; E Oppenheimer
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

5.  Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.

Authors:  C Hydén-Granskog; R Salonen; H von Koskull
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

  5 in total

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