Literature DB >> 1617223

Completion of the physical map of Xq28: the location of the gene for L1CAM on the human X chromosome.

A Dietrich1, B Korn, A Poustka.   

Abstract

The gene for the neural cell adhesion molecule L1 (L1CAM) has been shown to be located close to the color vision pigment genes in mouse and man. This location has been confirmed by a number of different mapping strategies in both species. With pulsed field gel electrophoresis it has been proposed that L1CAM lies between the RCP, GCP, and GDX, G6PD loci. We report here a reinterpretation of the location of this gene, based on the physical linkage of L1CAM to the more proximal locus DXS15. This places L1CAM between this marker and the color vision genes (RCP, GCP), a region very dense in CpG islands, expected to contain a large fraction of the disease genes assigned to the Xq28 region. In combination with the physical mapping data on Xq28 described previously, this closes the last remaining gap in the map of the Xq27-Xq28 region. This removes the last contradiction between the maps of this region in the genomes of man and mouse, and confirms the close similarity of order and distances of markers between these organisms.

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Year:  1992        PMID: 1617223     DOI: 10.1007/bf00352462

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  21 in total

1.  Structure and polymorphism of human telomere-associated DNA.

Authors:  W R Brown; P J MacKinnon; A Villasanté; N Spurr; V J Buckle; M J Dobson
Journal:  Cell       Date:  1990-10-05       Impact factor: 41.582

2.  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

3.  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

4.  The fragile X site in somatic cell hybrids: an approach for molecular cloning of fragile sites.

Authors:  S T Warren; F Zhang; G R Licameli; J F Peters
Journal:  Science       Date:  1987-07-24       Impact factor: 47.728

5.  A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion.

Authors:  B G Herrmann; D P Barlow; H Lehrach
Journal:  Cell       Date:  1987-03-13       Impact factor: 41.582

6.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

7.  Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Authors:  D Drayna; K Davies; D Hartley; J L Mandel; G Camerino; R Williamson; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

8.  Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.

Authors:  P Wieacker; K E Davies; H J Cooke; P L Pearson; R Williamson; S Bhattacharya; J Zimmer; H H Ropers
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

9.  Neural adhesion molecule L1 as a member of the immunoglobulin superfamily with binding domains similar to fibronectin.

Authors:  M Moos; R Tacke; H Scherer; D Teplow; K Früh; M Schachner
Journal:  Nature       Date:  1988-08-25       Impact factor: 49.962

10.  Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.

Authors:  J Nathans; D Thomas; D S Hogness
Journal:  Science       Date:  1986-04-11       Impact factor: 47.728

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  3 in total

Review 1.  X linked hydrocephalus and MASA syndrome.

Authors:  S Kenwrick; M Jouet; D Donnai
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

2.  Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.

Authors:  T A Angel; C J Faust; J C Gonzales; S Kenwrick; R A Lewis; G E Herman
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

3.  Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

Authors:  M D'Esposito; N A Quaderi; A Ciccodicola; P Bruni; T Esposito; M D'Urso; S D Brown
Journal:  Mamm Genome       Date:  1996-07       Impact factor: 2.957

  3 in total

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