Literature DB >> 7509228

The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23.

D Pham-Dinh1, Y Fourbil, F Blanquet, M G Mattéi, N Roeckel, P Latour, G Chazot, A Vandenberghe, A Dautigny.   

Abstract

We have characterized the human gene encoding the major peripheral myelin protein zero (P0) and assigned it, by in situ hybridization, to the q21.3-q23 region of human chromosome 1. This region is known to contain a cluster of interspersed genes coding for the related human leukocyte receptors of the Fc portion of the immunoglobulin G (Fc gamma RI, II, III). This colocalization was refined by the finding of a yeast artificial chromosome (YAC) of the Centre d'Etude du Polymorphisme Humain (CEPH) library, hybridizing to the P0 and Fc gamma RIIA genes, demonstrating their physical linkage. These data may have important implications in demyelinating diseases studies like Charcot-Marie-Tooth disease type 1B (CMT1B).

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Year:  1993        PMID: 7509228     DOI: 10.1093/hmg/2.12.2051

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  7 in total

1.  Gene assignment in Ateles paniscus chamek (Platyrrhini, Primates). Allocation of 18 markers of human syntenic groups 1, 2, 7, 14, 15, 17 and 22.

Authors:  H N Seuánez; C R Lima; B Lemos; C R Bonvicino; M A Moreira; F C Canavez
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

2.  Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.

Authors:  J Lopes; E LeGuern; R Gouider; S Tardieu; N Abbas; N Birouk; M Gugenheim; P Bouche; Y Agid; A Brice
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

3.  A comparison of methods for gene dosage analysis in HMSN type 1.

Authors:  J S Rowland; D E Barton; G R Taylor
Journal:  J Med Genet       Date:  2001-02       Impact factor: 6.318

4.  A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

Authors:  A Bouhouche; A Benomar; N Birouk; A Mularoni; F Meggouh; J Tassin; D Grid; A Vandenberghe; M Yahyaoui; T Chkili; A Brice; E LeGuern
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

5.  Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.

Authors:  F L Mastaglia; K J Nowak; R Stell; B A Phillips; J E Edmondston; S M Dorosz; S D Wilton; J Hallmayer; B A Kakulas; N G Laing
Journal:  J Neurol Neurosurg Psychiatry       Date:  1999-08       Impact factor: 10.154

6.  High frequency of mutations in codon 98 of the peripheral myelin protein P0 gene in 20 French CMT1 patients.

Authors:  H Rouger; E LeGuern; R Gouider; S Tardieu; N Birouk; M Gugenheim; P Bouche; Y Agid; A Brice
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

7.  Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene.

Authors:  E Nelis; V Timmerman; P De Jonghe; A Vandenberghe; D Pham-Dinh; A Dautigny; J J Martin; C Van Broeckhoven
Journal:  Hum Genet       Date:  1994-12       Impact factor: 4.132

  7 in total

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