Literature DB >> 7881410

A YAC clone map spanning 7.5 megabases of human chromosome band Xq28.

U C Rogner1, P Kioschis, K Wilke, W Gong, E Pick, A Dietrich, U Zechner, H Hameister, A Pragliola, G E Herman.   

Abstract

Xq28 has been of special interest in human genetics because a large number of diseases map to this region. As a step in the molecular analysis of the as yet uncloned disease genes, and as a test for the detailed analysis of larger regions of the genome, we have constructed YAC clone contigs covering the 7.5 Mb region between IDS to the telomere on the long arm of the human X chromosome. Contigs were assembled and verified by an integrated hybridization-based strategy. Data was combined from the physical map, from YAC and cosmid mapping experiments, and from the localization of specific transcripts in the region. Two gaps in the YAC map of 250 and 100 kb were covered in part by the aid of cosmid clones, but small gaps of 50 kb each remain. The cloned region is expected to contain yet unidentified genes for at least ten genetic diseases. The construction of ordered YAC clone contigs of Xq28 represents an important step in the molecular identification of these genes, and the further analysis of one of the genetically most interesting regions of the human genome.

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Year:  1994        PMID: 7881410     DOI: 10.1093/hmg/3.12.2137

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


  7 in total

1.  A gene for dominant nonspecific X-linked mental retardation is located in Xq28.

Authors:  V des Portes; P Billuart; A Carrié; L Bachner; T Bienvenu; M C Vinet; C Beldjord; G Ponsot; A Kahn; J Boué; J Chelly
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

2.  A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.

Authors:  J L Blouin; D H Christie; A Gos; A Lynn; M A Morris; D H Ledbetter; A Chakravarti; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

3.  Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region.

Authors:  B de Gouyon; A Chatterjee; A Monaco; N Quaderi; S D Brown; G E Herman
Journal:  Mamm Genome       Date:  1996-08       Impact factor: 2.957

4.  Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.

Authors:  N Dahl; L J Hu; M Chery; M Fardeau; S Gilgenkrantz; A Nivelon-Chevallier; I Sidaner-Noisette; F Mugneret; J B Gouyon; A Gal
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

5.  Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions.

Authors:  A Chatterjee; T Tanaka; J E Parrish; G E Herman
Journal:  Mamm Genome       Date:  1995-11       Impact factor: 2.957

6.  A compositional map of human chromosome band Xq28.

Authors:  A De Sario; E M Geigl; G Palmieri; M D'Urso; G Bernardi
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-06       Impact factor: 11.205

7.  The systematic functional characterisation of Xq28 genes prioritises candidate disease genes.

Authors:  Anja Kolb-Kokocinski; Alexander Mehrle; Stephanie Bechtel; Jeremy C Simpson; Petra Kioschis; Stefan Wiemann; Ruth Wellenreuther; Annemarie Poustka
Journal:  BMC Genomics       Date:  2006-02-17       Impact factor: 3.969

  7 in total

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