Literature DB >> 7782069

Construction of a YAC contig spanning the Xq13.3 subband.

L Villard1, J Gecz, L Colleaux, A M Lossi, J Chelly, Y Ishikawa-Brush, A P Monaco, M Fontes.   

Abstract

The loci involved in several X-linked mental retardation syndromes have been linked to the pericentromeric region of the X chromosome long arm (Xq12-q21). To isolate candidate genes for these diseases, we set up the construction of YAC contigs spanning this region. Two of these syndromes (the Juberg-Marsidi syndrome and the alpha-thalessemia mental retardation syndrome) have been recently linked, with high lod scores, to polymorphic probes previously assigned to Xq13.3. We therefore constructed a first YAC contig, encompassing this band, from DXS441 to PGK1. The physical map, deduced from the isolated clones, extends over 2.1 Mb of genomic DNA. Restriction analysis of the YAC contig allowed us to map precisely the loci previously assigned to that chromosomal region and to define their relative order. The validity of this physical map has been checked by comparing Sfi I digests of the YACs to genomic fragments obtained with the same enzyme. A cDNA selection approach, already performed with a previous partial contig, has been extended to cover the whole region.

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Year:  1995        PMID: 7782069     DOI: 10.1016/0888-7543(95)80089-5

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  5 in total

1.  Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbands.

Authors:  L Colleaux; M May; J Belougne; D Lepaslier; C Schwartz; M Fontes
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

2.  Use of interspersed repetitive sequences-PCR products for cDNA selection.

Authors:  L Villard; E Passage; L Colleaux; M Fontes
Journal:  Mamm Genome       Date:  1995-09       Impact factor: 2.957

3.  Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1.

Authors:  L Villard; S Briault; A M Lossi; C Paringaux; J Belougne; L Colleaux; D R Pincus; E Woollatt; J Lespinasse; A Munnich; C Moraine; M Fontès; J Gecz
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

4.  The human sex-reversing ATRX gene has a homologue on the marsupial Y chromosome, ATRY: implications for the evolution of mammalian sex determination.

Authors:  A Pask; M B Renfree; J A Marshall Graves
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-21       Impact factor: 11.205

5.  Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemia.

Authors:  L Villard; A Toutain; A M Lossi; J Gecz; C Houdayer; C Moraine; M Fontès
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

  5 in total

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