Literature DB >> 7607667

Refined physical map of the spinal muscular atrophy gene (SMA) region at 5q13 based on YAC and cosmid contiguous arrays.

N Roy1, M D McLean, A Besner-Johnston, C Lefebvre, M Salih, J D Carpten, A H Burghes, Z Yaraghi, J E Ikeda, R G Korneluk.   

Abstract

The gene for the autosomal recessive neurodegenerative disorder spinal muscular atrophy has been mapped to a region of 5q13 flanked proximally by CMS-1 and distally by D5S557. We present a 2-Mb yeast artificial chromosome (YAC) contig constructed from three libraries encompassing the D5S435/D5S629/CMS-1-SMA-D5S557/D5S112 interval. The D5S629/CMS-1-SMA-D5S557 interval is unusual insofar as chromosome 5-specific repetitive sequences are present and many of the simple tandem repeats (STR) are located at multiple loci that are unstable in our YAC clones. A long-range restriction map that demonstrates the SMA-containing interval to be 550 kb is presented. Moreover, a 210-kb cosmid array from both a YAC-specific and a chromosome 5-specific cosmid library encompassing the multilocus STRs CATT-1, CMS-1, D5F149, D5F150, and D5F153 has been assembled. We have recently reported strong linkage disequilibrium with Type I SMA for two of these STRs, indicating that the gene is located in close proximity to or within our cosmid clone array.

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Year:  1995        PMID: 7607667     DOI: 10.1016/0888-7543(95)80162-f

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


  7 in total

Review 1.  Molecular genetics of autosomal recessive spinal muscular atrophy.

Authors:  N R Rodrigues; K Talbot; K E Davies
Journal:  Mol Med       Date:  1996-07       Impact factor: 6.354

2.  Genetic and physical mapping of the mouse host resistance locus Lgn1.

Authors:  E Diez; M C Beckers; E Ernst; C J DiDonato; L R Simard; C Morissette; F Gervais; S I Yoshida; P Gros
Journal:  Mamm Genome       Date:  1997-09       Impact factor: 2.957

3.  Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype.

Authors:  L Campbell; A Potter; J Ignatius; V Dubowitz; K Davies
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

4.  A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy.

Authors:  Z Yaraghi; M D McLean; N Roy; L Surh; J E Ikeda; R G Korneluk; A MacKenzie
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

Review 5.  Spinal muscular atrophy: untangling the knot?

Authors:  I Biros; S Forrest
Journal:  J Med Genet       Date:  1999-01       Impact factor: 6.318

6.  Identification and characterization of the porcine (Sus scrofa) survival motor neuron (SMN1) gene: an animal model for therapeutic studies.

Authors:  Monique A Lorson; Lee D Spate; Randall S Prather; Christian L Lorson
Journal:  Dev Dyn       Date:  2008-08       Impact factor: 3.780

7.  Development and validation of a haplotype-free technique for non-invasive prenatal diagnosis of spinal muscular atrophy.

Authors:  Xianda Wei; Weigang Lv; Hu Tan; Desheng Liang; Lingqian Wu
Journal:  J Clin Lab Anal       Date:  2019-09-25       Impact factor: 2.352

  7 in total

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