Literature DB >> 7633422

A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.

N Chiannilkulchai1, P Pasturaud, I Richard, C Auffray, J S Beckmann.   

Abstract

Previous genetic and physical studies of LGMD2A, an autosomal recessive form of limb-girdle muscular dystrophy, have led to the establishment of a 10-12 Mb YAC contig encompassing the morbid locus. In order to progress toward the identification of the gene involved in LGMD2A, a primary transcription map of this genomic region was generated. The direct cDNA selection strategy was used with three YACs covering the candidate region and two different muscle cDNA libraries. Seventeen transcription units were identified among 171 cDNA fragments analysed. Five sequences corresponded to known genes, and twelve to new ones. They were characterized for their sequences, physical positions within the YAC contig, and expression patterns. Among those specifically transcribed in muscle, the calpain gene is a good positional and functional candidate for LGMD2A.

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Year:  1995        PMID: 7633422     DOI: 10.1093/hmg/4.4.717

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


  9 in total

1.  The genexpress IMAGE knowledge base of the human muscle transcriptome: a resource of structural, functional, and positional candidate genes for muscle physiology and pathologies.

Authors:  G Piétu; E Eveno; B Soury-Segurens; N A Fayein; R Mariage-Samson; C Matingou; E Leroy; C Dechesne; S Krieger; W Ansorge; I Reguigne-Arnould; D Cox; A Dehejia; M H Polymeropoulos; M D Devignes; C Auffray
Journal:  Genome Res       Date:  1999-12       Impact factor: 9.043

2.  Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.

Authors:  H Tamary; L Shalmon; H Shalev; A Halil; D Dobrushin; N Ashkenazi; M Zoldan; P Resnitzky; M Korostishevsky; B Bonne-Tamir; R Zaizov
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

3.  Recombinant expression and isolation of human L-arginine:glycine amidinotransferase and identification of its active-site cysteine residue.

Authors:  A Humm; E Fritsche; K Mann; M Göhl; R Huber
Journal:  Biochem J       Date:  1997-03-15       Impact factor: 3.857

4.  Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.

Authors:  V Allamand; O Broux; I Richard; F Fougerousse; N Chiannilkulchai; N Bourg; L Brenguier; C Devaud; P Pasturaud; A Pereira de Souza
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

5.  An STS map of the limb girdle muscular dystrophy type 2A region.

Authors:  I Richard; C Roudaut; F Fougerousse; N Chiannilkulchai; J S Beckmann
Journal:  Mamm Genome       Date:  1995-10       Impact factor: 2.957

6.  Calpainopathy-a survey of mutations and polymorphisms.

Authors:  I Richard; C Roudaut; A Saenz; R Pogue; J E Grimbergen; L V Anderson; C Beley; A M Cobo; C de Diego; B Eymard; P Gallano; H B Ginjaar; A Lasa; C Pollitt; H Topaloglu; J A Urtizberea; M de Visser; A van der Kooi; K Bushby; E Bakker; A Lopez de Munain; M Fardeau; J S Beckmann
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

Review 7.  Calpain chronicle--an enzyme family under multidisciplinary characterization.

Authors:  Hiroyuki Sorimachi; Shoji Hata; Yasuko Ono
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2011       Impact factor: 3.493

8.  The Classification, Natural History and Treatment of the Limb Girdle Muscular Dystrophies.

Authors:  Alexander Peter Murphy; Volker Straub
Journal:  J Neuromuscul Dis       Date:  2015-07-22

Review 9.  CAPN3: A muscle‑specific calpain with an important role in the pathogenesis of diseases (Review).

Authors:  Lin Chen; Fajuan Tang; Hu Gao; Xiaoyan Zhang; Xihong Li; Dongqiong Xiao
Journal:  Int J Mol Med       Date:  2021-09-22       Impact factor: 4.101

  9 in total

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