Literature DB >> 16141003

Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.

G Piluso1, L Politano, S Aurino, M Fanin, E Ricci, V M Ventriglia, A Belsito, A Totaro, V Saccone, H Topaloglu, A C Nascimbeni, L Fulizio, A Broccolini, N Canki-Klain, L I Comi, G Nigro, C Angelini, V Nigro.   

Abstract

BACKGROUND: The limb girdle muscular dystrophies (LGMD) are a heterogeneous group of Mendelian disorders highlighted by weakness of the pelvic and shoulder girdle muscles. Seventeen autosomal loci have been so far identified and genetic tests are mandatory to distinguish among the forms. Mutations at the calpain 3 locus (CAPN3) cause LGMD type 2A.
OBJECTIVE: To obtain unbiased information on the consequences of CAPN3 mutations. PATIENTS: 530 subjects with different grades of symptoms and 300 controls.
METHODS: High throughput denaturing HPLC analysis of DNA pools.
RESULTS: 141 LGMD2A cases were identified, carrying 82 different CAPN3 mutations (45 novel), along with 18 novel polymorphisms/variants. Females had a more favourable course than males. In 94% of the more severely affected patient group, the defect was also discovered in the second allele. This proves the sensitivity of the approach. CAPN3 mutations were found in 35.1% of classical LGMD phenotypes. Mutations were also found in 18.4% of atypical patients and in 12.6% of subjects with high serum creatine kinase levels.
CONCLUSIONS: A non-invasive and cost-effective strategy, based on the high throughput denaturing HPLC analysis of DNA pools, was used to obtain unbiased information on the consequences of CAPN3 mutations in the largest genetic study ever undertaken. This broadens the spectrum of LGMD2A phenotypes and sets the carrier frequency at 1:103.

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Year:  2005        PMID: 16141003      PMCID: PMC1736133          DOI: 10.1136/jmg.2004.028738

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  46 in total

1.  Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis.

Authors:  A C Jones; J Austin; N Hansen; B Hoogendoorn; P J Oefner; J P Cheadle; M C O'Donovan
Journal:  Clin Chem       Date:  1999-08       Impact factor: 8.327

2.  A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies.

Authors:  I Richard; N Bourg; S Marchand; O Alibert; B Eymard; A J van der Kooi; C E Jackson; C Garcia; J M Burgunder; C Legum; M de Visser; M Fardeau; J S Beckmann
Journal:  Neuromuscul Disord       Date:  1999-12       Impact factor: 4.296

Review 3.  XLMR genes: update 2000.

Authors:  P Chiurazzi; B C Hamel; G Neri
Journal:  Eur J Hum Genet       Date:  2001-02       Impact factor: 4.246

4.  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

5.  Myotilin is mutated in limb girdle muscular dystrophy 1A.

Authors:  M A Hauser; S K Horrigan; P Salmikangas; U M Torian; K D Viles; R Dancel; R W Tim; A Taivainen; L Bartoloni; J M Gilchrist; J M Stajich; P C Gaskell; J R Gilbert; J M Vance; M A Pericak-Vance; O Carpen; C A Westbrook; M C Speer
Journal:  Hum Mol Genet       Date:  2000-09-01       Impact factor: 6.150

6.  High incidence of 550delA mutation of CAPN3 in LGMD2 patients from Russia.

Authors:  T V Pogoda; I N Krakhmaleva; N A Lipatova; N I Shakhovskaya; S S Shishkin; S A Limborska
Journal:  Hum Mutat       Date:  2000-03       Impact factor: 4.878

7.  Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.

Authors:  G Bonne; M R Di Barletta; S Varnous; H M Bécane; E H Hammouda; L Merlini; F Muntoni; C R Greenberg; F Gary; J A Urtizberea; D Duboc; M Fardeau; D Toniolo; K Schwartz
Journal:  Nat Genet       Date:  1999-03       Impact factor: 38.330

8.  Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.

Authors:  E S Moreira; T J Wiltshire; G Faulkner; A Nilforoushan; M Vainzof; O T Suzuki; G Valle; R Reeves; M Zatz; M R Passos-Bueno; D E Jenne
Journal:  Nat Genet       Date:  2000-02       Impact factor: 38.330

9.  Clinical variability in calpainopathy: what makes the difference?

Authors:  Flávia de Paula; Mariz Vainzof; Maria Rita Passos-Bueno; Rita de Cássia M Pavanello; Sergio Russo Matioli; Louise V B Anderson; Vincenzo Nigro; Mayana Zatz
Journal:  Eur J Hum Genet       Date:  2002-12       Impact factor: 4.246

10.  Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy.

Authors:  C Minetti; F Sotgia; C Bruno; P Scartezzini; P Broda; M Bado; E Masetti; M Mazzocco; A Egeo; M A Donati; D Volonte; F Galbiati; G Cordone; F D Bricarelli; M P Lisanti; F Zara
Journal:  Nat Genet       Date:  1998-04       Impact factor: 38.330

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  35 in total

Review 1.  Calpain research for drug discovery: challenges and potential.

Authors:  Yasuko Ono; Takaomi C Saido; Hiroyuki Sorimachi
Journal:  Nat Rev Drug Discov       Date:  2016-11-11       Impact factor: 84.694

2.  Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity.

Authors:  Sabrina Sacconi; Pilar Camaño; Jessica C de Greef; Richard J L F Lemmers; Leonardo Salviati; Pascal Boileau; Adolfo Lopez de Munain Arregui; Silvère M van der Maarel; Claude Desnuelle
Journal:  J Med Genet       Date:  2011-10-07       Impact factor: 6.318

3.  Dynamic distribution of muscle-specific calpain in mice has a key role in physical-stress adaptation and is impaired in muscular dystrophy.

Authors:  Koichi Ojima; Yukiko Kawabata; Harumi Nakao; Kazuki Nakao; Naoko Doi; Fujiko Kitamura; Yasuko Ono; Shoji Hata; Hidenori Suzuki; Hiroyuki Kawahara; Julius Bogomolovas; Christian Witt; Coen Ottenheijm; Siegfried Labeit; Henk Granzier; Noriko Toyama-Sorimachi; Michiko Sorimachi; Koichi Suzuki; Tatsuya Maeda; Keiko Abe; Atsu Aiba; Hiroyuki Sorimachi
Journal:  J Clin Invest       Date:  2010-07-01       Impact factor: 14.808

4.  Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group.

Authors:  Marzieh Mojbafan; Seyed Hassan Tonekaboni; Maryam Abiri; Soudeh Kianfar; Ameneh Sarhadi; Yalda Nilipour; Javad Tavakkoly-Bazzaz; Sirous Zeinali
Journal:  J Mol Neurosci       Date:  2016-06-04       Impact factor: 3.444

5.  Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscle.

Authors:  Yanchao Huang; Antoine de Morrée; Alexandra van Remoortere; Kate Bushby; Rune R Frants; Johan T den Dunnen; Silvère M van der Maarel
Journal:  Hum Mol Genet       Date:  2008-03-11       Impact factor: 6.150

6.  Impaired regeneration in LGMD2A supported by increased PAX7-positive satellite cell content and muscle-specific microrna dysregulation.

Authors:  Xiomara Q Rosales; Vinod Malik; Amita Sneh; Lei Chen; Sarah Lewis; Janaiah Kota; Julie M Gastier-Foster; Caroline Astbury; Rob Pyatt; Shalini Reshmi; Louise R Rodino-Klapac; K Reed Clark; Jerry R Mendell; Zarife Sahenk
Journal:  Muscle Nerve       Date:  2013-03-29       Impact factor: 3.217

Review 7.  Calpain 3, the "gatekeeper" of proper sarcomere assembly, turnover and maintenance.

Authors:  Jacques S Beckmann; Melissa Spencer
Journal:  Neuromuscul Disord       Date:  2008-10-29       Impact factor: 4.296

8.  Insertion sequence 1 from calpain-3 is functional in calpain-2 as an internal propeptide.

Authors:  Christian-Scott E McCartney; Qilu Ye; Robert L Campbell; Peter L Davies
Journal:  J Biol Chem       Date:  2018-09-25       Impact factor: 5.157

9.  The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients.

Authors:  Marco Savarese; Giuseppina Di Fruscio; Annalaura Torella; Chiara Fiorillo; Francesca Magri; Marina Fanin; Lucia Ruggiero; Giulia Ricci; Guja Astrea; Luigia Passamano; Alessandra Ruggieri; Dario Ronchi; Giorgio Tasca; Adele D'Amico; Sandra Janssens; Olimpia Farina; Margherita Mutarelli; Veer Singh Marwah; Arcomaria Garofalo; Teresa Giugliano; Simone Sampaolo; Francesca Del Vecchio Blanco; Gaia Esposito; Giulio Piluso; Paola D'Ambrosio; Roberta Petillo; Olimpia Musumeci; Carmelo Rodolico; Sonia Messina; Anni Evilä; Peter Hackman; Massimiliano Filosto; Giuseppe Di Iorio; Gabriele Siciliano; Marina Mora; Lorenzo Maggi; Carlo Minetti; Sabrina Sacconi; Lucio Santoro; Kathleen Claes; Liliana Vercelli; Tiziana Mongini; Enzo Ricci; Francesca Gualandi; Rossella Tupler; Jan De Bleecker; Bjarne Udd; Antonio Toscano; Maurizio Moggio; Elena Pegoraro; Enrico Bertini; Eugenio Mercuri; Corrado Angelini; Filippo Maria Santorelli; Luisa Politano; Claudio Bruno; Giacomo Pietro Comi; Vincenzo Nigro
Journal:  Neurology       Date:  2016-06-08       Impact factor: 9.910

10.  Gene Correction of LGMD2A Patient-Specific iPSCs for the Development of Targeted Autologous Cell Therapy.

Authors:  Sridhar Selvaraj; Neha R Dhoke; James Kiley; Alba Judith Mateos-Aierdi; Sudheer Tungtur; Ricardo Mondragon-Gonzalez; Grace Killeen; Vanessa K P Oliveira; Adolfo López de Munain; Rita C R Perlingeiro
Journal:  Mol Ther       Date:  2019-08-28       Impact factor: 11.454

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