Literature DB >> 26934379

Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, Egypt.

Hemakumar M Reddy1, Sherifa A Hamed2, Monkol Lek3,4, Satomi Mitsuhashi5, Elicia Estrella5, Michael D Jones1, Lane J Mahoney5, Anna R Duncan5, Kyung-Ah Cho1, Daniel G Macarthur3,4, Louis M Kunkel5, Peter B Kang6,7.   

Abstract

INTRODUCTION: The genetic causes of limb-girdle muscular dystrophy (LGMD) have been studied in numerous countries, but such investigations have been limited in Egypt.
METHODS: A cohort of 30 families with suspected LGMD from Assiut, Egypt, was studied using immunohistochemistry, homozygosity mapping, Sanger sequencing, and whole exome sequencing.
RESULTS: Six families were confirmed to have pathogenic mutations, 4 in SGCA and 2 in DMD. Of these, 3 families harbored a single nonsense mutation in SGCA, suggesting that this may be a common mutation in Assiut, Egypt, originating from a founder effect.
CONCLUSIONS: The Assiut region in Egypt appears to share at least several of the common LGMD genes found in other parts of the world. It is notable that 4 of the 6 mutations were ascertained by means of whole exome sequencing, even though it was the last approach adopted. This illustrates the power of this technique for identifying causative mutations for muscular dystrophies. Muscle Nerve 54: 690-695, 2016.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  founder effect; homozygosity mapping; limb-girdle muscular dystrophy; sarcoglycanopathy; whole exome sequencing

Mesh:

Substances:

Year:  2016        PMID: 26934379      PMCID: PMC5453499          DOI: 10.1002/mus.25094

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  40 in total

1.  Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.

Authors:  E M McNally; M R Passos-Bueno; C G Bönnemann; M Vainzof; E de Sá Moreira; H G Lidov; K B Othmane; P H Denton; J M Vance; M Zatz; L M Kunkel
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

2.  Making sense of the muscular dystrophies: diagnosis and treatment guideline for limb-girdle muscular dystrophy.

Authors:  John D England
Journal:  Muscle Nerve       Date:  2014-11       Impact factor: 3.217

3.  MutationTaster2: mutation prediction for the deep-sequencing age.

Authors:  Jana Marie Schwarz; David N Cooper; Markus Schuelke; Dominik Seelow
Journal:  Nat Methods       Date:  2014-04       Impact factor: 28.547

4.  Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.

Authors:  M Brockington; Y Yuva; P Prandini; S C Brown; S Torelli; M A Benson; R Herrmann; L V Anderson; R Bashir; J M Burgunder; S Fallet; N Romero; M Fardeau; V Straub; G Storey; C Pollitt; I Richard; C A Sewry; K Bushby; T Voit; D J Blake; F Muntoni
Journal:  Hum Mol Genet       Date:  2001-12-01       Impact factor: 6.150

5.  Long-term skeletal muscle protection after gene transfer in a mouse model of LGMD-2D.

Authors:  Christina A Pacak; Glenn A Walter; Gabe Gaidosh; Nathan Bryant; Melissa A Lewis; Sean Germain; Cathryn S Mah; Kevin P Campbell; Barry J Byrne
Journal:  Mol Ther       Date:  2007-07-24       Impact factor: 11.454

6.  Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.

Authors:  A P Monaco; R L Neve; C Colletti-Feener; C J Bertelson; D M Kurnit; L M Kunkel
Journal:  Nature       Date:  1986 Oct 16-22       Impact factor: 49.962

7.  Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity.

Authors:  F Piccolo; S L Roberds; M Jeanpierre; F Leturcq; K Azibi; C Beldjord; A Carrié; D Récan; M Chaouch; A Reghis
Journal:  Nat Genet       Date:  1995-06       Impact factor: 38.330

8.  Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy.

Authors:  J Liu; M Aoki; I Illa; C Wu; M Fardeau; C Angelini; C Serrano; J A Urtizberea; F Hentati; M B Hamida; S Bohlega; E J Culper; A A Amato; K Bossie; J Oeltjen; K Bejaoui; D McKenna-Yasek; B A Hosler; E Schurr; K Arahata; P J de Jong; R H Brown
Journal:  Nat Genet       Date:  1998-09       Impact factor: 38.330

9.  Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes.

Authors:  Richard R Bennett; Hal E Schneider; Elicia Estrella; Stephanie Burgess; Andrew S Cheng; Caitlin Barrett; Va Lip; Poh San Lai; Yiping Shen; Bai-Lin Wu; Basil T Darras; Alan H Beggs; Louis M Kunkel
Journal:  BMC Genet       Date:  2009-10-18       Impact factor: 2.797

10.  Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models.

Authors:  Hashem A Shihab; Julian Gough; David N Cooper; Peter D Stenson; Gary L A Barker; Keith J Edwards; Ian N M Day; Tom R Gaunt
Journal:  Hum Mutat       Date:  2012-11-02       Impact factor: 4.878

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  7 in total

1.  Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan.

Authors:  Madhurima Saha; Hemakumar M Reddy; Mustafa A Salih; Elicia Estrella; Michael D Jones; Satomi Mitsuhashi; Kyung-Ah Cho; Silveli Suzuki-Hatano; Skylar A Rizzo; Muddathir H Hamad; Maowia M Mukhtar; Ahlam A Hamed; Maha A Elseed; Monkol Lek; Elise Valkanas; Daniel G MacArthur; Louis M Kunkel; Christina A Pacak; Isabelle Draper; Peter B Kang
Journal:  Physiol Genomics       Date:  2018-08-31       Impact factor: 3.107

2.  The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States.

Authors:  Hemakumar M Reddy; Kyung-Ah Cho; Monkol Lek; Elicia Estrella; Elise Valkanas; Michael D Jones; Satomi Mitsuhashi; Basil T Darras; Anthony A Amato; Hart Gw Lidov; Catherine A Brownstein; David M Margulies; Timothy W Yu; Mustafa A Salih; Louis M Kunkel; Daniel G MacArthur; Peter B Kang
Journal:  J Hum Genet       Date:  2016-10-06       Impact factor: 3.172

Review 3.  Limb-girdle Muscular Dystrophies in India: A Review.

Authors:  Satish V Khadilkar; Hinaben Dayalal Faldu; Sarika Bapuso Patil; Rakesh Singh
Journal:  Ann Indian Acad Neurol       Date:  2017 Apr-Jun       Impact factor: 1.383

Review 4.  The ties that bind: functional clusters in limb-girdle muscular dystrophy.

Authors:  Elisabeth R Barton; Christina A Pacak; Whitney L Stoppel; Peter B Kang
Journal:  Skelet Muscle       Date:  2020-07-29       Impact factor: 4.912

5.  Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.

Authors:  Uluç Yiş; Gülden Diniz; Filiz Hazan; Hülya Sevcan Daimagüler; Bahar Toklu Baysal; Figen Baydan; Gülçin Akinci; Aycan Ünalp; Gül Aktan; Erhan Bayram; Semra Hiz; Cem Paketçi; Derya Okur; Erdener Özer; Ayça Ersen Danyeli; Muzaffer Polat; Gökhan Uyanik; Sebahattin Çirak
Journal:  Acta Myol       Date:  2018-09-01

6.  Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites.

Authors:  Christine C Bruels; Chengcheng Li; Tonatiuh Mendoza; Jamillah Khan; Hemakumar M Reddy; Elicia A Estrella; Partha S Ghosh; Basil T Darras; Hart G W Lidov; Christina A Pacak; Louis M Kunkel; François Modave; Isabelle Draper; Peter B Kang
Journal:  Mol Genet Genomic Med       Date:  2019-01-28       Impact factor: 2.183

7.  Molecular diagnosis of muscular diseases in outpatient clinics: A Canadian perspective.

Authors:  Fanny Thuriot; Elaine Gravel; Caroline Buote; Marianne Doyon; Elvy Lapointe; Lydia Marcoux; Sandrine Larue; Amélie Nadeau; Sébastien Chénier; Paula J Waters; Pierre-Étienne Jacques; Serge Gravel; Sébastien Lévesque
Journal:  Neurol Genet       Date:  2020-03-13
  7 in total

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