Literature DB >> 26378787

The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy.

Davut Pehlivan1,2, Christine R Beck1, Yuji Okamoto1, Tamar Harel1, Zeynep H C Akdemir1, Shalini N Jhangiani3, Marjorie A Withers1, Meryem Tuba Goksungur4, Claudia M B Carvalho1, Dirk Czesnik5, Claudia Gonzaga-Jauregui1, Wojciech Wiszniewski1, Donna M Muzny3, Richard A Gibbs3, Bernd Rautenstrauss6,7, Michael W Sereda5,8, James R Lupski1,3,9,10.   

Abstract

PURPOSE: Charcot-Marie-Tooth (CMT) disease is a heterogeneous group of genetic disorders of the peripheral nervous system. Copy-number variants (CNVs) contribute significantly to CMT, as duplication of PMP22 underlies the majority of CMT1 cases. We hypothesized that CNVs and/or single-nucleotide variants (SNVs) might exist in patients with CMT with an unknown molecular genetic etiology.
METHODS: Two hundred patients with CMT, negative for both SNV mutations in several CMT genes and for CNVs involving PMP22, were screened for CNVs by high-resolution oligonucleotide array comparative genomic hybridization. Whole-exome sequencing was conducted on individuals with rare, potentially pathogenic CNVs.
RESULTS: Putatively causative CNVs were identified in five subjects (~2.5%); four of the five map to known neuropathy genes. Breakpoint sequencing revealed Alu-Alu-mediated junctions as a predominant contributor. Exome sequencing identified MFN2 SNVs in two of the individuals.
CONCLUSION: Neuropathy-associated CNV outside of the PMP22 locus is rare in CMT. Nevertheless, there is potential clinical utility in testing for CNVs and exome sequencing in CMT cases negative for the CMT1A duplication. These findings suggest that complex phenotypes including neuropathy can potentially be caused by a combination of SNVs and CNVs affecting more than one disease-associated locus and contributing to a mutational burden.Genet Med 18 5, 443-451.

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Year:  2015        PMID: 26378787      PMCID: PMC5322766          DOI: 10.1038/gim.2015.124

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  38 in total

1.  Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.

Authors:  Stephan Züchner; Irina V Mersiyanova; Maria Muglia; Nisrine Bissar-Tadmouri; Julie Rochelle; Elena L Dadali; Mario Zappia; Eva Nelis; Alessandra Patitucci; Jan Senderek; Yesim Parman; Oleg Evgrafov; Peter De Jonghe; Yuji Takahashi; Shoij Tsuji; Margaret A Pericak-Vance; Aldo Quattrone; Esra Battaloglu; Alexander V Polyakov; Vincent Timmerman; J Michael Schröder; Jeffery M Vance; Esra Battologlu
Journal:  Nat Genet       Date:  2004-04-04       Impact factor: 38.330

2.  Curcumin treatment abrogates endoplasmic reticulum retention and aggregation-induced apoptosis associated with neuropathy-causing myelin protein zero-truncating mutants.

Authors:  Mehrdad Khajavi; Ken Inoue; Wojciech Wiszniewski; Tomoko Ohyama; G Jackson Snipes; James R Lupski
Journal:  Am J Hum Genet       Date:  2005-09-30       Impact factor: 11.025

3.  Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defects.

Authors:  Ciprian M Bosoi; Valeria Capra; Redouane Allache; Vincent Quoc-Huy Trinh; Patrizia De Marco; Elisa Merello; Pierre Drapeau; Alexander G Bassuk; Zoha Kibar
Journal:  Hum Mutat       Date:  2011-09-23       Impact factor: 4.878

4.  Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability.

Authors:  Feng Zhang; Pavel Seeman; Pengfei Liu; Marian A J Weterman; Claudia Gonzaga-Jauregui; Charles F Towne; Sat Dev Batish; Els De Vriendt; Peter De Jonghe; Bernd Rautenstrauss; Klaus-Henning Krause; Mehrdad Khajavi; Jan Posadka; Antoon Vandenberghe; Francesc Palau; Lionel Van Maldergem; Frank Baas; Vincent Timmerman; James R Lupski
Journal:  Am J Hum Genet       Date:  2010-05-20       Impact factor: 11.025

Review 5.  Practice Parameter: evaluation of distal symmetric polyneuropathy: role of autonomic testing, nerve biopsy, and skin biopsy (an evidence-based review). Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation.

Authors:  J D England; G S Gronseth; G Franklin; G T Carter; L J Kinsella; J A Cohen; A K Asbury; K Szigeti; J R Lupski; N Latov; R A Lewis; P A Low; M A Fisher; D N Herrmann; J F Howard; G Lauria; R G Miller; M Polydefkis; A J Sumner
Journal:  Neurology       Date:  2008-12-03       Impact factor: 9.910

6.  Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.

Authors:  Cyril Goizet; Amir Boukhris; Emeline Mundwiller; Chantal Tallaksen; Sylvie Forlani; Annick Toutain; Nathalie Carriere; Véronique Paquis; Christel Depienne; Alexandra Durr; Giovanni Stevanin; Alexis Brice
Journal:  Hum Mutat       Date:  2009-02       Impact factor: 4.878

7.  The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans.

Authors:  Feng Zhang; Mehrdad Khajavi; Anne M Connolly; Charles F Towne; Sat Dev Batish; James R Lupski
Journal:  Nat Genet       Date:  2009-06-21       Impact factor: 38.330

8.  Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A.

Authors:  Kazuki Kijima; Chikahiko Numakura; Hiroko Izumino; Kazuo Umetsu; Atsuo Nezu; Toshihide Shiiki; Masafumi Ogawa; Yoshito Ishizaki; Takeshi Kitamura; Yasunobu Shozawa; Kiyoshi Hayasaka
Journal:  Hum Genet       Date:  2004-11-11       Impact factor: 4.132

9.  Copy number variation detection and genotyping from exome sequence data.

Authors:  Niklas Krumm; Peter H Sudmant; Arthur Ko; Brian J O'Roak; Maika Malig; Bradley P Coe; Aaron R Quinlan; Deborah A Nickerson; Evan E Eichler
Journal:  Genome Res       Date:  2012-05-14       Impact factor: 9.043

10.  A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.

Authors:  Alexander G Bassuk; Robyn H Wallace; Aimee Buhr; Andrew R Buller; Zaid Afawi; Masahito Shimojo; Shingo Miyata; Shan Chen; Pedro Gonzalez-Alegre; Hilary L Griesbach; Shu Wu; Marcus Nashelsky; Eszter K Vladar; Dragana Antic; Polly J Ferguson; Sebahattin Cirak; Thomas Voit; Matthew P Scott; Jeffrey D Axelrod; Christina Gurnett; Azhar S Daoud; Sara Kivity; Miriam Y Neufeld; Aziz Mazarib; Rachel Straussberg; Simri Walid; Amos D Korczyn; Diane C Slusarski; Samuel F Berkovic; Hatem I El-Shanti
Journal:  Am J Hum Genet       Date:  2008-10-30       Impact factor: 11.025

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  11 in total

1.  A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder.

Authors:  Brittany P Todd; Alexander G Bassuk
Journal:  J Neurogenet       Date:  2018-05-23       Impact factor: 1.250

2.  Comprehensive genomic analysis of patients with disorders of cerebral cortical development.

Authors:  Wojciech Wiszniewski; Pawel Gawlinski; Tomasz Gambin; Monika Bekiesinska-Figatowska; Ewa Obersztyn; Dorota Antczak-Marach; Zeynep Hande Coban Akdemir; Tamar Harel; Ender Karaca; Marta Jurek; Katarzyna Sobecka; Beata Nowakowska; Malgorzata Kruk; Iwona Terczynska; Alicja Goszczanska-Ciuchta; Mariola Rudzka-Dybala; Ewa Jamroz; Antoni Pyrkosz; Anna Jakubiuk-Tomaszuk; Piotr Iwanowski; Dorota Gieruszczak-Bialek; Malgorzata Piotrowicz; Maria Sasiadek; Iwona Kochanowska; Barbara Gurda; Barbara Steinborn; Mateusz Dawidziuk; Jennifer Castaneda; Pawel Wlasienko; Natalia Bezniakow; Shalini N Jhangiani; Dorota Hoffman-Zacharska; Jerzy Bal; Elzbieta Szczepanik; Eric Boerwinkle; Richard A Gibbs; James R Lupski
Journal:  Eur J Hum Genet       Date:  2018-04-30       Impact factor: 4.246

Review 3.  Biology in balance: human diploid genome integrity, gene dosage, and genomic medicine.

Authors:  James R Lupski
Journal:  Trends Genet       Date:  2022-04-18       Impact factor: 11.821

4.  Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease.

Authors:  J Mortreux; J Bacquet; A Boyer; E Alazard; R Bellance; A G Giguet-Valard; M Cerino; M Krahn; F Audic; B Chabrol; V Laugel; J P Desvignes; C Béroud; K Nguyen; A Verschueren; N Lévy; S Attarian; V Delague; C Missirian; N Bonello-Palot
Journal:  J Hum Genet       Date:  2019-12-18       Impact factor: 3.172

5.  Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.

Authors:  Angad Jolly; Yavuz Bayram; Serap Turan; Zehra Aycan; Tulay Tos; Zehra Yavas Abali; Bulent Hacihamdioglu; Zeynep Hande Coban Akdemir; Hadia Hijazi; Serpil Bas; Zeynep Atay; Tulay Guran; Saygin Abali; Firdevs Bas; Feyza Darendeliler; Roberto Colombo; Tahsin Stefan Barakat; Tuula Rinne; Janson J White; Gozde Yesil; Alper Gezdirici; Elif Yilmaz Gulec; Ender Karaca; Davut Pehlivan; Shalini N Jhangiani; Donna M Muzny; Sukran Poyrazoglu; Abdullah Bereket; Richard A Gibbs; Jennifer E Posey; James R Lupski
Journal:  J Clin Endocrinol Metab       Date:  2019-08-01       Impact factor: 6.134

6.  Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.

Authors:  Megan H Brewer; Rabia Chaudhry; Jessica Qi; Aditi Kidambi; Alexander P Drew; Manoj P Menezes; Monique M Ryan; Michelle A Farrar; David Mowat; Gopinath M Subramanian; Helen K Young; Stephan Zuchner; Stephen W Reddel; Garth A Nicholson; Marina L Kennerson
Journal:  PLoS Genet       Date:  2016-07-20       Impact factor: 5.917

Review 7.  Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.

Authors:  Giovanna Morello; Maria Guarnaccia; Antonio Gianmaria Spampinato; Valentina La Cognata; Velia D'Agata; Sebastiano Cavallaro
Journal:  Mol Neurobiol       Date:  2017-01-24       Impact factor: 5.590

Review 8.  Warning SINEs: Alu elements, evolution of the human brain, and the spectrum of neurological disease.

Authors:  Peter A Larsen; Kelsie E Hunnicutt; Roxanne J Larsen; Anne D Yoder; Ann M Saunders
Journal:  Chromosome Res       Date:  2018-02-19       Impact factor: 5.239

Review 9.  Structural variations causing inherited peripheral neuropathies: A paradigm for understanding genomic organization, chromatin interactions, and gene dysregulation.

Authors:  Anthony N Cutrupi; Megan H Brewer; Garth A Nicholson; Marina L Kennerson
Journal:  Mol Genet Genomic Med       Date:  2018-03-23       Impact factor: 2.183

10.  Improving molecular diagnosis of Chinese patients with Charcot-Marie-Tooth by targeted next-generation sequencing and functional analysis.

Authors:  Li-Xi Li; Shao-Yun Zhao; Zhi-Jun Liu; Wang Ni; Hong-Fu Li; Bao-Guo Xiao; Zhi-Ying Wu
Journal:  Oncotarget       Date:  2016-05-10
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