Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort

被引:43
作者
Nakamura, Ryoichi [1 ]
Sone, Jun [1 ]
Atsuta, Naoki [1 ]
Tohnai, Genki [1 ]
Watanabe, Hazuki [1 ,2 ]
Yokoi, Daichi [1 ]
Nakatochi, Masahiro [3 ]
Watanabe, Hirohisa [1 ,4 ]
Ito, Mizuki [1 ]
Senda, Jo [1 ,5 ]
Katsuno, Masahisa [1 ]
Tanaka, Fumiaki [6 ]
Li, Yuanzhe [7 ]
Izumi, Yuishin [8 ]
Morita, Mitsuya [9 ]
Taniguchi, Akira [10 ]
Kano, Osamu [11 ]
Oda, Masaya [12 ]
Kuwabara, Satoshi [13 ]
Abe, Koji [14 ]
Aiba, Ikuko [15 ]
Okamoto, Koichi [16 ]
Mizoguchi, Kouichi [17 ]
Hasegawa, Kazuko [18 ]
Aoki, Masashi [19 ]
Hattori, Nobutaka [7 ]
Tsuji, Shoji [20 ]
Nakashima, Kenji [21 ]
Kaji, Ryuji
Sobue, Gen [1 ,22 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Neurol, 65 Tsurumai Cho, Nagoya, Aichi 4668550, Japan
[2] Japanese Red Cross Nagoya Daiichi Hosp, Dept Neurol, Nagoya, Aichi, Japan
[3] Nagoya Univ Hosp, Ctr Adv Med & Clin Res, Bioinformat Sect, Nagoya, Aichi, Japan
[4] Nagoya Univ, Brain & Mind Res Ctr, Nagoya, Aichi 4648601, Japan
[5] Komaki City Hosp, Dept Neurol, Komaki, Japan
[6] Yokohama City Univ, Grad Sch Med, Dept Neurol & Stroke Med, Yokohama, Kanagawa 232, Japan
[7] Juntendo Univ, Sch Med, Dept Neurol, Tokyo 113, Japan
[8] Univ Tokushima, Grad Sch, Inst Biomed Sci, Dept Neurol, Tokushima, Japan
[9] Jichi Med Univ, Dept Internal Med, Div Neurol, Tochigi, Japan
[10] Mie Univ, Grad Sch Med, Dept Neurol, Tsu, Mie 514, Japan
[11] Toho Univ, Sch Med, Dept Internal Med, Div Neurol, Tokyo, Japan
[12] Vihara Hananosato Hosp, Dept Neurol, Miyoshi, Japan
[13] Chiba Univ, Grad Sch Med, Dept Neurol, 1-8-1 Inohana, Chiba, Japan
[14] Okayama Univ, Grad Sch Med, Dept Neurol, Okayama, Japan
[15] Natl Hosp Org Higashinagoya Natl Hosp, Dept Neurol, Nagoya, Aichi, Japan
[16] Geriatr Res Inst & Hosp, Dept Neurol, Maebashi, Gunma, Japan
[17] Natl Hosp Org Shizuoka Fuji Hosp, Dept Neurol, Fujinomiya, Japan
[18] Sagamihara Natl Hosp, Natl Hosp Org, Div Neurol, Sagamihara, Kanagawa, Japan
[19] Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 980, Japan
[20] Univ Tokyo, Grad Sch Sci, Dept Neurol, Tokyo 113, Japan
[21] Tottori Univ, Fac Med, Dept Brain & Neurosci, Div Neurol, Yonago, Tottori, Japan
[22] Nagoya Univ, Grad Sch Med, Res Div Dementia & Neurodegenerat Dis, Nagoya, Aichi 4648601, Japan
关键词
Amyotrophic lateral sclerosis; Japan; Genetic screening; Next-generation sequencer; AMYOTROPHIC-LATERAL-SCLEROSIS; HEXANUCLEOTIDE REPEAT EXPANSION; FAMILIAL ALS; MUTATIONS; FUS; C9ORF72; ANTICIPATION; PENETRANCE; GENETICS; JUVENILE;
D O I
10.1016/j.neurobiolaging.2015.11.030
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
We investigated the frequency and contribution of variants of the 28 known amyotrophic lateral sclerosis (ALS)-related genes in Japanese ALS patients. We designed a multiplex, polymerase chain reaction-based primer panel to amplify the coding regions of the 28 ALS-related genes and sequenced DNA samples from 257 Japanese ALS patients using an Ion Torrent PGM sequencer. We also performed exome sequencing and identified variants of the 28 genes in an additional 251 ALS patients using an Illumina HiSeq 2000 platform. We identified the known ALS pathogenic variants and predicted the functional properties of novel nonsynonymous variants in silico. These variants were confirmed by Sanger sequencing. Known pathogenic variants were identified in 19 (48.7%) of the 39 familial ALS patients and 14 (3.0%) of the 469 sporadic ALS patients. Thirty-two sporadic ALS patients (6.8%) harbored 1 or 2 novel nonsynonymous variants of ALS-related genes that might be deleterious. This study reports the first extensive genetic screening of Japanese ALS patients. These findings are useful for developing genetic screening and counseling strategies for such patients. (C) 2016 Elsevier Inc. All rights reserved.
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收藏
页码:219.e1 / 219.e8
页数:8
相关论文
共 53 条
[1]   Mapping Human Genetic Diversity in Asia [J].
Abdulla, Mahmood Ameen ;
Ahmed, Ikhlak ;
Assawamakin, Anunchai ;
Bhak, Jong ;
Brahmachari, Samir K. ;
Calacal, Gayvelline C. ;
Chaurasia, Amit ;
Chen, Chien-Hsiun ;
Chen, Jieming ;
Chen, Yuan-Tsong ;
Chu, Jiayou ;
Cutiongco-de la Paz, Eva Maria C. ;
De Ungria, Maria Corazon A. ;
Delfin, Frederick C. ;
Edo, Juli ;
Fuchareon, Suthat ;
Ghang, Ho ;
Gojobori, Takashi ;
Han, Junsong ;
Ho, Sheng-Feng ;
Hoh, Boon Peng ;
Huang, Wei ;
Inoko, Hidetoshi ;
Jha, Pankaj ;
Jinam, Timothy A. ;
Jin, Li ;
Jung, Jongsun ;
Kangwanpong, Daoroong ;
Kampuansai, Jatupol ;
Kennedy, Giulia C. ;
Khurana, Preeti ;
Kim, Hyung-Lae ;
Kim, Kwangjoong ;
Kim, Sangsoo ;
Kim, Woo-Yeon ;
Kimm, Kuchan ;
Kimura, Ryosuke ;
Koike, Tomohiro ;
Kulawonganunchai, Supasak ;
Kumar, Vikrant ;
Lai, Poh San ;
Lee, Jong-Young ;
Lee, Sunghoon ;
Liu, Edison T. ;
Majumder, Partha P. ;
Mandapati, Kiran Kumar ;
Marzuki, Sangkot ;
Mitchell, Wayne ;
Mukerji, Mitali ;
Naritomi, Kenji .
SCIENCE, 2009, 326 (5959) :1541-1545
[2]   High-ResolutionMelting (HRM) Analysis of the Cu/Zn Superoxide Dismutase (SOD1) Gene in Japanese Sporadic Amyotrophic Lateral Sclerosis (SALS) Patients [J].
Akimoto, Chizuru ;
Morita, Mitsuya ;
Atsuta, Naoki ;
Sobue, Gen ;
Nakano, Imaharu .
NEUROLOGY RESEARCH INTERNATIONAL, 2011, 2011
[3]   An estimate of amyotrophic lateral sclerosis heritability using twin data [J].
Al-Chalabi, A. ;
Fang, F. ;
Hanby, M. F. ;
Leigh, P. N. ;
Shaw, C. E. ;
Ye, W. ;
Rijsdijk, F. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2010, 81 (12) :1324-1326
[4]   Modelling the Effects of Penetrance and Family Size on Rates of Sporadic and Familial Disease [J].
Al-Chalabi, Ammar ;
Lewis, Cathryn M. .
HUMAN HEREDITY, 2011, 71 (04) :281-288
[5]   A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement [J].
Bannwarth, Sylvie ;
Ait-El-Mkadem, Samira ;
Chaussenot, Annabelle ;
Genin, Emmanuelle C. ;
Lacas-Gervais, Sandra ;
Fragaki, Konstantina ;
Berg-Alonso, Laetitia ;
Kageyama, Yusuke ;
Serre, Valerie ;
Moore, David G. ;
Verschueren, Annie ;
Rouzier, Cecile ;
Le Ber, Isabelle ;
Auge, Gaelle ;
Cochaud, Charlotte ;
Lespinasse, Francoise ;
N'Guyen, Karine ;
de Septenville, Anne ;
Brice, Alexis ;
Yu-Wai-Man, Patrick ;
Sesaki, Hiromi ;
Pouget, Jean ;
Paquis-Flucklinger, Veronique .
BRAIN, 2014, 137 :2329-2345
[6]   El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis [J].
Brooks, BR ;
Miller, RG ;
Swash, M ;
Munsat, TL .
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, 2000, 1 (05) :293-299
[7]   Absence of consensus in diagnostic criteria for familial neurodegenerative diseases [J].
Byrne, Susan ;
Elamin, Marwa ;
Bede, Peter ;
Hardiman, Orla .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2012, 83 (04) :365-367
[8]   Amyotrophic Lateral Sclerosis Onset Is Influenced by the Burden of Rare Variants in Known Amyotrophic Lateral Sclerosis Genes [J].
Cady, Janet ;
Allred, Peggy ;
Bali, Taha ;
Pestronk, Alan ;
Goate, Alison ;
Miller, Timothy M. ;
Mitra, Robi D. ;
Ravits, John ;
Harms, Matthew B. ;
Baloh, Robert H. .
ANNALS OF NEUROLOGY, 2015, 77 (01) :100-113
[9]   Extensive genetics of ALS A population-based study in Italy [J].
Chio, Adriano ;
Calvo, Andrea ;
Mazzini, Letizia ;
Cantello, Roberto ;
Mora, Gabriele ;
Moglia, Cristina ;
Corrado, Lucia ;
D'Alfonso, Sandra ;
Majounie, Elisa ;
Renton, Alan ;
Pisano, Fabrizio ;
Ossola, Irene ;
Brunetti, Maura ;
Traynor, Bryan J. ;
Restagno, Gabriella .
NEUROLOGY, 2012, 79 (19) :1983-1989
[10]   Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation [J].
Chio, Adriano ;
Restagno, Gabriella ;
Brunetti, Maura ;
Ossola, Irene ;
Calvo, Andrea ;
Mora, Gabriele ;
Sabatelli, Mario ;
Monsurro, Maria Rosaria ;
Battistini, Stefania ;
Mandrioli, Jessica ;
Salvi, Fabrizio ;
Spataro, Rossella ;
Schymick, Jennifer ;
Traynor, Bryan J. ;
La Bella, Vincenzo .
NEUROBIOLOGY OF AGING, 2009, 30 (08) :1272-1275