Elucidation of novel genes causing auditory neuropathy
| Project/Area Number |
24390391
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Partial Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Otorhinolaryngology
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| Research Institution | 独立行政法人国立病院機構(東京医療センター臨床研究センター) |
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Principal Investigator |
MATSUNAGA Tatsuo 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚・平衡覚研究部, 室長 (90245580)
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| Co-Investigator(Kenkyū-buntansha) |
MIYA Fuyuki 独立行政法人理化学研究所, 統合生命医科学研究センター, リサーチアソシエイト (50415311)
MUTAI Hideki 東京医療センター, 臨床研究センター聴覚障害研究室, 研究員 (60415891)
KUDOH Jun 慶應義塾大学医学部, 遺伝子医学研究室, 教授 (80178003)
鈴木 直大 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚・平衡覚研究部・聴覚障害研究室, 研究員 (90611195)
清水 厚志 慶應義塾大学, 医学部, 助教 (30327655)
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| Project Period (FY) |
2012-04-01 – 2015-03-31
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| Project Status |
Completed (Fiscal Year 2014)
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| Budget Amount *help |
¥17,810,000 (Direct Cost: ¥13,700,000、Indirect Cost: ¥4,110,000)
Fiscal Year 2014: ¥5,720,000 (Direct Cost: ¥4,400,000、Indirect Cost: ¥1,320,000)
Fiscal Year 2013: ¥5,720,000 (Direct Cost: ¥4,400,000、Indirect Cost: ¥1,320,000)
Fiscal Year 2012: ¥6,370,000 (Direct Cost: ¥4,900,000、Indirect Cost: ¥1,470,000)
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| Keywords | 遺伝子 / 医療・福祉 / ゲノム / 脳神経疾患 / バイオテクノロジー |
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| Outline of Final Research Achievements |
Auditory Neuropathy (AN) is a new concept of hearing loss with the clinical feature of poor recognition of words. The purpose of this study is to reveal novel genetic causes of AN. By Sanger sequencing analysis in 36 patients with AN, we detected 11 novel OTOF mutations in 25 patients and 1 known GJB2 mutation in a patient. By whole genome SNP analysis followed by real time PCR analysis in 4 patients with monoallelic OTOF mutations, we did not detect large deletions in OTOF. With exome analysis in 10 patients who had not been found genetic causes by previous genetic analyses, we detected 3 candidates of novel AN genes (PNPLA3, RYR3, TACC2) and a novel OPA1 mutation which is likely to be a de novo mutation.
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Report
(4 results)
Research Products
(25 results)
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[Journal Article] Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: A cross-sectional, multi-center next-generation sequencing study.2013
Author(s)
Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Morimoto N, Kudoh J, Kaga K, Kosaki K, Matsunaga T
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Journal Title
Orphanet Journal of Rare Diseases
Volume: 8
Pages: 172-172
DOI
Related Report
Peer Reviewed
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[Journal Article] A prevalent founder mutation and genotype-phenotype correlations of OTOF in Japanese patients with auditory neuropathy2012
Author(s)
Matsunaga T, Mutai H, Kunishima S, Namba K, Morimoto N, Shinjo Y, Arimoto Y, Kataoka Y, Shintani T, Morita N, Sugiuchi T, Masuda S, Nakano A, Taiji H, Kaga K.
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Journal Title
Clinical Genetics
Volume: 82(5)
Pages: 425-32
DOI
Related Report
Peer Reviewed
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