Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2

Satoshi Akamine, Noriaki Sagata, Yasunari Sakai, Takahiro Kato, Takeshi Nakahara, Yuki Matsushita, Osamu Togao, Hiwatashi Akio, Masafumi Sanefuji, Yoshito Ishizaki, Hiroyuki Torisu, Hirotomo Saitsu, Naomichi Matsumoto, Toshiro Hara, Akira Sawa, Shinichi Kano, Masutaka Furue, Shigenobu Kanba, Chad A. Shaw, Shoichi Ohga

研究成果: ジャーナルへの寄稿記事

1 引用 (Scopus)

抄録

Advance in the exome-wide sequencing analysis contributes to identifying hundreds of genes that are associated with early-onset epileptic encephalopathy and neurodevelopmental disorders. On the basis of massive sequencing data, functional interactions among different genes are suggested to explain the common molecular pathway underlying the pathogenic process of these disorders. However, the relevance of such interactions with the phenotypic severity or variety in an affected individual remains elusive. In this report, we present a 45-year-old woman with neurofibromatosis type 1 (NF1), infantile-onset epileptic encephalopathy, and severe developmental delay. Whole-exome sequencing identified de novo pathogenic mutations in NF1 and the Schaaf-Yang syndrome-associated gene, MAGEL2. Literature-curated interaction data predicted that NF1 and MAGEL2 proteins were closely connected in this network via their common interacting proteins. Direct conversion of fibroblasts into neurons in vitro showed that neuronal cells from 9 patients with NF1 expressed significantly lower levels of MAGEL2 (54%, p = 0.0047) than those from healthy individuals. These data provide the first evidence that pathogenic mutations of NF1 deregulate the expression of other neurodevelopmental disease-associated genes. De novo mutations in multiple genes may lead to severe developmental phenotypes through their cumulative effects or synergistic interactions.

元の言語英語
ページ(範囲)81-85
ページ数5
ジャーナルEpilepsia Open
3
発行部数1
DOI
出版物ステータス出版済み - 1 1 2018

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Neurofibromatosis 1
Brain Diseases
Mutation
Exome
Genes
Neurofibromin 1
Fibroblasts
Phenotype
Neurons
Proteins

All Science Journal Classification (ASJC) codes

  • Neurology
  • Clinical Neurology

これを引用

Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2. / Akamine, Satoshi; Sagata, Noriaki; Sakai, Yasunari; Kato, Takahiro; Nakahara, Takeshi; Matsushita, Yuki; Togao, Osamu; Akio, Hiwatashi; Sanefuji, Masafumi; Ishizaki, Yoshito; Torisu, Hiroyuki; Saitsu, Hirotomo; Matsumoto, Naomichi; Hara, Toshiro; Sawa, Akira; Kano, Shinichi; Furue, Masutaka; Kanba, Shigenobu; Shaw, Chad A.; Ohga, Shoichi.

:: Epilepsia Open, 巻 3, 番号 1, 01.01.2018, p. 81-85.

研究成果: ジャーナルへの寄稿記事

Akamine, S, Sagata, N, Sakai, Y, Kato, T, Nakahara, T, Matsushita, Y, Togao, O, Akio, H, Sanefuji, M, Ishizaki, Y, Torisu, H, Saitsu, H, Matsumoto, N, Hara, T, Sawa, A, Kano, S, Furue, M, Kanba, S, Shaw, CA & Ohga, S 2018, 'Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2', Epilepsia Open, 巻. 3, 番号 1, pp. 81-85. https://doi.org/10.1002/epi4.12085
Akamine, Satoshi ; Sagata, Noriaki ; Sakai, Yasunari ; Kato, Takahiro ; Nakahara, Takeshi ; Matsushita, Yuki ; Togao, Osamu ; Akio, Hiwatashi ; Sanefuji, Masafumi ; Ishizaki, Yoshito ; Torisu, Hiroyuki ; Saitsu, Hirotomo ; Matsumoto, Naomichi ; Hara, Toshiro ; Sawa, Akira ; Kano, Shinichi ; Furue, Masutaka ; Kanba, Shigenobu ; Shaw, Chad A. ; Ohga, Shoichi. / Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2. :: Epilepsia Open. 2018 ; 巻 3, 番号 1. pp. 81-85.
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AU - Nakahara, Takeshi

AU - Matsushita, Yuki

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AU - Sawa, Akira

AU - Kano, Shinichi

AU - Furue, Masutaka

AU - Kanba, Shigenobu

AU - Shaw, Chad A.

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