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Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy

Authors :
Masahiro Horiuchi
Osamu Onodera
Takamichi Hattori
Jun Mitsui
Jun Goto
Kenju Hara
Katsuhiko Shirahige
Sid Gilman
Laurie J. Ozelius
Hidehiro Mizusawa
Hidenao Sasaki
Hiroyuki Soma
Kazuaki Kanai
Ullrich Wallner
Alessandro Filla
Tatsushi Toda
Yoshiyuki Kuroiwa
Akiyoshi Kakita
Thomas Klockgether
Alexandra Durr
Yuishin Izumi
Yoshio Momose
Kinya Ishikawa
Susumu Kusunoki
Virginia M.-Y. Lee
Wataru Satake
Hidetoshi Date
Garth A. Nicholson
Budrul Ahsan
Makiko Komata
Alexis Brice
Yaeko Ichikawa
Atsushi Iwata
Kenichi Yasui
Caroline M. Tanner
Yorihiro Yamamoto
Satoshi Kuwabara
Masashi Aoki
Yuji Takahashi
Takeo Kato
Gen Sobue
Yasushi Osaki
Mitsutoshi Yamamoto
Ichiro Yabe
Hirohisa Watanabe
Paola Sandroni
Ryozo Kuwano
Hitoshi Takahashi
Eliezer Masliah
Hiroyuki Ishiura
Mizuki Ito
Tatsuhiko Yuasa
Tatiana Foroud
Shoji Tsuji
Kazuko Hasegawa
Kimihito Arai
Mitsunori Yamada
Takashi Matsukawa
Shigeo Murayama
John Q. Trojanowski
Shigeru Koyano
Tomoyoshi Kondo
Masatoyo Nishizawa
Yoko Fukuda
Kenji Nakashima
Nobutaka Hattori
Hiroshi Takashima
Miho Murata
Phillip A. Low
Clifford W. Shults
Walter A. Kukull
Hijiri Ito
Yasuo Nakahara
Ryuji Kaji
Mitsui, J
Matsukawa, T
Ishiura, H
Fukuda, Y
Ichikawa, Y
Date, H
Ahsan, B
Nakahara, Y
Momose, Y
Takahashi, Y
Iwata, A
Goto, J
Yamamoto, Y
Komata, M
Shirahige, K
Hara, K
Kakita, A
Yamada, M
Takahashi, H
Onodera, O
Nishizawa, M
Takashima, H
Kuwano, R
Watanabe, H
Ito, M
Sobue, G
Soma, H
Yabe, I
Sasaki, H
Aoki, M
Ishikawa, K
Mizusawa, H
Kanai, K
Hattori, T
Kuwabara, S
Arai, K
Koyano, S
Kuroiwa, Y
Hasegawa, K
Yuasa, T
Yasui, K
Nakashima, K
Ito, H
Izumi, Y
Kaji, R
Kato, T
Kusunoki, S
Osaki, Y
Horiuchi, M
Kondo, T
Murayama, S
Hattori, N
Yamamoto, M
Murata, M
Satake, W
Toda, T
Dürr, A
Brice, A
Filla, Alessandro
Klockgether, T
Wüllner, U
Nicholson, G
Gilman, S
Shults, Cw
Tanner, Cm
Kukull, Wa
Lee, Vm
Masliah, E
Low, Pa
Sandroni, P
Trojanowski, Jq
Ozelius, L
Foroud, T
Tsuji, S.
Source :
The New England journal of medicine 369(3), 233-244 (2013). doi:10.1056/NEJMoa1212115
Publication Year :
2013
Publisher :
Massachusetts Medical Society, 2013.

Abstract

Multiple-system atrophy is an intractable neurodegenerative disease characterized by autonomic failure in addition to various combinations of parkinsonism, cerebellar ataxia, and pyramidal dysfunction. Although multiple-system atrophy is widely considered to be a nongenetic disorder, we previously identified multiplex families with this disease, which indicates the involvement of genetic components.In combination with linkage analysis, we performed whole-genome sequencing of a sample obtained from a member of a multiplex family in whom multiple-system atrophy had been diagnosed on autopsy. We also performed mutational analysis of samples from members of five other multiplex families and from a Japanese series (363 patients and two sets of controls, one of 520 persons and one of 2383 persons), a European series (223 patients and 315 controls), and a North American series (172 patients and 294 controls). On the basis of these analyses, we used a yeast complementation assay and measured enzyme activity of parahydroxybenzoate-polyprenyl transferase. This enzyme is encoded by the gene COQ2 and is essential for the biosynthesis of coenzyme Q10. Levels of coenzyme Q10 in lymphoblastoid cells and brain tissue were measured on high-performance liquid chromatography.We identified a homozygous mutation (M78V-V343A/M78V-V343A) and compound heterozygous mutations (R337X/V343A) in COQ2 in two multiplex families. Furthermore, we found that a common variant (V343A) and multiple rare variants in COQ2, all of which are functionally impaired, are associated with sporadic multiple-system atrophy. The V343A variant was exclusively observed in the Japanese population.Functionally impaired variants of COQ2 were associated with an increased risk of multiple-system atrophy in multiplex families and patients with sporadic disease, providing evidence of a role of impaired COQ2 activities in the pathogenesis of this disease. (Funded by the Japan Society for the Promotion of Science and others.).

Details

ISSN :
15334406 and 00284793
Volume :
369
Database :
OpenAIRE
Journal :
New England Journal of Medicine
Accession number :
edsair.doi.dedup.....278e847779e0f61aaacdd8bf6c5654c5
Full Text :
https://doi.org/10.1056/nejmoa1212115