論文 ·日本語 ·未確認
An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease
Kae Koganebuchi ・ Kimitoshi Sato ・ Kiyotaka Fujii ・ Toshihiro Kumabe ・ Kuniaki Haneji ・ Takashi Toma ・ Hajime Ishida ・ Keiichiro Joh ・ Hidenobu Soejima ・ Shuhei Mano ・ Motoyuki Ogawa ・ Hiroki Oota
- 刊行年
- 2021-05-20
- 収録
- 『Annals of Human Genetics』 85(5) pp. 166-177
- 出版
- Wiley
- 言語
- 英語
- OpenAlex
- W3161223805
- DOI
- 10.1111/ahg.12424
- PubMed
- 34013582
- MAG
- 3161223805
- ISSN
- 0003-4800
- URL
- https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/ahg.12424
要旨
BACKGROUND: Ring finger protein 213 (RNF213) is a susceptibility gene of moyamoya disease (MMD). A previous case-control study and a family analysis demonstrated a strong association of the East Asian-specific variant, R4810K (rs112735431), with MMD. Our aim is to uncover evolutionary history of R4810K in East Asian populations. METHODS: The RNF213 locus of 24 MMD patients in Japan were sequenced using targeted-capture sequencing. Based on the sequence data, we conducted population genetic analysis and estimated the age of R4810K using coalescent simulation. RESULTS: The diversity of the RNF213 gene was higher in Africans than non-Africans, which can be explained by bottleneck effect of the out-of-Africa migration. Coalescent simulation showed that the risk variant was born in East Asia 14,500-5100 years ago and came to the Japanese archipelago afterward, probably in the period when the known migration based on archaeological evidences occurred. CONCLUSIONS: Although clinical data show that the symptoms varies, all sequences harboring the risk allele are almost identical with a small number of exceptions, suggesting the MMD phenotypes are unaffected by the variants of this gene and rather would be more affected by environmental factors.
主題
この書誌の出所
- openalex— W3161223805(2026-08-14取得)
引用
Kae Koganebuchi・Kimitoshi Sato・Kiyotaka Fujii・Toshihiro Kumabe・Kuniaki Haneji・Takashi Toma・Hajime Ishida・Keiichiro Joh・Hidenobu Soejima・Shuhei Mano・Motoyuki Ogawa・Hiroki Oota(2021-05-20) An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease 『Annals of Human Genetics』 85(5) pp. 166-177 Wiley