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RNF213 loss of function reshapes vascular transcriptome and spliceosome leading to disrupted angiogenesis and aggravated vascular inflammatory responses.RNF213 功能丧失重塑血管转录组和剪接体,导致血管生成受损和血管炎症反应加重。
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Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review.伴肺动脉高压的烟雾病中的无名指蛋白213:一篇综述
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Observation of p.R4810K, a Polymorphism of the Mysterin Gene, the Susceptibility Gene for Moyamoya Disease, in Two Female Japanese Diabetic Patients with Familial Partial Lipodystrophy 1.观察到 Mysterin 基因的 p.R4810K 多态性,该基因是家族性部分脂肪营养不良 1 型的易感性基因,在两名日本女性糖尿病患者中发现。
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本文引用的文献

1
Frequency of the moyamoya-related RNF213 p.Arg4810Lys variant in 1,516 Korean individuals.1516名韩国人脑中与烟雾病相关的RNF213基因p.Arg4810Lys变异的频率
BMC Med Genet. 2015 Nov 20;16:109. doi: 10.1186/s12881-015-0252-4.
2
Incidence, prevalence, and survival of moyamoya disease in Korea: a nationwide, population-based study.韩国烟雾病的发病率、患病率及生存率:一项基于全国人口的研究。
Stroke. 2014 Apr;45(4):1090-5. doi: 10.1161/STROKEAHA.113.004273. Epub 2014 Mar 4.
3
Genetic variant RNF213 c.14576G>A in various phenotypes of intracranial major artery stenosis/occlusion.RNF213 c.14576G>A 基因变异与颅内大血管狭窄/闭塞的多种表型相关。
Stroke. 2013 Oct;44(10):2894-7. doi: 10.1161/STROKEAHA.113.002477. Epub 2013 Aug 22.
4
Molecular analysis of RNF213 gene for moyamoya disease in the Chinese Han population.中国汉族人群中 moyamoya 病 RNF213 基因的分子分析。
PLoS One. 2012;7(10):e48179. doi: 10.1371/journal.pone.0048179. Epub 2012 Oct 23.
5
P.R4810K, a polymorphism of RNF213, the susceptibility gene for moyamoya disease, is associated with blood pressure.RNF213 的一种多态性 P.R4810K 是烟雾病的易感基因,与血压有关。
Environ Health Prev Med. 2013 Mar;18(2):121-9. doi: 10.1007/s12199-012-0299-1. Epub 2012 Aug 10.
6
Distribution of moyamoya disease susceptibility polymorphism p.R4810K in RNF213 in East and Southeast Asian populations.东亚和东南亚人群中RNF213基因的烟雾病易感性多态性p.R4810K的分布。
Neurol Med Chir (Tokyo). 2012;52(5):299-303. doi: 10.2176/nmc.52.299.
7
Epidemiological features of moyamoya disease in Japan.日本烟雾病的流行病学特征。
Neurol Med Chir (Tokyo). 2012;52(5):295-8. doi: 10.2176/nmc.52.295.
8
Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease.RNF213 c.14576G>A 纯合变异可预测早发型和严重型烟雾病。
Neurology. 2012 Mar 13;78(11):803-10. doi: 10.1212/WNL.0b013e318249f71f. Epub 2012 Feb 29.
9
Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development.鉴定 RNF213 为 moyamoya 病的易感基因及其在血管发育中的可能作用。
PLoS One. 2011;6(7):e22542. doi: 10.1371/journal.pone.0022542. Epub 2011 Jul 20.
10
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.一项全基因组关联研究确定 RNF213 为首个烟雾病基因。
J Hum Genet. 2011 Jan;56(1):34-40. doi: 10.1038/jhg.2010.132. Epub 2010 Nov 4.

烟雾病易感变异体RNF213 p.R4810K在日本人群中的频率及携带者的健康特征。

Frequency of RNF213 p.R4810K, a susceptibility variant for moyamoya disease, and health characteristics of carriers in the Japanese population.

作者信息

Cao Yang, Kobayashi Hatasu, Morimoto Takaaki, Kabata Risako, Harada Kouji H, Koizumi Akio

机构信息

Department of Health and Environmental Sciences, Kyoto University Graduate School of Medicine, Yoshida, Sakyo-ku, Kyoto, 606-8501, Japan.

Department of Neurosurgery, Kyoto University Graduate School of Medicine, Shogoin Kawahara, Sakyo-ku, Kyoto, 606-8507, Japan.

出版信息

Environ Health Prev Med. 2016 Sep;21(5):387-390. doi: 10.1007/s12199-016-0549-8. Epub 2016 Jun 30.

DOI:10.1007/s12199-016-0549-8
PMID:27365075
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5305994/
Abstract

OBJECTIVES

RNF213 p.R4810K is a founder polymorphism that confers genetic susceptibility to moyamoya disease in East Asia. Only a few studies have investigated the symptoms and disease histories of RNF213 p.R4810K carriers in Japan. This study investigated the frequency of RNF213 p.R4810K in the general Japanese population and the health characteristics of the carriers.

METHODS

Through a health-promotion campaign in the city of Uji, Japan, 519 subjects (120 males and 399 females) of the general Japanese population were genotyped for RNF213 p.R4810K and interviewed to determine health characteristics.

RESULTS

Nine RNF213 p.R4810K heterozygous carriers (GA genotype) and no RNF213 p.R4810K homozygous carriers (AA genotype) were found among the 519 individuals. The estimates of the genotypes and allele frequencies for RNF213 p.R4810K were 1.73 and 0.87 %, respectively. There were no obvious differences in age, gender ratio, body mass index, hypertension, dyslipidemia, diabetes, kidney disease, liver disease, heart disease, or drinking or smoking habits between carriers and non-carriers. Interestingly, one patient with moyamoya disease was found among the nine RNF213 p.R4810K carriers.

CONCLUSIONS

This study showed the genotypes and allele frequencies of RNF213 p.R4810K in the general Japanese population to be similar to results of previous reports.

摘要

目的

RNF213 p.R4810K是一种奠基者多态性,赋予东亚人群烟雾病的遗传易感性。在日本,仅有少数研究调查了RNF213 p.R4810K携带者的症状和疾病史。本研究调查了RNF213 p.R4810K在日本普通人群中的频率以及携带者的健康特征。

方法

通过在日本宇治市开展的一项健康促进活动,对519名日本普通人群受试者(120名男性和399名女性)进行RNF213 p.R4810K基因分型,并进行访谈以确定健康特征。

结果

在519名个体中,发现9名RNF213 p.R4810K杂合携带者(GA基因型),未发现RNF213 p.R4810K纯合携带者(AA基因型)。RNF213 p.R4810K的基因型频率和等位基因频率估计分别为1.73%和0.87%。携带者和非携带者在年龄、性别比例、体重指数、高血压、血脂异常、糖尿病、肾病、肝病、心脏病或饮酒或吸烟习惯方面没有明显差异。有趣的是,在9名RNF213 p.R4810K携带者中发现了1例烟雾病患者。

结论

本研究表明,RNF213 p.R4810K在日本普通人群中的基因型频率和等位基因频率与先前报道的结果相似。