Suppr超能文献

两个 EYS 基因中的新突变可能是日本人群常染色体隐性遗传视网膜色素变性的主要原因。

Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population.

机构信息

Department of Ophthalmology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

出版信息

PLoS One. 2012;7(2):e31036. doi: 10.1371/journal.pone.0031036. Epub 2012 Feb 17.

Abstract

Retinitis pigmentosa (RP) is a highly heterogeneous genetic disease including autosomal recessive (ar), autosomal dominant (ad), and X-linked inheritance. Recently, arRP has been associated with mutations in EYS (Eyes shut homolog), which is a major causative gene for this disease. This study was conducted to determine the spectrum and frequency of EYS mutations in 100 Japanese arRP patients. To determine the prevalence of EYS mutations, all EYS exons were screened for mutations by polymerase chain reaction amplification, and sequence analysis was performed. We detected 67 sequence alterations in EYS, of which 21 were novel. Of these, 7 were very likely pathogenic mutations, 6 were possible pathogenic mutations, and 54 were predicted non-pathogenic sequence alterations. The minimum observed prevalence of distinct EYS mutations in our study was 18% (18/100, comprising 9 patients with 2 very likely pathogenic mutations and the remaining 9 with only one such mutation). Among these mutations, 2 novel truncating mutations, c.4957_4958insA (p.S1653KfsX2) and c.8868C>A (p.Y2956X), were identified in 16 patients and accounted for 57.1% (20/35 alleles) of the mutated alleles. Although these 2 truncating mutations were not detected in Japanese patients with adRP or Leber's congenital amaurosis, we detected them in Korean arRP patients. Similar to Japanese arRP results, the c.4957_4958insA mutation was more frequently detected than the c.8868C>A mutation. The 18% estimated prevalence of very likely pathogenic mutations in our study suggests a major involvement of EYS in the pathogenesis of arRP in the Japanese population. Mutation spectrum of EYS in 100 Japanese patients, including 13 distinct very likely and possible pathogenic mutations, was largely different from the previously reported spectrum in patients from non-Asian populations. Screening for c.4957_4958insA and c.8868C>A mutations in the EYS gene may therefore be very effective for the genetic testing and counseling of RP patients in Japan.

摘要

色素性视网膜炎(RP)是一种高度异质性的遗传疾病,包括常染色体隐性(ar)、常染色体显性(ad)和 X 连锁遗传。最近,arRP 与 EYS(眼睛关闭同源物)的突变有关,EYS 是该病的主要致病基因。本研究旨在确定 100 名日本 arRP 患者 EYS 突变的谱和频率。为了确定 EYS 突变的流行率,通过聚合酶链反应扩增筛选所有 EYS 外显子的突变,并进行序列分析。我们在 EYS 中检测到 67 种序列改变,其中 21 种是新的。其中,7 种是极可能的致病性突变,6 种是可能的致病性突变,54 种是预测的非致病性序列改变。在我们的研究中,观察到的不同 EYS 突变的最小流行率为 18%(18/100,包括 9 名患者有 2 种极可能的致病性突变,其余 9 名只有 1 种此类突变)。在这些突变中,在 16 名患者中发现了 2 种新的截断突变,c.4957_4958insA(p.S1653KfsX2)和 c.8868C>A(p.Y2956X),占突变等位基因的 57.1%(20/35 个等位基因)。尽管这 2 种截断突变未在日本 adRP 或 Leber 先天性黑蒙患者中检测到,但在韩国 arRP 患者中检测到。与日本 arRP 结果相似,c.4957_4958insA 突变的检出频率高于 c.8868C>A 突变。我们的研究中估计的 18%极可能致病性突变的患病率表明 EYS 在日本人群中 arRP 的发病机制中起主要作用。100 名日本患者的 EYS 突变谱,包括 13 种不同的极可能和可能的致病性突变,与以前在非亚洲人群患者中报道的谱有很大不同。因此,在日本对 EYS 基因中的 c.4957_4958insA 和 c.8868C>A 突变进行筛查可能对 RP 患者的遗传检测和咨询非常有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af15/3281914/44e2beae8e03/pone.0031036.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验