Suppr超能文献

在 X 连锁显性低磷血症性佝偻病的致病基因 PHEX 中,对 22 个剪接位点突变进行功能分析。

Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets.

机构信息

Department of Genetics, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

Department of Genetics, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

出版信息

Bone. 2019 Aug;125:186-193. doi: 10.1016/j.bone.2019.05.017. Epub 2019 May 15.

Abstract

CONTEXT

X-linked hypophosphatemic rickets (XLH) is caused by inactivating mutations in the PHEX gene and is the most common form of hereditary rickets. The splice-site mutations account for 17% of all reported PHEX mutations. The functional consequence of these splice-site mutations has not been systemically investigated.

OBJECTIVE

The current study was undertaken to functionally annotate previously reported 22 splice-site mutations in the PHEX gene.

METHODS

PHEX mini-genes with different splice-site mutations were created by site-directed mutagenesis and expressed in HEK293 cells. The mRNA transcripts were analyzed by RT-PCR, cloning, and sequencing.

RESULTS

These splicing mutations led to a variety of consequences, including exon skipping, intron retention, and activation of cryptic splice sites. Among 22 splice-site mutations, exon skipping was the most common event accounting for 73% (16/22). Non-canonical splice-site mutations could result in splicing errors to the same extent as canonical splice-site mutations such as c.436+3G>C, c.436+4A>C, c.436+6T>C, c.437-3C>G, c.850-3C>G, c.1080-3C>A, c.1482+5G>C, c.1586+6T>C, c.1645+5G>A, c.1645+6T>C, c.1701-16T>A, c.1768+5G>A, and c.1899+5G>A. Interestingly, non-canonical (c.436+6T>C and c.1586+6T>C) and canonical splice-site mutations (c.1769-1G>C) could generate partial splicing errors (both wild-type and mutant transcripts were detected), resulting in incomplete inactivation of PHEX gene, which may explain the mild disease phenotype reported previously, providing evidence of genotype-phenotype correlation. c.1645C>T (p.R549*) had no impact on pre-mRNA splicing although it is located next to canonical splice donor site GT.

CONCLUSIONS

Exon skipping is the most common outcome due to splice-site mutations. Both canonical and non-canonical splice-site mutations can result in either severe or mild RNA splicing defects, contributing to phenotype heterogeneity. Non-canonical splice-site mutations should not be overlooked in genetic screening especially those located within 50 bp from canonical splice site.

摘要

背景

X 连锁低磷血症性佝偻病(XLH)是由 PHEX 基因突变引起的,是遗传性佝偻病最常见的形式。剪接位点突变占所有报道的 PHEX 突变的 17%。这些剪接位点突变的功能后果尚未系统研究。

目的

本研究旨在对先前报道的 PHEX 基因中的 22 个剪接位点突变进行功能注释。

方法

通过定点诱变创建具有不同剪接位点突变的 PHEX 迷你基因,并在 HEK293 细胞中表达。通过 RT-PCR、克隆和测序分析 mRNA 转录本。

结果

这些剪接突变导致多种后果,包括外显子跳跃、内含子保留和激活隐性剪接位点。在 22 个剪接位点突变中,外显子跳跃是最常见的事件,占 73%(16/22)。非典型剪接位点突变可导致与典型剪接位点突变(如 c.436+3G>C、c.436+4A>C、c.436+6T>C、c.437-3C>G、c.850-3C>G、c.1080-3C>A、c.1482+5G>C、c.1586+6T>C、c.1645+5G>A、c.1645+6T>C、c.1701-16T>A、c.1768+5G>A 和 c.1899+5G>A)相同程度的剪接错误。有趣的是,非典型(c.436+6T>C 和 c.1586+6T>C)和典型剪接位点突变(c.1769-1G>C)可导致部分剪接错误(均检测到野生型和突变型转录本),导致 PHEX 基因不完全失活,这可能解释了先前报道的轻度疾病表型,为基因型-表型相关性提供了证据。尽管 c.1645C>T(p.R549*)位于典型剪接供体位点 GT 附近,但它对前体 mRNA 剪接没有影响。

结论

剪接位点突变最常见的结果是外显子跳跃。典型和非典型剪接位点突变均可导致严重或轻度的 RNA 剪接缺陷,导致表型异质性。在遗传筛查中不应忽视非典型剪接位点突变,尤其是那些位于典型剪接位点 50bp 内的突变。

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