通过微型基因测定法确定 col4a1 基因中改变 RNA 剪接的七个变体。

IF 2.9 3区 医学 Q2 GENETICS & HEREDITY Clinical Genetics Pub Date : 2024-05-15 DOI:10.1111/cge.14546
Zhi Wang, Yan Sun, Yiyin Zhang, Yan Zhang, Ran Zhang, Changying Li, Xuyan Liu, Fengjiao Pan, Dan Qiao, Xiaomeng Shi, Bingying Zhang, Ning Xu, Irene Bottillo, Leping Shao
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引用次数: 0

摘要

IV 型胶原蛋白是基底膜不可或缺的组成部分。COL4A1 是编码 IV 型胶原蛋白的关键基因之一,其突变可导致多种疾病。很明显,很大一部分影响剪接的突变可直接导致疾病或导致疾病的易感性或严重性。在此,我们利用生物信息学程序分析了 COL4A1 基因中描述的外显子突变和内含子突变,并通过微型基因系统确定了可能改变正常剪接模式的候选突变。我们发现了七种变异,它们通过破坏正常剪接位点、创建新位点或改变剪接调控元件来诱导剪接改变。这些变异预计会影响蛋白质的功能。我们的研究结果有助于对 COL4A1 变异进行正确的分子鉴定,并有助于开发更多个性化治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Identification of seven variants in the col4a1 gene that alter RNA splicing by minigene assay

Type IV collagen is an integral component of basement membranes. Mutations in COL4A1, one of the key genes encoding Type IV collagen, can result in a variety of diseases. It is clear that a significant proportion of mutations that affect splicing can cause disease directly or contribute to the susceptibility or severity of disease. Here, we analyzed exonic mutations and intronic mutations described in the COL4A1 gene using bioinformatics programs and identified candidate mutations that may alter the normal splicing pattern through a minigene system. We identified seven variants that induce splicing alterations by disrupting normal splice sites, creating new ones, or altering splice regulatory elements. These mutations are predicted to impact protein function. Our results help in the correct molecular characterization of variants in COL4A1 and may help develop more personalized treatment options.

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来源期刊
Clinical Genetics
Clinical Genetics 医学-遗传学
CiteScore
6.50
自引率
0.00%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Clinical Genetics links research to the clinic, translating advances in our understanding of the molecular basis of genetic disease for the practising clinical geneticist. The journal publishes high quality research papers, short reports, reviews and mini-reviews that connect medical genetics research with clinical practice. Topics of particular interest are: • Linking genetic variations to disease • Genome rearrangements and disease • Epigenetics and disease • The translation of genotype to phenotype • Genetics of complex disease • Management/intervention of genetic diseases • Novel therapies for genetic diseases • Developmental biology, as it relates to clinical genetics • Social science research on the psychological and behavioural aspects of living with or being at risk of genetic disease
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