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大熊猫老年先天性白内障中 HSF4 基因的一种新错义突变。

A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts.

机构信息

Beijing Key Laboratory of Captive Wildlife Technologies, Beijing Zoo, Beijing, China.

Beijing Zoo, Beijing, China.

出版信息

Sci Rep. 2021 Mar 8;11(1):5411. doi: 10.1038/s41598-021-84741-5.

Abstract

Cataracts are a common cause of visual impairment and blindness in mammals. They are usually associated with aging, but approximately one third of cases have a significant genetic component. Cataracts are increasingly prevalent among aging populations of captive giant pandas (Ailuropoda melanoleuca) and it is therefore important to identify genetic determinants that influence the likelihood of cataract development in order to distinguish between congenital and age-related disease. Here we screened for cataract-related genetic effects using a functional candidate gene approach combined with bioinformatics to identify the underlying genetic defect in a giant panda with congenital cataracts. We identified a missense mutation in exon 10 of the HSF4 gene encoding heat shock transcription factor 4. The mutation causes the amino acid substitution R377W in a highly conserved segment of the protein between the isoform-specific and downstream hydrophobic regions. Predictive modeling revealed that the substitution is likely to increase the hydrophobicity of the protein and disrupt interactions with spatially adjacent amino acid side chains. The mutation was not found in 13 unaffected unrelated animals but was found in an unrelated animal also diagnosed with senile congenital cataract. The novel missense mutation in the HSF4 gene therefore provides a potential new genetic determinant that could help to predict the risk of cataracts in giant pandas.

摘要

白内障是哺乳动物视力障碍和失明的常见原因。它们通常与衰老有关,但大约三分之一的病例有明显的遗传成分。在圈养大熊猫(Ailuropoda melanoleuca)的老年群体中,白内障的发病率越来越高,因此,确定影响白内障发生可能性的遗传决定因素对于区分先天性和年龄相关性疾病非常重要。在这里,我们使用功能候选基因方法结合生物信息学来筛选与白内障相关的遗传效应,以确定一只先天性白内障大熊猫的潜在遗传缺陷。我们在编码热休克转录因子 4 的 HSF4 基因的第 10 外显子中发现了一个错义突变。该突变导致蛋白的高度保守区域内的氨基酸取代 R377W,该区域在同种型特异性和下游疏水区之间。预测建模表明,该取代可能会增加蛋白的疏水性并破坏与空间相邻氨基酸侧链的相互作用。该突变未在 13 只未受影响的无关动物中发现,但在另一只也被诊断为老年性先天性白内障的无关动物中发现。因此,HSF4 基因中的新型错义突变提供了一个潜在的新遗传决定因素,有助于预测大熊猫白内障的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31a5/7940430/216b78f7b2c1/41598_2021_84741_Fig1_HTML.jpg

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