A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts
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 mel...
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2021-03-01
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doaj-4ab9236ffd9b46af9de4e26bef8088162021-03-11T12:17:44ZengNature Publishing GroupScientific Reports2045-23222021-03-011111710.1038/s41598-021-84741-5A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataractsYuyan You0Chao Bai1Xuefeng Liu2Maohua Xia3Yanqiang Yin4Yucun Chen5Wei Wang6Ting Jia7Yan Lu8Tianchun Pu9Chenglin Zhang10Xiaoguang Li11Liqin Wang12Yunfang Xiu13Lili Niu14Jun Zhou15Yang Du16Yanhui Liu17Suhui Xu18Beijing Key Laboratory of Captive Wildlife Technologies, Beijing ZooBeijing Key Laboratory of Captive Wildlife Technologies, Beijing ZooBeijing ZooBeijing ZooChongqing ZooStrait (Fuzhou) Giant Panda Research and Exchange CentersBeijing Key Laboratory of Captive Wildlife Technologies, Beijing ZooBeijing Key Laboratory of Captive Wildlife Technologies, Beijing ZooBeijing ZooBeijing ZooBeijing Key Laboratory of Captive Wildlife Technologies, Beijing ZooBeijing ZooChengdu ZooStrait (Fuzhou) Giant Panda Research and Exchange CentersChengdu ZooChongqing ZooBeijing ZooBeijing ZooStrait (Fuzhou) Giant Panda Research and Exchange CentersAbstract 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.https://doi.org/10.1038/s41598-021-84741-5 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yuyan You Chao Bai Xuefeng Liu Maohua Xia Yanqiang Yin Yucun Chen Wei Wang Ting Jia Yan Lu Tianchun Pu Chenglin Zhang Xiaoguang Li Liqin Wang Yunfang Xiu Lili Niu Jun Zhou Yang Du Yanhui Liu Suhui Xu |
spellingShingle |
Yuyan You Chao Bai Xuefeng Liu Maohua Xia Yanqiang Yin Yucun Chen Wei Wang Ting Jia Yan Lu Tianchun Pu Chenglin Zhang Xiaoguang Li Liqin Wang Yunfang Xiu Lili Niu Jun Zhou Yang Du Yanhui Liu Suhui Xu A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts Scientific Reports |
author_facet |
Yuyan You Chao Bai Xuefeng Liu Maohua Xia Yanqiang Yin Yucun Chen Wei Wang Ting Jia Yan Lu Tianchun Pu Chenglin Zhang Xiaoguang Li Liqin Wang Yunfang Xiu Lili Niu Jun Zhou Yang Du Yanhui Liu Suhui Xu |
author_sort |
Yuyan You |
title |
A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts |
title_short |
A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts |
title_full |
A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts |
title_fullStr |
A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts |
title_full_unstemmed |
A novel missense mutation in the HSF4 gene of giant pandas with senile congenital cataracts |
title_sort |
novel missense mutation in the hsf4 gene of giant pandas with senile congenital cataracts |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-03-01 |
description |
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. |
url |
https://doi.org/10.1038/s41598-021-84741-5 |
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