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大熊猫单侧白内障形成相关基因编码主要内在蛋白的新型错义突变。

A novel missense mutation in the gene encoding major intrinsic protein (MIP) in a Giant panda with unilateral cataract formation.

机构信息

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

Beijing Zoo, Beijing, China.

出版信息

BMC Genomics. 2021 Feb 2;22(1):100. doi: 10.1186/s12864-021-07386-8.

DOI:10.1186/s12864-021-07386-8
PMID:33530927
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7856726/
Abstract

BACKGROUND

Cataracts are defects of the lens that cause progressive visual impairment and ultimately blindness in many vertebrate species. Most cataracts are age-related, but up to one third have an underlying genetic cause. Cataracts are common in captive zoo animals, but it is often unclear whether these are congenital or acquired (age-related) lesions.

RESULTS

Here we used a functional candidate gene screening approach to identify mutations associated with cataracts in a captive giant panda (Ailuropoda melanoleuca). We screened 11 genes often associated with human cataracts and identified a novel missense mutation (c.686G > A) in the MIP gene encoding major intrinsic protein. This is expressed in the lens and normally accumulates in the plasma membrane of lens fiber cells, where it plays an important role in fluid transport and cell adhesion. The mutation causes the replacement of serine with asparagine (p.S229N) in the C-terminal tail of the protein, and modeling predicts that the mutation induces conformational changes that may interfere with lens permeability and cell-cell interactions.

CONCLUSION

The c.686G > A mutation was found in a captive giant panda with a unilateral cataract but not in 18 controls from diverse regions in China, suggesting it is most likely a genuine disease-associated mutation rather than a single-nucleotide polymorphism. The mutation could therefore serve as a new genetic marker to predict the risk of congenital cataracts in captive giant pandas.

摘要

背景

白内障是晶状体的缺陷,会导致许多脊椎动物物种的视力逐渐受损,最终失明。大多数白内障与年龄有关,但多达三分之一的白内障有潜在的遗传原因。白内障在圈养的动物园动物中很常见,但通常不清楚这些是先天性的还是后天获得的(与年龄相关的)病变。

结果

在这里,我们使用功能候选基因筛选方法来鉴定与圈养大熊猫(Ailuropoda melanoleuca)白内障相关的突变。我们筛选了 11 个通常与人类白内障相关的基因,并在编码主要内在蛋白的 MIP 基因中发现了一个新的错义突变(c.686G > A)。该基因在晶状体中表达,正常情况下在晶状体纤维细胞的质膜中积累,在其中发挥重要的流体运输和细胞黏附作用。该突变导致蛋白质 C 末端尾部丝氨酸被天冬酰胺取代(p.S229N),建模预测该突变诱导的构象变化可能干扰晶状体通透性和细胞间相互作用。

结论

在一只患有单侧白内障的圈养大熊猫中发现了 c.686G > A 突变,但在中国不同地区的 18 个对照中没有发现,这表明它很可能是一种真正的与疾病相关的突变,而不是单核苷酸多态性。因此,该突变可以作为预测圈养大熊猫先天性白内障风险的新遗传标记。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/c5b8a3dfd798/12864_2021_7386_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/5755de0d2ea3/12864_2021_7386_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/f69fe85b6ca9/12864_2021_7386_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/78db6e3dc090/12864_2021_7386_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/8c7ae3ba266d/12864_2021_7386_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/c5b8a3dfd798/12864_2021_7386_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/5755de0d2ea3/12864_2021_7386_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/f69fe85b6ca9/12864_2021_7386_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/78db6e3dc090/12864_2021_7386_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/8c7ae3ba266d/12864_2021_7386_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/7856726/c5b8a3dfd798/12864_2021_7386_Fig5_HTML.jpg

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