Literature DB >> 33530927

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

Chao Bai1, Yuyan You2, Xuefeng Liu1, Maohua Xia3, Wei Wang1, Ting Jia1, Tianchun Pu3, Yan Lu3, Chenglin Zhang1, Xiaoguang Li3, Yanqiang Yin4, Liqin Wang5, Jun Zhou4, Lili Niu5.   

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.

Entities:  

Keywords:  Cataracts; Giant panda; Major intrinsic protein (MIP)

Mesh:

Year:  2021        PMID: 33530927      PMCID: PMC7856726          DOI: 10.1186/s12864-021-07386-8

Source DB:  PubMed          Journal:  BMC Genomics        ISSN: 1471-2164            Impact factor:   3.969


  73 in total

1.  Successful protein fold recognition by optimal sequence threading validated by rigorous blind testing.

Authors:  D T Jones; R T Miller; J M Thornton
Journal:  Proteins       Date:  1995-11

Review 2.  Ultraviolet radiation as a risk factor for cataract and macular degeneration.

Authors:  Joan E Roberts
Journal:  Eye Contact Lens       Date:  2011-07       Impact factor: 2.018

3.  Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2.

Authors:  M Litt; R Carrero-Valenzuela; D M LaMorticella; D W Schultz; T N Mitchell; P Kramer; I H Maumenee
Journal:  Hum Mol Genet       Date:  1997-05       Impact factor: 6.150

4.  A predominant form of C-terminally end-cleaved AQP0 functions as an open water channel and an adhesion protein in AQP0ΔC/ΔC mouse lens.

Authors:  S Sindhu Kumari; Kulandaiappan Varadaraj
Journal:  Biochem Biophys Res Commun       Date:  2019-02-27       Impact factor: 3.575

5.  Water permeability of C-terminally truncated aquaporin 0 (AQP0 1-243) observed in the aging human lens.

Authors:  Lauren E Ball; Mark Little; Mark W Nowak; Donita L Garland; Rosalie K Crouch; Kevin L Schey
Journal:  Invest Ophthalmol Vis Sci       Date:  2003-11       Impact factor: 4.799

6.  Confocal fluorescence microscopy study of interaction between lens MIP26/AQP0 and crystallins in living cells.

Authors:  Bing-Fen Liu; Jack J Liang
Journal:  J Cell Biochem       Date:  2008-05-01       Impact factor: 4.429

Review 7.  The lens circulation.

Authors:  Richard T Mathias; Joerg Kistler; Paul Donaldson
Journal:  J Membr Biol       Date:  2007-06-14       Impact factor: 2.426

8.  A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family.

Authors:  Kai Jie Wang; Sha Sha Li; Bo Yun; Wen Xian Ma; Tian Ge Jiang; Si Quan Zhu
Journal:  Mol Vis       Date:  2011-01-08       Impact factor: 2.367

9.  A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family.

Authors:  Guoxing Yang; Guisen Zhang; Qiang Wu; Jialiang Zhao
Journal:  Mol Vis       Date:  2011-05-13       Impact factor: 2.367

10.  A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family.

Authors:  Ke Yao; Chongfei Jin; Ning Zhu; Wei Wang; Renyi Wu; Jin Jiang; Xingchao Shentu
Journal:  Mol Vis       Date:  2008-07-09       Impact factor: 2.367

View more
  1 in total

1.  RNA-Seq analysis in giant pandas reveals the differential expression of multiple genes involved in cataract formation.

Authors:  Yuyan You; Chao Bai; Xuefeng Liu; Yan Lu; Ting Jia; Maohua Xia; Yanqiang Yin; Wei Wang; Yucun Chen; Chenglin Zhang; Yan Liu; Liqin Wang; Tianchun Pu; Tao Ma; Yanhui Liu; Jun Zhou; Lili Niu; Suhui Xu; Yanxia Ni; Xin Hu; Zengshuai Zhang
Journal:  BMC Genom Data       Date:  2021-10-27
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.