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AIM:To identify mutations in the genes of a fourgeneration Chinese family with congenital membranous cataracts and investigate the morphologic changes and possible functional damage underlying the role of the mutant gene.METHODS:Whole exome analysis of thirteen members of a four-generation pedigree affected with congenital membranous cataracts was performed;co-segregation analysis of identified variants was validated by Sanger sequencing.All members underwent detailed physical and complete eye examinations.The physical changes caused by the mutation were analyzed in silico through homology modeling.The lens fiber block from a patient was observed under a scanning electron microscope(SEM).Cell membrane proteins and cytoplasmic proteins from the human lenses donated by one patient with cataract in this family and from the dislocated lens resulted from the penetrating ocular trauma of a patient unrelated with this family were extracted,and the expression and localization of MP20 and Cx46 were detected by Western blot(WB)assay in these proteins.RESULTS:A novel LIM2 heterozygous mutation(c.388 C>T,p.R130 C)was identified with congenital membranous cataracts inherited by an autosomal dominant(AD)pattern.Nystagmus and amblyopia were observed in all patients of this family,and exotropia and long axial length were observed in most patients.A/B ultrasound scan and ultrasound biomicroscopy revealed obvious thin crystalline lenses from 1.7 to 2.7 mm in central thickness in all cataract eyes.The bioinformatic analysis showed that the mutation was deleterious to the physiological function of LIM2-encoded MP20.Furthermore,by SEM,ultrastructure of the cataract nucleus showed that lens fiber cells(LFCs)remained morphologic characteristics of immature fiber cells,including flap cell surface with straight edges and lacking normal ball-and-socket joint boundaries,which implied that the differentiation of LFCs might be inhibited.Accumulation of MP20 and Cx46 in the cytoplasm was observed in the cytoplasm of the LFCs in human cataract
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篇名 A novel mutation of LIM2 causes autosomal dominant membranous cataract in a Chinese family
来源期刊 国际眼科杂志:英文版 学科 医学
关键词 LIM2 MP20 congenital cataract missense mutation DIFFERENTIATION
年,卷(期) 2020,(10) 所属期刊栏目
研究方向 页码范围 1512-1520
页数 9页 分类号 R776.1
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LIM2
MP20
congenital
cataract
missense
mutation
DIFFERENTIATION
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国际眼科杂志:英文版
月刊
2222-3959
西安市友谊东路269号
出版文献量(篇)
2720
总下载数(次)
2
总被引数(次)
0
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