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HSF4 Mutation p.Arg116His Found in Age-related Cataracts and in Normal Populations Produces Childhood Lamellar Cataract in Transgenic Mice

机译:在与年龄有关的白内障和正常人群中发现的HSF4突变p.Arg116His在转基因小鼠中产生儿童层状白内障

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摘要

The p.Arg116His mutation in the heat shock transcription factor-4 (HSF4) has been associated with age-related cataracts, but it is also seen in 2% of the normal population indicating either reduced penetrance or that the normal subjects were not old enough to express the phenotype. Based on the proximity of p.Arg116His to two known mutations in the DNA binding domain of HSF4, namely p.Leu114Pro and p.Arg119Cys, which segregate with childhood lamellar cataract, we tested the possibility that this phenotype may have been missed by the ophthalmologist and/or that it did not spread to the visual axis so as to affect vision significantly. Here we demonstrate via BAC (bacterial artificial chromosome) transgenesis that p.Arg116His recreates the childhood lamellar cataract in mice suggesting that incomplete penetrance associated with early cataracts may not be an absence but a limitation of the detection of the phenotype.
机译:热休克转录因子-4(HSF4)中的p.Arg116His突变与年龄相关性白内障有关,但在2%的正常人群中也可见到,这表明外显率降低或正常人年龄不足表达表型。根据p.Arg116His与HSF4 DNA结合结构域中的两个已知突变即p.Leu114Pro和p.Arg119Cys的接近性,它们与儿童层状白内障隔离,我们测试了这种表型可能被眼科医生遗漏的可能性和/或它没有传播到视轴以显着影响视力。在这里,我们通过BAC(细菌人工染色体)转基因证明p.Arg116His在小鼠中重现了童年的层状白内障,提示与早期白内障相关的不完全外显性可能不是缺席,而是表型检测的局限。

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