Jing Zhe, Gangalum Rajendra K, Bhat Ankur M, Nagaoka Yoshiko, Jiang Meisheng, Bhat Suraj P
Jules Stein Eye Institute.
Hum Mutat. 2014 Sep;35(9):1068-71. doi: 10.1002/humu.22610. Epub 2014 Jul 23.
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.
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,这表明要么是外显率降低,要么是正常受试者年龄不够大,尚未表现出该表型。鉴于p.Arg116His与HSF4 DNA结合域中的两个已知突变p.Leu114Pro和p.Arg119Cys位置相近,这两个突变与儿童板层白内障相关,我们推测这种表型可能被眼科医生漏诊,和/或其尚未扩散至视轴从而未显著影响视力。在此,我们通过细菌人工染色体(BAC)转基因技术证明,p.Arg116His可在小鼠中重现儿童板层白内障,这表明与早期白内障相关的不完全外显可能并非是该表型不存在,而是检测存在局限性。