Ng Tsz Kin, Lam Ching Yan, Lam Dennis Shun Chiu, Chiang Sylvia Wai Yee, Tam Pancy Oi Sin, Wang Dan Yi, Fan Bao Jian, Yam Gary Hin-Fai, Fan Dorothy Shu Ping, Pang Chi Pui
Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong, Hong Kong S.A.R.
Mol Vis. 2009 Nov 5;15:2239-48.
The PAX6 gene, located at the reported myopia locus MYP7 on chromosome 11p13, was postulated to be associated with myopia development. This study investigated the association of PAX6 with high myopia in 379 high myopia patients and 349 controls.
High myopia patients had refractive errors of -6.00 diopters or greater and axial length longer than 26 mm. Control subjects had refractive errors less than -1.00 diopter and axial length shorter than 24 mm. The P1 promoter, all coding sequences, and adjacent splice-site regions of the PAX6 gene were screened in all study subjects by polymerase chain reaction and direct sequencing. PAX6 P1 promoter-luciferase constructs with variable AC and AG repeat lengths were prepared and transfected into human ARPE-19 cells prior to assaying for their transcriptional activities.
No sequence alterations in the coding or splicing regions showed an association with high myopia. Two dinucleotide repeats, (AC)(m) and (AG)(n), in the P1 promoter region were found to be highly polymorphic and significantly associated with high myopia. Higher repeat numbers were observed in high myopia patients for both (AC)(m) (empirical p = 0.013) and (AG)(n) (empirical p = 0.012) dinucleotide polymorphisms, with a 1.327-fold increased risk associated with the (AG)(n) repeat (empirical p = 0.016; 95% confidence interval: 1.059-1.663). Luciferase-reporter analysis showed elevated transcription activity with increasing individual (AC)(m) and (AG)(n) and combined (AC)(m)(AG)(n) repeat lengths.
Our results revealed an association between high myopia and AC and AG dinucleotide repeat lengths in the PAX6 P1 promoter, indicating the involvement of PAX6 in the pathogenesis of high myopia.
PAX6基因位于11号染色体p13上已报道的近视位点MYP7,推测其与近视发展有关。本研究调查了379例高度近视患者和349例对照中PAX6与高度近视的关联。
高度近视患者的屈光不正度数为-6.00屈光度或更高,眼轴长度超过26mm。对照受试者的屈光不正度数小于-1.00屈光度,眼轴长度短于24mm。通过聚合酶链反应和直接测序对所有研究对象的PAX6基因P1启动子、所有编码序列和相邻剪接位点区域进行筛选。制备了具有可变AC和AG重复长度的PAX6 P1启动子-荧光素酶构建体,并在检测其转录活性之前转染到人ARPE-19细胞中。
编码或剪接区域的序列改变与高度近视无关联。发现P1启动子区域的两个二核苷酸重复序列(AC)(m)和(AG)(n)具有高度多态性,且与高度近视显著相关。在高度近视患者中,(AC)(m)(经验p=0.013)和(AG)(n)(经验p=0.012)二核苷酸多态性的重复次数均较高,(AG)(n)重复的风险增加1.327倍(经验p=0.016;95%置信区间:1.059-1.663)。荧光素酶报告分析显示,随着个体(AC)(m)和(AG)(n)以及联合(AC)(m)(AG)(n)重复长度的增加,转录活性升高。
我们的结果揭示了高度近视与PAX6 P1启动子中AC和AG二核苷酸重复长度之间的关联,表明PAX6参与了高度近视的发病机制。