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TRIM44基因变异通过损害PAX6表达导致无虹膜症。

Variants in TRIM44 Cause Aniridia by Impairing PAX6 Expression.

作者信息

Zhang Xibo, Qin Gang, Chen Guilan, Li Tao, Gao Linghan, Huang Li, Zhang Ying, Ouyang Ke, Wang Yuqi, Pang Yu, Zeng Bo, Yu Ling

机构信息

Department of Ophthalmology, Affiliated Hospital of Luzhou Medical College, Luzhou, China.

Department of Otolaryngology, Head and Neck Surgery, Affiliated Hospital of Luzhou Medical College, Luzhou, China.

出版信息

Hum Mutat. 2015 Dec;36(12):1164-7. doi: 10.1002/humu.22907. Epub 2015 Oct 9.

Abstract

Congenital aniridia is a genetic disorder that manifests as iris hypoplasia and other associated ocular complications. Mutations in the paired box 6 (PAX6) gene are considered the major cause of aniridia. In this study, we identified four mutations exclusively presented in aniridia patients from a four-generation Chinese pedigree, including two single nucleotide substitutions in the 3'UTR of PAX6 (NM_000280.4:c.[*76G>A; *2977C>A]) and two missense mutations in tripartite motif containing 44 (TRIM44, NM_017583.4:c.[191C>A; 463G>A]), which lead to amino acid changes p.S64Y and p.G155R, respectively. Bioinformatic analyses revealed that the two 3'UTR mutations of PAX6 disrupted microRNA binding motifs in the wildtype 3'UTR sequence. Luciferase reporter assay and Western blotting with predicted microRNAs showed that the two 3'UTR mutations could only increase or have no effect on the expression of PAX6. Therefore, they would not be the cause of aniridia that resulted from PAX6 deficiency. Instead, we found that overexpression of TRIM44 significantly reduced the expression of PAX6 in human lens epithelial cells, and the p.G155R mutant exhibited much stronger effect than the wildtype form. We conclude that inhibition of PAX6 expression by mutant TRIM44 is a novel pathogenic mechanism for aniridia.

摘要

先天性无虹膜是一种遗传性疾病,表现为虹膜发育不全及其他相关眼部并发症。配对盒6(PAX6)基因突变被认为是无虹膜的主要病因。在本研究中,我们从一个四代中国家系中鉴定出四个仅在无虹膜患者中出现的突变,包括PAX6基因3'UTR中的两个单核苷酸替换(NM_000280.4:c.[*76G>A; *2977C>A])以及含三联基序蛋白44(TRIM44,NM_017583.4:c.[191C>A; 463G>A])中的两个错义突变,分别导致氨基酸变化p.S64Y和p.G155R。生物信息学分析显示,PAX6基因的两个3'UTR突变破坏了野生型3'UTR序列中的微小RNA结合基序。荧光素酶报告基因检测和用预测的微小RNA进行的蛋白质印迹分析表明,这两个3'UTR突变只能增加PAX6的表达或对其表达无影响。因此,它们不是PAX6缺乏导致无虹膜的原因。相反,我们发现TRIM44的过表达显著降低了人晶状体上皮细胞中PAX6的表达,且p.G155R突变体的作用比野生型更强。我们得出结论,突变型TRIM44对PAX6表达的抑制是无虹膜的一种新的致病机制。

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