Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome
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- 作者：R. Faridi ; A.U. Rehman ; R.J. Morell ; P.L. Friedman ; L. Demain ; S. Zahra ; A.A. Khan ; D. Tohlob ; M.Z. Assir ; G. Beaman ; S.N. Khan ; W.G. Newman ; S. Riazuddin and T.B. Friedman
- 刊名：Clinical Genetics
- 出版年：2017
- 出版时间：February 2017
- 年：2017
- 卷：91
- 期：2
- 页码：328-332
- 全文大小：572K
- ISSN：1399-0004
文摘
Perrault syndrome (PS) is a genetically heterogeneous disorder characterized by primary ovarian insufficiency (POI) in females and sensorineural hearing loss in males and females. In many PS subjects, causative variants have not been found in the five reported PS genes. The objective of this study was to identify the genetic cause of PS in an extended consanguineous family with six deaf individuals. Whole exome sequencing (WES) was completed on four affected members of a large family, and variants and co-segregation was confirmed by Sanger sequencing. All hearing impaired individuals, including the proband, are homozygous for a pathogenic variant of CLDN14, but this only explains the deafness. The PS proband is also homozygous for a frameshift variant (c.1453_1454delGA, p.(Glu485Lysfs*5)) in exon 7 of SGO2 encoding shugoshin 2, which is the likely cause of her concurrent ovarian insufficiency. In mouse, Sgol2a encoding shugoshin-like 2a is necessary during meiosis in both sexes to maintain the integrity of the cohesin complex that tethers sister chromatids. Human SGO2 has not previously been implicated in any disorder, but in this case of POI and perhaps others, it is a candidate for unexplained infertility.