Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology and Center for Human Genome Research, Huazhong University of Science and Technology, Wuhan, 430074, Hubei, China.
Reproductive Medicine Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
J Assist Reprod Genet. 2020 Apr;37(4):841-847. doi: 10.1007/s10815-020-01698-6. Epub 2020 Feb 11.
To identify the disease gene in 40 patients with female infertility due to oocyte maturation arrest.
Genomic DNA was extracted from peripheral blood of 40 patients and their family members. Whole-exome sequencing was performed on the patients, and the PATL2 mutations were identified and confirmed by Sanger sequencing. Harmfulness of the mutations was analyzed by SIFT, Polyphen-2, Mutation Taster, and M-CAP software, and we used western immunoblotting analysis to check the effect of mutations on PATL2 protein expression in vitro.
Two novel missense mutations c.1528C>A (p.Pro510Thr) and c.1376C>A (p.Ser459Tyr) in PATL2 were identified in three patients (7.5%) from two consanguineous families in our cohort. We found that mutations in PATL2 resulted in variable oocyte phenotypes, including GV arrest, MI arrest, and morphologic abnormalities. Western immunoblotting analysis showed that the expression levels of the two novel mutant PATL2 proteins decreased significantly.
We identified two novel PATL2 mutations that caused oocyte maturation arrest and abnormal morphology, and variable phenotypes in patients.
鉴定 40 例卵母细胞成熟阻滞所致女性不孕患者的疾病基因。
从 40 例患者及其家系成员的外周血中提取基因组 DNA。对患者进行全外显子组测序,并通过 Sanger 测序鉴定和确认 PATL2 突变。采用 SIFT、Polyphen-2、Mutation Taster 和 M-CAP 软件分析突变的危害性,并通过 Western 免疫印迹分析体外检测突变对 PATL2 蛋白表达的影响。
在我们的队列中,来自两个近亲家庭的 3 名患者(7.5%)中发现了 PATL2 中的两个新错义突变 c.1528C>A(p.Pro510Thr)和 c.1376C>A(p.Ser459Tyr)。我们发现 PATL2 突变导致卵母细胞表型发生变化,包括GV 阻滞、MI 阻滞和形态异常。Western 免疫印迹分析显示,两种新型突变 PATL2 蛋白的表达水平显著降低。
我们鉴定了两个导致卵母细胞成熟阻滞和形态异常以及患者表型变化的新型 PATL2 突变。