Maddirevula Sateesh, Coskun Serdar, Alhassan Saad, Elnour Atif, Alsaif Hessa S, Ibrahim Niema, Abdulwahab Firdous, Arold Stefan T, Alkuraya Fowzan S
Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Am J Hum Genet. 2017 Oct 5;101(4):603-608. doi: 10.1016/j.ajhg.2017.08.009. Epub 2017 Sep 28.
Infertility is a relatively common disorder of the reproductive system and remains unexplained in many cases. In vitro fertilization techniques have uncovered previously unrecognized infertility phenotypes, including oocyte maturation arrest, the molecular etiology of which remains largely unknown. We report two families affected by female-limited infertility caused by oocyte maturation failure. Positional mapping and whole-exome sequencing revealed two homozygous, likely deleterious variants in PATL2, each of which fully segregates with the phenotype within the respective family. PATL2 encodes a highly conserved oocyte-specific mRNP repressor of translation. Previous data have shown the strict requirement for PATL2 in oocyte-maturation in model organisms. Data gathered from the families in this study suggest that the role of PATL2 is conserved in humans and expand our knowledge of the factors that are necessary for female meiosis.
不孕症是一种相对常见的生殖系统疾病,在许多情况下病因不明。体外受精技术揭示了以前未被认识的不孕症表型,包括卵母细胞成熟停滞,其分子病因在很大程度上仍然未知。我们报告了两个受卵母细胞成熟失败导致的女性局限性不孕症影响的家族。定位作图和全外显子组测序揭示了PATL2基因中的两个纯合、可能有害的变异,每个变异在各自家族中均与该表型完全共分离。PATL2编码一种高度保守的卵母细胞特异性mRNA翻译阻遏物。先前的数据表明,模式生物中卵母细胞成熟严格需要PATL2。本研究中从这些家族收集的数据表明,PATL2的作用在人类中是保守的,并扩展了我们对女性减数分裂所需因素的认识。