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Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2.
Maddirevula, Sateesh; Coskun, Serdar; Alhassan, Saad; Elnour, Atif; Alsaif, Hessa S; Ibrahim, Niema; Abdulwahab, Firdous; Arold, Stefan T; Alkuraya, Fowzan S.
Afiliación
  • Maddirevula S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
  • Coskun S; 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.
  • Alhassan S; Department of Obstetrics and Gynecology, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
  • Elnour A; Dr. Sulaiman Al Habib Medical Group, Olaya Complex, Riyadh 11643, Saudi Arabia.
  • Alsaif HS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
  • Ibrahim N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
  • Abdulwahab F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
  • Arold ST; King Abdullah University of Science and Technology, Computational Bioscience Research Center, Division of Biological and Environmental Sciences and Engineering, Thuwal 23955-6900, Saudi Arabia.
  • Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh 11
Am J Hum Genet ; 101(4): 603-608, 2017 Oct 05.
Article en En | MEDLINE | ID: mdl-28965844
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Oocitos / Proteínas de Unión al ADN / Infertilidad Femenina / Mutación Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male / Pregnancy Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article País de afiliación: Arabia Saudita

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Oocitos / Proteínas de Unión al ADN / Infertilidad Femenina / Mutación Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male / Pregnancy Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article País de afiliación: Arabia Saudita