Literature DB >> 28965844

Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2.

Sateesh Maddirevula1, Serdar Coskun2, Saad Alhassan3, Atif Elnour4, Hessa S Alsaif1, Niema Ibrahim1, Firdous Abdulwahab1, Stefan T Arold5, Fowzan S Alkuraya6.   

Abstract

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.
Copyright © 2017 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  GVBD; IVF; P100; PAT1A; maturation arrest; meiosis

Mesh:

Substances:

Year:  2017        PMID: 28965844      PMCID: PMC5630161          DOI: 10.1016/j.ajhg.2017.08.009

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  30 in total

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Journal:  Bioinformatics       Date:  2004-09-03       Impact factor: 6.937

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Journal:  Mol Cell Biol       Date:  1997-11       Impact factor: 4.272

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4.  A dependent pathway of cytoplasmic polyadenylation reactions linked to cell cycle control by c-mos and CDK1 activation.

Authors:  S Ballantyne; D L Daniel; M Wickens
Journal:  Mol Biol Cell       Date:  1997-08       Impact factor: 4.138

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Authors:  S Maddirevula; S Coskun; K Awartani; H Alsaif; F M Abdulwahab; F S Alkuraya
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Authors:  Stephanie Beall; Carol Brenner; James Segars
Journal:  Fertil Steril       Date:  2010-04-07       Impact factor: 7.329

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Authors:  W Edelmann; P E Cohen; M Kane; K Lau; B Morrow; S Bennett; A Umar; T Kunkel; G Cattoretti; R Chaganti; J W Pollard; R D Kolodner; R Kucherlapati
Journal:  Cell       Date:  1996-06-28       Impact factor: 41.582

8.  Requirement of Cks2 for the first metaphase/anaphase transition of mammalian meiosis.

Authors:  Charles H Spruck; Maria P de Miguel; Adrian P L Smith; Aimee Ryan; Paula Stein; Richard M Schultz; A Jeannine Lincoln; Peter J Donovan; Steven I Reed
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9.  Purification, primary structure, bacterial expression and subcellular distribution of an oocyte-specific protein in Xenopus.

Authors:  R P Rother; M B Frank; P S Thomas
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2.  Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility.

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3.  Novel mutations in NLRP5 and PATL2 cause female infertility characterized by primarily oocyte maturation abnormality and consequent early embryonic arrest.

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5.  A genomics approach to females with infertility and recurrent pregnancy loss.

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8.  Origins and mechanisms leading to aneuploidy in human eggs.

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9.  Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic development.

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Review 10.  Meiosis interrupted: the genetics of female infertility via meiotic failure.

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