Literature DB >> 25899990

Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia.

Esther Maor-Sagie1, Yuval Cinnamon, Barak Yaacov, Avraham Shaag, Hannoch Goldsmidt, Shamir Zenvirt, Neri Laufer, Carmelit Richler, Ayala Frumkin.   

Abstract

PURPOSE: To determine the molecular basis of familial, autosomal-recessive, non-obstructive azoospermia in a consanguineous Iranian Jewish family.
METHODS: We investigated the genetic cause of non-obstructive azoospermia in two affected siblings from a consanguineous family. Homozygosity mapping in the DNA samples of the patients and their normospermic brother was followed by exome analysis of one of the patients. Other family members were genotyped for the mutation by Sanger sequencing. The mutation effect was demonstrated by immunostaining of the patients' testicular tissue.
RESULTS: The two patients were homozygous for a splice site mutation in SYCE1 which resulted in retention of intron three in the cDNA and premature stop codon. SYCE1 encodes a Synaptonemal Complex protein which plays an essential role during meiosis. Immunostaining of patient's testicular tissue with anti-Syce1 antibody revealed an undetectable level of Syce1. Histological examination of the patients' tissue disclosed immature-stages spermatocytes without mature forms, indicating maturation arrest.
CONCLUSION: The significance of most synaptonemal complex proteins was previously demonstrated in a mutant mouse model. The present report underscores the importance of synaptonemal complex proteins in spermatogenenesis in humans. Our new approach, combining homozygosity mapping and exome sequencing, resulted in one of the first reports of an autosomal-recessive form of NOA.

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Year:  2015        PMID: 25899990      PMCID: PMC4491075          DOI: 10.1007/s10815-015-0445-y

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  12 in total

Review 1.  The genetics and molecular biology of the synaptonemal complex.

Authors:  Scott L Page; R Scott Hawley
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2.  MutationTaster evaluates disease-causing potential of sequence alterations.

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3.  CUA Guideline: The workup of azoospermic males.

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4.  Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency.

Authors:  Liat de Vries; Doron M Behar; Pola Smirin-Yosef; Irina Lagovsky; Shay Tzur; Lina Basel-Vanagaite
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5.  Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.

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7.  Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11.

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8.  Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia.

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9.  A novel mouse synaptonemal complex protein is essential for loading of central element proteins, recombination, and fertility.

Authors:  Sabine Schramm; Johanna Fraune; Ronald Naumann; Abrahan Hernandez-Hernandez; Christer Höög; Howard J Cooke; Manfred Alsheimer; Ricardo Benavente
Journal:  PLoS Genet       Date:  2011-05-26       Impact factor: 5.917

10.  Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair.

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Journal:  PLoS Genet       Date:  2009-02-27       Impact factor: 5.917

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  38 in total

1.  A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.

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Journal:  J Assist Reprod Genet       Date:  2017-04-11       Impact factor: 3.412

2.  Linked homozygous BMPR1B and PDHA2 variants in a consanguineous family with complex digit malformation and male infertility.

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3.  Pathogenic variations in Germ Cell Nuclear Acidic Peptidase (GCNA) are associated with human male infertility.

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Review 4.  Male Infertility in Humans: An Update on Non-obstructive Azoospermia (NOA) and Obstructive Azoospermia (OA).

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5.  Genome-wide detection of imprinted differentially methylated regions using nanopore sequencing.

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6.  Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia.

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7.  Primary Ovarian Insufficiency and Azoospermia in Carriers of a Homozygous PSMC3IP Stop Gain Mutation.

Authors:  Abdulmoein Eid Al-Agha; Ihab Abdulhamed Ahmed; Esther Nuebel; Mika Moriwaki; Barry Moore; Katherine A Peacock; Tim Mosbruger; Deborah W Neklason; Lynn B Jorde; Mark Yandell; Corrine K Welt
Journal:  J Clin Endocrinol Metab       Date:  2018-02-01       Impact factor: 5.958

Review 8.  Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives.

Authors:  Laura Kasak; Maris Laan
Journal:  Hum Genet       Date:  2020-01-18       Impact factor: 4.132

9.  Recent advances and future opportunities to diagnose male infertility.

Authors:  Samantha L P Schilit
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10.  Targeted next-generation sequencing panel screening of 668 Chinese patients with non-obstructive azoospermia.

Authors:  Miao An; Yidong Liu; Ming Zhang; Kai Hu; Yan Jin; Shiran Xu; Hongxiang Wang; Mujun Lu
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