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Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model

Transmission Ratio Distortion (TRD), the uneven transmission of an allele from a parent to its offspring, can be caused by allelic differences affecting gametogenesis, fertilization or embryogenesis. However, TRD remains vaguely studied at a genomic scale. We sequenced the diploid and haploid genome...

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Autores principales: Gòdia, Marta, Casellas, Joaquim, Ruiz-Herrera, Aurora, Rodríguez-Gil, Joan E, Castelló, Anna, Sánchez, Armand, Clop, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750926/
https://www.ncbi.nlm.nih.gov/pubmed/32931559
http://dx.doi.org/10.1093/dnares/dsaa019
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author Gòdia, Marta
Casellas, Joaquim
Ruiz-Herrera, Aurora
Rodríguez-Gil, Joan E
Castelló, Anna
Sánchez, Armand
Clop, Alex
author_facet Gòdia, Marta
Casellas, Joaquim
Ruiz-Herrera, Aurora
Rodríguez-Gil, Joan E
Castelló, Anna
Sánchez, Armand
Clop, Alex
author_sort Gòdia, Marta
collection PubMed
description Transmission Ratio Distortion (TRD), the uneven transmission of an allele from a parent to its offspring, can be caused by allelic differences affecting gametogenesis, fertilization or embryogenesis. However, TRD remains vaguely studied at a genomic scale. We sequenced the diploid and haploid genomes of three boars from leukocytes and spermatozoa at 50x to shed light into the genetic basis of spermatogenesis-caused Allelic Ratio Distortion (ARD). We first developed a Binomial model to identify ARD by simultaneously analysing all three males. This led to the identification of 55 ARD SNPs, most of which were animal-specific. We then evaluated ARD individually within each pig by a Fisher’s exact test and identified two shared genes (TOP3A and UNC5B) and four shared genomic regions harbouring distinct ARD SNPs in the three boars. The shared genomic regions contained candidate genes with functions related to spermatogenesis including AK7, ARID4B, BDKRB2, GSK3B, NID1, NSMCE1, PALB2, VRK1 and ZC3H13. Using the Fisher’s test, we also identified 378 genes containing variants with protein damaging potential in at least one boar, a high proportion of which, including FAM120B, TDRD15, JAM2 or AOX4 among others, are associated to spermatogenesis. Overall, our results show that sperm is subjected to ARD with variants associated to a wide variety of genes involved in different stages of spermatogenesis.
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spelling pubmed-77509262020-12-28 Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model Gòdia, Marta Casellas, Joaquim Ruiz-Herrera, Aurora Rodríguez-Gil, Joan E Castelló, Anna Sánchez, Armand Clop, Alex DNA Res Research Article Transmission Ratio Distortion (TRD), the uneven transmission of an allele from a parent to its offspring, can be caused by allelic differences affecting gametogenesis, fertilization or embryogenesis. However, TRD remains vaguely studied at a genomic scale. We sequenced the diploid and haploid genomes of three boars from leukocytes and spermatozoa at 50x to shed light into the genetic basis of spermatogenesis-caused Allelic Ratio Distortion (ARD). We first developed a Binomial model to identify ARD by simultaneously analysing all three males. This led to the identification of 55 ARD SNPs, most of which were animal-specific. We then evaluated ARD individually within each pig by a Fisher’s exact test and identified two shared genes (TOP3A and UNC5B) and four shared genomic regions harbouring distinct ARD SNPs in the three boars. The shared genomic regions contained candidate genes with functions related to spermatogenesis including AK7, ARID4B, BDKRB2, GSK3B, NID1, NSMCE1, PALB2, VRK1 and ZC3H13. Using the Fisher’s test, we also identified 378 genes containing variants with protein damaging potential in at least one boar, a high proportion of which, including FAM120B, TDRD15, JAM2 or AOX4 among others, are associated to spermatogenesis. Overall, our results show that sperm is subjected to ARD with variants associated to a wide variety of genes involved in different stages of spermatogenesis. Oxford University Press 2020-09-15 /pmc/articles/PMC7750926/ /pubmed/32931559 http://dx.doi.org/10.1093/dnares/dsaa019 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Gòdia, Marta
Casellas, Joaquim
Ruiz-Herrera, Aurora
Rodríguez-Gil, Joan E
Castelló, Anna
Sánchez, Armand
Clop, Alex
Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model
title Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model
title_full Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model
title_fullStr Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model
title_full_unstemmed Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model
title_short Whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model
title_sort whole genome sequencing identifies allelic ratio distortion in sperm involving genes related to spermatogenesis in a swine model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750926/
https://www.ncbi.nlm.nih.gov/pubmed/32931559
http://dx.doi.org/10.1093/dnares/dsaa019
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