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Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men
BACKGROUND: The decrease in sperm motility has a potent influence on fertilisation. Sperm motility, represented as the percentage of motile sperm in ejaculated sperms, is influenced by lifestyle habits or environmental factors and by inherited factors. However, genetic factors contributing to indivi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992371/ https://www.ncbi.nlm.nih.gov/pubmed/29453196 http://dx.doi.org/10.1136/jmedgenet-2017-104991 |
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author | Sato, Youichi Tajima, Atsushi Sato, Takehiro Nozawa, Shiari Yoshiike, Miki Imoto, Issei Yamauchi, Aiko Iwamoto, Teruaki |
author_facet | Sato, Youichi Tajima, Atsushi Sato, Takehiro Nozawa, Shiari Yoshiike, Miki Imoto, Issei Yamauchi, Aiko Iwamoto, Teruaki |
author_sort | Sato, Youichi |
collection | PubMed |
description | BACKGROUND: The decrease in sperm motility has a potent influence on fertilisation. Sperm motility, represented as the percentage of motile sperm in ejaculated sperms, is influenced by lifestyle habits or environmental factors and by inherited factors. However, genetic factors contributing to individual differences in sperm motility remain unclear. To identify genetic factors that influence human sperm motility, we performed a genome-wide association study (GWAS) of sperm motility. METHODS: A two-stage GWAS was conducted using 811 Japanese men in a discovery stage, followed by a replication study using an additional 779 Japanese men. RESULTS: In the two-staged GWAS, a single nucleotide polymorphism rs3791686 in the intron of gene for erb-b2 receptor tyrosine kinase 4 (ERBB4) on chromosome 2q34 was identified as a novel locus for sperm motility, as evident from the discovery and replication results using meta-analysis (β=−4.01, combined P=5.40×10(−9)). CONCLUSIONS: Together with the previous evidence that Sertoli cell-specific Erbb4-knockout mice display an impaired ability to produce motile sperm, this finding provides the first genetic evidence for further investigation of the genome-wide significant association at the ERBB4 locus in larger studies across diverse human populations. |
format | Online Article Text |
id | pubmed-5992371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-59923712018-06-11 Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men Sato, Youichi Tajima, Atsushi Sato, Takehiro Nozawa, Shiari Yoshiike, Miki Imoto, Issei Yamauchi, Aiko Iwamoto, Teruaki J Med Genet Complex Traits BACKGROUND: The decrease in sperm motility has a potent influence on fertilisation. Sperm motility, represented as the percentage of motile sperm in ejaculated sperms, is influenced by lifestyle habits or environmental factors and by inherited factors. However, genetic factors contributing to individual differences in sperm motility remain unclear. To identify genetic factors that influence human sperm motility, we performed a genome-wide association study (GWAS) of sperm motility. METHODS: A two-stage GWAS was conducted using 811 Japanese men in a discovery stage, followed by a replication study using an additional 779 Japanese men. RESULTS: In the two-staged GWAS, a single nucleotide polymorphism rs3791686 in the intron of gene for erb-b2 receptor tyrosine kinase 4 (ERBB4) on chromosome 2q34 was identified as a novel locus for sperm motility, as evident from the discovery and replication results using meta-analysis (β=−4.01, combined P=5.40×10(−9)). CONCLUSIONS: Together with the previous evidence that Sertoli cell-specific Erbb4-knockout mice display an impaired ability to produce motile sperm, this finding provides the first genetic evidence for further investigation of the genome-wide significant association at the ERBB4 locus in larger studies across diverse human populations. BMJ Publishing Group 2018-06 2018-02-16 /pmc/articles/PMC5992371/ /pubmed/29453196 http://dx.doi.org/10.1136/jmedgenet-2017-104991 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Complex Traits Sato, Youichi Tajima, Atsushi Sato, Takehiro Nozawa, Shiari Yoshiike, Miki Imoto, Issei Yamauchi, Aiko Iwamoto, Teruaki Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men |
title | Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men |
title_full | Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men |
title_fullStr | Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men |
title_full_unstemmed | Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men |
title_short | Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men |
title_sort | genome-wide association study identifies erbb4 on 2q34 as a novel locus associated with sperm motility in japanese men |
topic | Complex Traits |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992371/ https://www.ncbi.nlm.nih.gov/pubmed/29453196 http://dx.doi.org/10.1136/jmedgenet-2017-104991 |
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