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Open Access Research article

Two-stage genome-wide association study identifies integrin beta 5 as having potential role in bull fertility

Jean M Feugang1, Abdullah Kaya2, Grier P Page3, Lang Chen3, Tapan Mehta3, Kashif Hirani4, Lynne Nazareth4, Einko Topper2, Richard Gibbs4 and Erdogan Memili1*

Author affiliations

1 Department of Animal and Dairy Sciences, Mississippi State University, Mississippi State, MS 39762, USA

2 Alta Genetics Inc. Watertown, WI, USA

3 School of Public Health, University of Alabama-Birmingham, Birmingham, AL, USA

4 Baylor College of Medicine, Houston, TX, USA

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Citation and License

BMC Genomics 2009, 10:176  doi:10.1186/1471-2164-10-176

Published: 24 April 2009

Abstract

Background

Fertility is one of the most critical factors controlling biological and financial performance of animal production systems and genetic improvement of lines. The objective of this study was to identify molecular defects in the sperm that are responsible for uncompensable fertility in Holstein bulls. We performed a comprehensive genome wide analysis of single nucleotide polymorphisms (SNP) for bull fertility followed by a second-stage replication in additional bulls for a restricted set of markers.

Results

In the Phase I association study, we genotyped the genomic sperm DNA of 10 low-fertility and 10 high-fertility bulls using Bovine SNP Gene Chips containing approximately 10,000 random SNP markers. In these animals, 8,207 markers were found to be polymorphic, 97 of which were significantly associated with fertility (p < 0.01). In the Phase II study, we tested the four most significant SNP from the Phase I study in 101 low-fertility and 100 high-fertility bulls, with two SNPs (rs29024867 and rs41257187) significantly replicated. Rs29024867 corresponds to a nucleotide change of C → G 2,190 bp 3' of the collagen type I alpha 2 gene on chromosome 4, while the rs41257187 (C → T) is in the coding region of integrin beta 5 gene on chromosome 1. The SNP rs41257187 induces a synonymous (Proline → Proline), suggesting disequilibrium with the true causative locus (i), but we found that the incubation of bull spermatozoa with integrin beta 5 antibodies significantly decreased the ability to fertilize oocytes. Our findings suggest that the bovine sperm integrin beta 5 protein plays a role during fertilization and could serve as a positional or functional marker of bull fertility.

Conclusion

We have identified molecular markers associated with bull fertility and established that at least one of the genes harboring such variation has a role in fertility. The findings are important in understanding mechanisms of uncompensatory infertility in bulls, and in other male mammals. The findings set the stage for more hypothesis-driven research aimed at discovering the role of variation in the genome that affect fertility and that can be used to identify molecular mechanisms of development.