Journal
ANIMAL REPRODUCTION SCIENCE
Volume 128, Issue 1-4, Pages 11-21Publisher
ELSEVIER
DOI: 10.1016/j.anireprosci.2011.08.008
Keywords
mRNA; Immunofluorescence; Spermatogenesis; Epididymis; Spermatozoa
Funding
- FBF (Forderverein Biotechnologieforschung e. V., Bonn, Germany)
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Male fertility is impaired through the lack of ESR1 (Estrogen Receptor 1) but little is known about the ESR1 roles in boar spermatogenesis and fertility. Therefore, this research was aimed at investigating the association with sperm quality and boar fertility traits in a total of 300 boars both from purebred Pietrain and Pietrain x Hampshire crosses. A SNP in coding region of ESR1 g.672C > T in exon 1 was associated with sperm motility (P < 0.05) and plasma droplet rate (P < 0.01) while the polymorphism in non-coding region of ESR1 g.35756T > C in inton 1 was associated with non-return rate (P < 0.05). Furthermore, to analyse the mRNA and protein expression of ESR1 in boar reproductive tissues, a total of six boars were divided into two groups [Group 1 (G-I) and Group II (G-II)], where G-I had relatively better sperm quality. ESR1 expression was higher in tissues collected from G-I boars than those of collected from G-II boars, and the difference in mRNA expression was significant (P < 0.01) in head of epididymis. The ESR1 protein expression results from western blot coincided with the results of qRT-PCR. The ESR1 protein localization observed a strong staining in the cytoplasm of Sertoli cell in the testis, in the epithelial cells in head and tail of epididymis, in smooth muscle in tail of epididymis, and in the post acrosomal region and tail of the spermatozoa. These results will improve the understanding of the functions of the ESR1 in spermatogenesis within the reproductive tract and will shed light on ESR1 as a candidate in the selection of boar with good sperm quality and fertility. (C) 2011 Elsevier B.V. All rights reserved.
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