A common mutation in the defensin DEFB126 causes impaired sperm function and subfertility

Theodore L Tollner, Scott A. Venners, Edward J. Hollox, Ashley I. Yudin, Xue Liu, Genfu Tang, Houxun Xing, Robert J. Kays, Tsang Lau, James W. Overstreet, Xiping Xu, Charles L Bevins, Gary N. Cherr

Research output: Contribution to journalArticle

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Abstract

A glycosylated polypeptide, β-defensin 126 (DEFB126), derived from the epididymis and adsorbed onto the sperm surface, has been implicated in immunoprotection and efficient movement of sperm in mucosal fluids of the female reproductive tract. Here, we report a sequence variant in DEFB126 that has a two-nucleotide deletion in the open reading frame, which generates an abnormal mRNA. The allele frequency of this variant sequence was high in both a European (0.47) and a Chinese (0.45) population cohort. Binding of the Agaricus bisporus lectin to the sperm surface glycocalyx was significantly lower in men with the homozygous variant (del/del) genotype than in those with either a del/wt or a wt/wt genotype, suggesting an altered sperm glycocalyx with fewer O-linked oligosaccharides in del/del men. Moreover, sperm from del/del carriers exhibited an 84% reduction in the rate of penetration of a hyaluronic acid gel, a surrogate for cervical mucus, compared to the other genotypes. This reduction in sperm performance in hyaluronic acid gels was not a result of decreased progressive motility (average curvilinear velocity) or morphological deficits. Nevertheless, DEFB126 genotype and lectin binding were correlated with sperm performance in the penetration assays. In a prospective cohort study of newly married couples who were trying to conceive by natural means, couples were less likely to become pregnant and took longer to achieve a live birth if the male partner was homozygous for the variant sequence. This common sequence variation in DEFB126, and its apparent effect of impaired reproductive function, will allow a better understanding, clinical evaluation, and possibly treatment of human infertility.

Original languageEnglish (US)
Article number92ra65
JournalScience Translational Medicine
Volume3
Issue number92
DOIs
StatePublished - Jul 20 2011

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Defensins
Infertility
Spermatozoa
Mutation
Genotype
Glycocalyx
Hyaluronic Acid
Gels
Cervix Mucus
Epididymis
Live Birth
Oligosaccharides
Lectins
Gene Frequency
Open Reading Frames
Cohort Studies
Nucleotides
Prospective Studies
Messenger RNA
Peptides

ASJC Scopus subject areas

  • Medicine(all)

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A common mutation in the defensin DEFB126 causes impaired sperm function and subfertility. / Tollner, Theodore L; Venners, Scott A.; Hollox, Edward J.; Yudin, Ashley I.; Liu, Xue; Tang, Genfu; Xing, Houxun; Kays, Robert J.; Lau, Tsang; Overstreet, James W.; Xu, Xiping; Bevins, Charles L; Cherr, Gary N.

In: Science Translational Medicine, Vol. 3, No. 92, 92ra65, 20.07.2011.

Research output: Contribution to journalArticle

Tollner, TL, Venners, SA, Hollox, EJ, Yudin, AI, Liu, X, Tang, G, Xing, H, Kays, RJ, Lau, T, Overstreet, JW, Xu, X, Bevins, CL & Cherr, GN 2011, 'A common mutation in the defensin DEFB126 causes impaired sperm function and subfertility', Science Translational Medicine, vol. 3, no. 92, 92ra65. https://doi.org/10.1126/scitranslmed.3002289
Tollner, Theodore L ; Venners, Scott A. ; Hollox, Edward J. ; Yudin, Ashley I. ; Liu, Xue ; Tang, Genfu ; Xing, Houxun ; Kays, Robert J. ; Lau, Tsang ; Overstreet, James W. ; Xu, Xiping ; Bevins, Charles L ; Cherr, Gary N. / A common mutation in the defensin DEFB126 causes impaired sperm function and subfertility. In: Science Translational Medicine. 2011 ; Vol. 3, No. 92.
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