Impaired sperm maturation in RNASE9 knockout mice

Ribonuclease, RNase A family, 9 (RNASE9) is a ribonuclease A superfamily member that is expressed only in the epididymis. It is a small, secreted polypeptide, it lacks ribonuclease activity, and its function(s) is unknown. However, epididymis-specific expression suggests a role in sperm maturation....

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Bibliographic Details
Published in:Biology of reproduction 2014-06, Vol.90 (6), p.120-120
Main Authors: Westmuckett, Andrew D, Nguyen, Edward B, Herlea-Pana, Oana M, Alvau, Antonio, Salicioni, Ana M, Moore, Kevin L
Format: Article
Language:English
Subjects:
Animals
Epididymis - physiology
Female
Male
Mice, 129 Strain
Mice, Knockout
Pregnancy
Proteins - genetics
Ribonucleases - genetics
Sperm Capacitation - genetics
Sperm Maturation - genetics
Sperm Motility - genetics
Spermatogenesis - genetics
Spermatozoa - cytology
Spermatozoa - physiology
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Summary:Ribonuclease, RNase A family, 9 (RNASE9) is a ribonuclease A superfamily member that is expressed only in the epididymis. It is a small, secreted polypeptide, it lacks ribonuclease activity, and its function(s) is unknown. However, epididymis-specific expression suggests a role in sperm maturation. We generated Rnase9(-/-) mice to study RNASE9 function in vivo. We confirm that RNASE9 expression is restricted to the epididymis. Within the epididymis, RNASE9 is first detected in midcaput, persists through the distal caput and corpus, and wanes in the cauda. Rnase9(-/-) mice are born at the expected Mendelian ratio, have normal postnatal growth and development, and have no outwardly apparent phenotype. Spermatogenesis is normal, and Rnase9-null sperm are morphologically normal. Rnase9(-/-) males have normal fertility in unrestricted mating trials, and fertilization rates in in vitro fertilization assays are indistinguishable from wild-type mice. Visual observations coupled with analyses of sperm velocities shortly after swim out from the corpus shows that motility of Rnase9-null sperm is significantly impaired. However, no differences between wild-type and Rnase9-null sperm are detected by computer-assisted sperm analysis 10-90 min after sperm isolation from the corpus or cauda. Assessment of capacitation-dependent signaling pathways in Rnase9-null sperm showed that, while levels of tyrosine phosphorylation of sperm proteins were normal, there was decreased phosphorylation of protein kinase A substrates upon capacitation compared to wild-type mice. In conclusion, RNASE9 is dispensable for fertility, but the absence of RNASE9 during epididymal transit results in impaired sperm maturation.
ISSN:1529-7268
DOI:10.1095/biolreprod.113.116863