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BOR - Papers in Press, published online ahead of print June 21, 2006.
Biol Reprod 2006, 10.1095/biolreprod.106.053512
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BIOLOGY OF REPRODUCTION 75, 492–500 (2006)
DOI: 10.1095/biolreprod.106.053512
© 2006 by the Society for the Study of Reproduction, Inc.


Research Article

Adenylate Kinases 1 and 2 Are Part of the Accessory Structures in the Mouse Sperm Flagellum1

Wenlei Cao , Lisa Haig-Ladewig , George L. Gerton 3, and Stuart B. Moss 2 3

Center for Research on Reproduction and Women's Health, Department of Obstetrics and Gynecology, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 19104

ABSTRACT

Proper sperm function depends on adequate ATP levels. In the mammalian flagellum, ATP is generated in the midpiece by oxidative respiration and in the principal piece by glycolysis. In locations where ATP is rapidly utilized or produced, adenylate kinases (AKs) maintain a constant adenylate energy charge by interconverting stoichiometric amounts of ATP and AMP with two ADP molecules. We previously identified adenylate kinase 1 and 2 (AK1 and AK2) by mass spectrometry as part of a mouse SDS-insoluble flagellar preparation containing the accessory structures (fibrous sheath, outer dense fibers, and mitochondrial sheath). A germ cell-specific cDNA encoding AK1 was characterized and found to contain a truncated 3' UTR and a different 5' UTR compared to the somatic Ak1 mRNA; however, it encoded an identical protein. Ak1 mRNA was upregulated during late spermiogenesis, a time when the flagellum is being assembled. AK1 was first seen in condensing spermatids and was associated with the outer microtubular doublets and outer dense fibers of sperm. This localization would allow the interconversion of ATP and ADP between the fibrous sheath where ATP is produced by glycolysis and the axonemal dynein ATPases where ATP is consumed. Ak2 mRNA was expressed at relatively low levels throughout spermatogenesis, and the protein was localized to the mitochondrial sheath in the sperm midpiece. AK1 and AK2 in the flagellar accessory structures provide a mechanism to buffer the adenylate energy charge for sperm motility.

gametogenesis, sperm, sperm motility and transport, spermatogenesis


FOOTNOTES

1 Supported by NICHD HD06427 (S.B.M. and G.L.G.). The germ cell-specific AK1 sequence described in this work has been assigned the GenBank database accession number DQ486026.

2 Correspondence: Stuart B. Moss, Center for Research on Reproduction and Women's Health, 1312 BRB II, 421 Curie Blvd., University of Pennsylvania Medical School, Philadelphia, PA 19104. FAX: 215 573 7627; smoss{at}mail.med.upenn.edu

3 Co-principal investigators.




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