Genetics, Gene Regulation, and Expression
Specific expression of soluble adenylyl cyclase in male germ cells
Article first published online: 22 MAR 2000
DOI: 10.1002/(SICI)1098-2795(200005)56:1<6::AID-MRD2>3.0.CO;2-M
Copyright © 2000 Wiley-Liss, Inc.
Additional Information
How to Cite
Sinclair, M. L., Wang, X.-Y., Mattia, M., Conti, M., Buck, J., Wolgemuth, D. J. and Levin, L. R. (2000), Specific expression of soluble adenylyl cyclase in male germ cells. Molecular Reproduction and Development, 56: 6–11. doi: 10.1002/(SICI)1098-2795(200005)56:1<6::AID-MRD2>3.0.CO;2-M
Publication History
- Issue published online: 22 MAR 2000
- Article first published online: 22 MAR 2000
- Manuscript Accepted: 18 NOV 1999
- Manuscript Received: 24 SEP 1999
Funded by
- National Institutes of Health. Grant Numbers: DK48022, DK52797, GM52891, DA07274, HD34915, HD31544
- Abstract
- References
- Cited By
Keywords:
- testis;
- cAMP;
- in situ hybridization;
- spermatogenesis;
- pachytene spermatocytes;
- spermatids
Abstract
The cAMP signaling pathway is an important mediator of extracellular signals in organisms from prokaryotes to higher eukaryotes. In mammals two types of adenylyl cyclase synthesize cAMP; a ubiquitous family of transmembrane isoforms regulated by G proteins in response to extracellular signals, and a recently isolated soluble enzyme insensitive to heterotrimeric G protein modulation. Using the very sensitive reverse transcription-polymerase chain reaction (RT-PCR), soluble adenylyl cyclase (sAC) expression is detectable in almost all tissues examined; however, Northern analysis and in situ hybridization indicate that high levels of sAC message are unique to male germ cells. Elevated levels of sAC mRNA are first observed in pachytene spermatocytes and expression increases through spermiogenesis. The accumulation of high levels of message in round spermatids suggests sAC protein plays an important role in the generation of cAMP in spermatozoa, implying possible roles in sperm maturation through the epididymis, capacitation, hypermotility, and/or the acrosome reaction. Mol. Reprod. Dev. 56:6–11, 2000. © 2000 Wiley-Liss, Inc.

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