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PMID: 9874775 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cytosolic adenylyl cyclase defines a unique signaling molecule in mammals.

Buck J, Sinclair ML, Schapal L, Cann MJ, Levin LR

Abstract

Mammals have nine differentially regulated isoforms of G protein-responsive transmembrane-spanning adenylyl cyclases. We now describe the existence of a distinct class of mammalian adenylyl cyclase that is soluble and insensitive to G protein or Forskolin regulation. Northern analysis indicates the gene encoding soluble adenylyl cyclase (sAC) is preferentially expressed in testis. As purified from rat testis cytosol, the active form of sAC appears to be a fragment derived from the full-length protein, suggesting a proteolytic mechanism for sAC activation. The two presumptive catalytic domains of sAC are closely related to cyanobacterial adenylyl cyclases, providing an evolutionary link between bacterial and mammalian signaling molecules.

MeSH Terms
Adenylyl Cyclases/genetics,isolation & purification Amino Acid Sequence Animals Catalytic Domain Cloning, Molecular Cytosol/enzymology DNA, Complementary/genetics Enzyme Activation Evolution, Molecular Male Molecular Sequence Data Protein Processing, Post-Translational Rats Sequence Homology, Amino Acid Signal Transduction Solubility Testis/enzymology Tissue Distribution
Chemicals
DNA, Complementary Adenylyl Cyclases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Buck J
Department of Pharmacology, Joan and Sanford I. Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021, USA.
Sinclair M L
Schapal L
Cann M J
Levin L R
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1999-01-05
Pages
79-84
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC15096
Subset
IM
Grants
NIDDK NIH HHS · DK48022 · United States
NIDDK NIH HHS · DK52797 · United States
NIGMS NIH HHS · GM52791 · United States
Databases
GENBANK
AF081941, AF176813
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