Proceedings of the National Academy of Sciences · 1999 · 526 citations · 24 references
Life SciencesBiochemistryMolecular BiologyCell SignalingGene ExpressionSignal TransductionCyclic Nucleotide SignalingG Protein-coupled Receptor SignalingProteolytic EnzymesProteolytic ProcessingAdenylate Cyclase SignalingAdenylyl Cyclase IsoformsAdenylyl Cyclase SignalingCatalytic DomainsCyclic Adenosine Monophosphate SignalingG Protein-coupled SignalingProteolytic ActivityProteolytic Pathways
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.
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