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J Biol Chem, Vol. 273, Issue 12, 6968-6975, March 20, 1998
From the Department of Biological Chemistry, University of Michigan
Medical School, Ann Arbor, Michigan 48109-0636
We describe the development of a genetic system
allowing for the isolation of mutant mammalian adenylyl cyclases
defective in their responses to G protein subunits, thus allowing for
the identification of structural elements within the cyclase that are
responsible for the recognition of these regulators. Expression of
mammalian type V adenylyl cyclase in a cyclase-deleted yeast strain can
conditionally complement the lethal phenotype of this strain. Type V
adenylyl cyclase-expressing yeast grow only when the cyclase is
activated by coexpression of Gs
or addition of
forskolin to the medium; however, growth arrest is observed in the
presence of both activators or under basal conditions. Utilizing this
genetic system, we have isolated 25 adenylyl cyclase mutants defective
in their response to Gs
. Sequence analysis and
biochemical characterization of these mutants have identified residues
in both cytoplasmic domains of the cyclase that are involved in the
specific binding of and regulation by Gs
.
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