
A cDNA coding for a new subunit of soluble guanylyl cyclase with a calculated molecular mass of 81.7 kDa was cloned and sequenced. On the basis of sequence homology, the new subunit appears to be an isoform of the alpha 1-subunit and was designated alpha 2 as the new subunit is very similar to the alpha 1-subunit in the middle and C-terminal part; it is quite diverse in the N-terminal part. Preceding experiments had shown that coexpression of the alpha 1- and beta 1-subunits is necessary to obtain a catalytically active guanylyl cyclase in COS cells [(1990) FEBS Lett. 272, 221-223]. The finding that the alpha 2-subunit was able to replace the alpha 1- but not the beta 1-subunit in expression experiments demonstrates the interchangeability of the alpha-subunit isoforms of soluble guanylyl cyclase.
Base Sequence, Molecular Sequence Data, Gene Expression, DNA, Opossums, Polymerase Chain Reaction, Blotting, Southern, Guanylate Cyclase, Animals, Amino Acid Sequence, Cloning, Molecular, Sequence Alignment
Base Sequence, Molecular Sequence Data, Gene Expression, DNA, Opossums, Polymerase Chain Reaction, Blotting, Southern, Guanylate Cyclase, Animals, Amino Acid Sequence, Cloning, Molecular, Sequence Alignment
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