Molecular cloning and expression of a new alpha-subunit of soluble guanylyl cyclase. Interchangeability of the alpha-subunits of the enzyme

FEBS Lett. 1991 Nov 4;292(1-2):217-22. doi: 10.1016/0014-5793(91)80871-y.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Southern
  • Cloning, Molecular
  • DNA / genetics
  • Gene Expression*
  • Guanylate Cyclase / genetics*
  • Guanylate Cyclase / metabolism
  • Molecular Sequence Data
  • Opossums
  • Polymerase Chain Reaction
  • Sequence Alignment

Substances

  • DNA
  • Guanylate Cyclase

Associated data

  • GENBANK/S62644
  • GENBANK/S62648
  • GENBANK/S62652
  • GENBANK/S67655
  • GENBANK/S67857
  • GENBANK/X58803
  • GENBANK/X63282
  • GENBANK/X63567
  • GENBANK/X63568
  • GENBANK/X63569