Second messengers and divergent HD-GYP enzymes regulate 3,3-cGAMP signaling Institutional Repository Document uri icon


  • ABSTRACT3,3-cyclic GMP-AMP (cGAMP) is the third cyclic dinucleotide (CDN) to be discovered in bacteria. No activators of cGAMP signaling have yet been identified, and the signaling pathways for cGAMP have appeared narrowly distributed based upon the characterized synthases, DncV and Hypr GGDEFs. Here we report that the ubiquitous second messenger cyclic AMP (cAMP) is an activator of the Hypr GGDEF enzyme GacB from Myxococcus xanthus. Furthermore, we show that GacB is inhibited directly by cyclic di-GMP, which provides evidence for cross-regulation between different CDN pathways. Finally, we reveal that the HD-GYP enzyme PmxA is a cGAMP-specific phosphodiesterase (GAP) that promotes resistance to osmotic stress in M. xanthus. A signature amino acid change in PmxA was found to reprogram substrate specificity and was applied to predict the presence of non-canonical HD-GYP phosphodiesterases in many bacterial species, including phyla previously not known to utilize cGAMP signaling.

altmetric score

  • 0.5

author list (cited authors)

  • Wright, T. A., Jiang, L., Park, J. J., Anderson, W. A., Chen, G. e., Hallberg, Z. F., Nan, B., & Hammond, M. C.

citation count

  • 0

complete list of authors

  • Wright, Todd A||Jiang, Lucy||Park, James J||Anderson, Wyatt A||Chen, Ge||Hallberg, Zachary F||Nan, Beiyan||Hammond, Ming C

Book Title

  • bioRxiv

publication date

  • April 2019