Phosphodiesterase Type 4 anchoring regulates cAMP signaling to Popeye domain-containing proteins.

Baillie, G. S.; Tibbo, A.; Dobi, S.; McFall, A.; Tejeda, G. S.; Blair, C.; MacLeod, R.; MacQuaide, N.; Gok, C.; Fuller, W.; Smith, B.; Smith, G.; Brand, T.

doi:10.1101/2020.09.10.290825

bioRxiv · 10.1101/2020.09.10.290825

Phosphodiesterase Type 4 anchoring regulates cAMP signaling to Popeye domain-containing proteins.

Baillie, G. S.·Tibbo, A.·Dobi, S.·McFall, A.·Tejeda, G. S.·Blair, C.·MacLeod, R.·MacQuaide, N.·Gok, C.·Fuller, W.·Smith, B.·Smith, G.·Brand, T.

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Abstract

Cyclic AMP is a ubiquitous second messenger used to transduce intracellular signals from a variety of Gs-coupled receptors. Compartmentalisation of protein intermediates within the cAMP signaling pathway underpins receptor-specific responses. The cAMP effector proteins protein-kinase A and EPAC are found in complexes that also contain phosphodiesterases whose presence ensures a coordinated cellular response to receptor activation events. Popeye proteins are the most recent class of cAMP effectors to be identified and have crucial roles in cardiac pacemaking and conduction. We report the first observation that Popeye proteins exist in complexes with members of the PDE4 family in cardiac myocytes thus restricting cAMP signaling. We show that POPDC1 preferentially binds the PDE4A sub-family via a specificity motif in the PDE4 UCR1 region and that PDE4s bind to the Popeye domain of POPDC1 in a region known to be susceptible to a mutation that causes human disease. Using a cell-permeable disruptor peptide that displaces the POPDC1-PDE4 complex we show that PDE4 activity localized to POPDC1 is essential to maintain action potential duration in beating cardiac myocytes.

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Baillie, G. S., Tibbo, A., Dobi, S., McFall, A., Tejeda, G. S., Blair, C., MacLeod, R., MacQuaide, N., Gok, C., Fuller, W., Smith, B., Smith, G., Brand, T.. 2020-09-11. Phosphodiesterase Type 4 anchoring regulates cAMP signaling to Popeye domain-containing proteins.. https://doi.org/10.1101/2020.09.10.290825

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