The C. elegans ASPP homolog APE-1 is a junctional protein phosphatase 1 modulator

Author:

Beacham Gwendolyn M.ORCID,Wei Derek T.ORCID,Beyrent ErikaORCID,Zhang Ying,Zheng JianORCID,Camacho Mari M. K.,Florens LaurenceORCID,Hollopeter GuntherORCID

Abstract

AbstractHow serine/threonine phosphatases are spatially and temporally tuned by regulatory subunits is a fundamental question in cell biology. Ankyrin repeat, SH3 domain, proline-rich-region-containing proteins (ASPPs) are protein phosphatase 1 (PP1) binding partners associated with cardiocutaneous diseases. ASPPs localize PP1 to cell-cell junctions, but how ASPPs localize and whether they regulate PP1 activity in vivo is unclear. Through a C. elegans genetic screen, we find that loss of the ASPP homolog, APE-1, suppresses a pathology called ‘jowls,’ providing us with an in vivo assay for APE-1 activity. Using structure-function analysis, we discover that APE-1’s N-terminal half directs the APE-1–PP1 complex to intercellular junctions. Additionally, we isolated mutations in highly conserved residues of APE-1’s ankyrin repeats that suppress jowls yet do not preclude PP1 binding, implying ASPPs do more than simply localize PP1. Indeed, in vivo reconstitution of APE-1 suggests the ankyrin repeats modulate phosphatase output, a function we find to be conserved among vertebrate homologs.

Publisher

Cold Spring Harbor Laboratory

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