Language

English

Publication Date

6-1-2025

Journal

Journal of Biological Chemistry

DOI

10.1016/j.jbc.2025.110279

PMID

40412525

PMCID

PMC12226364

PubMedCentral® Posted Date

5-22-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Exchange protein directly activated by cAMP (EPAC1), a multifunctional intracellular cAMP receptor, dynamically localizes to various cellular loci, engaging with diverse molecular partners to maintain cellular homeostasis. The study investigates the role of the SUMO-interacting motif (SIM) in the subcellular targeting and cellular functions of EPAC1. It reveals that the SIM is a critical structural element for EPAC1's association with RanBP2/nucleoporin 358, a nucleoporin of the cytoplasmic filament component of the nuclear pore complex. Mutational disruption of EPAC1 SIM interferes with EPAC1's ability to activate its canonical effectors, small GTPases, Rap1 and Rap2, and noncanonical functions, such as the formation of nuclear condensates and cellular SUMOylation. Because SIM is also directly involved in cAMP binding, RanBP2's association with EPAC1 with the SIM attenuates EPAC1's cAMP binding affinity to generate an EPAC1 signaling microdomain with reduced cAMP sensitivity around the nuclear pore complex. The coupling between EPAC1's scaffold association and cAMP binding enables EPAC1 to tune its sensitivity to stress stimuli spatially depending on the cellular locations. These findings provide novel structural insights into EPAC1 signaling, highlighting the importance of SIM in EPAC1's cellular functions and potential novel strategies for therapeutically targeting EPAC1.

Keywords

Guanine Nucleotide Exchange Factors, Humans, Cyclic AMP, Nuclear Pore Complex Proteins, Amino Acid Motifs, Sumoylation, HEK293 Cells, rap GTP-Binding Proteins, HeLa Cells, SUMO-1 Protein, rap1 GTP-Binding Proteins, Signal Transduction, Protein Binding, Molecular Chaperones

Published Open-Access

yes

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.