Unknown

Dataset Information

0

The Popeye Domain Containing Genes and their Function in Striated Muscle.


ABSTRACT: The Popeye domain containing (POPDC) genes encode a novel class of cAMP effector proteins, which are abundantly expressed in heart and skeletal muscle. Here we will review their role in striated muscle as deduced from work in cell and animal models and the recent analysis of patients carrying a missense mutation in POPDC1. Evidence suggests that POPDC proteins control membrane trafficking of interacting proteins. Furthermore, we will discuss the current catalogue of established protein-protein interactions. In recent years, the number of POPDC-interacting proteins is rising and currently includes ion channels (TREK-1), sarcolemma-associated proteins serving functions in mechanical stability (Dystrophin), compartmentalization (Caveolin 3), scaffolding (ZO-1), trafficking (NDRG4, VAMP2/3) and repair (Dysferlin), or acting as a guanine nucleotide exchange factor for Rho-family GTPases (GEFT). Recent evidence suggests that POPDC proteins might also control the cellular level of the nuclear proto-oncoprotein c-Myc. These data suggests that this family of cAMP-binding proteins probably serves multiple roles in striated muscle.

SUBMITTER: Schindler RF 

PROVIDER: S-EPMC4918794 | biostudies-literature | 2016 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

The Popeye Domain Containing Genes and their Function in Striated Muscle.

Schindler Roland Fr RF   Scotton Chiara C   French Vanessa V   Ferlini Alessandra A   Brand Thomas T  

Journal of cardiovascular development and disease 20160615 2


The Popeye domain containing (POPDC) genes encode a novel class of cAMP effector proteins, which are abundantly expressed in heart and skeletal muscle. Here we will review their role in striated muscle as deduced from work in cell and animal models and the recent analysis of patients carrying a missense mutation in <i>POPDC1</i>. Evidence suggests that POPDC proteins control membrane trafficking of interacting proteins. Furthermore, we will discuss the current catalogue of established protein-pr  ...[more]

Similar Datasets

| S-EPMC6726836 | biostudies-literature
| S-EPMC6562197 | biostudies-literature
| S-EPMC3677075 | biostudies-literature
| S-EPMC2849751 | biostudies-literature
| S-EPMC6952887 | biostudies-literature
| S-EPMC8788487 | biostudies-literature
| S-EPMC3774711 | biostudies-literature
| S-EPMC3287222 | biostudies-literature
| S-EPMC4863828 | biostudies-literature
| S-EPMC4821176 | biostudies-literature