Key result
Popeye domain containing (Popdc) proteins act as a novel class of cAMP effector proteins with important functions in striated muscle tissue, epithelial cells, and various types of cancer.
This review highlights the role of Popeye domain containing (Popdc) proteins as novel cAMP effectors with significant physiological and pathophysiological functions in cardiac and skeletal muscle.
Popdc proteins' complex cAMP interactions may affect cardiac signaling; leaves open their roles as therapeutic targets pending validation.
Popeye domain containing (Popdc) proteins are a unique family, which combine several different properties and functions in a surprisingly complex fashion. They are expressed in multiple tissues and cell types, present in several subcellular compartments, interact with different classes of proteins, and are associated with a variety of physiological and pathophysiological processes. Moreover, Popdc proteins bind the second messenger cAMP with high affinity and it is thought that they act as a novel class of cAMP effector proteins. Here, we will review the most important findings about the Popdc family, which accumulated since its discovery about 15 years ago. We will be focussing on Popdc protein interaction and function in striated muscle tissue. However, as a full picture only emerges if all aspects are taken into account, we will also describe what is currently known about the role of Popdc proteins in epithelial cells and in various types of cancer, and discuss these findings with regard to their relevance for cardiac and skeletal muscle.
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Schindler et al. (2016) reported a review. Popeye domain containing (Popdc) proteins was evaluated. Popeye domain containing (Popdc) proteins act as a novel class of cAMP effector proteins with important functions in striated muscle tissue, epithelial cells, and various types of cancer.
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