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Published on: June 3, 2016
The Role of the Popeye Domain Containing Gene Family in Organ Homeostasis
Johanna Ndamwena Amunjela1, Alexander H Swan2,3, Thomas Brand3
1Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Insights
The Popeye domain containing (POPDC) gene family, crucial for muscle and epithelial cells, plays roles in tissue repair and cancer suppression. Mutations link POPDC genes to muscular dystrophy and heart rhythm issues.
Area of Science:
- Molecular Biology
- Genetics
- Cell Biology
Background:
- The Popeye domain containing (POPDC) gene family, including POPDC1, POPDC2, and POPDC3, encodes cyclic adenosine monophosphate (cAMP) effector proteins.
- While known for 20 years, recent research has elucidated their roles in skeletal muscle regeneration, heart rhythm, and epithelial cell functions.
- POPDC genes are implicated in striated muscle homeostasis and act as tumor suppressors in epithelial cells.
Purpose of the Study:
- To summarize the recent advances in understanding the biological functions and disease associations of the POPDC gene family.
- To highlight the dual role of POPDC genes in both striated muscle and epithelial tissues.
- To explore the involvement of POPDC genes in various human cancers and their prognostic implications.
Main Methods:
- Loss-of-function experiments in mice and zebrafish to study muscle and heart functions.
- Analysis of patient data with muscular dystrophy and atrioventricular block to identify POPDC gene mutations.
- Investigation of POPDC gene expression and function in various human cancer cell lines and patient samples.
Main Results:
- Loss-of-function studies confirmed POPDC genes' importance in skeletal muscle regeneration, heart rhythm control, and stress signaling.
- Mutations in POPDC genes are associated with muscular dystrophy and atrioventricular block, indicating a role in striated muscle homeostasis.
- POPDC gene suppression promotes cancer progression (proliferation, migration, invasion, metastasis), while gain-of-function inhibits it, suggesting tumor suppressor activity. Downregulation often correlates with poor prognosis, though POPDC3 shows complex roles in head and neck cancer.
Conclusions:
- POPDC proteins are critical regulators of tissue homeostasis and cellular signaling in both epithelia and striated muscle.
- Dysregulation of POPDC genes contributes to muscle diseases and cancer development.
- Further research into POPDC gene function may reveal therapeutic targets for muscle disorders and cancer.
Abstract:
The Popeye domain containing (POPDC) gene family consists of POPDC1 (also known as BVES), POPDC2 and POPDC3 and encodes a novel class of cyclic adenosine monophosphate (cAMP) effector proteins. Despite first reports of their isolation and initial characterization at the protein level dating back 20 years, only recently major advances in defining their biological functions and disease association have been made. Loss-of-function experiments in mice and zebrafish established an important role in skeletal muscle regeneration, heart rhythm control and stress signaling. Patients suffering from muscular dystrophy and atrioventricular block were found to carry missense and nonsense mutations in either of the three POPDC genes, which suggests an important function in the control of striated muscle homeostasis. However, POPDC genes are also expressed in a number of epithelial cells and function as tumor suppressor genes involved in the control of epithelial structure, tight junction formation and signaling. Suppression of POPDC genes enhances tumor cell proliferation, migration, invasion and metastasis in a variety of human cancers, thus promoting a malignant phenotype. Moreover, downregulation of POPDC1 and POPDC3 expression in different cancer types has been associated with poor prognosis. However, high POPDC3 expression has also been correlated to poor clinical prognosis in head and neck squamous cell carcinoma, suggesting that POPDC3 potentially plays different roles in the progression of different types of cancer. Interestingly, a gain of POPDC1 function in tumor cells inhibits cell proliferation, migration and invasion thereby reducing malignancy. Furthermore, POPDC proteins have been implicated in the control of cell cycle genes and epidermal growth factor and Wnt signaling. Work in tumor cell lines suggest that cyclic nucleotide binding may also be important in epithelial cells. Thus, POPDC proteins have a prominent role in tissue homeostasis and cellular signaling in both epithelia and striated muscle.
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