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Published on: May 17, 2019
Analysis for Carom complex, signaling and function by database mining
Suxuan Liu, Xinyu Xiong, Sam Varghese Thomas
1Center for Metabolic Disease Research, Department of Pharmacology, Thrombosis Research Center, hongw@temple.edu.
Abstract:
Carom is a novel protein that regulates membrane curvature and transmits pathophysiological signaling. The tissue expression of Carom is unclear and its functional role and signaling are unknown. We employed a group of combined database mining strategies and established a working model of Carom signaling. We identified 26 Carom partners and established their expression profiles in human and mouse tissues. We classified three tiers of tissues for Carom/partner expression and found lymph node was the tier 1 tissue expressing Carom and most of its partners. Using GEO database, we discovered that four conditions (hypoxia, endometriosis, PPARgamma deletion and iPSC reprogramming) altered Carom/partner expression in endothelial cells. We identified 26 Carom partner signalings by Ingenuity pathway analysis. Ten of the 26 pathways and three genes (ITSN1, UBC and HSPA5) were reported to be regulated in the above four conditions. Paired induction of Carom/ITSN1 elevation was associated with pathological angiogenesis. Whereas, paired reduction of Carom/HSPA5 or UBC was associated with iPSC generation. These results provide an insight on identifying Carom complex model and predicting its functional implications.
Insights
Researchers mapped the Carom protein's tissue expression and identified 26 partners, revealing its role in signaling pathways. Lymph nodes are key tissues for Carom, which is linked to angiogenesis and stem cell generation.
Area of Science:
- Molecular Biology
- Cell Signaling
- Proteomics
Background:
- Carom is a novel protein regulating membrane curvature and pathophysiological signaling.
- Its tissue expression, functional role, and signaling pathways remain largely uncharacterized.
Purpose of the Study:
- To elucidate the tissue expression and signaling network of the Carom protein.
- To establish a working model for Carom's functional implications in biological processes.
Main Methods:
- Combined database mining strategies were employed to identify Carom partners and their expression profiles.
- Ingenuity pathway analysis was used to identify Carom partner signaling pathways.
- Gene expression data from the GEO database was analyzed for specific conditions.
Main Results:
- Twenty-six Carom partners were identified, with lymph nodes identified as a Tier 1 tissue for Carom and partner expression.
- Four conditions (hypoxia, endometriosis, PPARgamma deletion, iPSC reprogramming) altered Carom/partner expression in endothelial cells.
- Carom/ITSN1 elevation correlated with pathological angiogenesis, while Carom/HSPA5 or UBC reduction was linked to iPSC generation.
Conclusions:
- A Carom complex model was established, providing insights into its functional roles.
- The study highlights Carom's involvement in both pathological angiogenesis and induced pluripotent stem cell generation.
- Identified Carom partners and pathways offer potential targets for further research.
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