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Regulation of Phosphatidylethanolamine Homeostasis—The Critical Role of CTP:Phosphoethanolamine Cytidylyltransferase (Pcyt2)

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2013 Jan 29
PMID 23354482
Citations 39
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Abstract

Phosphatidylethanolamine (PE) is the most abundant lipid on the protoplasmatic leaflet of cellular membranes. It has a pivotal role in cellular processes such as membrane fusion, cell cycle regulation, autophagy, and apoptosis. CTP:phosphoethanolamine cytidylyltransferase (Pcyt2) is the main regulatory enzyme in de novo biosynthesis of PE from ethanolamine and diacylglycerol by the CDP-ethanolamine Kennedy pathway. The following is a summary of the current state of knowledge on Pcyt2 and how splicing and isoform specific differences could lead to variations in functional properties in this family of enzymes. Results from the most recent studies on Pcyt2 transcriptional regulation, promoter function, autophagy, and cell growth regulation are highlighted. Recent data obtained from Pcyt2 knockout mouse models is also presented, demonstrating the essentiality of this gene in embryonic development as well as the major physiological consequences of deletion of one Pcyt2 allele. Those include development of symptoms of the metabolic syndrome such as elevated lipogenesis and lipoprotein secretion, hypertriglyceridemia, liver steatosis, obesity, and insulin resistance. The objective of this review is to elucidate the nature of Pcyt2 regulation by linking its catalytic function with the regulation of lipid and energy homeostasis.

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References
1.
Bhoumik A, Fichtman B, DeRossi C, Breitwieser W, Kluger H, Davis S . Suppressor role of activating transcription factor 2 (ATF2) in skin cancer. Proc Natl Acad Sci U S A. 2008; 105(5):1674-9. PMC: 2234203. DOI: 10.1073/pnas.0706057105. View

2.
Ross B, Moszczynska A, Blusztajn J, Sherwin A, Lozano A, Kish S . Phospholipid biosynthetic enzymes in human brain. Lipids. 1997; 32(4):351-8. DOI: 10.1007/s11745-997-0044-x. View

3.
Leonardi R, Frank M, Jackson P, Rock C, Jackowski S . Elimination of the CDP-ethanolamine pathway disrupts hepatic lipid homeostasis. J Biol Chem. 2009; 284(40):27077-89. PMC: 2785637. DOI: 10.1074/jbc.M109.031336. View

4.
Kim B, Shin A, Hong C, Sohn D, Han K, Ryu K . Association of colorectal adenoma with components of metabolic syndrome. Cancer Causes Control. 2012; 23(5):727-35. DOI: 10.1007/s10552-012-9942-9. View

5.
Li H, Liu Y, Shin S, Sun Y, Loring J, Mattson M . Transcriptome coexpression map of human embryonic stem cells. BMC Genomics. 2006; 7:103. PMC: 1523211. DOI: 10.1186/1471-2164-7-103. View