Abstract
Phosphatidylinositol transfer proteins (PITP) are a family of monomeric proteins that bind and transfer phosphatidylinositol and phosphatidylcholine between membrane compartments. They are required for production of inositol and diacylglycerol second messengers, and are found in most metazoan organisms. While PITPs are known to carry out crucial cell-signaling roles in many organisms, the structure, function and evolution of the majority of family members remains unexplored; primarily because the ubiquity and diversity of the family thwarts traditional methods of global alignment. To surmount this obstacle, we instead took a novel approach, using MEME and a parsimony-based analysis to create a cladogram of conserved sequence motifs in 56 PITP family proteins from 26 species. In keeping with previous functional annotations, three clades were supported within our evolutionary analysis; two classes of soluble proteins and a class of membrane-associated proteins. By, focusing on conserved regions, the analysis allowed for in depth queries regarding possible functional roles of PITP proteins in both intra- and extra- cellular signaling.
Highlights
Phosphatidylinositol transfer proteins (PITP) are monomeric, lipid-binding proteins that bind and transfer phosphatidylinositol (PtdIns) and phosphatidylcholine (PtdCho) between membrane compartments
The derived nature of many of the proteins in the PITP family was already apparent; sequence motifs appeared in some classes but not others, rendering standard alignment and analysis methods ineffective
D. discoideum has been shown to have two genes, pitA and pitB, and expression has been demonstrated for both proteins, PITP1 and PITP2 [21]
Summary
Phosphatidylinositol transfer proteins (PITP) are monomeric, lipid-binding proteins that bind and transfer phosphatidylinositol (PtdIns) and phosphatidylcholine (PtdCho) between membrane compartments Inositol lipids have specialized functions in the regulation of eukaryotic cells, providing a source of second messengers and acting as signaling molecules. Published Online January 2010 in SciRes. http://www.scirp.org/journal/jbise. Biomedical Science and Engineering 3 (2010) 65-77
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