Abstract
Cholinephosphotransferase catalyses the final step in the synthesis of phosphatidylcholine (PtdCho) via the Kennedy pathway by the transfer of phosphocholine from CDP-choline to diacylglycerol. Ethanolaminephosphotransferase catalyses an analogous reaction with CDP-ethanolamine as the phosphobase donor for the synthesis of phosphatidylethanolamine (PtdEtn). Together these two enzyme activities determine both the site of synthesis and the fatty acyl composition of PtdCho and PtdEtn synthesized de novo. A human choline/ethanolaminephosphotransferase cDNA (hCEPT1) was cloned, expressed and characterized. Northern blot analysis revealed one hCEPT1 2.3 kb transcript that was ubiquitous and not enriched, with respect to actin, in any particular cell type. The open reading frame predicts a protein (hCEPT1p) of 416 amino acid residues with a molecular mass of 46550 Da containing seven membrane-spanning domains. A predicted amphipathic helix resides within the active site of the enzyme with the final two aspartic residues of the CDP-alcohol phosphotransferase motif, DG(X)2AR(X)8G(X)3D(X)3D, positioned within this helix. hCEPT1p was successfully expressed in a full-length, active form in Saccharomyces cerevisiae cells devoid of endogenous cholinephosphotransferase or ethanolaminephosphotransferase activities (HJ091, cpt1::LEU2 ept1-). In vitro, hCEPT1p displayed broad substrate specificity, utilizing both CDP-choline and CDP-ethanolamine as phosphobase donors to a broad range of diacylglycerols, resulting in the synthesis of both PtdCho and PtdEtn. In vivo, S. cerevisiae cells (HJ091, cpt1::LEU2 ept1-) expressing hCEPT1 efficiently incorporated both radiolabelled choline and ethanolamine into phospholipids, demonstrating that hCEPT1p has the ability to synthesize both choline- and ethanolamine- containing phospholipids in vitro and in vivo.
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- Akesson B., Arner A., Sundler R. Metabolism of different monoacylphospholipids in isolated hepatocytes and the intact rat. Biochim Biophys Acta. 1976 Sep 27;441(3):453–464. doi: 10.1016/0005-2760(76)90242-3. [DOI] [PubMed] [Google Scholar]
- Das S. K., Beg O., Mukherjee S. Partial characterization of guinea pig cholinephosphotransferase cDNA. Biochem Biophys Res Commun. 1997 Dec 18;241(2):504–508. doi: 10.1006/bbrc.1997.7862. [DOI] [PubMed] [Google Scholar]
- Dewey R. E., Wilson R. F., Novitzky W. P., Goode J. H. The AAPT1 gene of soybean complements a cholinephosphotransferase-deficient mutant of yeast. Plant Cell. 1994 Oct;6(10):1495–1507. doi: 10.1105/tpc.6.10.1495. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Feinberg A. P., Vogelstein B. "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum. Anal Biochem. 1984 Feb;137(1):266–267. doi: 10.1016/0003-2697(84)90381-6. [DOI] [PubMed] [Google Scholar]
- Gish W., States D. J. Identification of protein coding regions by database similarity search. Nat Genet. 1993 Mar;3(3):266–272. doi: 10.1038/ng0393-266. [DOI] [PubMed] [Google Scholar]
- Hjelmstad R. H., Bell R. M. The sn-1,2-diacylglycerol cholinephosphotransferase of Saccharomyces cerevisiae. Nucleotide sequence, transcriptional mapping, and gene product analysis of the CPT1 gene. J Biol Chem. 1990 Jan 25;265(3):1755–1764. [PubMed] [Google Scholar]
- Hjelmstad R. H., Bell R. M. sn-1,2-diacylglycerol choline- and ethanolaminephosphotransferases in Saccharomyces cerevisiae. Mixed micellar analysis of the CPT1 and EPT1 gene products. J Biol Chem. 1991 Mar 5;266(7):4357–4365. [PubMed] [Google Scholar]
- Hjelmstad R. H., Bell R. M. sn-1,2-diacylglycerol choline- and ethanolaminephosphotransferases in Saccharomyces cerevisiae. Nucleotide sequence of the EPT1 gene and comparison of the CPT1 and EPT1 gene products. J Biol Chem. 1991 Mar 15;266(8):5094–5103. [PubMed] [Google Scholar]
- Hjelmstad R. H., Morash S. C., McMaster C. R., Bell R. M. Chimeric enzymes. Structure-function analysis of segments of sn-1,2-diacylglycerol choline- and ethanolaminephosphotransferases. J Biol Chem. 1994 Aug 19;269(33):20995–21002. [PubMed] [Google Scholar]
- Holub B. J. Differential utilization of 1-palmitoyl and 1-stearoyl homologues of various unsaturated 1,2-diacyl-sn-glycerols for phosphatidylcholine and phosphatidylethanolamine synthesis in rat liver microsomes. J Biol Chem. 1978 Feb 10;253(3):691–696. [PubMed] [Google Scholar]
- Holub B. J., Kuksis A. Structural and metabolic interrelationships among glycerophosphatides of rat liver in vivo. Can J Biochem. 1971 Dec;49(12):1347–1356. doi: 10.1139/o71-195. [DOI] [PubMed] [Google Scholar]
- Jamil H., Utal A. K., Vance D. E. Evidence that cyclic AMP-induced inhibition of phosphatidylcholine biosynthesis is caused by a decrease in cellular diacylglycerol levels in cultured rat hepatocytes. J Biol Chem. 1992 Jan 25;267(3):1752–1760. [PubMed] [Google Scholar]
- Jobe A. H. Pulmonary surfactant therapy. N Engl J Med. 1993 Mar 25;328(12):861–868. doi: 10.1056/NEJM199303253281208. [DOI] [PubMed] [Google Scholar]
- KENNEDY E. P., WEISS S. B. The function of cytidine coenzymes in the biosynthesis of phospholipides. J Biol Chem. 1956 Sep;222(1):193–214. [PubMed] [Google Scholar]
- Kanoh H., Ohno K. Solubilization and purification of rat liver microsomal 1,2-diacylglycerol: CDP-choline cholinephosphotransferase and 1,2-diacylglycerol: CDP-ethanolamine ethanolaminephosphotransferase. Eur J Biochem. 1976 Jun 15;66(1):201–210. doi: 10.1111/j.1432-1033.1976.tb10440.x. [DOI] [PubMed] [Google Scholar]
- Kneller D. G., Cohen F. E., Langridge R. Improvements in protein secondary structure prediction by an enhanced neural network. J Mol Biol. 1990 Jul 5;214(1):171–182. doi: 10.1016/0022-2836(90)90154-E. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Leslie C. C. Properties and regulation of cytosolic phospholipase A2. J Biol Chem. 1997 Jul 4;272(27):16709–16712. doi: 10.1074/jbc.272.27.16709. [DOI] [PubMed] [Google Scholar]
- McGee T. P., Skinner H. B., Bankaitis V. A. Functional redundancy of CDP-ethanolamine and CDP-choline pathway enzymes in phospholipid biosynthesis: ethanolamine-dependent effects on steady-state membrane phospholipid composition in Saccharomyces cerevisiae. J Bacteriol. 1994 Nov;176(22):6861–6868. doi: 10.1128/jb.176.22.6861-6868.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McMaster C. R., Bell R. M. CDP-choline:1,2-diacylglycerol cholinephosphotransferase. Biochim Biophys Acta. 1997 Sep 4;1348(1-2):100–110. doi: 10.1016/s0005-2760(97)00097-0. [DOI] [PubMed] [Google Scholar]
- McMaster C. R., Bell R. M. Phosphatidylcholine biosynthesis in Saccharomyces cerevisiae. Regulatory insights from studies employing null and chimeric sn-1,2-diacylglycerol choline- and ethanolaminephosphotransferases. J Biol Chem. 1994 Nov 11;269(45):28010–28016. [PubMed] [Google Scholar]
- McMaster C. R., Morash S. C., Bell R. M. Phospholipid and cation activation of chimaeric choline/ethanolamine phosphotransferases. Biochem J. 1996 Feb 1;313(Pt 3):729–735. doi: 10.1042/bj3130729. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mumberg D., Müller R., Funk M. Yeast vectors for the controlled expression of heterologous proteins in different genetic backgrounds. Gene. 1995 Apr 14;156(1):119–122. doi: 10.1016/0378-1119(95)00037-7. [DOI] [PubMed] [Google Scholar]
- O K. M., Choy P. C. Effects of fasting on phosphatidylcholine biosynthesis in hamster liver: regulation of cholinephosphotransferase activity by endogenous argininosuccinate. Biochem J. 1993 Feb 1;289(Pt 3):727–733. doi: 10.1042/bj2890727. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O K. M., Siow Y. L., Choy P. C. Hamster liver cholinephosphotransferase and ethanolaminephosphotransferase are separate enzymes. Biochem Cell Biol. 1989 Oct;67(10):680–686. doi: 10.1139/o89-102. [DOI] [PubMed] [Google Scholar]
- Polokoff M. A., Wing D. C., Raetz C. R. Isolation of somatic cell mutants defective in the biosynthesis of phosphatidylethanolamine. J Biol Chem. 1981 Aug 10;256(15):7687–7690. [PubMed] [Google Scholar]
- Preiss J., Loomis C. R., Bishop W. R., Stein R., Niedel J. E., Bell R. M. Quantitative measurement of sn-1,2-diacylglycerols present in platelets, hepatocytes, and ras- and sis-transformed normal rat kidney cells. J Biol Chem. 1986 Jul 5;261(19):8597–8600. [PubMed] [Google Scholar]
- Roberts S. G., Green M. R. Activator-induced conformational change in general transcription factor TFIIB. Nature. 1994 Oct 20;371(6499):717–720. doi: 10.1038/371717a0. [DOI] [PubMed] [Google Scholar]
- Rost B., Sander C. Improved prediction of protein secondary structure by use of sequence profiles and neural networks. Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7558–7562. doi: 10.1073/pnas.90.16.7558. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ruetz S., Gros P. Phosphatidylcholine translocase: a physiological role for the mdr2 gene. Cell. 1994 Jul 1;77(7):1071–1081. doi: 10.1016/0092-8674(94)90446-4. [DOI] [PubMed] [Google Scholar]
- Samborski R. W., Ridgway N. D., Vance D. E. Evidence that only newly made phosphatidylethanolamine is methylated to phosphatidylcholine and that phosphatidylethanolamine is not significantly deacylated-reacylated in rat hepatocytes. J Biol Chem. 1990 Oct 25;265(30):18322–18329. [PubMed] [Google Scholar]
- Snyder F. CDP-choline:alkylacetylglycerol cholinephosphotransferase catalyzes the final step in the de novo synthesis of platelet-activating factor. Biochim Biophys Acta. 1997 Sep 4;1348(1-2):111–116. doi: 10.1016/s0005-2760(97)00109-4. [DOI] [PubMed] [Google Scholar]
- Steinberg D. Low density lipoprotein oxidation and its pathobiological significance. J Biol Chem. 1997 Aug 22;272(34):20963–20966. doi: 10.1074/jbc.272.34.20963. [DOI] [PubMed] [Google Scholar]
- Tijburg L. B., Houweling M., Geelen M. J., Van Golde L. M. Inhibition of phosphatidylethanolamine synthesis by glucagon in isolated rat hepatocytes. Biochem J. 1989 Feb 1;257(3):645–650. doi: 10.1042/bj2570645. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tronchère H., Record M., Tercé F., Chap H. Phosphatidylcholine cycle and regulation of phosphatidylcholine biosynthesis by enzyme translocation. Biochim Biophys Acta. 1994 May 13;1212(2):137–151. doi: 10.1016/0005-2760(94)90248-8. [DOI] [PubMed] [Google Scholar]
- Venable M. E., Zimmerman G. A., McIntyre T. M., Prescott S. M. Platelet-activating factor: a phospholipid autacoid with diverse actions. J Lipid Res. 1993 May;34(5):691–702. [PubMed] [Google Scholar]
- WEISS S. B., SMITH S. W., KENNEDY E. P. The enzymatic formation of lecithin from cytidine diphosphate choline and D-1,2-diglyceride. J Biol Chem. 1958 Mar;231(1):53–64. [PubMed] [Google Scholar]
- Williams J. G., McMaster C. R. Scanning alanine mutagenesis of the CDP-alcohol phosphotransferase motif of Saccharomyces cerevisiae cholinephosphotransferase. J Biol Chem. 1998 May 29;273(22):13482–13487. doi: 10.1074/jbc.273.22.13482. [DOI] [PubMed] [Google Scholar]
- Yang T. T., Kain S. R. Fast hybridization solution for the detection of immobilized nucleic acids. Biotechniques. 1995 Mar;18(3):498–503. [PubMed] [Google Scholar]