CYTIDINE DIPHOSPHATE DIACYLGLYCEROL
STRUCTURE, OCCURRENCE AND BIOCHEMISTRY
Nucleotides are the basic building blocks of DNA and RNA, and they are required for many aspects of intermediary metabolism. They consist of three elements – a heterocyclic nitrogenous base derived from purine (adenine and guanine) or pyrimidine (uracil, thymine and cytosine), a pentose (ribose or deoxyribose) and a molecule of phosphoric acid. From the standpoint of lipid metabolism, one of the most important of these is cytidine 5’-phosphoric acid, which is a key component of the phospholipid cytidine diphosphate diacylglycerol (CDP-diacylglycerol), a liponucleotide.

Cytidine diphosphate diacylglycerol per se is rarely noticed in analyses of lipid compositions of tissues, as it is present is such small amounts, perhaps only 0.05% or so of the total phospholipids. Indeed, the composition of the fatty acids or molecular species in this lipid in nature (as opposed to experiments in vitro) has hardly ever been reported. Data for ox brain are listed in Table 1. In this instance, the composition is closer to that of phosphatidylinositol than of any other lipid.
Table 1. Fatty acid compositions of positions sn-1 and sn-2 of cytidine diphosphate diacylglycerol of bovine brain. |
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| Fatty acids | |||||||
|---|---|---|---|---|---|---|---|
| 16:0 | 18:0 | 18:1 | 18:2 | 20:4 | 22:3 | 22:6 | |
| sn-1 | 15 | 78 | 6 | ||||
| sn-2 | 4 | 10 | 35 | 3 | 45 | 3 | 1 |
| Thompson, W. and MacDonald, G. Eur. J. Biochem., 65, 107-111 (1976). | |||||||
This lipid was first found in eukaryotic organisms, but it is now known to be ubiquitous and plays an even more important role in the biochemistry of prokaryotes.
Biosynthesis of CDP-diacylglycerol involves condensation of phosphatidic acid and cytidine triphosphate, with elimination of pyrophosphate, catalysed by an enzyme CDP-diacylglycerol synthase. This is found in all mammalian tissues, for example, but is especially active in liver and brain. The resulting CDP-diacylglycerol is utilized immediately for the synthesis of phosphatidylglycerol, and thence cardiolipin, and of phosphatidylinositol (see the appropriate web pages for these lipids for further discussion). In prokaryotes, CDP-diacylglycerol is the precursor for phosphatidylserine. CDP-diacylglycerol for phosphatidylinositol synthesis is produced in the endoplasmic reticulum, whereas that for phosphatidylglycerol production is produced in the mitochondria. However, some transfer of the liponucleotide between organelles may be possible.

It is not known whether the final fatty acid composition of the lipid is a result of the specificity of the CDP-diacylglycerol synthase in selecting particular molecular species of phosphatidic acid, or whether remodelling occurs via deacylation/re-acylation reactions. While CTP containing deoxyribose is a good substrate for the enzyme in vitro, it does not appear to be utilized in vivo.
Most studies of CDP-diacylglycerol have been concerned with its function as an intermediate in the biosynthesis of other lipids, and as such it is the first step in a pathway that is very different from that for phosphatidylcholine and phosphatidylethanolamine. These also require nucleotides for their biosynthesis, but do not form liponucleotides as intermediates. Similarly, another nucleotide uridine 5-diphosphate(UDP)-hexose (where hexose = glucose, galactose, etc) is required for the formation of glycolipids, including both the glycosyldiacylglycerols and sphingoglycolipids.
It is not known whether CDP-diacylglycerol has any biological functions other than as an intermediate, although anti-cancer activities in vitro have been reported.
Because it is such a minor component of tissues, isolation of cytidine diphosphate diacylglycerol appears to be a tedious task, involving ion-exchange column chromatography and thin-layer chromatography. The pyrophosphate bond is relatively labile and is very susceptible to alkaline hydrolysis. It remains to be seen whether modern mass spectrometric methods will make an impact.
Recommended Reading
- Heacock, A.M. and Agranoff, B.W. CDP-diacylglycerol synthase from mammalian tissues. Biochim. Biophys. Acta, 1348, 166-172 (1997).
- Vance, D.E. and Vance, J. (editors) Biochemistry of Lipids, Lipoproteins and Membranes. 4th Edition. (Elsevier, Amsterdam) (2002) – several chapters.
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Updated: 23/4/2007 |
Scottish Crop Research Institute (and MRS Lipid Analysis Unit), Invergowrie, Dundee (DD2 5DA), Scotland
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