Abstract

In the vertebrate retina, a number of proteins involved in signal transduction are known to be N-terminal acylated with the unusual 14 carbon fatty acids 14:1n-9 and 14:2n-6. We have explored possible pathways for producing these fatty acids in the frog retina by incubation in vitro with candidate precursor fatty acids bearing radiolabels, including [3H]14:0, [3H]18:1n-9, [3H]18:2n-6, and [3H]18:3n-3. Rod outer segments were prepared from the radiolabeled retinas for analysis of protein-linked fatty acids, and total lipids were extracted from the remaining retinal pellet. Following saponification of extracted lipids, fatty acid phenacyl esters were prepared and analyzed by high pressure liquid chromatography (HPLC) with detection by continuous scintillation counting. Transducin, whose alpha-subunit (Gt alpha) is known to bear N-terminal acyl chains, was extracted from the rod outer segments and subjected to SDS-polyacrylamide gel electrophoresis and fluorography to detect radiolabeled proteins. Gt alpha was also subjected to methanolysis, and the resulting fatty acyl methyl esters were analyzed by HPLC. The identities of HPLC peaks coinciding with unsaturated species of both phenacyl esters and methyl esters were confirmed by reanalyzing them after catalytic hydrogenation. The results showed that 14:1n-9 can be derived in the retina from 18:1n-9 and 14:2n-6 from 18:2n-6, most likely by two rounds of beta-oxidation, but that neither is produced in detectable amounts from 14:0. Retroconversion of unsaturated 18 carbon fatty acids to the corresponding 14 carbon species showed specificity, in that 18:3n-3 was not converted to 14 carbon fatty acids in detectable amounts. Myristic acid (14:0), 14:1n-9, and 14:2n-6 were all incorporated into Gt alpha. A much less efficient incorporation of 18:1n-9 into Gt alpha was also observed, but no radiolabeling of Gt alpha was observed in retinas incubated with 18:3n-3. Thus, retroconversion by limited beta-oxidation of longer chain unsaturated fatty acids appears to be the most likely metabolic source of the unusual fatty acids found on the N termini of signal transducing proteins in the retina.

Highlights

  • The work presented in this paper is based on platform presentations given by James C

  • We describe here experiments designed to determine if retroconversion pathways can produce 14:1n-9 and 14:2n-6 in the frog retina and if they are used for N-terminal fatty acylation of Gt␣

  • Incubation with [9,10-3H]14:0—high pressure liquid chromatography (HPLC) of FAPEs derived from the total retinal lipid pool after incubation with [3H]14:0 (Fig. 1A) revealed only chain elongation to [3H]16:0 (ϳ11% of [3H]14:0) and [3H]18:0 (ϳ7%)

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Summary

The abbreviations used are

Gt␣, transducin ␣-subunit; FAME, fatty acid methyl ester; FAPE, fatty acid phenacyl ester; Gt␤, transducin ␤-subunit; Gt␥, transducin ␥-subunit; HPLC, high pressure liquid chromatography; PAGE, polyacrylamide gel electrophoresis; ROS, rod outer segments; GTP␥S, guanosine 5Ј-3-O-(thio)triphosphate. It has been hypothesized that 14:2n-6 is generated within the photoreceptor cell in this manner (Hansen, 1993; Wang and Anderson, 1993) Such partial ␤-oxidation is characteristic of peroxisomal metabolism in contrast to mitochondrial ␤-oxidation, which favors complete degradation to acetyl-CoA (Schulz, 1991). Retroconversion pathways of this kind have been demonstrated to convert 13-hydroxy-9,11-octadecadienoic acid (13-OH, 18:2n-6) to. We describe here experiments designed to determine if retroconversion pathways can produce 14:1n-9 and 14:2n-6 in the frog retina and if they are used for N-terminal fatty acylation of Gt␣

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