Abstract

BackgroundThe only hitherto known biological role of yeast Saccharomyces cerevisiae Tum1 protein is in the tRNA thiolation pathway. The mammalian homologue of the yeast TUM1 gene, the thiosulfate sulfurtransferase (a.k.a. rhodanese) Tst, has been proposed as an obesity-resistance and antidiabetic gene. To assess the role of Tum1 in cell metabolism and the putative functional connection between lipid metabolism and tRNA modification, we analysed evolutionary conservation of the rhodanese protein superfamily, investigated the role of Tum1 in lipid metabolism, and examined the phenotype of yeast strains expressing the mouse homologue of Tum1, TST.ResultsWe analysed evolutionary relationships in the rhodanese superfamily and established that its members are widespread in bacteria, archaea and in all major eukaryotic groups. We found that the amount of sterol esters was significantly higher in the deletion strain tum1Δ than in the wild-type strain. Expression of the mouse TST protein in the deletion strain did not rescue this phenotype. Moreover, although Tum1 deficiency in the thiolation pathway was complemented by re-introducing TUM1, it was not complemented by the introduction of the mouse homologue Tst. We further showed that the tRNA thiolation pathway is not involved in the regulation of sterol ester content in S. cerevisiae, as overexpression of the tEUUC, tKUUU and tQUUG tRNAs did not rescue the lipid phenotype in the tum1Δ deletion strain, and, additionally, deletion of the key gene for the tRNA thiolation pathway, UBA4, did not affect sterol ester content.ConclusionsThe rhodanese superfamily of proteins is widespread in all organisms, and yeast TUM1 is a bona fide orthologue of mammalian Tst thiosulfate sulfurtransferase gene. However, the mouse TST protein cannot functionally replace yeast Tum1 protein, neither in its lipid metabolism-related function, nor in the tRNA thiolation pathway. We show here that Tum1 protein is involved in lipid metabolism by decreasing the sterol ester content in yeast cells, and that this function of Tum1 is not exerted through the tRNA thiolation pathway, but through another, currently unknown pathway.

Highlights

  • The only hitherto known biological role of yeast Saccharomyces cerevisiae Tum1 protein is in the tRNA thiolation pathway

  • In this study we examined the molecular role of the yeast Tum1 protein which has been previously described only as a protein with a non-essential function in the tRNA wobble uridine modification pathway [9, 10]

  • Effect of Tum1 on the lipid content in S. cerevisiae we investigated the involvement of TUM1 in lipid metabolism of S. cerevisiae

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Summary

Introduction

The only hitherto known biological role of yeast Saccharomyces cerevisiae Tum protein is in the tRNA thiolation pathway. In this study we examined the molecular role of the yeast Tum protein which has been previously described only as a protein with a non-essential function in the tRNA wobble uridine modification pathway [9, 10]. This pathway consists of Uba, Ncs, Ncs and Nfs proteins and is required for the thiolation of three tRNA molecules, specific for glutamine (tQUUG), lysine (tKUUU), and glutamic acid (tEUUC) tRNAs, which contain 2-thiouridine derivate as the wobble nucleoside [11]. We analysed evolutionary conservation of the rhodanese protein superfamily, investigated the role of Tum in lipid metabolism, and examined the putative functional connection between lipid metabolism and tRNA modification processes

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