Abstract

The human genome encodes 53 members of the solute carrier family 25 (SLC25), also called the mitochondrial carrier family, many of which have been shown to transport inorganic anions, amino acids, carboxylates, nucleotides, and coenzymes across the inner mitochondrial membrane, thereby connecting cytosolic and matrix functions. Here two members of this family, SLC25A33 and SLC25A36, have been thoroughly characterized biochemically. These proteins were overexpressed in bacteria and reconstituted in phospholipid vesicles. Their transport properties and kinetic parameters demonstrate that SLC25A33 transports uracil, thymine, and cytosine (deoxy)nucleoside di- and triphosphates by an antiport mechanism and SLC25A36 cytosine and uracil (deoxy)nucleoside mono-, di-, and triphosphates by uniport and antiport. Both carriers also transported guanine but not adenine (deoxy)nucleotides. Transport catalyzed by both carriers was saturable and inhibited by mercurial compounds and other inhibitors of mitochondrial carriers to various degrees. In confirmation of their identity (i) SLC25A33 and SLC25A36 were found to be targeted to mitochondria and (ii) the phenotypes of Saccharomyces cerevisiae cells lacking RIM2, the gene encoding the well characterized yeast mitochondrial pyrimidine nucleotide carrier, were overcome by expressing SLC25A33 or SLC25A36 in these cells. The main physiological role of SLC25A33 and SLC25A36 is to import/export pyrimidine nucleotides into and from mitochondria, i.e. to accomplish transport steps essential for mitochondrial DNA and RNA synthesis and breakdown.

Highlights

  • SLC25A33 and SLC25A36 are two human uncharacterized proteins encoded by the mitochondrial carrier solute carrier family 25 (SLC25) genes

  • Chinese hamster ovary (CHO) cells were transfected with the pcDNA3-SLC25A36-enhanced green fluorescent protein (EGFP) plasmid, and images were acquired 40 – 45 h after transfection. ϳ35% of cells were transfected, and green fluorescence revealed typical mitochondrial localization of SLC25A36 (Fig. 1)

  • The recombinant proteins were not detected in bacteria harvested immediately before induction of expression (Fig. 2, lane 2, for SLC25A33) nor in cells harvested after induction but lacking the coding sequence in the expression vector (Fig. 2, lane 3 for SLC25A33 and lane 6 for SLC25A36)

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Summary

Introduction

SLC25A33 and SLC25A36 are two human uncharacterized proteins encoded by the mitochondrial carrier SLC25 genes. Two members of this family, SLC25A33 and SLC25A36, have been thoroughly characterized biochemically These proteins were overexpressed in bacteria and reconstituted in phospholipid vesicles. Their transport properties and kinetic parameters demonstrate that SLC25A33 transports uracil, thymine, and cytosine (deoxy)nucleoside diand triphosphates by an antiport mechanism and SLC25A36 cytosine and uracil (deoxy)nucleoside mono-, di-, and triphosphates by uniport and antiport. Both carriers transported guanine but not adenine (deoxy)nucleotides. The main physiological role of SLC25A33 and SLC25A36 is to import/export

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