1. Academic Validation
  2. The human mitochondrial Mrs2 protein functionally substitutes for its yeast homologue, a candidate magnesium transporter

The human mitochondrial Mrs2 protein functionally substitutes for its yeast homologue, a candidate magnesium transporter

  • Genomics. 2001 Mar 1;72(2):158-68. doi: 10.1006/geno.2000.6407.
G Zsurka 1 J Gregán R J Schweyen
Affiliations

Affiliation

  • 1 Vienna Biocenter, Department of Microbiology and Genetics, University of Vienna, Dr. Bohrgasse 9, Vienna, A-1030, Austria.
Abstract

We report here on the human MRS2 gene that encodes a protein, hsaMrs2p, the first molecularly characterized candidate for a magnesium transporter in metazoa. The protein, like the yeast mitochondrial Mrs2 and Lpe10 proteins, contains two predicted transmembrane domains in its carboxyl-terminus, the first of which terminates with the conserved motif F/Y-G-M-N. These are typical features of the CorA family of magnesium transporters. Expression of hsaMrs2p in mrs2-1 knock-out mutant yeast partly restores mitochondrial magnesium concentrations that are significantly reduced in this mutant. It also alleviates other defects of this mutant, which may be secondary to the reduction in magnesium concentrations. These findings suggest that hsaMrs2p and yMrs2p are functional homologues. Like its yeast homologues, hsaMrs2p has been localized in mitochondria. The hsaMRS2 gene is located on chromosome 6 (6p22.1-p22.3) and is composed of 11 exons. A low level of the transcript is detected in various mouse tissues.

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