A novel Drosophila mitochondrial carrier protein acts as a Mg(2+) exporter in fine-tuning mitochondrial Mg(2+) homeostasis

Biochim Biophys Acta. 2016 Jan;1863(1):30-9. doi: 10.1016/j.bbamcr.2015.10.004. Epub 2015 Oct 14.

Abstract

The homeostasis of magnesium (Mg(2+)), an abundant divalent cation indispensable for many biological processes including mitochondrial functions, is underexplored. In yeast, the mitochondrial Mg(2+) homeostasis is accurately controlled through the combined effects of importers, Mrs2 and Lpe10, and an exporter, Mme1. However, little is known about this Mg(2+) homeostatic process in multicellular organisms. Here, we identified the first mitochondrial Mg(2+) transporter in Drosophila, the orthologue of yeast Mme1, dMme1, by homologous comparison and functional complementation. dMme1 can mediate the exportation of mitochondrial Mg(2+) when heterologously expressed in yeast. Altering the expression of dMme1, although only resulting in about a 10% change in mitochondrial Mg(2+) levels in either direction, led to a significant survival reduction in Drosophila. Furthermore, the reduced survival resulting from dMme1 expression changes could be completely rescued by feeding the dMME1-RNAi flies Mg(2+)-restricted food or the dMME1-over-expressing flies the Mg(2+)-supplemented diet. Our studies therefore identified the first Drosophila mitochondrial Mg(2+) exporter, which is involved in the precise control of mitochondrial Mg(2+) homeostasis to ensure an optimal state for survival.

Keywords: CG3476; Drosophila melanogaster; Mitochondrial Mg(2+) exporter; Mme1; Yeast; dMME1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cation Transport Proteins* / genetics
  • Cation Transport Proteins* / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster
  • Homeostasis / physiology*
  • Ion Transport / physiology
  • Magnesium / metabolism*
  • Mitochondria* / genetics
  • Mitochondria* / metabolism
  • Mitochondrial Proteins* / genetics
  • Mitochondrial Proteins* / metabolism

Substances

  • Cation Transport Proteins
  • Drosophila Proteins
  • Mitochondrial Proteins
  • Magnesium