Abstract

Signal-anchored proteins are a class of mitochondrial outer membrane proteins that expose a hydrophilic domain to the cytosol and are anchored to the membrane by a single transmembrane domain in the N-terminal region. Like the vast majority of mitochondrial proteins, signal-anchored proteins are synthesized on cytosolic ribosomes and are subsequently imported into the organelle. We have studied the mechanisms by which precursors of these proteins are recognized by the mitochondria and are inserted into the outer membrane. The import of signal-anchored proteins was found to be independent of the known import receptors, Tom20 and Tom70, but to require the major Tom component, Tom40. In contrast to precursors destined to internal compartments of mitochondria and those of outer membrane beta-barrel proteins, precursors of signal-anchored proteins appear not to be inserted via the general import pore. Taken together, we propose a novel pathway for insertion of these proteins into the outer membrane of mitochondria.

Highlights

  • The mitochondrial outer membrane mediates numerous interactions between the metabolic and genetic systems of mitochondria and the rest of the eukaryotic cell

  • Like the vast majority of mitochondrial proteins, signalanchored proteins are synthesized on cytosolic ribosomes and are subsequently imported into the organelle

  • Is the TOM complex involved at all in the import of signalanchored proteins? We investigated the insertion of Tom20ext into mitochondria isolated from a strain harboring the temperature-sensitive allele of tom40

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Summary

Introduction

The mitochondrial outer membrane mediates numerous interactions between the metabolic and genetic systems of mitochondria and the rest of the eukaryotic cell. We have studied the mechanisms by which precursors of these proteins are recognized by the mitochondria and are inserted into the outer membrane. In contrast to precursors destined to internal compartments of mitochondria and those of outer membrane ␤-barrel proteins, precursors of signal-anchored proteins appear not to be inserted via the general import pore.

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