Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10871071 | FEBS Letters | 2013 | 7 Pages |
Abstract
Sdh3/Shh3, a subunit of mitochondrial succinate dehydrogenase, contains transmembrane domains with a hydrophobicity comparable to that of endoplasmic reticulum (ER) proteins. Here, we show that a C-terminal reporter fusion to Sdh3/Shh3 results in partial mis-targeting of the protein to the ER. This mis-targeting is mediated by the signal recognition particle (SRP) and depends on the length of the C-terminal tail. These results imply that if nuclear-encoded mitochondrial proteins contain strongly hydrophobic transmembrane domains and a long C-terminal tail, they have the potential to be recognized by SRP and mis-targeted to the ER.
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Authors
Johannes H. Reithinger, Chewon Yim, Kwangjin Park, Patrik Björkholm, Gunnar von Heijne, Hyun Kim,