Abstract
Translocation of proteins across membranes of the endoplasmic reticulum, mitochondrion, and chloroplast has been shown to be mediated by targeting signals present in the transported proteins. To test whether the transport of proteins into peroxisomes is also mediated by a peptide targeting signal, we have studied the firefly luciferase gene that encodes a protein transported to peroxisomes in both insect and mammalian cells. We have identified two regions of luciferase which are necessary for transport of this protein into peroxisomes. We demonstrate that one of these, region II, represents a peroxisomal targeting signal because it is both necessary and sufficient for directing cytosolic proteins to peroxisomes. The signal is no more than twelve amino acids long and is located at the extreme carboxy-terminus of luciferase. The location of the targeting signal for translocation across the peroxisomal membrane therefore differs from the predominantly amino-terminal location of signals responsible for transport across the membranes of the endoplasmic reticulum, chloroplast, or mitochondrion.
MeSH Terms
Acetyltransferases/metabolism
Biological Transport
Cell Compartmentation
Chloramphenicol O-Acetyltransferase
Cloning, Molecular
DNA Mutational Analysis
Luciferases/metabolism
Microbodies/metabolism
Recombinant Fusion Proteins/metabolism
Structure-Activity Relationship
Tetrahydrofolate Dehydrogenase/metabolism
Chemicals
Recombinant Fusion Proteins
Luciferases
Tetrahydrofolate Dehydrogenase
Acetyltransferases
Chloramphenicol O-Acetyltransferase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Gould S G
Department of Biology, University of California, San Diego, La Jolla 92093.
Keller G A
Subramani S
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