Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 Oct 18:4:297.
doi: 10.3389/fphys.2013.00297.

Dual targeting of peroxisomal proteins

Affiliations
Review

Dual targeting of peroxisomal proteins

Julia Ast et al. Front Physiol. .

Abstract

Cellular compartmentalization into organelles serves to separate biological processes within the environment of a single cell. While some metabolic reactions are specific to a single organelle, others occur in more than one cellular compartment. Specific targeting of proteins to compartments inside of eukaryotic cells is mediated by defined sequence motifs. To achieve multiple targeting to different compartments cells use a variety of strategies. Here, we focus on mechanisms leading to dual targeting of peroxisomal proteins. In many instances, isoforms of peroxisomal proteins with distinct intracellular localization are encoded by separate genes. But also single genes can give rise to differentially localized proteins. Different isoforms can be generated by use of alternative transcriptional start sites, by differential splicing or ribosomal read-through of stop codons. In all these cases different peptide variants are produced, of which only one carries a peroxisomal targeting signal. Alternatively, peroxisomal proteins contain additional signals that compete for intracellular targeting. Dual localization of proteins residing in both the cytoplasm and in peroxisomes may also result from use of inefficient targeting signals. The recent observation that some bona fide cytoplasmic enzymes were also found in peroxisomes indicates that dual targeting of proteins to both the cytoplasm and the peroxisome might be more widespread. Although current knowledge of proteins exhibiting only partial peroxisomal targeting is far from being complete, we speculate that the metabolic capacity of peroxisomes might be larger than previously assumed.

Keywords: alternative splicing; glycolysis; peroxisomes; protein import; ribosomal read-through.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Schematic overview on the diversity of mechanism leading to dual targeting of peroxisomal proteins. Peroxisomal targeting signals are indicated in pink, while mitochondrial signal sequences are indicated in yellow. For further explanations see text.

References

    1. Antonenkov V. D. (1989). Dehydrogenases of the pentose phosphate pathway in rat liver peroxisomes. Eur. J. Biochem. 183, 75–82 10.1111/j.1432-1033.1989.tb14898.x - DOI - PubMed
    1. Antonenkov V. D., Sormunen R. T., Hiltunen J. K. (2004). The rat liver peroxisomal membrane forms a permeability barrier for cofactors but not for small metabolites in vitro. J. Cell. Sci. 117, 5633–5642 10.1242/jcs.01485 - DOI - PubMed
    1. Arand M., Knehr M., Thomas H., Zeller H. D., Oesch F. (1991). An impaired peroxisomal targeting sequence leading to an unusual bicompartmental distribution of cytosolic epoxide hydrolase. FEBS Lett. 294, 19–22 10.1016/0014-5793(91)81333-4 - DOI - PubMed
    1. Ashmarina L. I., Pshezhetsky A. V., Branda S. S., Isaya G., Mitchell G. A. (1999). 3-Hydroxy-3-methylglutaryl coenzyme A lyase: targeting and processing in peroxisomes and mitochondria. J. Lipid Res. 40, 70–75 - PubMed
    1. Bakker B. M., Overkamp K. M., van Maris A. J., Kotter P., Luttik M. A., van Dijken J. P., et al. (2001). Stoichiometry and compartmentation of NADH metabolism in Saccharomyces cerevisiae. FEMS Microbiol. Rev. 25, 15–37 10.1111/j.1574-6976.2001.tb00570.x - DOI - PubMed

LinkOut - more resources