Intra-ER sorting of the peroxisomal membrane protein Pex3 relies on its luminal domain
| Autor: | Ewald H. Hettema, Peter J. M. Drake, Alison M. Motley, Mohammad H. Fakieh, Joanne Lacey, Joanne M. Munck |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2013 |
| Předmět: |
Peroxisomal ER
QH301-705.5 Science Intra-ER sorting Peroxin Biology Peroxisome Bioinformatics Transport Pathway General Biochemistry Genetics and Molecular Biology 03 medical and health sciences 0302 clinical medicine Biology (General) 030304 developmental biology 0303 health sciences Wild type Fusion protein Transmembrane protein Pex3 Cell biology Transmembrane domain Cytoplasm General Agricultural and Biological Sciences 030217 neurology & neurosurgery Research Article |
| Zdroj: | Biology Open, Vol 2, Iss 8, Pp 829-837 (2013) Biology Open |
| ISSN: | 2046-6390 |
| Popis: | Summary Pex3 is an evolutionarily conserved type III peroxisomal membrane protein required for peroxisome formation. It is inserted into the ER membrane and sorted via an ER subdomain (the peroxisomal ER, or pER) to peroxisomes. By constructing chimeras between Pex3 and the type III ER membrane protein Sec66, we have been able to separate the signals that mediate insertion of Pex3 into the ER from those that mediate sorting within the ER to the pER subdomain. The N-terminal 17-amino acid segment of Pex3 contains two signals that are each sufficient for sorting to the pER: a chimeric protein containing the N-terminal domain of Pex3 fused to the transmembrane and cytoplasmic segments of Sec66 sorts to the pER in wild type cells, and does not colocalise with peroxisomes. Subsequent transport to existing peroxisomes requires the Pex3 transmembrane segment. When expressed in Drosophila S2R+ cells, ScPex3 targeting to peroxisomes is dependent on the intra-ER sorting signals in the N-terminal segment. The N-terminal segments of both human and Drosophila Pex3 contain intra-ER sorting information and can replace that of ScPex3. Our analysis has uncovered the signals within Pex3 required for the various steps of its transport to peroxisomes. Our generation of versions of Pex3 that are blocked at each stage along its transport pathway provides a tool to dissect the mechanism, as well as the molecular machinery required at each step of the pathway. |
| Databáze: | OpenAIRE |
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