4.7 Article

Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and TRC40-independent class I pathway

Journal

JOURNAL OF CELL BIOLOGY
Volume 200, Issue 5, Pages 651-666

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201211077

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Funding

  1. Core Research for Evolutional Science and Technology grant from the Science and Technology Agency of Japan
  2. Global Center of Excellence Program
  3. Grants for Excellent Graduate Schools from the Ministry of Education, Culture, Sports, Science and Technology of Japan
  4. Japan Foundation for Applied Enzymology
  5. Takeda Science Foundation
  6. [19058011]
  7. [20370039]
  8. [24247038]

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Tail-anchored (TA) proteins are anchored into cellular membranes by a single transmembrane domain (TMD) close to the C terminus. Although the targeting of TA proteins to peroxisomes is dependent on PEX19, the mechanistic details of PEX19-dependent targeting and the signal that directs TA proteins to peroxisomes have remained elusive, particularly in mammals. The present study shows that PEX19 formed a complex with the peroxisomal TA protein PEX26 in the cytosol and translocated it directly to peroxisomes by interacting with the peroxisomal membrane protein PEX3. Unlike in yeast, the adenosine triphosphatase TRC40, which delivers TA proteins to the endoplasmic reticulum, was dispensable for the peroxisomal targeting of PEX26. Moreover, the basic amino acids within the luminal domain of PEX26 were essential for binding to PEX19 and thereby for peroxisomal targeting. Finally, our results suggest that a TMD that escapes capture by TRC40 and is followed by a highly basic luminal domain directs TA proteins to peroxisomes via the PEX19-dependent route.

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