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Mol Biol Cell. 2016 Sep 14. pii: mbc.E16-02-0116. [Epub ahead of print]

Syndapin/SDPN-1 is required for endocytic recycling and endosomal actin association in the C. elegans intestine.

Author information

1
Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854.
2
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461.
3
Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854 grant@biology.rutgers.edu.

Abstract

Syndapin/Pascin family F-BAR domain proteins bind directly to membrane lipids and are associated with actin dynamics at the plasma membrane. Previous reports have also implicated mammalian syndapin 2 in endosome function during receptor recycling, but precise analysis of a putative recycling function for syndapin in mammalian systems is difficult because of syndapin effects on the earlier step of endocytic uptake, and potential redundancy among the three separate genes that encode mammalian syndapin isoforms. Here we analyze the endocytic transport function of the only C. elegans syndapin, SDPN-1. We find that SDPN-1 is a resident protein of the early and basolateral recycling endosomes in the C. elegans intestinal epithelium, and sdpn-1 deletion mutants display phenotypes indicating a block in basolateral recycling transport. sdpn-1 mutants accumulate abnormal endosomes positive for early endosome and recycling endosome markers that are normally separate, and such endosomes accumulate high levels of basolateral recycling cargo. Furthermore, we observed strong colocalization of endosomal SDPN-1 with the F-actin biosensor Lifeact, and found that loss of SDPN-1 greatly reduced Lifeact accumulation on early endosomes. Taken together our results provide strong evidence for an in vivo function of syndapin in endocytic recycling, and suggest that syndapin promotes transport via endosomal fission.

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