PLoS Genetics (Jan 2012)

CED-10/Rac1 regulates endocytic recycling through the RAB-5 GAP TBC-2.

  • Lin Sun,
  • Ou Liu,
  • Jigar Desai,
  • Farhad Karbassi,
  • Marc-André Sylvain,
  • Anbing Shi,
  • Zheng Zhou,
  • Christian E Rocheleau,
  • Barth D Grant

DOI
https://doi.org/10.1371/journal.pgen.1002785
Journal volume & issue
Vol. 8, no. 7
p. e1002785

Abstract

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Rac1 is a founding member of the Rho-GTPase family and a key regulator of membrane remodeling. In the context of apoptotic cell corpse engulfment, CED-10/Rac1 acts with its bipartite guanine nucleotide exchange factor, CED-5/Dock180-CED-12/ELMO, in an evolutionarily conserved pathway to promote phagocytosis. Here we show that in the context of the Caenorhabditis elegans intestinal epithelium CED-10/Rac1, CED-5/Dock180, and CED-12/ELMO promote basolateral recycling. Furthermore, we show that CED-10 binds to the RAB-5 GTPase activating protein TBC-2, that CED-10 contributes to recruitment of TBC-2 to endosomes, and that recycling cargo is trapped in recycling endosomes in ced-12, ced-10, and tbc-2 mutants. Expression of GTPase defective RAB-5(Q78L) also traps recycling cargo. Our results indicate that down-regulation of early endosome regulator RAB-5/Rab5 by a CED-5, CED-12, CED-10, TBC-2 cascade is an important step in the transport of cargo through the basolateral recycling endosome for delivery to the plasma membrane.