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Distinct roles of the two VPS33 proteins in the endolysosomal system in Caenorhabditis elegans
Author(s) -
GengyoAndo Keiko,
KageNakadai Eriko,
Yoshina Sawako,
Otori Muneyoshi,
KagawaNagamura Yuko,
Nakai Junichi,
Mitani Shohei
Publication year - 2016
Publication title -
traffic
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.677
H-Index - 130
eISSN - 1600-0854
pISSN - 1398-9219
DOI - 10.1111/tra.12430
Subject(s) - caenorhabditis elegans , biology , microbiology and biotechnology , caenorhabditis , computational biology , genetics , gene
Sec1/Munc‐18 ( SM ) family proteins are essential regulators in intracellular transport in eukaryotic cells. The SM protein Vps33 functions as a core subunit of two tethering complexes, class C core vacuole/endosome tethering (CORVET) and homotypic fusion and vacuole protein sorting (HOPS) in the endocytic pathway in yeast. Metazoan cells possess two Vps33 proteins, VPS33A and VPS33B , but their precise roles remain unknown. Here, we present a comparative analysis of Caenorhabditis elegans null mutants for these proteins. We found that the vps‐33.1 ( VPS33A ) mutants exhibited severe defects in both endocytic function and endolysosomal biogenesis in scavenger cells. Furthermore, vps‐33.1 mutations caused endocytosis defects in other tissues, and the loss of maternal and zygotic VPS ‐33.1 resulted in embryonic lethality. By contrast, vps‐33.2 mutants were viable but sterile, with terminally arrested spermatocytes. The spermatogenesis phenotype suggests that VPS33 .2 is involved in the formation of a sperm‐specific organelle. The endocytosis defect in the vps‐33.1 mutant was not restored by the expression of VPS ‐33.2, which indicates that these proteins have nonredundant functions. Together, our data suggest that VPS ‐33.1 shares most of the general functions of yeast Vps33 in terms of tethering complexes in the endolysosomal system, whereas VPS ‐33.2 has tissue/organelle specific functions in C. elegans .