By genetic analysis of Caenorhabditis elegans mutants defective in yolk uptake, we have identified new molecules functioning in the endocytosis pathway. Here we describe a novel J-domain-containing protein, RME-8, identified by such genetic analysis. RME-8 is required for receptor-mediated endocytosis and fluid-phase endocytosis in various cell types and is essential for C. elegans development and viability. In the macrophage-like coelomocytes, RME-8 localizes to the limiting membrane of large endosomes. Endocytosis markers taken up by the coelomocytes rapidly accumulate in these large RME-8-positive endosomes, concentrate in internal subendosomal structures, and later appear in RME-8-negative lysosomes. rme-8 mutant coelomocytes fail to accumulate visible quantities of endocytosis markers. These observations show that RME-8 functions in endosomal trafficking before the lysosome. RME-8 homologues are found in multicellular organisms from plants to humans but not in the yeast Saccharomyces cerevisiae. These sequence homologies suggest that RME-8 fulfills a conserved function in multicellular organisms.
RME-8, a conserved J-domain protein, is required for endocytosis in Caenorhabditis elegans.
RME-8 是一种保守的 J 结构域蛋白,是秀丽隐杆线虫内吞作用所必需的
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作者:Zhang Y, Grant B, Hirsh D
| 期刊: | Molecular Biology of the Cell | 影响因子: | 2.700 |
| 时间: | 2001 | 起止号: | 2001 Jul;12(7):2011-21 |
| doi: | 10.1091/mbc.12.7.2011 | 研究方向: | 免疫/内分泌 |
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