Kowalewski-Nimmerfall Elisabeth, Schähs Philipp, Maresch Daniel, Rendic Dubravko, Krämer Helmut, Mach Lukas
Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Muthgasse 18, A-1190 Vienna, Austria.
Department of Chemistry, University of Natural Resources and Life Sciences, Muthgasse 18, A-1190 Vienna, Austria.
Biochim Biophys Acta. 2014 Dec;1843(12):2900-12. doi: 10.1016/j.bbamcr.2014.08.012. Epub 2014 Aug 27.
Mammalian cellular repressor of E1A-stimulated genes is a lysosomal glycoprotein implicated in cellular growth and differentiation. The genome of the fruit fly Drosophila melanogaster encodes a putative orthologue (dCREG), suggesting evolutionarily conserved physiological functions of this protein. In D. melanogaster S2 cells, dCREG was found to localize in lysosomes. Further studies revealed that intracellular dCREG is subject of proteolytic maturation. Processing and turnover could be substantially reduced by RNAi-mediated silencing of cathepsin L. In contrast to mammalian cells, lysosomal delivery of dCREG does not depend on its carbohydrate moiety. Furthermore, depletion of the putative D. melanogaster lysosomal sorting receptor lysosomal enzyme receptor protein did not compromise cellular retention of dCREG. We also investigated the developmental consequences of dCREG ablation in whole D. melanogaster flies. Ubiquitous depletion of dCREG proved lethal at the late pupal stage once a knock-down efficiency of >95% was achieved. These results demonstrate that dCREG is essential for proper completion of fly development.
E1A 刺激基因的哺乳动物细胞阻遏物是一种溶酶体糖蛋白,与细胞生长和分化有关。果蝇黑腹果蝇的基因组编码一种假定的直系同源物(dCREG),表明该蛋白具有进化上保守的生理功能。在黑腹果蝇 S2 细胞中,发现 dCREG 定位于溶酶体。进一步的研究表明,细胞内的 dCREG 是蛋白水解成熟的对象。通过 RNAi 介导的组织蛋白酶 L 沉默,加工和周转可大幅减少。与哺乳动物细胞不同,dCREG 的溶酶体递送不依赖于其碳水化合物部分。此外,假定的黑腹果蝇溶酶体分选受体溶酶体酶受体蛋白的缺失并不影响 dCREG 在细胞内的保留。我们还研究了在整个黑腹果蝇中 dCREG 缺失的发育后果。一旦敲低效率达到>95%,dCREG 的普遍缺失在蛹后期被证明是致命的。这些结果表明,dCREG 对于果蝇发育的正常完成至关重要。