Pringa E, Meier I, Müller U, Martinez-Noel G, Harbers K
Heinrich-Pette-Institut für experimentelle Virologie und Immunologie an der Universität Hamburg, Martinistr. 52, D-20251, Hamburg, Germany.
Biochim Biophys Acta. 2000 Nov 15;1494(1-2):75-82. doi: 10.1016/s0167-4781(00)00221-9.
The ubiquitin-conjugating enzyme UbcM4, which is identical to the human enzyme UbcH7, was previously shown to be essential for normal mouse development. In order to study the possible role of UbcM4 for cell proliferation and in vitro differentiation, we here describe the establishment and characterization of fibroblast and embryonic stem cell lines with partial or complete inactivation of the UbcM4 gene. ES cell lines in which both alleles of the gene were inactivated by targeted mutagenesis showed no differences in growth rates, cell cycle progression and in vitro differentiation when compared to wild-type ES cells. Fibroblast cell lines with a partially inactivated UbcM4 gene were derived from embryos of the previously described A6 mouse mutant, where retrovirus integration has resulted in a recessive lethal mutation. As in the mutant embryos, steady levels of RNA and protein in the cell lines were reduced by about 70%. The mutant cell lines showed no differences in immortalization kinetics, growth rates and cell cycle progression when compared to wild-type fibroblasts. Taken together, our results strongly suggest that UbcM4-mediated ubiquitination and degradation are not necessary for proteins involved in the maintenance and growth of cells.
泛素结合酶UbcM4与人类酶UbcH7相同,先前已证明它对正常小鼠发育至关重要。为了研究UbcM4在细胞增殖和体外分化中的可能作用,我们在此描述了UbcM4基因部分或完全失活的成纤维细胞和胚胎干细胞系的建立及特性。通过靶向诱变使该基因的两个等位基因均失活的胚胎干细胞系,与野生型胚胎干细胞相比,在生长速率、细胞周期进程和体外分化方面没有差异。UbcM4基因部分失活的成纤维细胞系源自先前描述的A6小鼠突变体的胚胎,其中逆转录病毒整合导致了隐性致死突变。与突变胚胎一样,细胞系中RNA和蛋白质的稳定水平降低了约70%。与野生型成纤维细胞相比,突变细胞系在永生化动力学、生长速率和细胞周期进程方面没有差异。综上所述,我们的结果强烈表明,UbcM4介导的泛素化和降解对于参与细胞维持和生长的蛋白质而言并非必需。