Ohmori Y, Tanabe J, Takada S, Lee W M, Obinata M
Department of Cell Biology, Tohoku University, Sendai, Japan.
Oncogene. 1993 Feb;8(2):379-86.
In the early event of the induction of mouse erythroleukemia (MEL) cell differentiation, c-myc mRNA levels show a drastic change. The elevated expression of a transfected c-myc gene inhibits the commitment and differentiation of MEL cell transformants. In the present work, we have introduced human c-myc mutants into MEL cells under the inducible promoter to define the functional domains of c-Myc involved in erythroid differentiation. The c-Myc domains necessary for commitment and differentiation are not co-localized; almost entire regions are required for inhibition of commitment, whereas domains II and IV that are essential for co-transforming activity with ras are required for inhibition of differentiation. Interestingly, mutants that delete domains for c-Myc dimerization motifs enhanced differentiation. These results suggest that c-Myc may regulate commitment and differentiation by interacting with proteins through different domains.
在诱导小鼠红白血病(MEL)细胞分化的早期事件中,c-myc mRNA水平呈现出剧烈变化。转染的c-myc基因的高表达抑制了MEL细胞转化体的定向分化。在本研究中,我们将人c-myc突变体导入到诱导型启动子调控下的MEL细胞中,以确定参与红系分化的c-Myc功能结构域。定向分化和分化所必需的c-Myc结构域并非共定位;几乎整个区域对于抑制定向分化是必需的,而与ras协同转化活性所必需的结构域II和IV对于抑制分化是必需的。有趣的是,缺失c-Myc二聚化基序结构域的突变体增强了分化。这些结果表明,c-Myc可能通过不同结构域与蛋白质相互作用来调节定向分化和分化。