Fox E J, Wright S C
School of Biochemistry and Molecular Biology, University of Leeds, Mount Preston Street, Leeds LS2 9JT, UK.
Biochem J. 2001 Oct 15;359(Pt 2):361-7. doi: 10.1042/0264-6021:3590361.
The Myc/Max/Mad transcription factor network plays a central role in the control of cellular proliferation, differentiation and apoptosis. In order to elucidate the biological function of Mad3, we have analysed the precise temporal patterns of Mad3 mRNA expression during the cell cycle and differentiation in cultured cells. We show that Mad3 is induced at the G1/S transition in proliferating cells; expression persists throughout S-phase, and then declines as cells pass through G2 and mitosis. The expression pattern of Mad3 is coincident with that of Cdc2 throughout the cell cycle. In contrast, the expression of Mad3 during differentiation of cultured mouse erythroleukemia cells shows two transient peaks of induction. The first of these occurs at the onset of differentiation, and does not correlate with the S-phase of the cell cycle, whereas the second is coincident with the S-phase burst that precedes the terminal stages of differentiation. Our results therefore suggest that Mad3 serves a cell-cycle-related function in both proliferating and differentiating cells, and that it may also have a distinct role at various stages of differentiation.
Myc/Max/Mad转录因子网络在细胞增殖、分化和凋亡的调控中起着核心作用。为了阐明Mad3的生物学功能,我们分析了培养细胞在细胞周期和分化过程中Mad3 mRNA表达的精确时间模式。我们发现,Mad3在增殖细胞的G1/S期转换时被诱导;其表达在整个S期持续存在,然后随着细胞进入G2期和有丝分裂而下降。在整个细胞周期中,Mad3的表达模式与Cdc2的表达模式一致。相比之下,在培养的小鼠红白血病细胞分化过程中,Mad3的表达出现两个短暂的诱导峰值。其中第一个峰值出现在分化开始时,与细胞周期的S期无关,而第二个峰值与分化末期之前的S期爆发一致。因此,我们的结果表明,Mad3在增殖细胞和分化细胞中都发挥着与细胞周期相关的功能,并且它在分化的各个阶段可能也具有独特的作用。