Yamano H, Kitamura K, Kominami K, Lehmann A, Katayama S, Hunt T, Toda T
Laboratory of Cell Cycle Control, Imperial Cancer Research Fund, South Mimms, Herts EN6 3LD, United Kingdom.
Mol Cell. 2000 Dec;6(6):1377-87. doi: 10.1016/s1097-2765(00)00135-0.
We describe a novel set of oscillation mechanisms for the fission yeast S phase cyclin Cig2, which contains an authentic destruction box and is destroyed at anaphase via the APC/cyclosome (APC/C). Unlike the mitotic cyclin Cdc13, however, Cig2 mRNA and protein peak at the G1/S boundary and decline to low levels in G2 and M phases. We show here that SCF(Pop1, Pop2) plays a role in transcriptional periodicity, as pop mutations result in constitutive cig2(+) transcripts. The instability of Cig2 during G2 and M is independent of either the APC/C or Pop1/Pop2, but requires Skp1, a core component of SCF. These data indicate that the APC/C and SCF control Cig2 levels differentially at different stages of the cell cycle.
我们描述了裂殖酵母S期细胞周期蛋白Cig2的一组新的振荡机制,Cig2含有一个真正的破坏框,并在后期通过后期促进复合物/细胞周期体(APC/C)被降解。然而,与有丝分裂细胞周期蛋白Cdc13不同,Cig2 mRNA和蛋白在G1/S边界达到峰值,并在G2和M期降至低水平。我们在此表明,SCF(Pop1,Pop2)在转录周期性中起作用,因为pop突变导致组成型cig2(+)转录本。Cig2在G2和M期的不稳定性与APC/C或Pop1/Pop2无关,但需要Skp1,它是SCF的核心成分。这些数据表明,APC/C和SCF在细胞周期的不同阶段差异地控制Cig2的水平。