Fersht Naomi, Hermand Damien, Hayles Jacqueline, Nurse Paul
Cell Cycle Group, Cancer Research UK London Institute, London WC2A 3PX, UK.
Nucleic Acids Res. 2007;35(16):5323-37. doi: 10.1093/nar/gkm527. Epub 2007 Aug 8.
A screen for genes that can ectopically activate a Rad3-dependent checkpoint block over mitosis in fission yeast has identified the DNA replication initiation factor cdc18 (known as CDC6 in other organisms). Either a stabilized form of Cdc18, the Cdc18-T6A phosphorylation mutant, or overexpression of wild type Cdc18, activate the Rad3-dependent S-M checkpoint in the apparent absence of detectable replication structures and gross DNA damage. This cell cycle block relies on the Rad checkpoint pathway and requires Chk1 phosphorylation and activation. Unexpectedly, Cdc18-T6A induces changes in the mobility of Chromosome III, affecting the size of a restriction fragment containing rDNA repeats and producing aberrant nucleolar structures. Recombination events within the rDNA appear to contribute at least in part to the cell cycle delay. We propose that an elevated level of Cdc18 activates the Rad3-dependent checkpoint either directly or indirectly, and additionally causes expansion of the rDNA repeats on Chromosome III.
一项针对能够异位激活裂殖酵母有丝分裂过程中Rad3依赖性检查点阻滞的基因的筛选,鉴定出了DNA复制起始因子cdc18(在其他生物体中称为CDC6)。无论是稳定形式的Cdc18、Cdc18-T6A磷酸化突变体,还是野生型Cdc18的过表达,在明显没有可检测到的复制结构和严重DNA损伤的情况下,都会激活Rad3依赖性的S-M检查点。这种细胞周期阻滞依赖于Rad检查点途径,并且需要Chk1磷酸化和激活。出乎意料的是,Cdc18-T6A会诱导III号染色体迁移率的变化,影响包含rDNA重复序列的限制性片段的大小,并产生异常的核仁结构。rDNA内的重组事件似乎至少部分导致了细胞周期延迟。我们提出,Cdc18水平的升高直接或间接激活了Rad3依赖性检查点,并且还导致了III号染色体上rDNA重复序列的扩增。