Elledge S J, Davis R W
Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030.
Genes Dev. 1990 May;4(5):740-51. doi: 10.1101/gad.4.5.740.
Ribonucleotide reductase activity is essential for progression through the cell cycle, catalyzing the rate-limiting step for the production of deoxyribonucleotides needed for DNA synthesis. The enzymatic activity of the enzyme fluctuates in the cell cycle with an activity maximum in S phase. We have identified and characterized two Saccharomyces cerevisiae genes encoding the regulatory subunit of ribonucleotide reductase, RNR1 and RNR3. They share approximately 80% amino acid identity with each other and 60% with the mammalian homolog, M1. Genetic disruption reveals that the RNR1 gene is essential for mitotic viability, whereas the RNR3 gene is not essential. A high-copy-number clone of RNR3 is able to suppress the lethality of rnr1 mutations. Analysis of mRNA levels in cell-cycle-synchronized cultures reveals that the RNR1 mRNA is tightly cell-cycle regulated, fluctuating 15- to 30-fold, and is coordinately regulated with the POL1 mRNA, being expressed in the late G1 and S phases of the cell cycle. Progression from the alpha-factor-induced G1 block to induction of RNR1 mRNA is blocked by cycloheximide, further defining the requirement for protein synthesis in the G1- to S-phase transition. Both RNR1 and RNR3 transcripts are inducible by treatments that damage DNA, such as 4-nitroquinoline-1-oxide and methylmethanesulfonate, or block DNA replication, such as hydroxyurea. RNR1 is inducible 3- to 5-fold, and RNR3 is inducible greater than 100-fold. When MATa cells are arrested in G1 by alpha-factor, RNR1 and RNR3 mRNA is still inducible by DNA damage, indicating that the observed induction can occur outside of S phase. Inhibition of ribonucleotide reductase activity by hydroxyurea treatment results in arrest of the cell cycle in S phase as large budded, uninucleate cells. This specific cell-cycle arrest is independent of the RAD9 gene, defining a separate pathway for the coordination of DNA synthesis and cell-cycle progression.
核糖核苷酸还原酶活性对于细胞周期进程至关重要,它催化DNA合成所需脱氧核糖核苷酸产生的限速步骤。该酶的酶活性在细胞周期中波动,在S期活性最高。我们已鉴定并表征了两个编码核糖核苷酸还原酶调节亚基的酿酒酵母基因,即RNR1和RNR3。它们彼此间氨基酸同一性约为80%,与哺乳动物同源物M1的氨基酸同一性为60%。基因破坏表明RNR1基因对于有丝分裂活力至关重要,而RNR3基因并非必需。RNR3的高拷贝数克隆能够抑制rnr1突变的致死性。对细胞周期同步培养物中mRNA水平的分析表明,RNR1 mRNA受到严格的细胞周期调控,波动幅度为15至30倍,并且与POL1 mRNA协同调控,在细胞周期的G1晚期和S期表达。从α因子诱导的G1阻滞到RNR1 mRNA诱导的进程被环己酰亚胺阻断,这进一步明确了G1期到S期转变中蛋白质合成的需求。RNR1和RNR3转录本均可被损伤DNA的处理诱导,如4 - 硝基喹啉 - 1 - 氧化物和甲基磺酸甲酯,或阻断DNA复制的处理,如羟基脲。RNR1可诱导3至5倍,RNR3可诱导超过100倍。当MATa细胞被α因子阻滞在G1期时,RNR1和RNR3 mRNA仍可被DNA损伤诱导,表明观察到的诱导可在S期之外发生。羟基脲处理抑制核糖核苷酸还原酶活性会导致细胞周期在S期停滞,形成大芽、单核细胞。这种特定的细胞周期停滞独立于RAD9基因,定义了一条用于协调DNA合成和细胞周期进程的单独途径。