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The D-type cyclin CYCD3;1 is limiting for the G1-to-S-phase transition in Arabidopsis

机译:D型细胞周期蛋白CYCD3; 1限制了拟南芥中G1到S相的转变。

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The G1-to-S-phase transition is a key regulatory point in the cell cycle, but the rate-limiting component in plants is unknown. Overexpression of CYCLIN D3;1 (CYCD3;1) in transgenic plants increases mitotic cycles and reduces endocycles, but its effects on cell cycle progression cannot be unambiguously determined. To analyze the cell cycle roles of plant D-type cyclins, we overexpressed CYCD3;1 in Arabidopsis thaliana cell suspension cultures. Changes in cell number and doubling time were insignificant, but cultures exhibited an increased proportion of G2- over G1-phase cells, as well as increased G2 arrest in response to stationary phase and sucrose starvation. Synchronized cultures confirm that CYCD3;1-expressing (but not CYCD2;1-expressing) cells show increased G2-phase length and delayed activation of mitotic genes such as B-type cyclins, suggesting that CYCD3;1 has a specific G1/S role. Analysis of putative cyclin-dependent kinase phosphorylation sites within CYCD3;1 shows that mutating Ser-343 to Ala enhances CYCD3;1 potency without affecting its rate of turnover and results in a fivefold increase in the level of cell death in response to sucrose removal. We conclude that CYCD3;1 dominantly drives the G1/S transition, and in sucrose-depleted cells the decline in CYCD3;1 levels leads to G1 arrest, which is overcome by ectopic CYCD3;1 expression. Ser-343 is likely a key residue in modulating CYCD3;1 activity in response to sucrose depletion.
机译:从G1到S相的过渡是细胞周期中的关键调控点,但植物中的限速成分尚不清楚。 CYCLIN D3; 1(CYCD3; 1)在转基因植物中的过表达增加了有丝分裂周期并减少了内周期,但不能明确确定其对细胞周期进程的影响。若要分析植物D型细胞周期蛋白的细胞周期作用,我们在拟南芥细胞悬浮培养物中过表达CYCD3; 1。细胞数量和倍增时间的变化微不足道,但培养物显示G2相对于G1期细胞的比例增加,并且响应于固定相和蔗糖饥饿而增加了G2阻滞。同步培养证实表达CYCD3; 1的细胞(但不表达CYCD2; 1的细胞)显示出G2期长度增加和有丝分裂基因如B型细胞周期蛋白的激活延迟,提示CYCD3; 1具有特定的G1 / S作用。 CYCD3; 1中假定的细胞周期蛋白依赖性激酶磷酸化位点的分析表明,将Ser-343突变为Ala可增强CYCD3; 1的效力,而不会影响其转化率,并且响应于蔗糖去除,细胞死亡水平增加了五倍。我们得出的结论是,CYCD3; 1主导了G1 / S的转变,在蔗糖耗尽的细胞中,CYCD3; 1的水平下降导致G1阻滞,这被异位CYCD3; 1的表达所克服。 Ser-343可能是调节CYCD3; 1活性的关键残基,以响应蔗糖的消耗。

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