Cheng Haili, Bao Xin, Rao Hai
From the Department of Molecular Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229.
From the Department of Molecular Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229
J Biol Chem. 2016 May 6;291(19):10372-7. doi: 10.1074/jbc.M115.701813. Epub 2016 Mar 14.
Cse4, a histone H3-like centromeric protein, plays critical functions in chromosome segregation. Cse4 level is tightly regulated, but the underlying mechanism remains poorly understood. We employed a toxicity-based screen to look for the degradation components involved in Cse4 regulation. Here, we show that the F-box containing protein Rcy1 is required for efficient Cse4 turnover as Cse4 degradation is compromised in yeast cells lacking RCY1 Excessive Cse4 accumulation in rcy1Δ cells leads to growth retardation. Furthermore, the deletion of RCY1 is tied to enhanced chromosome instability and temperature-sensitive cell growth. Our results reveal the involvement of Rcy1 in chromosome regulation and another regulatory pathway controlling the Cse4 level and activity.
Cse4是一种组蛋白H3样着丝粒蛋白,在染色体分离中发挥关键作用。Cse4的水平受到严格调控,但其潜在机制仍知之甚少。我们采用基于毒性的筛选方法来寻找参与Cse4调控的降解成分。在此,我们表明含F-box的蛋白Rcy1是Cse4有效周转所必需的,因为在缺乏RCY1的酵母细胞中Cse4降解受损。rcy1Δ细胞中Cse4的过度积累导致生长迟缓。此外,RCY1的缺失与染色体不稳定性增强和温度敏感型细胞生长有关。我们的结果揭示了Rcy1参与染色体调控以及另一条控制Cse4水平和活性的调控途径。