Hildebrandt E R, Hoyt M A
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218, USA.
Mol Biol Cell. 2001 Nov;12(11):3402-16. doi: 10.1091/mbc.12.11.3402.
Saccharomyces cerevisiae Cin8p belongs to the BimC family of kinesin-related motor proteins that are essential for spindle assembly. Cin8p levels were found to oscillate in the cell cycle due in part to a high rate of degradation imposed from the end of mitosis through the G1 phase. Cin8p degradation required the anaphase-promoting complex ubiquitin ligase and its late mitosis regulator Cdh1p but not the early mitosis regulator Cdc20p. Cin8p lacks a functional destruction box sequence that is found in the majority of anaphase-promoting complex substrates. We carried out an extensive mutagenesis study to define the cis-acting sequence required for Cin8p degradation in vivo. The C terminus of Cin8p contains two elements required for its degradation: 1) a bipartite destruction sequence composed of a KEN-box plus essential residues within the downstream 22 amino acids and 2) a nuclear localization signal. The bipartite destruction sequence appears in other BimC kinesins as well. Expression of nondegradable Cin8p showed very mild phenotypic effects, with an increase in the fraction of mitotic cells with broken spindles.
酿酒酵母Cin8p属于驱动蛋白相关运动蛋白的BimC家族,对纺锤体组装至关重要。研究发现,Cin8p水平在细胞周期中振荡,部分原因是从有丝分裂末期到G1期存在较高的降解速率。Cin8p的降解需要后期促进复合物泛素连接酶及其有丝分裂后期调节因子Cdh1p,但不需要有丝分裂早期调节因子Cdc20p。Cin8p缺乏大多数后期促进复合物底物中存在的功能性破坏框序列。我们进行了广泛的诱变研究,以确定体内Cin8p降解所需的顺式作用序列。Cin8p的C末端包含其降解所需的两个元件:1)由一个KEN框加上下游22个氨基酸内的必需残基组成的二分破坏序列,以及2)一个核定位信号。二分破坏序列也出现在其他BimC驱动蛋白中。不可降解的Cin8p的表达显示出非常轻微的表型效应,有纺锤体断裂的有丝分裂细胞比例增加。