Breeding C S, Hudson J, Balasubramanian M K, Hemmingsen S M, Young P G, Gould K L
Department of Cell Biology, Vanderbilt University, Nashville, Tennessee, 37212, USA.
Mol Biol Cell. 1998 Dec;9(12):3399-415. doi: 10.1091/mbc.9.12.3399.
Schizosaccharomyces pombe cells respond to nutrient deprivation by altering G2/M cell size control. The G2/M transition is controlled by activation of the cyclin-dependent kinase Cdc2p. Cdc2p activation is regulated both positively and negatively. cdr2(+) was identified in a screen for regulators of mitotic control during nutrient deprivation. We have cloned cdr2(+) and have found that it encodes a putative serine-threonine protein kinase that is related to Saccharomyces cerevisiae Gin4p and S. pombe Cdr1p/Nim1p. cdr2(+) is not essential for viability, but cells lacking cdr2(+) are elongated relative to wild-type cells, spending a longer period of time in G2. Because of this property, upon nitrogen deprivation cdr2(+) mutants do not arrest in G1, but rather undergo another round of S phase and arrest in G2 from which they are able to enter a state of quiescence. Genetic evidence suggests that cdr2(+) acts as a mitotic inducer, functioning through wee1(+), and is also important for the completion of cytokinesis at 36 degrees C. Defects in cytokinesis are also generated by the overproduction of Cdr2p, but these defects are independent of wee1(+), suggesting that cdr2(+) encodes a second activity involved in cytokinesis.
粟酒裂殖酵母细胞通过改变G2/M期细胞大小控制来响应营养剥夺。G2/M期转换由细胞周期蛋白依赖性激酶Cdc2p的激活所控制。Cdc2p的激活受到正向和负向调节。cdr2(+)是在营养剥夺期间有丝分裂控制调节因子筛选中鉴定出来的。我们已经克隆了cdr2(+),并发现它编码一种推定的丝氨酸 - 苏氨酸蛋白激酶,与酿酒酵母Gin4p和粟酒裂殖酵母Cdr1p/Nim1p相关。cdr2(+)对细胞生存力不是必需的,但缺乏cdr2(+)的细胞相对于野生型细胞伸长,在G2期花费更长时间。由于这种特性,在氮剥夺时,cdr2(+)突变体不会在G1期停滞,而是经历另一轮S期并在G2期停滞,从该期它们能够进入静止状态。遗传证据表明cdr2(+)作为有丝分裂诱导剂,通过wee1(+)发挥作用,并且对于在36℃时胞质分裂的完成也很重要。胞质分裂缺陷也由Cdr2p的过量产生引起,但这些缺陷与wee1(+)无关,表明cdr2(+)编码参与胞质分裂的第二种活性。