Ayscough K, Hayles J, MacNeill S A, Nurse P
Department of Biochemistry, University of Oxford, UK.
Mol Gen Genet. 1992 Apr;232(3):344-50. doi: 10.1007/BF00266236.
The p34cdc2 protein kinase plays a central role in the regulation of the eukaryotic cell cycle, being required both in late G1 for the commitment to S-phase and in late G2 for the initiation of mitosis. p34cdc2 also determines the precise timing of entry into mitosis in fission yeast, where a number of gene products that regulate p34cdc2 activity have been identified and characterised. To investigate further the mitotic role of p34cdc2 in this organism we have isolated new cold-sensitive p34cdc2 mutants. These are defective only in their G2 function and are extragenic suppressors of the lethal premature entry into mitosis brought about by mutating the mitotic inhibitor p107wee1 and overproducing the mitotic activator p80cdc25. One of the mutant proteins p34cdc2-E8 is only functional in the absence of p107wee1, and all the mutant strains have reduced histone H1 kinase activity in vitro. Each mutant allele has been cloned and sequenced, and the lesions responsible for the cold-sensitive phenotypes identified. All the mutations were found to map to regions that are conserved between the fission yeast p34cdc2 and functional homologues from higher eukaryotes.
p34cdc2蛋白激酶在真核细胞周期调控中起核心作用,在G1晚期进入S期以及G2晚期启动有丝分裂时均发挥作用。p34cdc2还决定了裂殖酵母进入有丝分裂的精确时间,在裂殖酵母中已鉴定并表征了许多调节p34cdc2活性的基因产物。为了进一步研究p34cdc2在该生物体中的有丝分裂作用,我们分离出了新的冷敏感型p34cdc2突变体。这些突变体仅在其G2功能上存在缺陷,并且是由有丝分裂抑制剂p107wee1突变和有丝分裂激活剂p80cdc25过量产生导致的致死性过早进入有丝分裂的基因外抑制子。突变蛋白之一p34cdc2-E8仅在不存在p107wee1时才具有功能,并且所有突变菌株在体外均具有降低的组蛋白H1激酶活性。每个突变等位基因均已克隆并测序,并确定了导致冷敏感表型的损伤。所有突变均定位于裂殖酵母p34cdc2与高等真核生物功能同源物之间保守的区域。