Vallen E A, Ho W, Winey M, Rose M D
Department of Molecular Biology, Princeton University, New Jersey 08544-1014.
Genetics. 1994 Jun;137(2):407-22. doi: 10.1093/genetics/137.2.407.
KAR1 encodes an essential component of the yeast spindle pole body (SPB) that is required for karyogamy and SPB duplication. A temperature-sensitive mutation, kar1-delta 17, mapped to a region required for SPB duplication and for localization to the SPB. To identify interacting SPB proteins, we isolated 13 dominant mutations and 3 high copy number plasmids that suppressed the temperature sensitivity of kar1-delta 17. Eleven extragenic suppressor mutations mapped to two linkage groups, DSK1 and DSK2. The extragenic suppressors were specific for SPB duplication and did not suppress karyogamy-defective alleles. The major class, DSK1, consisted of mutations in CDC31. CDC31 is required for SPB duplication and encodes a calmodulin-like protein that is most closely related to caltractin/centrin, a protein associated with the Chlamydomonas basal body. The high copy number suppressor plasmids contained the wild-type CDC31 gene. One CDC31 suppressor allele conferred a temperature-sensitive defect in SPB duplication, which was counter-suppressed by recessive mutations in KAR1. In spite of the evidence for a direct interaction, the strongest CDC31 alleles, as well as both DSK2 alleles, suppressed a complete deletion of KAR1. However, the CDC31 alleles also made the cell supersensitive to KAR1 gene dosage, arguing against a simple bypass mechanism of suppression. We propose a model in which Kar1p helps localize Cdc31p to the SPB and that Cdc31p then initiates SPB duplication via interaction with a downstream effector.
KAR1编码酵母纺锤体极体(SPB)的一个必需成分,该成分是核融合和SPB复制所必需的。一个温度敏感突变体kar1-δ17,定位于SPB复制和定位于SPB所需的区域。为了鉴定相互作用的SPB蛋白,我们分离出13个显性突变和3个高拷贝数质粒,它们抑制了kar1-δ17的温度敏感性。11个基因外抑制突变定位于两个连锁群,DSK1和DSK2。这些基因外抑制子对SPB复制具有特异性,并不抑制核融合缺陷等位基因。主要类别DSK1由CDC31中的突变组成。CDC31是SPB复制所必需的,编码一种类钙调蛋白,与衣藻基体相关蛋白钙牵蛋白/中心蛋白关系最为密切。高拷贝数抑制质粒包含野生型CDC31基因。一个CDC31抑制等位基因在SPB复制中导致温度敏感缺陷,该缺陷被KAR1中的隐性突变反抑制。尽管有直接相互作用的证据,但最强的CDC31等位基因以及两个DSK2等位基因都抑制了KAR1的完全缺失。然而,CDC31等位基因也使细胞对KAR1基因剂量超敏感,这与简单的旁路抑制机制相悖。我们提出一个模型,其中Kar1p帮助将Cdc31p定位到SPB,然后Cdc31p通过与下游效应器相互作用启动SPB复制。