Winey M, Goetsch L, Baum P, Byers B
Department of Genetics, University of Washington, Seattle 98195.
J Cell Biol. 1991 Aug;114(4):745-54. doi: 10.1083/jcb.114.4.745.
It is crucial to the eucaryotic cell cycle that the centrosome undergo precise duplication to generate the two poles of the mitotic spindle. In the budding yeast Saccharomyces cerevisiae, centrosomal functions are provided by the spindle pole body (SPB), which is duplicated at the time of bud emergence in G1 of the cell cycle. Genetic control of this process has previously been revealed by the characterization of mutants in CDC31 and KAR1, which prevent SPB duplication and lead to formation of a monopolar spindle. Newly isolated mutations described here (mps1 and mps2, for monopolar spindle) similarly cause monopolar mitosis but their underlying effects on SPB duplication are unique. The MPS1 gene is found by electron microscopy to be essential for proper formation of the site at which the new SPB normally arises adjacent to the existing one. By contrast, a mutation in MPS2 permits duplication to proceed, but the newly formed SPB is structurally defective and unable to serve as a functional spindle pole. Distinct temporal requirements for the CDC31, MPS1, and MPS2 gene functions during the SPB duplication cycle further demonstrate the individual roles of these genes in the morphogenetic pathway.
中心体进行精确复制以形成有丝分裂纺锤体的两极,这对于真核细胞周期至关重要。在芽殖酵母酿酒酵母中,中心体功能由纺锤体极体(SPB)提供,它在细胞周期G1期芽出现时进行复制。此前通过对CDC31和KAR1突变体的表征揭示了这一过程的遗传控制,这些突变体阻止SPB复制并导致单极纺锤体的形成。这里描述的新分离的突变(mps1和mps2,代表单极纺锤体)同样会导致单极有丝分裂,但其对SPB复制的潜在影响是独特的。通过电子显微镜发现,MPS1基因对于新SPB通常在现有SPB附近正常出现的位点的正确形成至关重要。相比之下,MPS2中的突变允许复制进行,但新形成的SPB在结构上有缺陷,无法作为功能性纺锤体极发挥作用。在SPB复制周期中,CDC31、MPS1和MPS2基因功能的不同时间要求进一步证明了这些基因在形态发生途径中的各自作用。