Wittenberg C, Richardson S L, Reed S I
Department of Biological Sciences, University of California, Santa Barbara 93106.
J Cell Biol. 1987 Oct;105(4):1527-38. doi: 10.1083/jcb.105.4.1527.
The product of the Saccharomyces cerevisiae gene CDC28, a protein kinase required for initiation of the cell division cycle, was localized within yeast cells. By using immunofluorescence methods, the CDC28 product was shown to be primarily cytoplasmic in distribution. The gene product was localized largely to the particulate fraction by differential centrifugation after mechanical disruption in aqueous buffers. The particulate association was not affected by the presence of nonionic detergent. To refine this localization further, a procedure was developed for the preparation of yeast cytoplasmic matrices which resemble the cytoskeletons of vertebrate cells on the basis of methodology, immunochemistry, and gross ultrastructure. A portion of the CDC28 product was found to be tightly associated with these detergent-insoluble cytoplasmic matrices by both immunofluorescence and immunoblotting procedures. Although, for technical reasons, precise quantitation was not possible, it is estimated that a minimum of 2-15% of the total CDC28 product pool is involved in the association with the insoluble matrix. Alcohol dehydrogenase, a soluble cytoplasmic protein, was found not to be associated with the cytoplasmic matrices at any detectable level, whereas, in contrast, approximately 10-40% of the total cellular actin, a bonafide cytoskeletal protein, was present in these structures. The proportion of CDC28 gene product associated with the particulate fraction, and perhaps the insoluble matrix, appears to be substantially decreased during the preparation of spheroplasts.
酿酒酵母基因CDC28的产物是一种细胞分裂周期启动所需的蛋白激酶,已在酵母细胞内定位。通过免疫荧光方法显示,CDC28产物主要分布在细胞质中。在水性缓冲液中机械破碎后,通过差速离心,该基因产物大部分定位于颗粒部分。颗粒结合不受非离子去污剂存在的影响。为了进一步优化这种定位,开发了一种制备酵母细胞质基质的方法,该基质在方法学、免疫化学和总体超微结构方面类似于脊椎动物细胞的细胞骨架。通过免疫荧光和免疫印迹程序发现,一部分CDC28产物与这些去污剂不溶性细胞质基质紧密结合。尽管由于技术原因无法进行精确定量,但据估计,至少2 - 15%的总CDC28产物库参与了与不溶性基质的结合。醇脱氢酶是一种可溶性细胞质蛋白,未在任何可检测水平与细胞质基质结合,而相比之下,约10 - 40%的总细胞肌动蛋白(一种真正的细胞骨架蛋白)存在于这些结构中。在原生质球制备过程中,与颗粒部分(可能还有不溶性基质)结合的CDC28基因产物比例似乎大幅下降。