Haarer B K, Pringle J R
Department of Biology, University of Michigan, Ann Arbor 48109.
Mol Cell Biol. 1987 Oct;7(10):3678-87. doi: 10.1128/mcb.7.10.3678-3687.1987.
Budding cells of the yeast Saccharomyces cerevisiae possess a ring of 10-nm-diameter filaments, of unknown biochemical nature, that lies just inside the plasma membrane in the neck connecting the mother cell to its bud (B. Byers and L. Goetsch, J. Cell Biol. 69:717-721, 1976). Mutants defective in any of four genes (CDC3, CDC10, CDC11, and CDC12) lack these filaments and display a pleiotropic phenotype that involves abnormal bud growth and cell-wall deposition and an inability to complete cytokinesis. We fused the cloned CDC12 gene to the Escherichia coli lacZ and trpE genes and used the resulting fusion proteins to raise polyclonal antibodies specific for the CDC12 gene product. In immunofluorescence experiments with affinity-purified antibodies, the neck region of wild-type and mutant cells stained in patterns consistent with the hypothesis that the CDC12 gene product is a constituent of the ring of 10-nm filaments. Without careful affinity purification of the CDC12-specific antibodies, these staining patterns were completely obscured by the staining of residual cell wall components in the neck by antibodies present even in the "preimmune" sera of all rabbits tested.
酿酒酵母的出芽细胞在连接母细胞与其芽体的颈部质膜内侧有一圈直径为10纳米的丝状结构,其生化性质未知(B. 拜尔斯和L. 戈奇,《细胞生物学杂志》69:717 - 721, 1976年)。四个基因(CDC3、CDC10、CDC11和CDC12)中任何一个有缺陷的突变体都缺乏这些丝状结构,并表现出多效性表型,包括异常的芽体生长、细胞壁沉积以及无法完成胞质分裂。我们将克隆的CDC12基因与大肠杆菌的lacZ和trpE基因融合,并利用产生的融合蛋白制备针对CDC12基因产物的多克隆抗体。在用亲和纯化抗体进行的免疫荧光实验中,野生型和突变体细胞的颈部区域染色模式与以下假设一致,即CDC12基因产物是10纳米丝状环的一个组成部分。如果没有对CDC12特异性抗体进行仔细的亲和纯化,即使在所有测试兔子的“免疫前”血清中存在的抗体对颈部残留细胞壁成分的染色也会完全掩盖这些染色模式。