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通过两个检查点基因的过表达抑制α-微管蛋白中的条件突变。

Suppression of a conditional mutation in alpha-tubulin by overexpression of two checkpoint genes.

作者信息

Guénette S, Magendantz M, Solomon F

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

J Cell Sci. 1995 Mar;108 ( Pt 3):1195-204. doi: 10.1242/jcs.108.3.1195.

Abstract

To identify proteins that regulate microtubule assembly in Saccharomyces cerevisiae, we screened for multicopy suppressors of a conditional mutation in alpha-tubulin. Cells expressing the recessive allele tub1-729 as their sole alpha-tubulin gene grow normally at permissive temperature. However, at 15 degrees C the cells lose viability and arrest primarily with large buds and quantitatively diminished microtubule structures. Transformation of mutant cells with genomic libraries repeatedly identified three different suppressors: the two wild-type alpha-tubulin genes, TUB1 and TUB3; and BUB3. BUB3 is a checkpoint gene that permits entry into mitosis depending upon the assembly state of microtubules. Excess BUB3 rescues both the loss of viability and microtubule defects but not the benomyl supersensitivity associated with tub1-729. The suppression is specific for the mutation ALA422VAL in TUB1, and does not affect several other mutations in TUB1 that produce the 'no microtubule' phenotype. Overexpression of BUB1, which interacts genetically with BUB3 and which is involved in the same checkpoint pathway, also rescues the cold sensitivity of tub1-729, but another checkpoint gene, MAD2, does not. Overexpression of BUB3 in wild-type cells has no detectable growth or microtubule defect, but disruption of the BUB3 gene produces slow growth and benomyl supersensitivity. Our results suggest that BUB1 and BUB3 overexpression modulate an event required for mitotic spindle function which is rate limiting for tub1-729 cells at the restrictive temperature.

摘要

为了鉴定酿酒酵母中调节微管组装的蛋白质,我们筛选了α-微管蛋白条件突变的多拷贝抑制子。将隐性等位基因tub1-729作为唯一α-微管蛋白基因表达的细胞在允许温度下正常生长。然而,在15摄氏度时,细胞失去活力并主要停滞于大芽阶段,微管结构在数量上减少。用基因组文库转化突变细胞反复鉴定出三种不同的抑制子:两个野生型α-微管蛋白基因,TUB1和TUB3;以及BUB3。BUB3是一个检查点基因,它根据微管的组装状态允许进入有丝分裂。过量的BUB3可挽救活力丧失和微管缺陷,但不能挽救与tub1-729相关的苯菌灵超敏感性。这种抑制作用对TUB1中的ALA422VAL突变具有特异性,并且不影响TUB1中产生“无微管”表型的其他几个突变。与BUB3发生遗传相互作用且参与相同检查点途径的BUB1的过表达也可挽救tub1-729的冷敏感性,但另一个检查点基因MAD2则不能。野生型细胞中BUB3的过表达没有可检测到的生长或微管缺陷,但BUB3基因的破坏会导致生长缓慢和苯菌灵超敏感性。我们的结果表明,BUB1和BUB3的过表达调节有丝分裂纺锤体功能所需的一个事件,该事件在限制温度下对tub1-729细胞是限速的。

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