Kopski K M, Huffaker T C
Section of Biochemistry, Molecular and Cellular Biology, Cornell University, Ithaca, New York 14853-2703, USA.
Genetics. 1997 Oct;147(2):409-20. doi: 10.1093/genetics/147.2.409.
We have isolated a new conditional-lethal mutation, ndc10-2, in the NDC10/CBF2/CTF14 gene that encodes the 110-kD subunit of the Saccharomyces cerevisiae CBF3 kinetochore complex. At the restrictive temperature of 37 degrees, ndc10-2 cells are able to assemble anaphase spindles, but fail to segregate their DNA, consistent with a defect in kinetochore function. To identify other factors that play a role in kinetochore assembly or function, we isolated both dosage and second site suppressors of the ndc10-2 mutation. These screens identified UBC6 as a dosage suppressor, and mutations in UBC6 and UBC7 as second-site suppressors of ndc10-2 heat sensitivity. Both UBC6 and UBC7 encode ubiquitin-conjugating enzymes that function in ubiquitin-mediated protein degradation. Furthermore, overexpression of a mutant ubiquitin suppresses the ndc10-2 mutation. These results implicate the ubiquitin system in the regulation of ndc10-2 function and suggest a role for the ubiquitin system in kinetochore function.
我们在编码酿酒酵母CBF3动粒复合体110-kD亚基的NDC10/CBF2/CTF14基因中分离出一种新的条件致死突变体ndc10-2。在37摄氏度的限制温度下,ndc10-2细胞能够组装后期纺锤体,但无法分离其DNA,这与动粒功能缺陷一致。为了鉴定在动粒组装或功能中起作用的其他因子,我们分离了ndc10-2突变的剂量和第二位点抑制子。这些筛选确定UBC6为剂量抑制子,UBC6和UBC7中的突变作为ndc10-2热敏感性的第二位点抑制子。UBC6和UBC7都编码在泛素介导的蛋白质降解中起作用的泛素结合酶。此外,突变泛素的过表达抑制了ndc10-2突变。这些结果表明泛素系统参与了ndc10-2功能的调节,并提示泛素系统在动粒功能中发挥作用。