Kimura Y, Yahara I, Lindquist S
Department of Molecular Genetics and Cell Biology, University of Chicago, IL 60637, USA.
Science. 1995 Jun 2;268(5215):1362-5. doi: 10.1126/science.7761857.
The substrate-specific protein chaperone Hsp90 (heat shock protein 90) from Saccharomyces cerevisiae functions in diverse signal transduction pathways. A mutation in YDJ1, a member of the DnaJ chaperone family, was recovered in a synthetic-lethal screen with Hsp90 mutants. In an otherwise wild-type background, the ydj1 mutation exerted strong and specific effects on three Hsp90 substrates, derepressing two (the estrogen and glucocorticoid receptors) and reducing the function of the third (the tyrosine kinase p60v-src). Analysis of one of these substrates, the glucocorticoid receptor, indicated that Ydj1 exerts its effects through physical interaction with Hsp90 substrates.
来自酿酒酵母的底物特异性蛋白质伴侣Hsp90(热休克蛋白90)在多种信号转导途径中发挥作用。在与Hsp90突变体的合成致死筛选中,发现了DnaJ伴侣家族成员YDJ1的一个突变。在其他方面为野生型的背景下,ydj1突变对三种Hsp90底物产生了强烈而特异的影响,解除了对其中两种底物(雌激素和糖皮质激素受体)的抑制,并降低了第三种底物(酪氨酸激酶p60v-src)的功能。对其中一种底物糖皮质激素受体的分析表明,Ydj1通过与Hsp90底物的物理相互作用发挥其作用。