Department of Basic Medical Sciences, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Genes Cells. 2009 May;14(5):659-68. doi: 10.1111/j.1365-2443.2009.01297.x. Epub 2009 Apr 15.
[PIN(+)] is a prion form of Rnq1 in Saccharomyces cerevisiae and is necessary for the de novo induction of a second prion, [PSI(+)]. We previously isolated a truncated form of Rnq1, named Rnq1Delta100, as a [PSI(+)]-eliminating factor in S. cerevisiae. Rnq1Delta100 deletes the N-terminal non-prion domain of Rnq1, and eliminates [PSI(+)] in [PIN(+)] yeast. Here we found that [PIN(+)] is transmissible to Rnq1Delta100 in the absence of full-length Rnq1, forming a novel prion variant [RNQ1Delta100(+)]. [RNQ1Delta100(+)] has similar [PIN(+)] properties as it stimulates the de novo induction of [PSI(+)] and is eliminated by the null hsp104Delta mutation, but not by Hsp104 overproduction. In contrast, [RNQ1Delta100(+)] inherits the inhibitory activity and hampers the maintenance of [PSI(+)] though less efficiently than [PIN(+)] made of Rnq1-Rnq1Delta100 co-aggregates. Interestingly, [RNQ1Delta100(+)] prion was eliminated by de novo [PSI(+)] induction. Thus, the [RNQ1Delta100(+)] prion demonstrates selfish activity to eliminate a heterologous prion in S. cerevisiae, showing the first instance of a selfish prion variant in living organisms.
[PIN(+)]是酿酒酵母中 Rnq1 的朊病毒形式,是从头诱导第二种朊病毒[PSI(+)]所必需的。我们之前分离到一种 Rnq1 的截断形式,命名为 Rnq1Delta100,它是酿酒酵母中[PSI(+)]消除因子。Rnq1Delta100 删除了 Rnq1 的 N 端非朊病毒结构域,并消除了[PIN(+)]酵母中的[PSI(+)]。在这里,我们发现[PIN(+)]可以在没有全长 Rnq1 的情况下传递给 Rnq1Delta100,形成一种新的朊病毒变体[RNQ1Delta100(+)]。[RNQ1Delta100(+)]具有与[PIN(+)]相似的特性,因为它刺激[PSI(+)]的从头诱导,并被 null hsp104Delta 突变消除,但不受 Hsp104 过表达的影响。相比之下,[RNQ1Delta100(+)]继承了抑制活性,并通过阻碍[PSI(+)]的维持来干扰其活性,但其效率不如由 Rnq1-Rnq1Delta100 共聚集形成的[PIN(+)]。有趣的是,[RNQ1Delta100(+)]朊病毒被新诱导的[PSI(+)]消除。因此,[RNQ1Delta100(+)]朊病毒在酿酒酵母中表现出自私活性,以消除异源朊病毒,这是在活生物体中首次发现自私朊病毒变体。