Oling David, Masoom Rehan, Kvint Kristian
Department of Chemistry and Molecular Biology, University of Gothenburg, 413 90 Gothenburg, Sweden.
Department of Chemistry and Molecular Biology, University of Gothenburg, 413 90 Gothenburg, Sweden
Mol Biol Cell. 2014 Jun 15;25(12):1916-24. doi: 10.1091/mbc.E13-10-0591. Epub 2014 Apr 23.
Ubp3 is a conserved ubiquitin protease that acts as an antisilencing factor in MAT and telomeric regions. Here we show that ubp3∆ mutants also display increased silencing in ribosomal DNA (rDNA). Consistent with this, RNA polymerase II occupancy is lower in cells lacking Ubp3 than in wild-type cells in all heterochromatic regions. Moreover, in a ubp3∆ mutant, unequal recombination in rDNA is highly suppressed. We present genetic evidence that this effect on rDNA recombination, but not silencing, is entirely dependent on the silencing factor Sir2. Further, ubp3∆ sir2∆ mutants age prematurely at the same rate as sir2∆ mutants. Thus our data suggest that recombination negatively influences replicative life span more so than silencing. However, in ubp3∆ mutants, recombination is not a prerequisite for aging, since cells lacking Ubp3 have a shorter life span than isogenic wild-type cells. We discuss the data in view of different models on how silencing and unequal recombination affect replicative life span and the role of Ubp3 in these processes.
Ubp3是一种保守的泛素蛋白酶,在MAT和端粒区域作为抗沉默因子发挥作用。在此我们表明,ubp3∆突变体在核糖体DNA(rDNA)中也表现出增强的沉默作用。与此一致的是,在所有异染色质区域,缺乏Ubp3的细胞中RNA聚合酶II的占有率低于野生型细胞。此外,在ubp3∆突变体中,rDNA中的不等位重组受到高度抑制。我们提供了遗传学证据,表明这种对rDNA重组而非沉默的影响完全依赖于沉默因子Sir2。此外,ubp3∆ sir2∆突变体与sir2∆突变体以相同的速率过早衰老。因此,我们的数据表明,重组对复制寿命的负面影响比沉默更大。然而,在ubp3∆突变体中,重组不是衰老的先决条件,因为缺乏Ubp3的细胞比同基因野生型细胞的寿命更短。我们根据关于沉默和不等位重组如何影响复制寿命的不同模型以及Ubp3在这些过程中的作用来讨论这些数据。