Institute of Biomedicine, University of Eastern Finland, Kuopio, Finland.
Institute for Research in Immunology and Cancer, University of Montréal, Montréal, Québec, Canada.
PLoS Biol. 2022 Mar 3;20(3):e3001548. doi: 10.1371/journal.pbio.3001548. eCollection 2022 Mar.
Commitment to cell division at the end of G1 phase, termed Start in the budding yeast Saccharomyces cerevisiae, is strongly influenced by nutrient availability. To identify new dominant activators of Start that might operate under different nutrient conditions, we screened a genome-wide ORF overexpression library for genes that bypass a Start arrest caused by absence of the G1 cyclin Cln3 and the transcriptional activator Bck2. We recovered a hypothetical gene YLR053c, renamed NRS1 for Nitrogen-Responsive Start regulator 1, which encodes a poorly characterized 108 amino acid microprotein. Endogenous Nrs1 was nuclear-localized, restricted to poor nitrogen conditions, induced upon TORC1 inhibition, and cell cycle-regulated with a peak at Start. NRS1 interacted genetically with SWI4 and SWI6, which encode subunits of the main G1/S transcription factor complex SBF. Correspondingly, Nrs1 physically interacted with Swi4 and Swi6 and was localized to G1/S promoter DNA. Nrs1 exhibited inherent transactivation activity, and fusion of Nrs1 to the SBF inhibitor Whi5 was sufficient to suppress other Start defects. Nrs1 appears to be a recently evolved microprotein that rewires the G1/S transcriptional machinery under poor nitrogen conditions.
在芽殖酵母酿酒酵母中,G1 期结束时对细胞分裂的承诺,称为 Start,强烈受到营养物质可用性的影响。为了鉴定新的 Start 优势激活因子,这些因子可能在不同的营养条件下发挥作用,我们筛选了一个全基因组 ORF 过表达文库,以寻找能够绕过因缺乏 G1 周期蛋白 Cln3 和转录激活因子 Bck2 引起的 Start 停滞的基因。我们回收了一个假定的基因 YLR053c,将其重新命名为 NRS1,用于氮响应 Start 调节因子 1,它编码一种特征较差的 108 个氨基酸的微蛋白。内源性 Nrs1 定位于核内,仅限于氮匮乏条件,TORC1 抑制后诱导,细胞周期调控峰值出现在 Start 时。NRS1 在遗传上与编码主要 G1/S 转录因子复合物 SBF 的亚基 SWI4 和 SWI6 相互作用。相应地,Nrs1 与 Swi4 和 Swi6 发生物理相互作用,并定位于 G1/S 启动子 DNA 上。Nrs1 表现出固有的转录激活活性,并且 Nrs1 与 SBF 抑制剂 Whi5 的融合足以抑制其他 Start 缺陷。Nrs1 似乎是一种最近进化的微蛋白,它在氮匮乏条件下重新连接 G1/S 转录机制。