Shcherbakova Ksenia, Nakayama Hideki, Shimamoto Nobuo
Faculty of Life Sciences, Kyoto Sangyo University, Kamigamo-Motoyama, Kita-Ku, 603-8555, Kyoto, Japan.
Genes Cells. 2015 Oct;20(10):789-801. doi: 10.1111/gtc.12273. Epub 2015 Aug 20.
Ribosomal proteins S10 and S2 were each fused with GFP to track the fates of these proteins in the stationary growth phase and the following decay period in Escherichia coli. The fused proteins localized mainly in the cytoplasm, and their amounts were proportional to the colony-forming unit. S10-GFP strains that lacked genes responsible for regulating 100S ribosomes and S2-GFP strain that was unable to form 100S both showed shortened stationary phases. This result indicates that these strains exhibit earlier death in the absence of 100S formation (S2-GFP, S10-GFP∆rmf and S10-GFP∆hpf) and breakdown (S10-GFP∆yfiA). Therefore, in addition to the mere presence of 100S, the correct timing of 100S formation and breakdown is required to maintain viability. We propose a model in which 100S acts as a tentative repository of ribosomes that are protected from degradation and provide a source of amino acids in later growth period.
核糖体蛋白S10和S2分别与绿色荧光蛋白(GFP)融合,以追踪这些蛋白质在大肠杆菌稳定生长期及随后衰退期的命运。融合蛋白主要定位于细胞质中,其含量与菌落形成单位成正比。缺乏负责调控100S核糖体的基因的S10 - GFP菌株以及无法形成100S的S2 - GFP菌株,其稳定期均缩短。这一结果表明,在无法形成100S(S2 - GFP、S10 - GFP∆rmf和S10 - GFP∆hpf)以及100S解体(S10 - GFP∆yfiA)的情况下,这些菌株会更早死亡。因此,除了100S的单纯存在外,100S形成和解体的正确时间对于维持生存能力也是必需的。我们提出了一个模型,其中100S作为核糖体的临时储存库,免受降解,并在后期生长阶段提供氨基酸来源。