Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Avenue, Bronx, NY 10461, USA.
Mol Cell Biol. 2010 Dec;30(23):5562-71. doi: 10.1128/MCB.00618-10. Epub 2010 Sep 27.
A set of genome-wide screens for proteins whose absence exacerbates growth defects due to pseudo-haploinsufficiency of ribosomal proteins in Saccharomyces cerevisiae identified Dom34 as being particularly important for cell growth when there is a deficit of 40S ribosomal subunits. In contrast, strains with a deficit of 60S ribosomal proteins were largely insensitive to the loss of Dom34. The slow growth of cells lacking Dom34 and haploinsufficient for a protein of the 40S subunit is caused by a severe shortage of 40S subunits available for translation initiation due to a combination of three effects: (i) the natural deficiency of 40S subunits due to defective synthesis, (ii) the sequestration of 40S subunits due to the large accumulation of free 60S subunits, and (iii) the accumulation of ribosomes "stuck" in a distinct 80S form, insensitive to the Mg(2+) concentration, and at least temporarily unavailable for further translation. Our data suggest that these stuck ribosomes have neither mRNA nor tRNA. We postulate, based on our results and on previously published work, that the stuck ribosomes arise because of the lack of Dom34, which normally resolves a ribosome stalled due to insufficient tRNAs, to structural problems with its mRNA, or to a defect in the ribosome itself.
一组针对蛋白质的全基因组筛选,这些蛋白质的缺失会加剧由于酿酒酵母核糖体蛋白的假单倍不足导致的生长缺陷,结果发现 Dom34 在 40S 核糖体亚基缺乏时对细胞生长特别重要。相比之下,60S 核糖体蛋白缺乏的菌株对 Dom34 的缺失基本上不敏感。由于三种效应的结合,缺乏 Dom34 和单倍不足的 40S 亚基蛋白的细胞生长缓慢:(i)由于合成缺陷导致 40S 亚基的天然缺乏,(ii)由于游离 60S 亚基的大量积累导致 40S 亚基的隔离,以及(iii)核糖体“卡住”在独特的 80S 形式中,对镁离子浓度不敏感,并且至少暂时无法进一步翻译。我们的数据表明,这些卡住的核糖体既没有 mRNA 也没有 tRNA。根据我们的结果和以前发表的工作,我们推测这些卡住的核糖体是由于缺乏 Dom34 引起的,Dom34 通常可以解决由于 tRNA 不足、其 mRNA 的结构问题或核糖体本身的缺陷而导致的核糖体停滞。