Harnpicharnchai P, Jakovljevic J, Horsey E, Miles T, Roman J, Rout M, Meagher D, Imai B, Guo Y, Brame C J, Shabanowitz J, Hunt D F, Woolford J L
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Mol Cell. 2001 Sep;8(3):505-15. doi: 10.1016/s1097-2765(01)00344-6.
The pathway and complete collection of factors that orchestrate ribosome assembly are not clear. To address these problems, we affinity purified yeast preribosomal particles containing the nucleolar protein Nop7p and developed means to separate their components. Nop7p is associated primarily with 66S preribosomes containing either 27SB or 25.5S plus 7S pre-rRNAs. Copurifying proteins identified by mass spectrometry include ribosomal proteins, nonribosomal proteins previously implicated in 60S ribosome biogenesis, and proteins not known to be involved in ribosome production. Analysis of strains mutant for eight of these proteins not previously implicated in ribosome biogenesis showed that they do participate in this pathway. These results demonstrate that proteomic approaches in concert with genetic tools provide powerful means to purify and characterize ribosome assembly intermediates.
协调核糖体组装的途径和完整的因子集合尚不清楚。为了解决这些问题,我们通过亲和纯化了含有核仁蛋白Nop7p的酵母前核糖体颗粒,并开发了分离其组分的方法。Nop7p主要与含有27SB或25.5S加7S前体rRNA的66S前核糖体相关。通过质谱鉴定的共纯化蛋白包括核糖体蛋白、先前已涉及60S核糖体生物发生的非核糖体蛋白,以及未知参与核糖体产生的蛋白。对其中八种先前未涉及核糖体生物发生的蛋白的突变菌株进行分析表明,它们确实参与了这一途径。这些结果表明,蛋白质组学方法与遗传工具相结合,为纯化和表征核糖体组装中间体提供了强大的手段。