Department of Biochemistry and Biomedical Sciences, and M.G. DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, Ontario, L8N3Z5, Canada.
RNA. 2013 Jun;19(6):789-802. doi: 10.1261/rna.037523.112. Epub 2013 Apr 23.
Assembly of the Escherichia coli 30S ribosomal subunits proceeds through multiple parallel pathways. The protein factors RimM, YjeQ, RbfA, and Era work in conjunction to assist at the late stages of the maturation process of the small subunit. However, it is unclear how the functional interplay between these factors occurs in the context of multiple parallel pathways. To understand how these factors work together, we have characterized the immature 30S subunits that accumulate in ΔrimM cells and compared them with immature 30S subunits from a ΔyjeQ strain. The cryo-EM maps obtained from these particles showed that the densities representing helices 44 and 45 in the rRNA were partially missing, suggesting mobility of these motifs. These 30S subunits were also partially depleted in all tertiary ribosomal proteins, particularly those binding in the head domain. Using image classification, we identified four subpopulations of ΔrimM immature 30S subunits differing in the amount of missing density for helices 44 and 45, as well as the amount of density existing in these maps for the underrepresented proteins. The structural defects found in these immature subunits resembled those of the 30S subunits that accumulate in the ΔyjeQ strain. These findings are consistent with an "early convergency model" in which multiple parallel assembly pathways of the 30S subunit converge into a late assembly intermediate, as opposed to the mature state. Functionally related factors will bind to this intermediate to catalyze the last steps of maturation leading to the mature 30S subunit.
大肠杆菌 30S 核糖体亚基的组装是通过多个平行途径进行的。蛋白质因子 RimM、YjeQ、RbfA 和 Era 协同作用,协助小亚基成熟过程的后期阶段。然而,这些因素在多个平行途径的背景下如何相互作用尚不清楚。为了了解这些因素如何协同工作,我们对在 ΔrimM 细胞中积累的不成熟 30S 亚基进行了表征,并将其与来自 ΔyjeQ 菌株的不成熟 30S 亚基进行了比较。从这些颗粒获得的 cryo-EM 图谱显示,rRNA 中代表螺旋 44 和 45 的密度部分缺失,表明这些基序的移动性。这些 30S 亚基也部分缺乏所有三级核糖体蛋白,特别是那些结合在头部结构域的蛋白。通过图像分类,我们鉴定了 4 种不同 ΔrimM 不成熟 30S 亚基的亚群,这些亚基的区别在于螺旋 44 和 45 的缺失密度以及这些图谱中代表性不足的蛋白质的密度存在量。这些不成熟亚基中的结构缺陷与在 ΔyjeQ 菌株中积累的 30S 亚基相似。这些发现与“早期收敛模型”一致,即 30S 亚基的多个平行组装途径收敛到一个晚期组装中间体,而不是成熟状态。功能相关的因子将结合到这个中间体上,催化成熟过程的最后几步,从而产生成熟的 30S 亚基。