Zhang Jingyu, Harnpicharnchai Piyanun, Jakovljevic Jelena, Tang Lan, Guo Yurong, Oeffinger Marlene, Rout Michael P, Hiley Shawna L, Hughes Timothy, Woolford John L
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, USA.
Genes Dev. 2007 Oct 15;21(20):2580-92. doi: 10.1101/gad.1569307.
More than 170 proteins are necessary for assembly of ribosomes in eukaryotes. However, cofactors that function with each of these proteins, substrates on which they act, and the precise functions of assembly factors--e.g., recruiting other molecules into preribosomes or triggering structural rearrangements of pre-rRNPs--remain mostly unknown. Here we investigated the recruitment of two ribosomal proteins and 5S ribosomal RNA (rRNA) into nascent ribosomes. We identified a ribonucleoprotein neighborhood in preribosomes that contains two yeast ribosome assembly factors, Rpf2 and Rrs1, two ribosomal proteins, rpL5 and rpL11, and 5S rRNA. Interactions between each of these four proteins have been confirmed by binding assays in vitro. These molecules assemble into 90S preribosomal particles containing 35S rRNA precursor (pre-rRNA). Rpf2 and Rrs1 are required for recruiting rpL5, rpL11, and 5S rRNA into preribosomes. In the absence of association of these molecules with pre-rRNPs, processing of 27SB pre-rRNA is blocked. Consequently, the abortive 66S pre-rRNPs are prematurely released from the nucleolus to the nucleoplasm, and cannot be exported to the cytoplasm.
在真核生物中,核糖体组装需要170多种蛋白质。然而,与这些蛋白质各自发挥作用的辅因子、它们作用的底物以及组装因子的精确功能——例如,将其他分子招募到前核糖体中或触发前核糖体核糖核蛋白(pre - rRNP)的结构重排——大多仍不清楚。在这里,我们研究了两种核糖体蛋白和5S核糖体RNA(rRNA)被招募到新生核糖体中的情况。我们在核糖体前体中鉴定出一个核糖核蛋白区域,其中包含两种酵母核糖体组装因子Rpf2和Rrs1、两种核糖体蛋白rpL5和rpL11以及5S rRNA。这四种蛋白质之间的相互作用已通过体外结合试验得到证实。这些分子组装成含有35S rRNA前体(pre - rRNA)的90S核糖体前体颗粒。Rpf2和Rrs1是将rpL5、rpL11和5S rRNA招募到核糖体前体中所必需的。在这些分子与前核糖体核糖核蛋白不结合的情况下,27SB pre - rRNA的加工被阻断。因此,有缺陷的66S前核糖体核糖核蛋白会过早地从核仁释放到核质中,并且无法输出到细胞质中。