Phelps Steven S, Gaudin Cyril, Yoshizawa Satoko, Benitez Cesar, Fourmy Dominique, Joseph Simpson
Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Dr., La Jolla, CA 92093-0314, USA.
J Mol Biol. 2006 Jul 14;360(3):610-22. doi: 10.1016/j.jmb.2006.05.016. Epub 2006 May 22.
Coordinated translocation of the tRNA-mRNA complex by the ribosome occurs in a precise, stepwise movement corresponding to a distance of three nucleotides along the mRNA. Frameshift suppressor tRNAs generally contain an extra nucleotide in the anticodon loop and they subvert the normal mechanisms used by the ribosome for frame maintenance. The mechanism by which suppressor tRNAs traverse the ribosome during translocation is poorly understood. Here, we demonstrate translocation of a tRNA by four nucleotides from the A site to the P site, and from the P site to the E site. We show that translocation of a punctuated mRNA is possible with an extra, unpaired nucleotide between codons. Interestingly, the NMR structure of the four nucleotide anticodon stem-loop reveals a conformation different from the canonical tRNA structure. Flexibility within the loop may allow conformational adjustment upon A site binding and for interacting with the four nucleotide codon in order to shift the mRNA reading frame.
核糖体对tRNA-mRNA复合物的协同易位以精确的、逐步的方式进行,该方式对应于沿着mRNA移动三个核苷酸的距离。移码抑制tRNA通常在反密码子环中含有一个额外的核苷酸,它们破坏了核糖体用于维持读框的正常机制。目前对抑制tRNA在易位过程中穿过核糖体的机制了解甚少。在这里,我们证明了tRNA从A位点到P位点以及从P位点到E位点进行了四个核苷酸的易位。我们表明,在密码子之间存在一个额外的未配对核苷酸的情况下,间断mRNA的易位是可能的。有趣的是,四核苷酸反密码子茎环的NMR结构揭示了一种与经典tRNA结构不同的构象。环内的灵活性可能允许在A位点结合时进行构象调整,并与四核苷酸密码子相互作用,从而改变mRNA的阅读框。