Kindgren Peter, Yap Aaron, Bond Charles S, Small Ian
Australian Research Council Centre of Excellence in Plant Energy Biology, The University of Western Australia, Crawley, WA 6009, Australia.
School of Chemistry and Biochemistry, The University of Western Australia, Crawley, WA 6009, Australia.
Plant Cell. 2015 Feb;27(2):403-16. doi: 10.1105/tpc.114.134189. Epub 2015 Feb 3.
RNA editing factors of the pentatricopeptide repeat (PPR) family show a very high degree of sequence specificity in the recognition of their target sites. A molecular basis for target recognition by editing factors has been proposed based on statistical correlations but has not been tested experimentally. To achieve this, we systematically mutated the pentatricopeptide motifs in the Arabidopsis thaliana RNA editing factor CLB19 to investigate their individual contribution to RNA recognition. We find that the motifs contributing significantly to the specificity of binding follow the previously proposed recognition rules, distinguishing primarily between purines and pyrimidines. Our results are consistent with proposals that each motif recognizes one nucleotide in the RNA target with the protein aligned parallel to the RNA and contiguous motifs aligned with contiguous nucleotides such that the final PPR motif aligns four nucleotides upstream of the edited cytidine. By altering S motifs in CLB19 and another editing factor, OTP82, and using the modified proteins to attempt to complement the respective mutants, we demonstrate that we can predictably alter the specificity of these factors in vivo.
五肽重复序列(PPR)家族的RNA编辑因子在识别其靶位点时表现出高度的序列特异性。基于统计相关性提出了编辑因子识别靶标的分子基础,但尚未经过实验验证。为了实现这一点,我们系统地突变了拟南芥RNA编辑因子CLB19中的五肽重复基序,以研究它们对RNA识别的各自贡献。我们发现,对结合特异性有显著贡献的基序遵循先前提出的识别规则,主要区分嘌呤和嘧啶。我们的结果与以下提议一致:每个基序识别RNA靶标中的一个核苷酸,蛋白质与RNA平行排列,相邻基序与相邻核苷酸对齐,使得最终的PPR基序与编辑的胞嘧啶上游的四个核苷酸对齐。通过改变CLB19和另一个编辑因子OTP82中的S基序,并使用修饰后的蛋白质来尝试互补各自的突变体,我们证明我们可以在体内可预测地改变这些因子的特异性。