Zhang Libin, Bao Penghui, Leibowitz Michael J, Zhang Yi
State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072, People's Republic of China.
RNA. 2009 Nov;15(11):1986-92. doi: 10.1261/rna.1638609. Epub 2009 Aug 26.
Pseudoknots play critical roles in packing the active structure of various functional RNAs. The importance of the P3-P7 pseudoknot in refolding of group I intron ribozymes has been recently appreciated, while little is known about the pseudoknot function in co-transcriptional folding. Here we used the Candida group I intron as a model to address the question. We show that co-transcriptional folding of the active self-splicing intron is twice as fast as refolding. The P3-P7 pseudoknot folds slowly during co-transcriptional folding at a rate constant similar to the folding of the active ribozyme, and folding of both P3-P7 and P1-P10 pseudoknots are inhibited by antisense oligonucleotides. We conclude that when RNA folding is coupled with transcription, formation of pseudoknot structures dominates the productive folding pathway and serves as a rate-limiting step in producing the self-splicing competent Candida intron.
假结在多种功能性RNA的活性结构组装中发挥着关键作用。最近人们认识到P3 - P7假结在I组内含子核酶重折叠中的重要性,而对于共转录折叠过程中假结的功能却知之甚少。在此,我们以念珠菌I组内含子为模型来解决这个问题。我们发现,活性自我剪接内含子的共转录折叠速度是重折叠速度的两倍。在共转录折叠过程中,P3 - P7假结折叠缓慢,其速率常数与活性核酶的折叠速率常数相似,并且P3 - P7和P1 - P10假结的折叠均受到反义寡核苷酸的抑制。我们得出结论,当RNA折叠与转录偶联时,假结结构的形成主导了有效的折叠途径,并成为产生具有自我剪接能力的念珠菌内含子的限速步骤。