Pawlica Paulina, Sheu-Gruttadauria Jessica, MacRae Ian J, Steitz Joan A
Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06536, USA.
Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Cold Spring Harb Symp Quant Biol. 2019;84:179-183. doi: 10.1101/sqb.2019.84.039321. Epub 2020 Feb 4.
microRNAs (miRNAs) are crucial for posttranscriptional regulation of messenger RNAs. "Classical" miRNA targets predominantly interact with the miRNA seed sequence located near the miRNA 5' end. Interestingly, certain transcripts that exhibit extensive complementarity to the miRNAs 3' region, instead of being subjected to regulation, induce miRNA decay in a process termed target-directed miRNA degradation (TDMD). Here, we review recent advances in understanding the molecular mechanisms of TDMD. Specifically, we discuss how extensive miRNA complementarity to TDMD-inducing targets results in displacement of the miRNA 3' end from its protective pocket in the Argonaute protein. Unprotected miRNA 3' ends are then available for enzymatic attack by still-unidentified cellular enzymes. Identification of these cellular enzymes and discovery of additional TDMD-inducing transcripts are subjects for future research.
微小RNA(miRNA)对于信使核糖核酸的转录后调控至关重要。“经典”的miRNA靶标主要与位于miRNA 5'端附近的miRNA种子序列相互作用。有趣的是,某些与miRNA 3'区域具有广泛互补性的转录本,非但受到调控,反而在一个称为靶标导向的miRNA降解(TDMD)的过程中诱导miRNA降解。在此,我们综述了在理解TDMD分子机制方面的最新进展。具体而言,我们讨论了miRNA与TDMD诱导靶标的广泛互补性如何导致miRNA 3'端从其在AGO蛋白中的保护口袋中被置换出来。未受保护的miRNA 3'端随后可供仍未鉴定的细胞酶进行酶促攻击。鉴定这些细胞酶以及发现更多TDMD诱导转录本是未来研究的课题。