New class of microRNA targets containing simultaneous 5'-UTR and 3'-UTR interaction sites.

TitleNew class of microRNA targets containing simultaneous 5'-UTR and 3'-UTR interaction sites.
Publication TypeJournal Article
Year of Publication2009
AuthorsLee, Inhan, Ajay Subramanian S., Yook Jong In, Kim Hyun Sil, Hong Su Hyung, Kim Nam Hee, Dhanasekaran Saravana M., Chinnaiyan Arul M., and Athey Brian D.
JournalGenome Res
Volume19
Issue7
Pagination1175-83
Date Published2009 Jul
ISSN1088-9051
Keywords3' Untranslated Regions, 5' Untranslated Regions, Axin Protein, Base Sequence, Blotting, Western, Cell Culture Techniques, Cytoskeletal Proteins, Humans, Kidney, MicroRNAs, Molecular Sequence Data, Reverse Transcriptase Polymerase Chain Reaction, RNA, Messenger, Sequence Homology, Nucleic Acid, Transfection, Wnt1 Protein
Abstract

MicroRNAs (miRNAs) are known to post-transcriptionally regulate target mRNAs through the 3'-UTR, which interacts mainly with the 5'-end of miRNA in animals. Here we identify many endogenous motifs within human 5'-UTRs specific to the 3'-ends of miRNAs. The 3'-end of conserved miRNAs in particular has significant interaction sites in the human-enriched, less conserved 5'-UTR miRNA motifs, while human-specific miRNAs have significant interaction sites only in the conserved 5'-UTR motifs, implying both miRNA and 5'-UTR are actively evolving in response to each other. Additionally, many miRNAs with their 3'-end interaction sites in the 5'-UTRs turn out to simultaneously contain 5'-end interaction sites in the 3'-UTRs. Based on these findings we demonstrate combinatory interactions between a single miRNA and both end regions of an mRNA using model systems. We further show that genes exhibiting large-scale protein changes due to miRNA overexpression or deletion contain both UTR interaction sites predicted. We provide the predicted targets of this new miRNA target class, miBridge, as an efficient way to screen potential targets, especially for nonconserved miRNAs, since the target search space is reduced by an order of magnitude compared with the 3'-UTR alone. Efficacy is confirmed by showing SEC24D regulation with hsa-miR-605, a miRNA identified only in primate, opening the door to the study of nonconserved miRNAs. Finally, miRNAs (and associated proteins) involved in this new targeting class may prevent 40S ribosome scanning through the 5'-UTR and keep it from reaching the start-codon, preventing 60S association.

DOI10.1101/gr.089367.108
Alternate JournalGenome Res.
PubMed ID19336450
PubMed Central IDPMC2704433
Grant ListU54-DA021519 / DA / NIDA NIH HHS / United States