Abstract

Mature microRNAs (miRNAs) are single-stranded RNAs of 18–24 nucleotides that repress post-transcriptional gene expression. However, it is unknown whether the functions of mature miRNAs can be regulated. Here we report that expression of versican 3′UTR induces organ adhesion in transgenic mice by modulating miR-199a* activities. The study was initiated by the hypothesis that the non-coding 3′UTR plays a role in the regulation of miRNA function. Transgenic mice expressing a construct harboring the 3′UTR of versican exhibits the adhesion of organs. Computational analysis indicated that a large number of microRNAs could bind to this fragment potentially including miR-199a*. Expression of versican and fibronectin, two targets of miR-199a*, are up-regulated in transgenic mice, suggesting that the 3′UTR binds and modulates miR-199a* activities, freeing mRNAs of versican and fibronectin from being repressed by miR-199a*. Confirmation of the binding was performed by PCR using mature miR-199a* as a primer and the targeting was performed by luciferase assays. Enhanced adhesion by expression of the 3′UTR was confirmed by in vitro assays. Our results demonstrated that upon arrival in cytoplasm, miRNA activities can be modulated locally by the 3′UTR. Our assay may be developed as sophisticated approaches for studying the mutual regulation of miRNAs and mRNAs in vitro and in vivo. We anticipate that expression of the 3′UTR may be an approach in the development of gene therapy.

Highlights

  • Human Genome Project identified approximately 25,000 protein-coding genes, occupying 1.9% of total genomic DNA

  • Analysis of chromosome 22 indicated that approximately 20% of the pseudogenes are potentially transcribed [3]

  • The fragment containing the transcription unit was cropped for the generation of transgenic mice and we obtained four versican 39-Untranslated Region (39UTR) transgenic founder animals

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Summary

Introduction

Human Genome Project identified approximately 25,000 protein-coding genes, occupying 1.9% of total genomic DNA. We found that the expression of the versican 39UTR induced cell, tissue, and organ adhesion by arresting miR-199a* functions. Cells that were transfected with different concentrations of lu-VUTR always produced lower levels of luciferase activity than cells transfected with a control construct (Fig S3a), suggesting repression of luciferase expression by endogenous miRNAs. with increased concentrations of lu-VUTR, the relative luciferase activities increased when normalized with the control construct.

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