Cargando…
A 3′-Untranslated Region (3′UTR) Induces Organ Adhesion by Regulating miR-199a* Functions
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 mod...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638016/ https://www.ncbi.nlm.nih.gov/pubmed/19223980 http://dx.doi.org/10.1371/journal.pone.0004527 |
_version_ | 1782164392055406592 |
---|---|
author | Lee, Daniel Y. Shatseva, Tatiana Jeyapalan, Zina Du, William W. Deng, Zhaoqun Yang, Burton B. |
author_facet | Lee, Daniel Y. Shatseva, Tatiana Jeyapalan, Zina Du, William W. Deng, Zhaoqun Yang, Burton B. |
author_sort | Lee, Daniel Y. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2638016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26380162009-02-18 A 3′-Untranslated Region (3′UTR) Induces Organ Adhesion by Regulating miR-199a* Functions Lee, Daniel Y. Shatseva, Tatiana Jeyapalan, Zina Du, William W. Deng, Zhaoqun Yang, Burton B. PLoS One Research Article 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. Public Library of Science 2009-02-18 /pmc/articles/PMC2638016/ /pubmed/19223980 http://dx.doi.org/10.1371/journal.pone.0004527 Text en Lee et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lee, Daniel Y. Shatseva, Tatiana Jeyapalan, Zina Du, William W. Deng, Zhaoqun Yang, Burton B. A 3′-Untranslated Region (3′UTR) Induces Organ Adhesion by Regulating miR-199a* Functions |
title | A 3′-Untranslated Region (3′UTR) Induces Organ Adhesion by Regulating miR-199a* Functions |
title_full | A 3′-Untranslated Region (3′UTR) Induces Organ Adhesion by Regulating miR-199a* Functions |
title_fullStr | A 3′-Untranslated Region (3′UTR) Induces Organ Adhesion by Regulating miR-199a* Functions |
title_full_unstemmed | A 3′-Untranslated Region (3′UTR) Induces Organ Adhesion by Regulating miR-199a* Functions |
title_short | A 3′-Untranslated Region (3′UTR) Induces Organ Adhesion by Regulating miR-199a* Functions |
title_sort | 3′-untranslated region (3′utr) induces organ adhesion by regulating mir-199a* functions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638016/ https://www.ncbi.nlm.nih.gov/pubmed/19223980 http://dx.doi.org/10.1371/journal.pone.0004527 |
work_keys_str_mv | AT leedaniely a3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT shatsevatatiana a3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT jeyapalanzina a3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT duwilliamw a3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT dengzhaoqun a3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT yangburtonb a3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT leedaniely 3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT shatsevatatiana 3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT jeyapalanzina 3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT duwilliamw 3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT dengzhaoqun 3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions AT yangburtonb 3untranslatedregion3utrinducesorganadhesionbyregulatingmir199afunctions |