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Translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region
Transposable elements constitute a substantial portion of eukaryotic genomes and contribute to genomic variation, function, and evolution. Miniature inverted-repeat transposable elements (MITEs), as DNA transposons, are widely distributed in plant and animal genomes. Previous studies have suggested...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338036/ https://www.ncbi.nlm.nih.gov/pubmed/28256530 http://dx.doi.org/10.1038/ncomms14651 |
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author | Shen, Jianqiang Liu, Juhong Xie, Kabin Xing, Feng Xiong, Fang Xiao, Jinghua Li, Xianghua Xiong, Lizhong |
author_facet | Shen, Jianqiang Liu, Juhong Xie, Kabin Xing, Feng Xiong, Fang Xiao, Jinghua Li, Xianghua Xiong, Lizhong |
author_sort | Shen, Jianqiang |
collection | PubMed |
description | Transposable elements constitute a substantial portion of eukaryotic genomes and contribute to genomic variation, function, and evolution. Miniature inverted-repeat transposable elements (MITEs), as DNA transposons, are widely distributed in plant and animal genomes. Previous studies have suggested that retrotransposons act as translational regulators; however, it remains unknown how host mRNAs are influenced by DNA transposons. Here we report a translational repression mechanism mediated by a stowaway-like MITE (sMITE) embedded in the 3′-untranslated region (3′-UTR) of Ghd2, a member of the CCT (CONSTANS [CO], CO-LIKE and TIMING OF CAB1) gene family in rice. Ghd2 regulates important agronomic traits, including grain number, plant height and heading date. Interestingly, the translational repression of Ghd2 by the sMITE mainly relies on Dicer-like 3a (OsDCL3a). Furthermore, other MITEs in the 3′-UTRs of different rice genes exhibit a similar effect on translational repression, thus suggesting that MITEs may exert a general regulatory function at the translational level. |
format | Online Article Text |
id | pubmed-5338036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53380362017-03-09 Translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region Shen, Jianqiang Liu, Juhong Xie, Kabin Xing, Feng Xiong, Fang Xiao, Jinghua Li, Xianghua Xiong, Lizhong Nat Commun Article Transposable elements constitute a substantial portion of eukaryotic genomes and contribute to genomic variation, function, and evolution. Miniature inverted-repeat transposable elements (MITEs), as DNA transposons, are widely distributed in plant and animal genomes. Previous studies have suggested that retrotransposons act as translational regulators; however, it remains unknown how host mRNAs are influenced by DNA transposons. Here we report a translational repression mechanism mediated by a stowaway-like MITE (sMITE) embedded in the 3′-untranslated region (3′-UTR) of Ghd2, a member of the CCT (CONSTANS [CO], CO-LIKE and TIMING OF CAB1) gene family in rice. Ghd2 regulates important agronomic traits, including grain number, plant height and heading date. Interestingly, the translational repression of Ghd2 by the sMITE mainly relies on Dicer-like 3a (OsDCL3a). Furthermore, other MITEs in the 3′-UTRs of different rice genes exhibit a similar effect on translational repression, thus suggesting that MITEs may exert a general regulatory function at the translational level. Nature Publishing Group 2017-03-03 /pmc/articles/PMC5338036/ /pubmed/28256530 http://dx.doi.org/10.1038/ncomms14651 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Shen, Jianqiang Liu, Juhong Xie, Kabin Xing, Feng Xiong, Fang Xiao, Jinghua Li, Xianghua Xiong, Lizhong Translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region |
title | Translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region |
title_full | Translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region |
title_fullStr | Translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region |
title_full_unstemmed | Translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region |
title_short | Translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region |
title_sort | translational repression by a miniature inverted-repeat transposable element in the 3′ untranslated region |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338036/ https://www.ncbi.nlm.nih.gov/pubmed/28256530 http://dx.doi.org/10.1038/ncomms14651 |
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