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Global translational reprogramming is a fundamental layer of immune regulation in plants
In the absence of specialized immune cells, the need for plants to reprogram transcription to transition from growth-related activities to defence is well understood(1, 2). However, little is known about translational changes that occur during immune induction. Using ribosome footprinting (RF), we p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485861/ https://www.ncbi.nlm.nih.gov/pubmed/28514447 http://dx.doi.org/10.1038/nature22371 |
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author | Xu, Guoyong Greene, George H. Yoo, Heejin Liu, Lijing Marqués, Jorge Motley, Jonathan Dong, Xinnian |
author_facet | Xu, Guoyong Greene, George H. Yoo, Heejin Liu, Lijing Marqués, Jorge Motley, Jonathan Dong, Xinnian |
author_sort | Xu, Guoyong |
collection | PubMed |
description | In the absence of specialized immune cells, the need for plants to reprogram transcription to transition from growth-related activities to defence is well understood(1, 2). However, little is known about translational changes that occur during immune induction. Using ribosome footprinting (RF), we performed global translatome profiling on Arabidopsis exposed to the microbe-associated molecular pattern (MAMP) elf18. We found that during this pattern-triggered immunity (PTI), translation was tightly regulated and poorly correlated with transcription. Identification of genes with altered translational efficiency (TE) led to the discovery of novel regulators of this immune response. Further investigation of these genes showed that mRNA sequence features are major determinants of the observed TE changes. In the 5′ leader sequences of transcripts with increased TE, we found a highly enriched mRNA consensus sequence, R-motif, consisting of mostly purines. We showed that R-motif regulates translation in response to PTI induction through interaction with poly(A)-binding proteins. Therefore, this study provides not only strong evidence, but also a molecular mechanism for global translational reprogramming during PTI in plants. |
format | Online Article Text |
id | pubmed-5485861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-54858612017-11-17 Global translational reprogramming is a fundamental layer of immune regulation in plants Xu, Guoyong Greene, George H. Yoo, Heejin Liu, Lijing Marqués, Jorge Motley, Jonathan Dong, Xinnian Nature Article In the absence of specialized immune cells, the need for plants to reprogram transcription to transition from growth-related activities to defence is well understood(1, 2). However, little is known about translational changes that occur during immune induction. Using ribosome footprinting (RF), we performed global translatome profiling on Arabidopsis exposed to the microbe-associated molecular pattern (MAMP) elf18. We found that during this pattern-triggered immunity (PTI), translation was tightly regulated and poorly correlated with transcription. Identification of genes with altered translational efficiency (TE) led to the discovery of novel regulators of this immune response. Further investigation of these genes showed that mRNA sequence features are major determinants of the observed TE changes. In the 5′ leader sequences of transcripts with increased TE, we found a highly enriched mRNA consensus sequence, R-motif, consisting of mostly purines. We showed that R-motif regulates translation in response to PTI induction through interaction with poly(A)-binding proteins. Therefore, this study provides not only strong evidence, but also a molecular mechanism for global translational reprogramming during PTI in plants. 2017-05-17 2017-05-25 /pmc/articles/PMC5485861/ /pubmed/28514447 http://dx.doi.org/10.1038/nature22371 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms Reprints and permissions information is available at www.nature.com/reprints |
spellingShingle | Article Xu, Guoyong Greene, George H. Yoo, Heejin Liu, Lijing Marqués, Jorge Motley, Jonathan Dong, Xinnian Global translational reprogramming is a fundamental layer of immune regulation in plants |
title | Global translational reprogramming is a fundamental layer of immune regulation in plants |
title_full | Global translational reprogramming is a fundamental layer of immune regulation in plants |
title_fullStr | Global translational reprogramming is a fundamental layer of immune regulation in plants |
title_full_unstemmed | Global translational reprogramming is a fundamental layer of immune regulation in plants |
title_short | Global translational reprogramming is a fundamental layer of immune regulation in plants |
title_sort | global translational reprogramming is a fundamental layer of immune regulation in plants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485861/ https://www.ncbi.nlm.nih.gov/pubmed/28514447 http://dx.doi.org/10.1038/nature22371 |
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