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A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA
All known riboswitches use their aptamer to senese one metabolite signal and their expression platform to regulate gene expression. Here, we characterize a SAM-I riboswitch (SAM-I(Xcc)) from the Xanthomonas campestris that regulates methionine synthesis via the met operon. In vitro and in vivo exper...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270179/ https://www.ncbi.nlm.nih.gov/pubmed/32493973 http://dx.doi.org/10.1038/s41467-020-16417-z |
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author | Tang, Dong-Jie Du, Xinyu Shi, Qiang Zhang, Jian-Ling He, Yuan-Ping Chen, Yan-Miao Ming, Zhenhua Wang, Dan Zhong, Wan-Ying Liang, Yu-Wei Liu, Jin-Yang Huang, Jian-Ming Zhong, Yun-Shi An, Shi-Qi Gu, Hongzhou Tang, Ji-Liang |
author_facet | Tang, Dong-Jie Du, Xinyu Shi, Qiang Zhang, Jian-Ling He, Yuan-Ping Chen, Yan-Miao Ming, Zhenhua Wang, Dan Zhong, Wan-Ying Liang, Yu-Wei Liu, Jin-Yang Huang, Jian-Ming Zhong, Yun-Shi An, Shi-Qi Gu, Hongzhou Tang, Ji-Liang |
author_sort | Tang, Dong-Jie |
collection | PubMed |
description | All known riboswitches use their aptamer to senese one metabolite signal and their expression platform to regulate gene expression. Here, we characterize a SAM-I riboswitch (SAM-I(Xcc)) from the Xanthomonas campestris that regulates methionine synthesis via the met operon. In vitro and in vivo experiments show that SAM-I(Xcc) controls the met operon primarily at the translational level in response to cellular S-adenosylmethionine (SAM) levels. Biochemical and genetic data demonstrate that SAM-I(Xcc) expression platform not only can repress gene expression in response to SAM binding to SAM-I(Xcc) aptamer but also can sense and bind uncharged initiator Met tRNA, resulting in the sequestering of the anti-Shine-Dalgarno (SD) sequence and freeing the SD for translation initiation. These findings identify a SAM-I riboswitch with a dual functioning expression platform that regulates methionine synthesis through a previously unrecognized mechanism and discover a natural tRNA-sensing RNA element. This SAM-I riboswitch appears to be highly conserved in Xanthomonas species. |
format | Online Article Text |
id | pubmed-7270179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72701792020-06-15 A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA Tang, Dong-Jie Du, Xinyu Shi, Qiang Zhang, Jian-Ling He, Yuan-Ping Chen, Yan-Miao Ming, Zhenhua Wang, Dan Zhong, Wan-Ying Liang, Yu-Wei Liu, Jin-Yang Huang, Jian-Ming Zhong, Yun-Shi An, Shi-Qi Gu, Hongzhou Tang, Ji-Liang Nat Commun Article All known riboswitches use their aptamer to senese one metabolite signal and their expression platform to regulate gene expression. Here, we characterize a SAM-I riboswitch (SAM-I(Xcc)) from the Xanthomonas campestris that regulates methionine synthesis via the met operon. In vitro and in vivo experiments show that SAM-I(Xcc) controls the met operon primarily at the translational level in response to cellular S-adenosylmethionine (SAM) levels. Biochemical and genetic data demonstrate that SAM-I(Xcc) expression platform not only can repress gene expression in response to SAM binding to SAM-I(Xcc) aptamer but also can sense and bind uncharged initiator Met tRNA, resulting in the sequestering of the anti-Shine-Dalgarno (SD) sequence and freeing the SD for translation initiation. These findings identify a SAM-I riboswitch with a dual functioning expression platform that regulates methionine synthesis through a previously unrecognized mechanism and discover a natural tRNA-sensing RNA element. This SAM-I riboswitch appears to be highly conserved in Xanthomonas species. Nature Publishing Group UK 2020-06-03 /pmc/articles/PMC7270179/ /pubmed/32493973 http://dx.doi.org/10.1038/s41467-020-16417-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tang, Dong-Jie Du, Xinyu Shi, Qiang Zhang, Jian-Ling He, Yuan-Ping Chen, Yan-Miao Ming, Zhenhua Wang, Dan Zhong, Wan-Ying Liang, Yu-Wei Liu, Jin-Yang Huang, Jian-Ming Zhong, Yun-Shi An, Shi-Qi Gu, Hongzhou Tang, Ji-Liang A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA |
title | A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA |
title_full | A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA |
title_fullStr | A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA |
title_full_unstemmed | A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA |
title_short | A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA |
title_sort | sam-i riboswitch with the ability to sense and respond to uncharged initiator trna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270179/ https://www.ncbi.nlm.nih.gov/pubmed/32493973 http://dx.doi.org/10.1038/s41467-020-16417-z |
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