Abstract
There is growing evidence that post-transcriptional RNA modifications are highly dynamic and can be used to improve crop production. Although more than 172 unique types of RNA modifications have been identified throughout the kingdom of life, we are yet to leverage upon the understanding to optimize RNA modifications in crops to improve productivity. The contributions of internal mRNA modifications such as N6-methyladenosine (m6A) and 5-methylcytosine (m5C) methylations to embryonic development, root development, leaf morphogenesis, flowering, fruit ripening and stress response are sufficiently known, but the roles of the two most abundant RNA modifications, pseudouridine (Ψ) and 2′-O-methylation (Nm), in the cell remain unclear due to insufficient advances in high-throughput technologies in plant development. Therefore, in this review, we discuss the latest methods and insights gained in mapping internal Ψ and Nm and their unique properties in plants and other organisms. In addition, we discuss the limitations that remain in high-throughput technologies for qualitative and quantitative mapping of these RNA modifications and highlight future challenges in regulating the plant epitranscriptome.
Original language | English |
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Pages (from-to) | 1241-1256 |
Number of pages | 16 |
Journal | Plant Biotechnology Journal |
Volume | 20 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2022 |
Bibliographical note
Publisher Copyright:© 2022 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.
Funding
KSR is supported by post‐doctoral fellowships from Koshland Foundation and the Dean, Faculty of Chemistry, Weizmann Institute of Science. The authors apologize to those whose original work(s) could not be included in this review due to space limitations. Figure 1 was created with BioRender.com. The authors are grateful for support from the National Natural Science Foundation of China (32071848), a grant from the Jiangxi ‘Shuangqian’ Program (S2019DQKJ2030), the Natural Science Foundation for Distinguished Young Scholars of Nanjing Forestry University (JC2019004), the Qing Lan Project of Jiangsu Higher Education Institutions, and a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions. This work was also supported by the Metasequoia Faculty Research Start‐up Funding (grant number 163100028) at Bamboo Research Institute, Nanjing Forestry University for the first author MR. The authors are grateful for support from the National Natural Science Foundation of China (32071848), a grant from the Jiangxi ‘Shuangqian’ Program (S2019DQKJ2030), the Natural Science Foundation for Distinguished Young Scholars of Nanjing Forestry University (JC2019004), the Qing Lan Project of Jiangsu Higher Education Institutions, and a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions. This work was also supported by the Metasequoia Faculty Research Start-up Funding (grant number 163100028) at Bamboo Research Institute, Nanjing Forestry University for the first author MR. KSR is supported by post-doctoral fellowships from Koshland Foundation and the Dean, Faculty of Chemistry, Weizmann Institute of Science. The authors apologize to those whose original work(s) could not be included in this review due to space limitations. Figure 1 was created with BioRender.com.
Funders | Funder number |
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Bamboo Research Institute | |
Metasequoia Faculty Research Start-up Funding | |
Natural Science Foundation for Distinguished Young Scholars of Nanjing Forestry University | JC2019004 |
Qing Lan Project of Jiangsu Higher Education Institutions | |
Nanjing Forestry University | |
Koshland Foundation | |
Weizmann Institute of Science | |
National Natural Science Foundation of China | S2019DQKJ2030, 32071848 |
Priority Academic Program Development of Jiangsu Higher Education Institutions | 163100028 |
Keywords
- 2′-O-methylation
- RNA modifications
- epitranscriptomics
- next-generation sequencing
- pseudouridine