Plants are subjected to high levels of DNA damage resulting from their essential dependence on sunlight and exposure to environmental stresses. Accumulation of DNA lesions generated by genotoxic stress disturb genome stability, which hinders plant development and crop productivity. To ensure the maintenance of genome stability, plants developed a range of mechanisms aiming at detecting and repairing DNA damage. The intricated DNA damage response (DDR) network consists of an impressive array of DNA damage sensing and signal transduction pathways leading to DNA repair and cell survival or, alternatively, triggering cell death. Although DDR is highly conserved in eukaryotes, peculiar plant-specific features are described (Yoshiyama et al., ; Nikitaki et al., ; Nisa et al., ). DDR is generally far less studied in plants as compared to mammals (Gimenez and Manzano-Agugliaro, ). Due to the essential role of DNA repair in maintaining genomic stability, tightly controlled regulatory mechanism are required, where different players, including phytohormones (Donà et al., ) or epigenetic regulators (Kim, ), are implicated.
The role played by miRNAs on the post-transcriptional regulation of the DDR has been less considered, particularly in plants when compared to animal systems. Indeed, miRNAs-mediated regulation of DDR gene expression has been already demonstrated in mammalian systems, highly explored in view of therapeutic applications (He et al., ; Majidinia and Yousefi, ; Rezaeian et al., ). In plants, the role of miRNAs in the regulation of DNA damage sensing and repair mechanisms remains to be elucidated.
The present collection of articles gathered within the scope of this Research Topic aims to focus on the implication of miRNAs in genome integrity and response to genotoxic stresses, through direct or indirect interactions with DDR components.
In an extensive review article, Cimini et al. discussed the interconnections between DDR and redox systems, painting a dynamic picture intertwined with regulatory mechanism mediated by miRNAs. Based on their literature analysis, the authors propose a triangular model for redox balance, DDR and miRNAs, where reactive oxygen species (ROS) act as common denominators. At the level of the nucleus, accumulation of ROS results in excessive DNA damage and cell cycle inhibition whereas DDR aid plants to cope with these alterations. Disturbances in the antioxidant and oxidant balance can influence cell cycle progression. Hence, ROS and redox signals are involved in the regulation of gene expression at transcriptional (redox-sensitive transcription factors) and post-transcriptional (miRNAs) levels. The manuscript enlists a series of miRNAs targeting genes involved in ROS production and scavenging along with putative miRNAs implicated in DDR-associated pathways. While more miRNAs associated with ROS metabolism have been experimentally tested, in the case of DDR most examples arrive from in silico studies.
Similarly, the review work by Chowdhury and Basak reinforce the fact that only few plant miRNAs have been identified as active players in combating genotoxic stresses and underlines specific challenges related to miRNA research in this context. As previously mentioned, the lack of in-depth information is a consequence of DDR being significantly less studied in plants compared to animals (Hurdle I) and this combines with the limited information on miRNA targets specifically involved in coping with genotoxic stress (Hurdle II). To address these hurdles, the authors encourage the development of more focused experimental designs combined with the application of omics techniques.
Differently, the review work by Valdés-López et al. provides a different vision on the topic, by looking into the Argonaute (AGO) proteins and their implications in the symbiotic relations between bacteria and legumes, with a stopover on DNA damage/repair-related issues. Being a highly complex process, the regulation of legume-rhizobia symbiosis (LRS) is genetically controlled while some miRNAs are known to play active roles in the post-transcriptional regulation of LRS. AGO proteins (key players in all small-RNA-guided gene-silencing processes) also appear to be involved in LRS, supported by evidence that legumes possess more genes coding for these proteins compared to other non-symbiotic species. In relation to DDR, it is underlined that during rhizobial infection, nodule cells are subjected to endoreduplication, a plant-specific response to DNA damage, cell-cycle arrest, and cell death. Weather AGO proteins with known roles in DNA repair (AGO2, AGO9) are involved in this specific process, still remains to be elucidated.
The “xenomiR” hypothesis proposes that miRNAs can be transferred from one species to another and potentially target genes across distant species. The research work by Bellato et al. combine this cross-kingdom topic with the evolutionary conserved DDR pathway aiming to answer if plant miRNAs could target DDR-related processes in both plant and human cells. The authors have developed a series of bioinformatic approaches to investigate and compare miRNA targets, attesting that these methodologies can be standardized for different species whereas the generated results can serve as starting point for experimental validation of such data. This work succeeded to identify a list of miRNAs predicted to target genes involved in DNA repair, recombination, and replication, chromatin remodeling, cell cycle, and cell death in the model legume Medicago truncatula.
Finally, as a follow up of the bioinformatic study by Bellato et al., the research work of Gualtieri et al. provides experimental evidence on the involvement of selected miRNAs in DDR-associated pathways. The authors have developed an experimental system based on the use of specific chemical agents (camptothecin and NSC120686) know to inhibit the activity of topoisomerase 1 and tyrosyl-DNA phosphodiesterase 1 enzymes. These chemical agents were found to affect the DDR as evidenced by the accumulation of DNA damage and cell death combined with altered transcription profiles of key DDR players in DNA repair and cell cycle regulation. The expression of miRNA-target gene pairs was investigated evidencing that when a miRNA is upregulated, its predicted DDR-target gene is downregulated. The contrasting expression profiles observed support the evidence that these miRNAs (miR156a, miR172c-5p, miR2600e, miR395e, and miR5741a) could repress the expression of these targets (UBE2A, RAD54-like, 5AT, DMAP1, and E2FE-like).
Overall, this collection of articles attentively underlines the gaps-of-knowledge existing with regards to the miRNA-mediated regulation of DDR in plants, while encouraging further research still needed to shed light on this complex topic.
Statements
Author contributions
All authors equally contributed to write the Editorial and discuss about the articles published in the Research Topic.
Acknowledgments
AM acknowledged the support of the Italian Ministry of Education, University and Research (MIUR): Dipartimenti di Eccellenza Program (2018-2022), DBB-UNIPV. The MoRE Lab was supported by grants from the Spanish Ministry of Science awarded to IR-S (RTI2018-097262-B-I00). SA acknowledged the support of FCT (Fundação para a Ciência e a Tecnologia) throughout Research Unit GREEN-IT (UID/Multi/04551/2020), 3i Bioeconomy POCI-01-0246-FEDER-026758 (FEDER, COMPETE 2020), and NORTE-06-3559-FSE-000103 (NORTE 2020, FSE). JAPP acknowledged FCT support throughout the PTDC/AGR-FOR/0931/2014 project.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
MicroRNAs, genotoxicity, DNA damage response, DNA repair, genome stability
Citation
Macovei A, Rubio-Somoza I, Paiva JAP, Araújo S and Donà M (2021) Editorial: MicroRNA Signatures in Plant Genome Stability and Genotoxic Stress. Front. Plant Sci. 12:683302. doi: 10.3389/fpls.2021.683302
Received
20 March 2021
Accepted
25 March 2021
Published
22 April 2021
Volume
12 - 2021
Edited and reviewed by
Jean Molinier, UPR2357 Institut de biologie moléculaire des plantes (IBMP), France
Updates
Copyright
© 2021 Macovei, Rubio-Somoza, Paiva, Araújo and Donà.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Anca Macovei anca.macovei@unipv.it
†Present address: Jorge Almiro Pinto Paiva, CECOLAB, Lagares da Beira, Portugal
This article was submitted to Plant Cell Biology, a section of the journal Frontiers in Plant Science
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