Elsevier

Journal of Plant Physiology

Volume 169, Issue 16, 1 November 2012, Pages 1664-1672
Journal of Plant Physiology

Role of microRNAs and other sRNAs of plants in their changing environments

https://doi.org/10.1016/j.jplph.2012.03.009Get rights and content

Abstract

Plants constantly face a complex array of environmental biotic and abiotic stimuli. Recent studies in various plants have highlighted the key roles of microRNAs and of different siRNA classes in the post-transcriptional regulation of plant genes essential for conserved responses of plants to individual stress conditions. It is not yet clear how these different signals and responses are integrated in nature. In the present review, we summarize current knowledge on sRNA-mediated responses to stress, and highlight possible directions of future research.

Introduction

In nature, plants are exposed to a wide array of environmental stimuli and stresses that trigger various functional and/or structural responses. Plants are sessile organisms. They must cope with stressful environmental conditions, to integrate these various stresses and to adjust a proper molecular response that might eventually lead to their adaptation or acclimation to the stresses. A large proportion of plant genes are regulated by biotic (e.g. bacterial pathogen, virus, fungi, insects, nematodes, etc.) (Fagard et al., 2007, Brotman et al., 2012) and abiotic stresses (e.g. drought, soil salinity, extreme temperatures, heavy metals, etc.) (Chao et al., 2005, Si et al., 2009). These regulations potentially affect all the different levels of gene expression, i.e. transcription, RNA processing, translation or even posttranslational modifications.

RNA silencing encompasses a wide variety of mechanisms that commonly depend on guide RNA molecules. In plants, RNA silencing plays key roles in defense against viruses and in orchestrating the expression, stability, and inheritance of eukaryotic genomes (Chen, 2009, Vazquez et al., 2010). To reach these latter goals, plants have evolved a complex variety of small RNA (sRNA) regulators that control virtually every aspect of plant life. These sRNAs are generated through different pathways that depend on core highly conserved proteins of the DICER-LIKE, Double-strand RNA Binding, and ARGONAUTE family proteins (for details see Vazquez, 2006, Brodersen and Voinnet, 2006, Mallory and Vaucheret, 2010). sRNAs are called microRNAs when they are produced as discrete sRNA species from MIR genes and siRNAs when produced as complex sRNA pools from long dsRNA precursors.

MicroRNAs, trans-acting siRNAs and other siRNA species play crucial roles in plant development and act as bandmasters of genome expression. Several studies have also highlighted the key roles of these sRNA regulators in the post-transcriptional regulation of genes essential for plant response to various stress conditions. In this review, we summarize current knowledge on sRNA-mediated response to stress (Fig. 1, Table 1 and S1).

Section snippets

The role of microRNAs in nutrient homeostasis

Plants require at least 14 essential mineral elements, predominately acquired from the soil, to maintain normal growth and development and to ensure the completion of their life cycles. Systematic and integrative genomic approaches have been applied to understand the processes of nutrient acquisition, assimilation, metabolism and adaptations in response to low nutrient concentrations. In this respect, sRNAs have emerged as crucial players to fine-regulate and optimize nutrient homeostasis (Fig.

Role of miR398 in response to oxidative stress

In plants, various environmental stresses, including salinity, heavy metals, drought, and nutrient deficiency result in the rapid accumulation of reactive oxygen species (ROS) such as superoxide radicals (O2), hydrogen peroxide (H2O2) and hydroxyl radicals (OH−) (Mittler, 2002, Bartels and Sunkar, 2005). ROS accumulation causes oxidative damage to nucleic acids, proteins and membrane lipids. In plants, enzymatic (superoxide dismutases, catalases and peroxidases) and non-enzymatic scavenging

Involvement of microRNAs in response to biotic stress

In addition to deprivation of nutrients and abiotic stresses, the quality and yield of crops can be strongly affected by attack by viruses, bacteria, fungi, insects and nematodes. While the role of RNA silencing in defense against viruses was unraveled several years ago, the involvement of miRNA-guided regulations have emerged only recently as one of the many strategies developed by plants to protect against bacterial pathogens (Navarro et al., 2006). Perception of flagellin is crucial for

Involvement of other classes of plant small RNAs in response to stress

Plant siRNAs derive mainly from heterochromatic regions and DNA repeats, and mediate the silencing maintenance of the regions from which they originate (Chen, 2009). Certain plant siRNAs like the trans-acting siRNAs or the nat-siRNAs regulate the expression of important target transcripts (Baulcombe, 2004, Ding and Voinnet, 2007, Vazquez et al., 2010). The dsRNA precursors of siRNAs are generated either by the function of different cellular RDRs (RNA-dependent RNA Polymerases) or by annealing

Outlook

The data we have reviewed here demonstrate the involvement of different classes of small RNAs, such as miRNAs, siRNAs, ta-siRNAs and nat-siRNAs in response to biotic and abiotic stresses. The role of these various sRNAs and especially of npcRNAs are highly promising areas of research for the future understanding of the diversity and specificities of plant responses to stresses. These responses involve coordinating the regulation of complex hormonal pathways. Thus, one important challenge will

Acknowledgments

The authors are grateful to EC (POLAPGEN-BD Project, grant no. UDA.POIG.01.03.01-00-101/08/01 to K.K.), the Ministry of Science and Higher Education for funding the research in Z.S.K. laboratory (KBN grant no. N302 236938 to M.P. and MNiSW grant no. 3011/B/PO1/2009/37) and to the Swiss National Science Foundation (SNSF) for funding the research in F.V. laboratory (Ambizione grant no. PZ00P3_126329/1 to F.V.). M. Pieczynski is a scholarship holder within the project “Scholarship support for

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