Expression of miRNAs involved in phosphate homeostasis and senescence is altered in glyphosate-treated maize
- 1.2k Downloads
Glyphosate is a systemic, nonselective and most widely used herbicide in the world. The introduction of glyphosate-resistant crops in the mid-1990s resulted in a dramatic increase in the use of glyphosate herbicide making it most widely used herbicide in the world. The average maize yield loss in the field caused by pests is around 20 % but in many regions it is much higher. It is now clear that glyphosate causes broader range of physiological alterations than previously assumed and some plants gain higher level of resistance to glyphosate without the need to use genetic engineering methods. To understand the mechanisms of such heightened resistance we must first know the processes mediating the plants’ death in response to glyphosate treatment. Here, we show that 12 miRNAs, belonging to miR167, miR396, miR159, miR156, miR169, miR444 and miR827 families, are significantly upregulated, and one, miR166, downregulated following glyphosate treatment. These miRNAs have been previously shown to be involved in abiotic stress responses and implicated in senescence. Strikingly, two of the induced miRNAs, miR444 and miR827, have been shown to regulate phosphate transport pathways, which seem to be common for Pi and glyphosate uptake.
KeywordsMaize Herbicidal stress Glyphosate miRNAs Pi homeostasis Senescence
Glyphosate, a glycine derivative (N-(phosphonomethyl)glycine), is a broad-spectrum, post-emergence herbicide. Concurrently with the release of genetically engineered glyphosate-resistant soybean in 1996, there was a dramatic increase in the use of glyphosate; it has now become the most widely used herbicide in the world. Glyphosate is active as a salt and effective only when it comes into contact with green, growing parts of plants (Duke and Powles 2008) after which it becomes distributed throughout the organism. There appear to be at least two mechanisms of glyphosate uptake (active and passive) in plants; however, they are not well understood to date. An active system operates at low concentrations of herbicide and may presumably involve a phosphate transporter since it has been shown that the glyphosate uptake is inhibited by sodium phosphate and phosphonoformic acid, competitive inhibitors of phosphate assimilation in plant cells (Denis and Delrot 1993; Hetherington et al. 1998; Morin et al. 1997; Shaner 2009). The interruption of essential metabolic pathways manifests as yellowing and wilting of the plant leaves followed by browning. Concurrently glyphosate induces decomposition of the plant’s roots and rhizomes. Plants sprayed with glyphosate die within 10–14 days. The symptoms resulting from glyphosate administration resemble those occurring during senescence. Leaf senescence is manifested by a tissue-specific changes like chloroplasts degeneration and disintegration of photosynthetic apparatus. The senescence hypothesis, known as the nutrient relocalization hypothesis, states that annual plants at the end of growing season face limited supplies of micro- and macronutrients and therefore relocate resources such as copper, phosphate and nitrate into vegetative tissues to enhance seed yields (Gregersen et al. 2008; Himelblau and Amasino 2001). Interestingly, large-scale expression profiling experiments indicate the existence of cross-talk between developmental senescence and responses to abiotic stresses (Allu et al. 2014; Buchanan-Wollaston et al. 2005).
Administration of herbicide Roundup® to plant causes glyphosate-mediated inhibition of the 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) resulting in the disruption of synthesis of aromatic amino acids and their derivatives (Duke and Powles 2008). However, some studies dispute that glyphosate toxic effect is strictly linked to EPSPS inhibition; it has not been verified that a depletion in concentration of aromatic amino acids occurs in glyphosate-treated plants (Serra et al. 2013). Instead, acting as a metal chelator, glyphosate could negatively contribute to the activity of many enzymes, altering plant physiological processes such as photosynthesis, carbon metabolism, mineral nutrition and oxidative events (Geiger et al. 1986; Orcaray et al. 2012; Romero et al. 2011).
The major drawback of wide use of herbicides is a continuous selection of plants able to both survive and reproduce under herbicide treatment. As a consequence, plants with improved survival properties are able to become dominant and distributed over large areas (Menne and Köcher 2008). There are currently 447 unique cases among 244 species (142 dicots and 102 monocots) of herbicide resistant weeds. Strikingly, they cover 22 of the 25 known mechanisms of herbicide action (156 different herbicides) (Heap 2015). The development of resistance to herbicides, however, is not restricted to weeds. Maize, Zea mays, is one of the world’s most cultivated crop plants. Its great economic potential is shown in its broad base use in food, fodder and textile industry as well as in bioethanol production. Unexpectedly the value of maize crop is nowadays threatened by its susceptibility to chemicals used for weeds and pests control. The average pest-induced yield loss of maize in the field is around 20 %, and often much higher. Field observation has shown that some of maize lines are more sensitive than others to herbicide spraying (K. Adamczewski, J. Adamczyk, personal communication).
Plants, as well as other organisms, have employed gene expression regulation by small RNA molecules in addition to regulatory DNA sequences and different types of regulatory proteins to achieve precise and timely regulation of stress-responsive gene networks. Small non-coding RNAs, discovered two decades ago, not only regulate gene expression on post-transcriptional and transcriptional levels, but also affect the organization and modification of chromatin. Moreover, they regulate growth and development of organisms, organ development, hormone signaling, and defense against pathogens among other physiological functions (Moazed 2009). They also function during environmental stress adaptation, providing precise regulation of gene expression. In plants small RNAs exhibit unexpected complexity, however, two main categories are distinguished based on their biogenesis and function. These are miRNAs (microRNAs) and siRNAs (short interfering RNAs).
To date little is known about the involvement of miRNAs in response to herbicide treatment in plants. Here, we describe the roles of miRNA in late response to one of the most commonly used herbicide worldwide—glyphosate. We performed the miRNA expression profiling in maize leaves 7 days after glyphosate administration, which is a crucial time point for selection of the death or survival pathway.
Materials and methods
For analyses we used maize inbred line S79757, seeds were obtained from a local breeder HR Smolice. We chose maize lines based on field tests conducted to verify the response of 25 maize inbred lines to Roundup® stress (K. Adamczewski, data not published). Based on these tests we chose the line S79757 as it showed the most prominent response to herbicide stress. Maize seedlings were grown in a greenhouse in controlled temperature (22 °C), humidity and light conditions (16/8 h, light/dark). Uniform-sized seedlings were selected and divided into two groups. The experimental group was sprayed with a sublethal dose of herbicide Roundup® (1.0 l/ha, 300 g glyphosate) with adjuvant AS 500 SL (4.0 l/ha) 2 weeks after plants’ emergence (at the 4–5 leaf), the control group was cultured without Roundup® treatment. Leaves were harvested 7 days after Roundup® application, to evaluate the late response to stress conditions. Leaves were harvested at the same times for both experimental and control plants. Plant material samples were immediately frozen in liquid nitrogen and stored at −80 °C.
RNA isolation, cDNA library preparation and sequencing
The small RNA fractions <200 nt were isolated from 250 mg of leaves collected and pooled from six plants. Isolation was performed using mirVana miRNA Isolation Kit (Ambion) following the manufacturer’s instructions. RNA concentration was measured with Nanodrop 2000 and the quality was determined with Bioanalizator 2100 (Agilent; Small RNA Kit). cDNA libraries were prepared for sequencing with TruSeq SmallRNA Preparation Kit (Illumina), this included the following steps: ligation of adapters, RT-PCR amplification, gel purification of small RNA libraries and validation. Genome Analyzer IIx (Illumina) was used for 72 nt single-read sequencing.
Analysis of sequencing data
Raw sequencing reads were examined for quality using FastQC software. Next, 3′ adaptor sequences were trimmed using cutadapt tool (Martin 2011). Only sequences with removed adaptors and resulting length of 18–24 nt were selected for downstream analysis. After adaptor removal, library quality was examined with FastQC software to verify that no further quality filtering or trimming was necessary. In order to enable identification of conserved miRNAs not observed previously in maize, the non-redundant subset of Magnoliophyta miRNAs obtained from miRBase (release 21) (Kozomara and Griffiths-Jones 2014) was used as reference miRNA sequences. This was prepared by clustering miRBase sequences with cdhit-est program (sequence identity 100 %, minimum overlap 80 %) (Fu et al. 2012). Maize miRNA was selected as the cluster representative, if present within a cluster. Expression profiling was performed with quantifier.pl script from the mirdeep2 package (Friedländer et al. 2012) with one mismatch between read and reference allowed. The high confidence set of expressed miRNAs was constructed by selection of miRNAs present in minimum of two samples with at least 10 reads. The resulting table of raw miRNA read counts is available in the Supporting Information section (Table S1).
Differential gene expression analysis was performed using R statistical environment and edgeR package (Robinson et al. 2010). For miRNA target prediction, the psRNA Target web server (Dai and Zhao 2011) was used. Functional annotation of the target mRNAs was done using the in-house script based on information downloaded from Plant Ensembl portal. For the Gene Ontology enrichment analysis the g:Profiler web server (Reimand et al. 2011) was used.
We found that 21 nt was the most prominent length of sequence reads from our experiments that mapped to miRNAs (Fig. 1b); this size is canonical for plant miRNAs. With few exceptions, this general trend was also observed for most of the analyzed individual miRNA length distributions.
Novel conserved miRNAs in maize
Novel maize miRNAs identified in this study
Number of supporting reads
Number of supporting libraries
Novel/known maize miRNA family
miRNAs involved in response to glyphosate treatment
Differentially expressed miRNAs upon glyphosate treatment
mRNA targets of differentially expressed miRNAs
All identified differentially expressed maize miRNAs are described in the literature and their mRNA targets are well documented. However, to verify if novel miRNA family members, differentially expressed following herbicide administration, differ in functional potential from known maize miRNAs, we predicted their putative targets, based on sequence complementarity to mRNA sequences. For all differentially expressed miRNAs we identified 264 potential target transcripts, corresponding to 122 genes, of which 48 were encoding for uncharacterized proteins. Gene Ontology (GO) enrichment analysis showed that most of the proteins with known function encoded by miRNAs-targeted mRNAs were localized in nucleus and were involved in the regulation of transcription (Supporting Information File 1). The only enriched GO category not related to gene expression regulation was regulation or involvement in hydrolase activity with 17 representatives. This function was assigned mostly to ATP-binding proteins. Noticeably, all predicted miRNA targets, including those for novel members of known maize miRNA families, were consistent with previous reports.
The holistic understanding of Roundup® mechanism of action is of great importance since it has been shown that glyphosate affects the growth of plants not only by inhibiting EPSPS but also through altering several crucial plant physiological processes (e.g., photosynthesis, carbon metabolism, mineral nutrition, oxidative events) (Geiger et al. 1986; Orcaray et al. 2012; Romero et al. 2011). Here, we focused our efforts on profiling of miRNA levels in a maize line sensitive to Roundup® 7 days after herbicide administration. We identified twelve miRNAs with statistically significant upregulation in glyphosate treated plants and one downregulated (Fig. 4; Table 2). Four of them, including two isoforms observed for the first time in maize, belong to miR167 family, two are miR396 family members and two are processed from both arms of miR827 precursor. The remaining ones include miR156, miR166, and novel miR159, miR169, miR444 isoforms.
Differentially expressed members of seven out of eight microRNA families, found in our study, have previously been implicated in abiotic stress responses (Liu et al. 2012; Li et al. 2011; Kulcheski et al. 2011). In Arabidopsis (Gao et al. 2010) as well as in maize (Ding et al. 2009) miR396c is downregulated during salinity and alkali treatment. In contrast, other differentiating in our samples miRNAs, namely miR167, miR156, miR396a and miR396d, have been previously reported to be upregulated in salinity and ABA treated plants but downregulated or unchanged in plants under cold or drought stress (Jian et al. 2010; Shen et al. 2010). Interestingly, most of microRNAs that differentiate in our samples have been recently linked with senescence. It has been shown that overexpression of miR396 in transgenic Arabidopsis lines causes faster senescence of leaves when compared to wild-type plants thus suggesting its primary role in this process (Debernardi et al. 2014). miR396a-5p, newly discovered in maize, similar to miR827, is induced in Arabidopsis during senescence in leaves but repressed in siliques (Thatcher et al. 2015). Representatives of three other miRNA families (miR156, miR159, miR167) also induced upon glyphosate treatment have been implicated in senescence (Meng et al. 2012). It has been established that miR156/157 family members all target SPL transcription factors controlling development and transition from the juvenile to adult phase of the plant (Wu et al. 2009). It has been observed in siliques that miR156 is strongly induced in late senescence. This could in turn repress some members of SPL family of proteins (Thatcher et al. 2015). Members of remaining two miRNA families differentially expressed under glyphosate treatment, miR167 and miR159, might be involved in a mechanism of senescence-resistance through ABA-dependent pathway (Xu et al. 2014). As shown in (Xu et al. 2014) the expression levels of miR167f-3p together with miR159b and miR159a.1 were significantly lower in age-resistant rice line (N2Y6) compared to age-sensitive rice line (LYP9) that is thought to contribute to the delay of leaf senescence. Moreover, miR159, miR166 and miR167 differentiating in our study, are significantly overexpressed and functionally implicated in hybrid necrosis in wheat (Zhou et al. 2015). Both these processes (senescence and necrosis) are phenotypically closely related to changes observed in glyphosate treated maize plants.
The remaining miRNAs found unique upon glyphosate treatment, including miR159, miR166, miR167, miR169 and miR396 were also shown to be differentially expressed under Pi starvation in Arabidopsis, wheat, maize, soybean and white lupin (Lundmark et al. 2010; Pei et al. 2013; Zeng et al. 2010; Zhao et al. 2013; Zhu et al. 2010).
Our study revealed 13 miRNAs with significantly altered expression upon treatment of the plants with glyphosate-based herbicide. Most of them are known to be involved in response to abiotic stresses and senescence. Our results suggest that prominent role in mechanism of glyphosate toxicity could be associated with the disruption of phosphate transport pathways (enabling glyphosate uptake into cells by using the transporters specific for Pi and thus diminishing Pi uptake) and regulated through the action of miR827-3p and miR444.
Author contribution statement
A.T., J.G. performed wet lab experiments; M.Ż. performed sequencing data and differential expression analysis; M.Ż., A.T., W.K., T.T. interpreted the results; M.Ż., A.T., J.G., W.K., T.T. wrote the manuscript.
We thank prof. K. Adamczewski for plant breeding. Small RNA sequencing was performed at ECBiG in Poznań, Poland. Authors declare no conflict of interest. This work was supported by grants from Ministry of Science and Higher Education of the Republic of Poland no. 7690/B/P01/2011/40, National Science Center Poland nos. UMO-2011/01/D/NZ9/03631, UMO-2012/06/A/NZ9/00125 and Ministry of Science and Higher Education of the Republic of Poland by KNOW program.
- Hackenberg M, Shi B-J, Gustafson P, Langridge P (2013) Characterization of phosphorus-regulated miR399 and miR827 and their isomirs in barley under phosphorus-sufficient and phosphorus-deficient conditions. BMC Plant Biol 13:214. doi:10.1186/1471-2229-13-214 PubMedCentralCrossRefPubMedGoogle Scholar
- Heap I (2015) International Survey of Herbicide Resistant Weeds. Online. Internet. Available: http://www.weedscience.com. Accessed 21 May 2015
- Lin W-Y, Huang T-K, Chiou T-J (2013) Nitrogen limitation adaptation, a target of microRNA827, mediates degradation of plasma membrane-localized phosphate transporters to maintain phosphate homeostasis in Arabidopsis. Plant Cell 25:4061–4074. doi:10.1105/tpc.113.116012 PubMedCentralCrossRefPubMedGoogle Scholar
- Martin M (2011) Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet.journal 17: 10Google Scholar
- Menne H, Köcher H (2008) HRAC Classification of Herbicides and Resistance Development. In: Modern Crop Protection Compounds. Hedelberg, Germany pp 5–26 doi:10.1002/9783527619580.ch1
- Serra A-A, Nuttens A, Larvor V et al (2013) Low environmentally relevant levels of bioactive xenobiotics and associated degradation products cause cryptic perturbations of metabolism and molecular stress responses in Arabidopsis thaliana. J Exp Bot 64:2753–2766. doi:10.1093/jxb/ert119 CrossRefPubMedGoogle Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.