Jagesh Kumar Tiwari
Tanuja Buckseth
Rajesh Kumar Singh
Manoj Kumar
Surya Kant- 1Indian Council of Agricultural Research (ICAR)-Central Potato Research Institute, Shimla, India
- 2Agriculture Victoria, Grains Innovation Park, Horsham, VIC, Australia
- 3Faculty of Veterinary and Agricultural Sciences, Centre for Agricultural Innovation, School of Agriculture and Food, The University of Melbourne, Melbourne, VIC, Australia
Introduction
Feeding the world population increasing from current 7.7 to 9.7 billion by 2050 is a big challenge (United Nations, 2019). This is further serious in developing countries where degradation of soil health, increasing fertilizers cost and reducing cultivable lands are the major constraints (St Clair and Lynch, 2010). Presently, 119.41 million tons of nitrogen (N) fertilizers are applied worldwide in crops to achieve desirable yield (FAO, 2018). Plant N uptake, transport, utilization/assimilation and remobilization are controlled by a complex network of genes involved in these biological processes. Significant research advancements have been made in nitrogen use efficiency (NUE) in plants like Arabidopsis, rice, maize and wheat (Li et al., 2017), and physiological and molecular mechanisms underlying N pathways have been elucidated in plants (Kant et al., 2011). Although, many studies have been undertaken in different N regimes and candidate genes have been identified for increasing NUE but success in achieving N-use efficient genotypes is limited due to its complex genetics and genotype by environment interaction (Baligar et al., 2001). Interestingly, a considerable number of transgenic plants with increased NUE have been developed in cereals (Li et al., 2020). Notably, progress in CRISPR/Cas9 [clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated nuclease 9] genome editing combined with base-editing technology provides a great opportunity for enhancing NUE in plants (Khatodia et al., 2016; Li et al., 2018).
Potato (Solanum tuberosum L.) is the fourth most important food crop of the world after rice, wheat and maize. Potato is an N fertilizer intensive crop that requires 180–240 kg N/ha fertilizers to produce high tuber yield (35–45 t/ha); of total applied N, plants acquire only 40–50% and remaining N is lost in environment (Trehan and Singh, 2013). Owing to the adverse impacts and high production cost caused by excess N fertilizers application, improving NUE of plant is an environmental-friendly approach to achieve sustainable crop yield (Fageria et al., 2008). This opinion article highlights prospects for improving NUE in potato based on the lessons learnt from the transgenics to the CRISPR/Cas9 genome editing research in plants.
Applications of Transgenics and CRISPR-Cas Technologies for Improving NUE in Plants
Transgenic technology has been applied in plants to create genetically modified organism (GMO) by overexpression or knockout/silencing of genes. Genes have been transferred within or across the species to introduce new or enhance/alter endogenous gene expression (Good et al., 2007). Whereas, gene silencing (RNAi) process inhibits gene expression or translation by disrupting targeted mRNA (Liang et al., 2014). N metabolism pathways genes such as nitrate or ammonium transporters, assimilation genes and transcription factors (TFs) have been manipulated for improving NUE in cereals (Li et al., 2020). Generally, overexpression of genes driven by the constitutive (Ubiquitin and CaMV35S) or tissue-specific (e.g., OsNAR2.1) promoters has been deployed to develop N-use efficient transgenic plants (Chen J. et al., 2016). Hu et al. (2015) have demonstrated overexpression of OsNRT1.1B allele of indica rice into japonica to increase NUE. RNAi technology has been deployed to knockdown the NAC-like TF OsNAP to improve NUE in rice (Liang et al., 2014).
The recently discovered CRISPR/Cas9 system has revolutionized the plant research. CRISPR/Cas9 (type-II, originates from Streptococcus pyogenes) is an adaptive immunity found in bacteria or archaea to combat with invading nucleic acids (Khatodia et al., 2016). The unprecedented advances in CRISPR/Cas9 facilitate an easy, versatile and robust technology to accelerate genomics-assisted crop improvement. CRISPR/Cas9 has been successfully deployed to edit N transporter gene to enhance NUE by introgression of NRT1.1B-indica allele into japonica rice (Li et al., 2018). Until now, CRISPR/Cas9 has been mostly applied to mutate negative regulators, instead of overexpression of positive regulators. The gene BT2, a member of the Bric-a-Brac/Tramtrack/Broad gene family, suppresses nitrate uptake and NUE; and overexpression of BT2 decreased NUE in rice under low nitrate by decreasing expression of NRT2.1 and NRT2.4 genes (Araus et al., 2016). Further, symbiotic N fixation (SNF)-associated genes have also been inactivated by CRISPR/Cas9 in Lotus japonicus (Wang et al., 2016), and thus progress in genome editing would accelerate SNF research in legumes and non-legumes. Recently, cytosine- and adenine- base editors (CBEs/ABEs) called base-editing, based on CRISPR/Cas9, have emerged as a newer technology for precise modification of nucleotides [C to T (or G to A), and A to G (or T to C)] for gain or loss of gene functions in eukaryotes (Li et al., 2018; Mishra et al., 2020). The base-editing has been demonstrated in rice for nitrate transporter gene OsNRT1.1B to improve NUE (Lu and Zhu, 2017; Zong et al., 2018). Collectively, the successful examples of a few N-use efficient plants (transgenics and genome-edited) are summarized in Supplementary Table 1.
Recent Results in Crops NUE Modification
Increasing N Uptake and Transport Efficiency
A number of N transporter genes such as low-affinity nitrate transporter NRT1.1b (Fan et al., 2015; Hu et al., 2015), high-affinity nitrate transporters NRT2.1 (Chen J. et al., 2016; Chen et al., 2017), NAR2.1 and NRT2.3a (Chen et al., 2020), NRT2.3 (Fu et al., 2015), and NRT2.3b (Fan et al., 2016), peptide transporter PTR9 (Fang et al., 2013), ammonium transporter AMT1;1 (Ranathunge et al., 2014), and quantitative trait loci qNGR9, synonymous with gene DEP1 (Sun et al., 2014) have shown to enhance NUE in rice. Similarly, TFs such as MADS25 (Yu et al., 2015) and NAC2-5A (He et al., 2015) have also been found effective in developing N use efficient rice and wheat, respectively. The roles of microRNA miR166 targeting Dof TF RDD1 have also been confirmed to promote ammonium uptake and transport in rice (Iwamoto and Tagiri, 2016). Recently, functions of several genes have been elucidated in plants for high NUE such as nitrate transporter OsNPF4.5 (Wang et al., 2020), NAC42-activated nitrate transporter (Tang et al., 2019) and nitrate reductase gene OsNR2 (Gao et al., 2019). Collectively, genetic engineering in N transporters have been proven successful to increase plant growth, root architecture, N uptake and transport and total N content, and thus improved NUE of plants (Supplementary Table 1).
Increasing Plant N Utilization and Remobilization Efficiency
Several genes have been engineered to enhance N utilization efficiency in plants. For example NIN-LIKE PROTEIN 7 (NLP7) (Yu et al., 2016), asparagine synthetase ASN1 (Lam et al., 2003), autophagy-related gene ATG7-1 (Wada et al., 2015) and glutamine synthetase GS1;2 (Brauer et al., 2011) have improved NUE in Arabidopsis/rice. The functions of TFs such as bZIP AtTGA4 (Zhong et al., 2015), HY5 (Chen X. B. et al., 2016), NAC-like NAP (Liang et al., 2014), Dof1 ZmDof1 (Yanagisawa et al., 2004; Kurai et al., 2011), NAC1-type NAC-S (Zhao et al., 2015) and Nuclear Factor Y NFYA-B1 (Qu et al., 2015) have been demonstrated in development of N-use efficient plants of Arabidopsis/rice/wheat. Importantly, barley AlaAT (alanine aminotransferase) has most successful in increasing NUE in rice (Shrawat et al., 2008), canola (Good et al., 2007) and sugarcane (Snyman et al., 2015). The miR166 targeting Dof TF RDD1 enhances transport of nutrients including ammonium and sucrose, N uptake and content, and grain yield under low N in rice (Iwamoto and Tagiri, 2016) (Supplementary Table 1).
Results and Targets for Improving NUE in Potato
In potato, several studies have reported on application of soil and agronomic practices for N management (review by Trehan and Singh, 2013), but very limited on genomics uses to enhance NUE. Hence, knowledge about genes and regulatory elements such as TFs and microRNAs (miRNAs) are important to improve NUE. Moreover, the underlying molecular and physiological mechanisms and genetic factors remain elusive in potato for root system architecture, carbon-nitrogen economy and N metabolism (uptake, transport, utilization and remobilization). Recently, we have reviewed application of integrated genomics, physiology and breeding approaches for improving NUE (Tiwari et al., 2018) and traits phenotyping under aeroponic in potato (Tiwari et al., 2020d). Further, recent studies provide information about the genes and miRNAs associated with N stress in potato (Tiwari et al., 2020a,b,c; Zhang et al., 2020). Potato is highly amenable to tissue culture and therefore transgenics protocols are well established. Also, CRISPR/Cas9 tool has been applied in potato such as creation of homozygous mutants, knockdown of steroidal glycoalkaloids, caroteinoid biosynthesis and phosphate transport (review by Nadakuduti et al., 2018; Dangol et al., 2019).
We summarize here potential candidate genes for improving NUE in potato based on the recent research (Tiwari et al., 2020a,b,c; Zhang et al., 2020). Our studies indicate that in potato roots, high-affinity nitrate transporters are the key candidate genes for manipulation in N uptake and transport. Moreover, genes like ferric chelate reductase, protein phosphatase 2 C, glutaredoxin, GDSL esterase/lipase, cytochrome P450 hydroxylase and TFs also appear important in roots. In stolons, nitrate transporter, urea active transporter and sodium/proline symporter facilitate N transport. We have also elucidated miRNAs (up-regulated: miR156/157 and miR482, and down-regulated: miR397 and miR398) in roots under N stress. Further, glutaredoxin gene family has been found the most prominent candidate gene under N stress in shoots. Another study shows effect of overexpression of glutaredoxin gene OsGRX6 on signaling and N status in rice (El-Kereamy et al., 2015). We have identified tartrate-resistant acid phosphatase, glycerophosphodiester phosphodiesterase and TFs (Myb and WRKY), and miRNAs (up-regulated: miR156 and miR319, and down-regulated: miR398 and miR5303) in shoots under N stress. Indeed, stolon formation is a critical stage of tuber formation in potato. Hence, carbohydrate metabolism genes like glucose-6-phosphate/phosphate translocator 2 and glucose-1-phosphate adenylyltransferase, and amino acid synthesis genes such as 2-oxoglutaratedependent dioxygenase, malate synthase and branched-chainamino-acid aminotransferase play crucial roles in potato tuberization. Likewise, inhibitors (cysteine protease and metallocarboxypeptidase), storage protein (patatin), TFs (heat stress, BTB/POZ and LOB domains, F-box), dehydration-responsive protein RD22 and hydroxyproline-rich glycoprotein are essentially involved in potato tuberization. Recently, Zhang et al. (2020) have observed key roles of nitrate transporters (StNRT2. 4, StNRT2. 5, and StNRT2. 7), glutamate dehydrogenase, glutamine synthetase and carbonic anhydrase in N metabolism in potato. Thus, like other plants, gene manipulation of N transporters in roots and assimilatory genes of carbohydrate and amino acids metabolism in shoots/stolons, and TFs (Myb and WRKY) could be manipulated by constitutive or tissue-specific promoters. Further, gene knockdown could be applied via RNAi (miR156, miR397, miR398, miR319, and miR482) or others targeting N pathways genes for improving NUE in potato (Figure 1). Moreover, CRISPR/Cas9 has been deployed in potato for multiple genes like Acetolactate synthase 1 (Butler et al., 2015) and granule-bound starch synthase (GBSS) (Andersson et al., 2017). Overall, candidate genes, TFs and miRNAs could be attempted for genetic manipulation to increase NUE in potato via transgenic or CRISPR/Cas9 or base-editing technologies.
Figure 1. An outline of selected differentially expressed genes identified in potato under N stress based on transcriptome (RNA-seq and small RNA) sequencing of plant grown in aeroponic culture (Tiwari et al., 2020a,b,c). It summarizes the potential candidate genes, transcription factors and microRNAs in different potato tissues (root, shoot/leaf, and stolon) for improving nitrogen use efficiency in potato by gene manipulation via transgenics and/or CRISPR/Cas9 genome editing coupled with based-editing technologies.
Potato is a tetraploid and therefore application of CRISPR/Cas9 is more challenging. Albeit, all four alleles of StGBSS gene in potato have been knocked out and genome-edited mutants have been regenerated (Andersson et al., 2017). Moreover, various transformation methods like Agrobacterium, geminivirus replicon, protoplasts and polyethylene glycol have been suggested for Cas9 application in potato (Butler et al., 2015; Nadakuduti et al., 2018), of which protoplasts is an excellent one (Andersson et al., 2017). Further, suitable sgRNA promoters like Arabidopsis (AtUp) and potato (StU6p), and plant promoters like CAMV35S have been suggested for potato (Belhaj et al., 2013). Nevertheless, selection of target gene, design of guide RNA, efficient CRISPR/Cas9, plant transformation and off-target mutants are the major issues of genome editing in potato.
Conclusions
Plant N metabolism involves a network of genes associated in N uptake, transport, utilization, remobilization and storage processes. NUE is a complex multigenic trait and therefore its improvement becomes difficult particularly in tetraploid potato. However, a substantial success has been achieved through transgenic and little via CRISPR/Cas in plants. CRISPR/Cas9 has been mostly applied to negative regulators of genes, and therefore in future it is expected to discover such additional genes. Here, we have suggested a few candidate genes based on our research findings for improving NUE in potato applying transgenics or CRISPR/Cas9 technologies. Further, strengthening the knowledge on genes, TFs, and microRNAs and elucidating underlying molecular and physiological mechanisms of N pathways are vital for NUE research. Collectively, CRISPR/Cas9 coupled with base-editing strategies represents an invaluable system for precise genome editing. Nonetheless, robust Cas9 array system with multiplexing of targets, transformation and regeneration, phenotypes and people awareness would be challenges in genome editing research.
Author Contributions
JT conceived the idea and wrote the manuscript. JT, TB, RS, and MK performed research work and improved the manuscript. SK critically read and edited the manuscript. All authors contributed to the article and approved the submitted version.
Funding
The work was funded by the Indian Council of Agricultural Research-Central Potato Research Institute, Shimla, Himachal Pradesh, India under the institute Biotechnology research programme and CABin Scheme (ICAR-IASRI, New Delhi).
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.
Acknowledgments
The authors thank the Competent Authority, Indian Council of Agricultural Research-Central Potato Research Institute, Shimla, Himachal Pradesh, India and CABin Scheme (ICAR-IASRI, New Delhi) for necessary support.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2020.597481/full#supplementary-material
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Keywords: CRISPR-Cas9, nitrogen use efficiency, plant, potato, transgenic
Citation: Tiwari JK, Buckseth T, Singh RK, Kumar M and Kant S (2020) Prospects of Improving Nitrogen Use Efficiency in Potato: Lessons From Transgenics to Genome Editing Strategies in Plants. Front. Plant Sci. 11:597481. doi: 10.3389/fpls.2020.597481
Received: 21 August 2020; Accepted: 10 December 2020;
Published: 23 December 2020.
Edited by:
Laura De Gara, Campus Bio-Medico University, ItalyReviewed by:
Jingguang Chen, Sun Yat-sen University, ChinaSergio Esposito, University of Naples Federico II, Italy
Copyright © 2020 Tiwari, Buckseth, Singh, Kumar and Kant. 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: Jagesh Kumar Tiwari, amFnZXNodGl3YXJpJiN4MDAwNDA7Z21haWwuY29t