NAC transcription factors in plant multiple abiotic stress responses: progress and prospects.

Abiotic stresses adversely affect plant growth and agricultural productivity. According to the current climate prediction models, crop plants will face a greater number of environmental stresses, which are likely to occur simultaneously in the future. So it is very urgent to breed broad-spectrum tolerant crops in order to meet an increasing demand for food productivity due to global population increase. As one of the largest families of transcription factors (TFs) in plants, NAC TFs play vital roles in regulating plant growth and development processes including abiotic stress responses. Lots of studies indicated that many stress-responsive NAC TFs had been used to improve stress tolerance in crop plants by genetic engineering. In this review, the recent progress in NAC TFs was summarized, and the potential utilization of NAC TFs in breeding abiotic stress tolerant transgenic crops was also be discussed. In view of the complexity of field conditions and the specificity in multiple stress responses, we suggest that the NAC TFs commonly induced by multiple stresses should be promising candidates to produce plants with enhanced multiple stress tolerance. Furthermore, the field evaluation of transgenic crops harboring NAC genes, as well as the suitable promoters for minimizing the negative effects caused by over-expressing some NAC genes, should be considered.

Introduction

As sessile organisms, plants continuously suffer from a broad range of environmental stresses including abiotic and biotic stresses. Abiotic stresses such as drought, salinity, heat and cold, adversely affect plant growth and agriculture productivity, and cause more than 50% of worldwide yield loss for major crops every year (Boyer, 1982; Bray et al., 2000; Shao et al., 2009; Ahuja et al., 2010; Lobell et al., 2011). Further to this, plants are also attacked by a vast range of pests and pathogens, including fungi, bacteria, viruses, nematodes, and herbivorous insects (Hammond-Kosack and Jones, 2000). In addition, current climate prediction models indicate the deterioration of climate including an increasing average temperature, a changing distribution of annual precipitation, a rise of sea level, and so on. This will be concurrent with an increased frequency of drought, flood, heat wave, and salinization (Easterling et al., 2000; IPCC, 2007, 2008; Mittler and Blumwald, 2010). Climate change will also affect the spread of pests and pathogens. For example, the increasing temperature can facilitate pathogen spread (Bale et al., 2002; Luck et al., 2011; Nicol et al., 2011), and many abiotic stress can weaken the defense mechanism of plants and increase their susceptibility to pathogen infection (Amtmann et al., 2008; Goel et al., 2008; Mittler and Blumwald, 2010; Atkinson and Urwin, 2012). Taken together, crop plants will face a greater range and number of environmental stresses, which are likely to occur simultaneously. So it is very urgent to breed stress-tolerant crop varieties to satisfy an increasing demand for food productivity due to global population increase (Takeda and Matsuoka, 2008; Newton et al., 2011).

To cope with these recurrent environmental stresses, plants can activate a number of defense mechanisms which include signal perception, signal transduction through either ABA-dependent or ABA-independent pathways, stress-responsive gene expression, in turn the activation of physiological and metabolic responses (Xiong et al., 2002; Chaves et al., 2003; Yamaguchi-Shinozaki and Shinozaki, 2006; Perez-Clemente et al., 2013). To date, a large array of stress responsive genes have been identified in many plants, including Arabidopsis and rice. These genes are generally classified into two types (Shinozaki et al., 2003). One is functional genes encoding important enzymes and metabolic proteins (functional proteins), such as detoxification enzyme, water channel, late embryogenesis abundant (LEA) protein, which directly function to protect cells from stresses. The other is regulatory genes encoding various regulatory proteins including transcription factors (TFs) and protein kinases, which regulate signal transduction and gene expression in the stress response. In the signal transduction processes, TFs play pivotal roles in the conversion of stress signal perception to stress-responsive gene expression. TFs and their interacting cis-elements function in the promoter region of different stress-related genes acting as molecular switches for gene expression. In plants ~7% of the genome encodes for putative TFs, which often belong to large gene families, such as WRKY, bZIP, MYB, AP2/EREBP, and NAC families (Udvardi et al., 2007; Golldack et al., 2011). In light of the key importance of TFs in controlling a wide range of downstream events, lots of studies have aimed to identify and characterize various TFs involved in stress responses. However, these studies have mostly focused on understanding the responses of model plants and crops to a single stress such as drought, salinity, heat or cold, pathogen infection, and so on (Hirayama and Shinozaki, 2010; Chew and Halliday, 2011). Unlike the controlled conditions in the laboratory, crops and other plants are often simultaneously subjected to multiple stresses in the field conditions (Ahuja et al., 2010). Recent studies have showed that plant response to a combination of drought and heat is not a simple additive effect of the individual stress, and the combination of multiple stresses produces a unique pattern of gene expression, which is distinct from the study of either stress individually (Rizhsky et al., 2002, 2004; Prasch and Sonnewald, 2013; Rasmussen et al., 2013). Therefore, the results of studies performed under individual stress factors are not suitable for the complex field conditions, and it is crucial to characterize the response of plants to multiple stresses and identify multiple stress responsive genes by imposing multiple stresses simultaneously as an entirely new stress (Mittler, 2006). Maybe, manipulation of these multiple stress responsive genes, especially multifunctional TFs, will provide the opportunity to breed the broad-spectrum tolerant crops with high yields. Based on these considerations above, this paper reviews the progress of NAC TFs involved in plant abiotic stress responses, and also prospects the future study direction for the challenge of multiple environmental stresses in agriculture, particularly concerning their potential utilization for plant multiple stress tolerance in the field conditions.

NAC transcription factors in plants

As one of the largest family of TFs in plants, the NAC TFs comprise a complex plant-specific superfamily and are present in a wide range of species. The NAC acronym is derived from three earliest characterized proteins with a particular domain (NAC domain) from petunia NAM (no apical meristem), Arabidopsis ATAF1/2 and CUC2 (cup-shaped cotyledon; Souer et al., 1996; Aida et al., 1997). By the availability of an ever-increasing number of complete plant genomes and EST sequences, large numbers of putative NAC genes have been identified in many sequenced species at genome-wide scale (As shown in Table 1), such as 117 in Arabidopsis, 151 in rice, 74 in grape, 152 in soybean, 204 in Chinese cabbage, 152 in maize, and so on. The large size of NAC family inevitably complicates the unraveling of their regulatory process.

Table 1

.

Species	Number of NAC family	References
Arabidopsis thaliana	117	Nuruzzaman et al., 2010
Rice (Oryza sativa)	151	Nuruzzaman et al., 2010
Grape (Vitis vinifera)	74	Wang et al., 2013
Soybean (Glycine max)	152	Le et al., 2011
Pigeonpea (Cajanus cajan)	88	Satheesh et al., 2014
Foxtail millet (Setaria italica L.)	147	Puranik et al., 2013
Chinese cabbage (Brassica rapa)	204	Liu et al., 2014
Brachypodium distachyon	101	You et al., 2015
Physic Nut (Jatropha curcas L.)	100	Wu et al., 2015
Maize (Zea mays)	152	Shiriga et al., 2014
Apple (Malus domestica)	180	Su et al., 2013
Chickpea (Cicer arietinum L.)	71	Ha et al., 2014
Potato (Solanum tuberosum)	110	Singh et al., 2013
Poplar (Populus trichocarpa)	163	Hu et al., 2010
Banana (Musa acuminata)	167	Cenci et al., 2014
Tobacco (Nicotiana tabacum)	152	Rushton et al., 2008
Tomato (Solanum lycopersicum)	104	Su et al., 2015
Cassava (Manihot esculenta Crantz)	96	Hu et al., 2015
Gossypium raimondii	145	Shang et al., 2013

.

The NAC family has been found to function in various processes including shoot apical meristem (Takada et al., 2001), flower development (Sablowski and Meyerowitz, 1998), cell division (Kim et al., 2006), leaf senescence (Breeze et al., 2011), formation of secondary walls (Zhong et al., 2010), and biotic and abiotic stress responses (Olsen et al., 2005; Christianson et al., 2010; Tran et al., 2010; Nakashima et al., 2012). Nonetheless, only a few of these genes have been characterized to date and most of the NAC family members have not yet been studied, even though these genes are likely to play important roles in plants, and a great deal of work will be required to determine the specific biological function of each NAC gene. The intensive study on model plants including Arabidopsis and rice reveals that a typical NAC protein contains a highly conserved N-terminal DNA-binding NAC domain and a variable transcriptional regulatory region in the C-terminal region. The NAC domain with ~150–160 amino acids is divided into five sub-domains (A to E; Ooka et al., 2003). The function of the NAC domain has been associated with nuclear localization, DNA binding, and the formation of homodimers or heterodimers with other NAC domain-containing proteins (Olsen et al., 2005). In contrast, the highly diverged C-terminal region functions as a transcription regulatory region, acting as a transcriptional activator or repressor, but it has frequent occurrence of simple amino acid repeats and regions rich in serine and threonine, proline and glutamine, or acidic residues (Olsen et al., 2005; Puranik et al., 2012). Some NAC TFs also contain transmembrane motifs in the C-terminal region which are responsible for anchoring to plasma membrane or endoplasmic reticulum, and these NAC TFs are membrane-associated and designated as NTLs (Seo et al., 2008; Seo and Park, 2010).

The expression of NAC genes can firstly be regulated at the level of transcription because there are some stress-responsive cis-acting elements contained in the promoter region such as ABREs (ABA-responsive elements), DREs (Dehydration-responsive elements), jasmonic acid responsive element and salicylic acid responsive element. Then the complex post-transcriptional regulation involves microRNA-mediated cleavage of genes or alternative splicing. NAC TFs also undergo intensive post-translational regulation including ubiquitinization, dimerization, phosphorylation or proteolysis (Nakashima et al., 2012; Puranik et al., 2012). These regulatory steps help NAC TFs playing multiple roles in the majority of plant processes as mentioned above. The NAC TFs regulate the transcription of downstream target genes by binding to a consensus sequence in their promoters. The NAC recognition sequence (NACRS) containing the CACG core-DNA binding motif has been identified in the promoter of the drought inducible EARLY RESPONSE TO DEHYDRATION1 (ERD1) gene in Arabidopsis (Simpson et al., 2003; Tran et al., 2004). The rice drought-inducible ONAC TFs also can bind to a similar NACRS, demonstrating that the NACRS might be conserved across plants at least for stress-inducible NAC TFs (Hu et al., 2006; Fang et al., 2008). In addition, other sequences have also been reported as NAC binding sites (NACBS), such as an Arabidopsis calmodulin-binding NAC with GCTT as core-binding motif (Kim et al., 2007), the iron deficiency-responsive IDE2 motif containing the core sequence CA(A/C)G(T/C) (T/C/A) (T/C/A) (Ogo et al., 2008) and the secondary wall NAC binding element (SNBE) with (T/A)NN(C/T) (T/C/G)TNNNNNNNA(A/C)GN(A/C/T) (A/T) as consensus sequence (Zhong et al., 2010). The sequences flanking the core site in promoter of target genes may define the binding specificity of different NAC TFs. Thus, the NAC TF family can recognize a vast array of DNA-Binding sequences and regulate multiple downstream target genes. These target genes regulated by NAC TFs comprise regulatory genes encoding regulatory proteins which function in signal transduction and regulation of gene expression and functional genes encoding proteins which are involved in osmolyte production, reactive oxygen species scavenging and detoxification, macromolecule protection and ubiquitination (Puranik et al., 2012). Taken together, the existence of NACRS in promoter of some of these genes makes them to be the potential direct targets, whereas those that do not have this motif may not be direct targets. In future more other novel NACRS remain to be elucidated by microarrays combined with chromatin immunoprecipitation (Taverner et al., 2004).

NAC transcription factors function in abiotic stress

The NAC TFs play a vital role in the complex signaling networks during plant stress responses. Because of the large number of NAC TFs from different plants and their unknown roles, it is still a great challenge to uncover their roles in abiotic stress. Recently, whole-genome expression profiling and transcriptome studies have enabled researchers to identify a number of putative NAC TFs involved in abiotic stress responses. For example, 33 NAC genes changed significantly in Arabdopsis under salt treatment (Jiang and Deyholos, 2006), 38 NAC genes were involved in response to drought in soybean (Le et al., 2011), 40 NAC genes responded to drought or salt stress in rice (Fang et al., 2008), 32 NAC genes responded to at least two kinds of treatments in Chrysanthemum lavandulifolium (Huang et al., 2012). It appears that a significant proportion of NAC genes function in stress response according to the expression data from genome-wide transcriptome analyses in many plants. Phylogenetic analyses of NAC TFs showed that most of the stress responsive NAC TFs appeared to contain a closely homologous NAC domain (Ernst et al., 2004; Fang et al., 2008). Moreover, the stress-responsive NAC genes exhibit a large diversity in expression patterns, indicating their involvement in the regulation of a wide spectrum of responses to different abiotic stresses. The precise regulations of NAC genes during plant abiotic stress responses contribute to the establishment of complex signaling networks, and the important roles of NAC genes in plant abiotic stress responses make them promising candidates for the generation of stress tolerant transgenic plants. The functional studies of NAC TFs by over-expression techniques will directly improve our understanding of the regulatory functions of NAC members to abiotic stresses. Transgenic constructs over-expressing the selected NAC genes have been made in Arabidopsis, rice and other plants. Some successful examples are summarized in Table 2.

Table 2

Abiotic stress tolerance of transgenic plant over-expressing .

Transgenic plant	Genotype	Enhanced tolerance	References
A. thaliana	ANAC019 overexpression	Drought, high-salinity, ABA signaling	Tran et al., 2004
	ANAC055 overexpression	Drought, high-salinity, ABA signaling	Tran et al., 2004
	ANAC72 overexpression	Drought, high-salinity, ABA signaling	Tran et al., 2004
	RD26 overexpression	Drought, salt, ABA signaling	Fujita et al., 2004
	ANAC019 overexpression	Cold, ABA signaling	Jensen et al., 2010
	ATAF1 overexpression	Positive regulator of drought tolerance	Wu et al., 2009
	ONAC063 overexpression	Higher seed germination under high salinity and osmotic stress	Yokotani et al., 2009
	GmNAC20 overexpression	Salt and freezing tolerance	Hao et al., 2011
	ZmSNAC1 overexpression	Low temperature, high-salinity, drought, and ABA signaling	Lu et al., 2012
	TaNAC2 overexpression	Drought, salt, and freezing stresses	Mao et al., 2012
	ANAC042 overexpression	Heat stress	Shahnejat-Bushehri et al., 2012
O. sativa	SNAC1 overexpression	Increased stomatal closure and drought resistance in dry field conditions, salt toleranc	Hu et al., 2006
	SNAC2 overexpression	Salt, drought, disease resistance drought, salinity, cold, wounding, and ABA treatment	Sindhu et al., 2008
	OsNAC4 overexpression	Drought, salt, cold tolerance	Zheng et al., 2009
	OsNAC5 overexpression	ABA, salt, cold tolerance, grain filling	Sperotto et al., 2009
	OsNAC6 overexpression	Drought and salt tolerance	Nakashima et al., 2007
	ONAC10 overexpression	Drought, high salinity, low temperature toleranc	Jeong et al., 2010
	ONAC045 overexpression	Drought and salt tolerance	Song et al., 2011
N. tabacum	TaNAC2a overexpression	Drought tolerance	Tang et al., 2012
	DgNAC1 overexpression	ABA, NaCl, drought, and cold	Liu et al., 2011a
	EcNAC1 overexpression	Water-deficit and salt stress	Ramegowda et al., 2012
T. aestivum	TaNAC69 overexpression	PEG-induced dehydration and mild salt tolerance	Xue et al., 2011
G. max	GmNAC11 overexpression	Salt tolerance in soybean transgenic hairy roots	Hao et al., 2011

Conclusions and perspectives

Considerable information has been gained about NAC TFs since the discovery of NAC TFs, but the research in this area is still in its infancy. Genome-wide identification and expression profiling will undoubtedly open new avenues for describing the key features of NAC TFs. As a result, our current understandings of the regulatory functions of the NAC TFs in various plant species will be definitely accelerated. In particular, the stress-responsive NAC TFs can be used as promising candidates for generation of stress tolerant transgenic plants possessing high productivity under adverse conditions. As a matter of fact, many transgenic studies have been proved successful by gene manipulation of NAC TFs for conferring different stresses tolerance to plants (As shown in Table 2), but there are still some problems to be solved. Firstly, the constitutive overexpression of NAC genes occasionally may lead to negative effects in transgenic plants such as dwarfing, late flowering and lower yields (Fujita et al., 2004; Nakashima et al., 2007; Hao et al., 2011; Liu et al., 2011b). Secondly, the transgenic plants overexpressing NAC genes may occasionally have antagonistic responses to different stresses. For example, drought tolerant Arabidopsis plants overexpressing ATAF1 were highly sensitive to ABA, high-salt, oxidative stress and necrotrophic fungus (B. cinerea; Wu et al., 2009). Overexpressing ANAC019 and ANAC055 not only increased drought tolerance but also decreased resistance to B. cinerea (Fujita et al., 2004; Bu et al., 2008). Thirdly, only a few of transgenic plants overexpressing NAC genes were evaluated in the field trials so far, and most of them were tested in greenhouse conditions and focused on plant vegetative stages rather than reproductive stages (Valliyodan and Nguyen, 2006). Lastly, most of the studies on NAC TFs only investigated the molecular mechanisms of individual occurring stress situations. Although recent studies have conducted multi-parallel stress experiments and identified different NAC TFs responding to single stress situations (Huang et al., 2012), the knowledge concerning responses to combinations of several stress factors is scarce, especially interactions among stress factors.

As everyone knows, one of the most important aims for plant stress research is to provide targets for the improvement of stress tolerance in crop plants. With the forecast changes in climatic conditions leading to a more complex stress environment in the fields, we will face new challenges in creating the multiple stress-tolerant crops. Breeding such plants will depend on understanding the crucial stress-regulatory networks and the potential effects of different combinations of adverse conditions. Studies of multiple stress responses in Arabidopsis have provided us with several possible avenues. Master regulatory genes such as members of the MYC, MYB, and NAC TF families that act in multiple abiotic stress responses are excellent candidates for manipulating multiple stress tolerance. So in the future, it is crucial to impose multiple stresses simultaneously that simulate natural field conditions and regard each set of stress combinations as an entirely new stress in order to identify the corresponding NAC TFs commonly induced by multiple stresses. Manipulation of these genes should be the major target of attempts to produce plants with enhanced multiple stress tolerance. Furthermore, the potential NAC genes which confer multiple abiotic stress tolerance in model plant species must be tested in crop plants and greater emphasis should be placed on the field evaluation of the transgenic crops harboring NAC genes, especially focusing on their reproductive success. Another lesson is the selection and/or improvement of suitable promoters (such as a stress-inducible promoter) which can maximize the positive effects and minimize the negative effects caused by over-expressing some NAC genes. In summary, NAC TFs are the key components of the signaling pathway in stress response which carry out their function by interacting with both downstream and upstream partners (Figure 1). Understanding the molecular mechanisms of NAC TFs networks integrating multiple stress responses will be essential for the development of broad-spectrum stress tolerant crop plants that can better cope with environmental challenges in future climates.

Figure 1

Schematic diagram of NAC TFs as key components in transcriptional regulatory networks during abiotic stress. NACRS is NAC recognition sequence.

Conflict of interest statement

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.