Abstract
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This review summarizes the molecular basis and emerging applications of developmental regulatory genes and nanoparticles in plant transformation and discusses strategies to overcome the obstacles of genotype dependency in plant transformation.
Abstract
Plant transformation is an important tool for plant research and biotechnology-based crop breeding. However, Plant transformation and regeneration are highly dependent on species and genotype. Plant regeneration is a process of generating a complete individual plant from a single somatic cell, which involves somatic embryogenesis, root and shoot organogeneses. Over the past 40 years, significant advances have been made in understanding molecular mechanisms of embryogenesis and organogenesis, revealing many developmental regulatory genes critical for plant regeneration. Recent studies showed that manipulating some developmental regulatory genes promotes the genotype-independent transformation of several plant species. Besides, nanoparticles penetrate plant cell wall without external forces and protect cargoes from degradation, making them promising materials for exogenous biomolecule delivery. In addition, manipulation of developmental regulatory genes or application of nanoparticles could also bypass the tissue culture process, paving the way for efficient plant transformation. Applications of developmental regulatory genes and nanoparticles are emerging in the genetic transformation of different plant species. In this article, we review the molecular basis and applications of developmental regulatory genes and nanoparticles in plant transformation and discuss how to further promote genotype-independent plant transformation.
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Introduction
Plant transformation is a method that delivers foreign DNA into regeneration-competent cells through the Agrobacterium-mediated method, biolistic (also called particle bombardment), pollen tube transformation, electroporation and so on. Among them, Agrobacterium-mediated and biolistic methods are the most common plant transformation methods (An et al. 2019, 2020; Zhang et al. 2018, 2021b; Zhu et al. 2020). Regenerative cells can derive from the proliferation of undifferentiated meristem cells of explants and then develop into intact plants through direct organogenesis. However, in many plants, regenerative cells are derived from the reprogramming of differentiated somatic cells and regain the ability for proliferation competence through dedifferentiation. Regenerative cells derived in this way develop into intact plants by de novo organogenesis and somatic embryogenesis (Feher 2019; Gaillochet and Lohmann 2015; Ikeuchi et al. 2016; Steward et al. 1958; Sugimoto et al. 2011; Xu and Hu 2020). Direct organogenesis regenerates adventitious shoots or roots directly from explants, while indirect organogenesis requires induction of pluripotent non-embryonic callus on the callus-inducing medium (CIM), and the callus then develops into adventitious shoots or roots. The callus is a highly heterogeneous group of cells, and its organized structure resembles lateral root primordia (Atta et al. 2009). Somatic embryo regeneration, namely somatic embryogenesis, depends on the totipotency of plant cells (Feher 2019). Somatic embryogenesis can induce somatic embryos directly without an intermediate embryonic callus or indirectly following an embryonic callus stage. In plant research, both plant genetic engineering and genome editing technologies that promote functional genomic research and accelerate crop trait improvement greatly depend on plant transformation (Altpeter et al. 2016; Fang et al. 2022; Hou et al. 2022a; Jiang et al. 2021; Liu et al. 2022a, b; Wei et al. 2022, 2023). However, plant transformation and regeneration rely highly on species and genotype, which are major limiting factors for developing and applying genetic engineering and genome editing technologies.
Since various factors influence callus formation and regeneration, successful plant transformation has to optimize several external factors such as explant types, pH, and basal media composition. Considering that most regeneration initiates from the cut place, the wound stress may be a trigger of plant regeneration (Ikeuchi et al. 2013). Recent studies showed that hormones and developmental regulatory genes play critical roles in callus induction and plant regeneration. Exogenous hormones induce callus formation in aerial explants with the elimination of leaf identity (He et al. 2012; Lee and Seo 2018). Then, developmental regulatory genes regulate de novo shoot and root regeneration in root and aerial explants (Kareem et al. 2015; Liu et al. 2014). In aerial explant-initiated plant regeneration, the elimination of leaf identity is primarily achieved through epigenetic regulation (He et al. 2012; Lee and Seo 2018). Overall, wounds, hormones, developmental regulatory genes, and epigenetic modifications are essential factors for plant regeneration. Recent studies showed the successful transformation of recalcitrant species through manipulating developmental regulatory genes (Aregawi et al. 2022; Hoerster et al. 2020; Lowe et al. 2018). Alternatively, nanoparticles (NPs) could penetrate the plant cell wall without external force and can be broadly applied to different plant species. In addition, nanomaterials (NMs) can protect cargoes from degradation and reach previously inaccessible plant tissues, cellular and subcellular locations. All these properties make NPs promising materials for exogenous biomolecule delivery and several recent studies showed the successful usage of NPs to deliver genes into plant cells for genetic engineering and genome editing (Demirer et al. 2019a; Kwak et al. 2019; Wang et al. 2020).
In this review, we performed a bibliometric analysis of 2414 publications selected by the related searches of plant transformation methods to gain a brief overview of the research history and status. We summarize and discuss the molecular basis of wounds, hormones, developmental regulatory genes, and epigenetic modifications in plant regeneration and the application of developmental regulatory genes in plant transformation. In addition, we also summarize the uptake and translocation of recently emerged NPs in plant cells and their application in plant transformation. Finally, we discuss the potential for genotype-independent plant transformation based on these advances.
A brief overview of plant transformation methods
The mechanism of Agrobacterium-mediated plant transformation is the transfer of foreign genes carried between the Ti plasmid T-DNA boundaries to the plant cell nucleus and subsequent transient transgene expression or integration into the plant genome. In 1983, with the successful regeneration of the transgenic Nicotiana tabacum transformed using the Agrobacterium-mediated method, the “starting line” was drawn for plant transformation (Fraley et al. 1983; Herrera-Estrella et al. 1983). Meanwhile, a study reported that a pollen tube-mediated method could successfully transform Gossypium hirsutum (Zhou et al. 1983). From then, leaf discs of a wide range of dicotyledon plants were successfully infected by Agrobacterium (Horsch et al. 1985). However, monocots, particularly the graminaceous crops, cannot be infected for a long time via this method. Other methods, such as biolistic, electroporation and silicon carbide fiber-mediated methods, are developed and applied to monocot transformation (Fromm et al. 1985; Kaeppler et al. 1990; Klein et al. 1987). In 1990, the first fertile transgenic Zea mays plants transformed by the biolistic method were regenerated (Gordon-Kamm et al. 1990). This method can deliver biomolecules to a broader range of plant species, but plant tissue is often damaged under high bombardment pressures. In addition, biolistic technology requires specialized equipment, which limits its wide application. It is necessary to develop Agrobacterium infecting method for monocots because the Agrobacterium-mediated method is easy to perform, low cost, and shows higher transformation efficiency than other methods. Several studies found that monocots can not produce enough inducers, such as phenolic compounds, at injury sites (Stachel et al. 1985). This could be the reason for the recalcitrance to Agrobacterium infection as these compounds are required for the activation of virulence (Vir) genes on the Ti plasmid, which is needed for inducing plant tumor production (Stachel et al. 1985). Indeed, transgenic Oryza sativa is obtained through Agrobacterium-mediated infection of immature embryos with the addition of phenolic compounds (Chan et al. 1993). These landmark events in plant transformation are illustrated in Fig. 1A. These methods were widely used in plant transformation from 2000 to 2022, among which the Agrobacterium-mediated method is the most used, followed by the biolistic method (Fig. 1B). However, the bottleneck of plant transformation and regeneration is species and genotype dependence.
Several studies have recently attempted to transform recalcitrant plant species and genotypes. For example, a method called in planta particle bombardment (iPB) is developed for Triticum aestivum transformation (Hamada et al. 2018). The iPB method is used to deliver Cas9/gRNA plasmids to shoot apical meristem (SAM) of imbibed seeds and regenerated genome-edited plants (Hamada et al. 2018). This method makes it possible to transform other recalcitrant plant species. Agrobacterium-mediated Vigna unguiculata embryonic axis transformation achieved transformation frequencies between 4 and 37% in many genotypes (Che et al. 2021). In addition, SAM cells were used as explants to transform recalcitrant G. hirsutum genotypes and successfully obtained transgenic plants (Ge et al. 2023). However, few studies showed the use of SAM or embryonic axis as explants to promote genotype-independent transformation. Another strategy for transforming recalcitrant species and genotypes is manipulating developmental regulatory genes and this strategy is widely used in genotype-independent plant transformation (Aregawi et al. 2022; Hoerster et al. 2020; Lowe et al. 2018). Recently, several plant species have achieved stable genetic transformation via magnetic nanoparticles (MNPs) technology (Wang et al. 2022b; Zhao et al. 2017). In the following sections, we will discuss in detail the mechanism and application of developmental regulatory genes and NPs to promote genotype-independent plant transformation.
Molecular basis of somatic embryogenesis, root and shoot organogeneses
Intact plant regeneration from a single somatic cell has to experience somatic embryogenesis, root and shoot organogeneses, and these processes require proper in vitro conditions and involve complicated in vivo signaling and transcriptional networks triggered or regulated by wounds, hormones, developmental regulatory genes and epigenetic reprogramming. Factors affecting somatic embryogenesis, root and shoot organogeneses and their molecular basis are summarized in the succeeding texts.
Molecular basis of somatic embryogenesis
Somatic embryogenesis occurs in many plant species when they are incubated on an auxin-containing medium and then transferred to an auxin-free medium (Ikeda-Iwai et al. 2002; Lu et al. 1983; Wernicke and Brettell 1980). During indirect somatic embryogenesis, embryonic callus formation is first activated on an auxin-rich medium (Ikeda-Iwai et al. 2002). The subsequent absence of auxin in the medium leads to the de novo establishment of auxin gradients in the embryonic callus (Fig. 2A). The gradient auxin distribution initiates a developmental program similar to zygotic embryogenesis, possibly activating the auxin transporter PIN-PORMED1 (PIN1) polar localization (Liu et al. 1993; Su et al. 2009). WUSCHEL (WUS), which determines stem cell fate in SAM, is induced by the established auxin gradient and polar auxin transport, and promotes somatic embryogenesis (Su et al. 2009).
Since most regeneration occurs at wounded loci, wound stress has long been considered a trigger for plant regeneration (Ikeuchi et al. 2013). Wound stress is perceived via damage-associated molecular modules, including cell wall-derived oligogalacturonic acid (Bishop et al. 1981) and extracellular adenosine triphosphate (ATP) (Choi et al. 2014; Tanaka et al. 2014). The ATP is released as a danger signal during plant damage, inducing cytoplasmic calcium signaling and a burst of reactive oxygen species (Choi et al. 2014; Tanaka et al. 2014). The local wound signals are further translated into electrical signals, such as cation channel GLUTAMATE RECEPTOR-LIKEs, which are transmitted to other parts of the plant to induce epigenetic modifications, transcriptional changes and phytohormone synthesis (Ikeuchi et al. 2017; Mousavi et al. 2013).
Somatic embryogenesis receptor-like kinase1 (SERK1) is a Leu-rich repeat (LRR) transmembrane receptor-like kinase (PLK) that might co-regulate the plant differentiation process with other specific receptor-like kinases. Ectopic expression of SERK1 has been taken as a strategy for improving the somatic embryogenesis efficiency of Coffea canephora (Perez-Pascual et al. 2018), Arabidopsis thaliana (Hecht et al. 2001), and O. sativa (Hu et al. 2005). SERK1 regulates somatic embryogenesis by activation of auxin biosynthesis, auxin transport, and probably also auxin perception, leading to the expression of early-stage homeotic genes, including WUS, the AP2/ERF transcription factor Baby boom (BBM) and the MADS-box transcription factor Agamous-like15 (AGL15), and the repression of late-stage homeotic genes such as Leafy cotyledon1 (LEC1) (Perez-Pascual et al. 2018). The BBM, LEC1, LEC2, and AGL15 transcription factors play essential roles in early embryogenesis. LEC1 and LEC2, as well as two other transcription factors, Abscisic acid insensitive3 (ABI3) and FUSCA3 (FUS3) are up-regulated by BBM in somatic embryogenesis (Horstman et al. 2017). In addition, LEC2 rapidly activates the expression of AGL15 (Braybrook et al. 2006). Interestingly, LEC2, FUS3, and ABI3 were identified as direct target genes of AGL15 (Zheng et al. 2009). These data suggest that feedback regulation exists in gene regulatory networks during embryogenesis. In addition, LEC2 is a mediator of auxin biosynthesis and signaling. LEC2 induces YUCCA2 (YUC2) and YUC4 (Stone et al. 2008), which encode auxin biosynthesis enzymes, while LEC1 activates the YUC10 (Junker et al. 2012). AGL15 directly upregulates GA2ox6, a GA catabolic enzyme, and represses the GA biosynthesis gene GA3ox2 leading to a reduction of biologically active GA in Arabidopsis (Wang et al. 2004; Zheng et al. 2009). Ga3ox2 is also repressed by LEC2 and FUS3 and is ectopically activated in the loss-of-function mutants of lec2 and fus3 (Curaba et al. 2004).
Epigenetic reprogramming occurs in many plant developmental processes and regeneration (Hou and Wan 2021; Hou et al. 2022b). Studies have shown that epigenetic modifications, including histone modifications and DNA methylation, suppress regenerative potential and maintain the differentiated status of plant cells (Chen and Dent 2014; Ikeuchi et al. 2015a; Lee and Seo 2018). A chromatin regulator POLYCOMB REPRESSIVE COMPLEX 2 (PRC2) promotes trimethylation on lysine 27 of histone H3 (H3K27me3) to represses gene expression (Holec and Berger 2012). In Arabidopsis, loss-of-function mutants in PRC2 complex develop normal root hairs but fail to maintain the differentiated state and generate callus and somatic embryos (Ikeuchi et al. 2015b). The Wound-induced dedifferentiation 3 (WIND3) and LEC2 are target genes of PRC2, and ectopic overexpression of WIND3 and LEC2 partly phenocopies the prc2 mutants (Ikeuchi et al. 2015b). These findings suggested that PRC2-mediated gene repression is essential for maintaining the differentiated cell state. Histone acetylation is a permissive histone mark and plays an essential role in somatic embryogenesis (Kadosh and Struhl 1998; Rundlett et al. 1998). Arabidopsis plants treated with trichostatin A (TSA), an inhibitor of histone deacetylases (HDAC), resulted in growth arrest and enhanced transcription of LEC1, FUS3, and ABI3 during germination (Tanaka et al. 2008). In addition, an HAD6/HAD19 double-repression line generated embryo-like structures on the true leaves. These phenotypes of the repression line can be rescued by lec1 (Tanaka et al. 2008). Thus, HDA6 and HDA19 redundantly regulate the inhibition of embryonic properties by repressing embryo-specific genes during germination in Arabidopsis. In Brassica napus, repressing histone deacetylase activity with TSA resulted in a significant increase in cell transition from pollen to embryogenic growth in male gametophytes (Li et al. 2014). Interestingly, TSA with heat treatment greatly increased the formation of somatic embryos (Li et al. 2014). Thus, heat stress and histone deacetylation may synergistically regulate somatic embryogenesis (Fig. 2B).
Molecular basis of de novo root organogenesis
The pericycle cells between the endodermis and stele have the potential to generate new lateral roots (Beeckman and De Smet 2014). Arabidopsis explants incubation on CIM and the root-inducing medium (RIM) strongly promote root regeneration from pericycle cells. Culturing hypocotyl explants on RIM after pretreatment on CIM induces a large number of roots, whereas only a few roots form when they are inoculated on RIM without the pretreatment. In contrast to hypocotyl explants, root explants with lateral root meristem primordia efficiently promote root formation when directly cultured on RIM. These results suggest that CIM induces the pluripotent non-embryonic callus generation and these cells then further develop into adventitious roots on RIM (Fig. 3A).
Several studies have shown that wounds, hormones, developmental regulatory genes, and epigenetic modifications affect de novo root organogenesis. Under either light or dark conditions, YUC1 and YUC4 are rapidly activated in response to wounding, promoting auxin biogenesis in mesophyll and competent cells, while YUC5, YUC8, and YUC9 mainly respond to dark conditions. Overall, YUC genes enhanced the auxin level in leaf explants during de novo root organogenesis (Chen et al. 2016). Wuschel related homeobox11 (WOX11), a homeobox gene, responds to wounding-induced auxin signaling together with its homolog WOX12 to upregulate Lateral organ boundaries domain 16 (LBD16) and LBD29, resulting in the fate transition from leaf procambium or parenchyma cells to root founder cells (Liu et al. 2014). Notably, the auxin response elements (AuxREs) in the promotor of WOX11 are essential for its induction in leaf explants, indicating that the auxin signaling pathway directly activates WOX11 expression during root regeneration (Liu et al. 2014). Thus, this novel regulatory mechanism links wounding and hormonal signaling to organ formation during regeneration. The other two LBD genes, LBD17 and LBD18 are also rapidly and significantly induced by CIM. In Arabidopsis, ectopic expression of each of the four LBD genes is sufficient for spontaneous callus formation in the absence of exogenous phytohormones, and inhibition of LBD function suppresses CIM-induced callus formation (Fan et al. 2012). These results support that LBD transcription factors play essential roles during the callus induction process. Collectively, these regulatory pathways together promote the auxin-mediated establishment of root meristems.
Epigenetic regulation, such as PRC2-mediated repression, regulates WOX11 to influence plant cell fate transition (Ikeuchi et al. 2013; Liu et al. 2014). In addition, JUMONJI C domain-containing protein 30 (JMJ30) binds to the promoters of LBD16 and LBD29 with Auxin response factor 7/19 (ARF7/ARF19) which are transcriptional activators of early auxin response, removes the methyl groups from H3K9me3, and promotes LBD expression (Lee et al. 2018). Arabidopsis trithorax-related 2 (ATXR2) is recruited to LBD16 and LBD29 promoters through ARF-JMJ30 complex and promotes trimethylation on lysine 36 of histone H3 (H3K36me3) to further promotes LBD expression during callus formation (Lee et al. 2017). A schematic gene regulatory network during root organogenesis is illustrated in Fig. 3B.
Molecular basis of de novo shoot organogenesis
Like many other plants, Arabidopsis explants do not readily regenerate shoots. However, culturing Arabidopsis explants on CIM and the shoot-inducing medium (SIM) rich in cytokinin strongly promotes shoot regeneration from pericycle cells (Atta et al. 2009; Che et al. 2007; Valvekens et al. 1988). The CIM-induced callus possesses root meristem characteristics. Thus, it is easy to regenerate roots when the CIM-induced callus is transferred to RIM. Establishing the identity of root meristem and further root development can be regulated through auxin-induced transcriptional cascade (Ozawa et al. 1998). In contrast, shoot regeneration may be more complex because it requires the transition from root meristem fate to shoot meristem fate. CIM induces pluripotent non-embryonic callus, which develops into adventitious shoots through two developmental processes: shoot progenitor cell regeneration and shoot formation after transferring to SIM (Kareem et al. 2015) (Fig. 4A).
De novo shoot organogenesis is also regulated by wounds, hormones, developmental regulatory genes, and epigenetic modifications. Studies showed an AP2/ERF transcription factor, WIND1 and its close homologs WIND2, WIND3, and WIND4 are rapidly induced by wounding, and these genes promote cell dedifferentiation and subsequent callus formation in Arabidopsis (Iwase et al. 2011a, b). WIND1 upregulates enhancer of shoot regeneration1/dornröschen (ESR1/DRN), encoding another AP2/ERF transcription factor, and promotes shoot regeneration in Arabidopsis (Banno et al. 2001; Iwase et al. 2017). In addition, WIND1 induces the B-type Arabidopsis response regulators (ARRs)-mediated cytokinin response (Iwase et al. 2011a). Double mutants of type-B ARRs (arr1-3arr12-1 and arr1-3arr10-5) display reduced callus formation. The expression of core cell cycle regulator Cyclin D3 (CYCD3;1) is downregulated in the arr1-3arr12-1 double mutant and triple loss-of-function mutants of cycd3;1–3 have low callus formation efficiency (Ikeuchi et al. 2017). Thus, these results suggest that wounding induces cytokinin signaling and then promotes cell cycle activation at wounded sites. Other AP2/ERF transcription factors, PLETHORA3 (PLT3), PLT5, and PLT7, are also induced after wounding, and plt357 triple mutants are less effective in callus formation (Ikeuchi et al. 2017). In addition, overexpression of PLT5 successfully obtained transgenic plants of Antirrhinum majus and Brassica rapa (Lian et al. 2022).
Induction of PLT3, PLT5, and PLT7 are among the earliest transcriptional responses induced by CIM and then the essential root meristem regulators PLT1 and PLT2 are activated (Aida et al. 2004; Galinha et al. 2007; Kareem et al. 2015). In addition, Cup-shaped cotyledon2 (CUC2), encoding a NAC family transcription factor, is also activated by PLT3, PLT5, and PLT7. Several pieces of evidence showed that CUC proteins are critical for shoot formation in the callus (Kareem et al. 2015). Overexpression of CUC1 or CUC2 enhances the adventitious shoot formation of calli derived from Arabidopsis hypocotyls (Daimon et al. 2003). Other transcription factors, such as ESR2, enhance shoot regeneration by directly regulating CUC1 transcription (Ikeda et al. 2006). After transferring to SIM, the essential shoot stem cell regulator WUS is induced (Gordon et al. 2007). The CUC2-expressing cells continue to proliferate and form promeristems in which PIN1 and a homeodomain transcription factor shoot meristemless (STM) are upregulated and further promote the formation of functional shoot meristems (Gordon et al. 2007). Overexpression of BnSTM induces type-B ARRs and represses type-A ARRs (Elhiti and Stasolla 2012). Activation of STM using an inducible system resulted in a rapid and dramatic increase of isopentenyl transferase 7 (IPT7), encoding a cytokinin biosynthesis gene (Yanai et al. 2005). In addition, MPΔ, an irrepressible variant of Monopteros (MP)/ARF5, promotes de novo shoot formation by activating the expression of STM and repressing the expression of ARRs-A (Ckurshumova et al. 2014; Krogan et al. 2012; Zhao et al. 2010).
WUS is essential for the maintenance of the stem cell niche in SAMs (Laux et al. 1996). Recent studies revealed that type-B ARRs activate the transcription of WUS. Type-B ARRs also inhibit auxin accumulation by repressing YUCs and indirectly inducing the expression of WUS (Meng et al. 2017). In addition, WUS directly represses the transcription of type-A ARRs (Leibfried et al. 2005). Like many other regeneration regulators, epigenetic marks modulate WUS expression during shoot regeneration (Li et al. 2011). Loss-of-function of a DNA methyltransferase 1 (MET1) led to increased WUS expression and accelerated developmental speed of in vitro shoot regeneration (Li et al. 2011) (Fig. 4B).
Application of developmental regulatory genes for genotype-independent plant transformation
Developmental regulatory genes that promote plant regeneration have been used to improve transformation efficiency and promote genotype-independent plant transformation. Ectopic expression of LEC1, L1L, or LEC2 in Arabidopsis (Lotan et al. 1998), Picea abies (Uddenberg et al. 2016), Citrus sinensis (Zhu et al. 2014) and Theobroma cacao (Shires et al. 2017) promotes embryo-like structure and somatic embryo formation but cannot obtain regenerated transgenic plants. However, inducible expression of LEC2 by β-estradiol could regenerate transgenic plants, though the regenerated plant displayed abnormal phenotypes (Rashid et al. 2007). AGL15 promotes the generation of secondary embryos from zygotic embryos and these secondary embryos maintain the potential for embryogenic development (Harding et al. 2003). Ectopic expression of AGL15 also enhances somatic embryo formation from the shoot apical meristem (Harding et al. 2003). Overexpression of GmAGL15, an ortholog of Arabidopsis AGL15, promotes somatic embryo development in Glycine max (Thakare et al. 2008). In G. hirsutum, overexpression of either GhAGL15-1, GhAGL15-3, or GhAGL15-4 promotes the embryogenic potential of transgenic calli (Yang et al. 2014).
Overexpression of TaWOX5 increases the transformation efficiency of multiple T. aestivum varieties without genotype dependency (Wang et al. 2022a). Ectopic expression of AtWOX2/8/9 led to a range of abnormal phenotypes in tobacco (Kyo et al. 2018). Overexpression of Z. mays homeobox gene knotted1 (Zmkn1) obtains a large number of transgenic calli and shoots on a hormone-free medium without antibiotic selection in tobacco. Under the same conditions, no callus or shoot was generated from explants that were infected with an Agrobacterium strain harboring the NPTII selection gene or uninfected controls. The use of 35S:ZmKn1 resulted in a three-fold increase in shoot organogenesis relative to the NPTII selection. These results suggest that ZmKn1 could be used as an effective selection marker with the potential to enhance plant transformation efficiency (Luo et al. 2006). Similarly, overexpression of ZmKn1 in transgenic citrus enhanced transformation efficiency by 3- to 15-fold (Hu et al. 2016). However, overexpression of Nicotiana tabacum homeobox (NTH) genes, knotted1-type homeobox genes, resulted in a range of abnormal leaf morphology. Transgenic plants overexpressing NTH1 or NTH9 displayed a relatively weak phenotype compared to NTH15 or NTH20 overexpression lines, which exhibited ectopic shoot formation on the leaf surface (Nishimura et al. 2000).
Overexpression of BBM enhances the spontaneous formation of somatic embryos in Arabidopsis and B. napus (Boutilier et al. 2002). BBM has also been used as an ectopic regulator in T. cacao (Florez et al. 2015) and tobacco (Srinivasan et al. 2007) genetic transformation. However, the BBM overexpression transgenic plants exhibited abnormal phenotypes. Thus, strategies that use inducible promoters or transgene excision to control the restricted spatiotemporal expression of BBM have been applied in tobacco (Srinivasan et al. 2007), Capsicum annuum (Heidmann et al. 2011) and Arabidopsis (Lutz et al. 2015). In Populus tomentosa genetic transformation, the generated transgenic plants are phenotypically normal when using a heat shock-inducible FRT/FLP system to excise BBM expression cassette from the callus stage (Deng et al. 2009). Transgenic plants generated by overexpression of WUS also exhibit negative pleiotropic phenotypes such as swollen hypocotyls, distorted leaves, and coiled root tips (Arroyo-Herrera et al. 2008; Bouchabke-Coussa et al. 2013; Rashid et al. 2007), suggesting that expression of WUS has to be strictly controlled.
A recent groundbreaking study showed that fine-tuning the expression of WUS and BBM enhanced the transformation efficiency of monocot plants (Lowe et al. 2016). Overexpression of ZmWUS2 driven by a strong callus promoter often causes callus necrosis. To solve this problem and to induce somatic embryogenesis in immature embryos, a relatively weak Agrobacterium-derived nopaline synthase promoter and a strong maize Ubiquitin promoter were used to drive ZmWUS2 (Nos:ZmWUS2) and ZmBBM (Ubi:ZmBBM) expression simultaneously (Lowe et al. 2016). Results showed that ectopic expression of ZmWUS2 and ZmBBM significantly enhanced callus transformation efficiency in Z. mays, Sorghum bicolor, O. sativa and Saccharum officinarum. However, the continuous expression of ZmWUS2 and ZmBBM leads to aberrant phenotypes, such as thick, short roots, stunted, twisted and sterile plants (Lowe et al. 2016). Thus, using desiccation-inducible promoter rab17 to activate CRE (a recombinase enzyme isolated from the P1 bacteriophage) expression, and remove the ZmWUS2, ZmBBM and CRE expression cassettes between two loxP sites in the transformed embryogenic calli generate healthy, fertile T0 transgenic plants (Lowe et al. 2016). This strategy could also obtain transgenic plants from previously non-transformable Z. mays and S. bicolor varieties (Mookkan et al. 2017, 2018). Another strategy for solving the phenotypic abnormalities is to select suitable endogenous promoters to trigger the required spatiotemporal expression of ZmWUS2 and ZmBBM. The promoter of a Z. mays phospholipid transferase protein gene (ZmPLTP) was selected to drive ZmBBM as ZmPLTP is highly expressed in leaves, embryos, and callus but has very low expression levels in roots, meristems, and reproductive tissues (Lowe et al. 2018). Somatic embryo formation was rapidly induced when ZmPLTP:ZmBBM and Nos:ZmWUS2 were co-transformed into Z. mays immature zygotic embryos, and these somatic embryos developed into healthy fertile plants without a callus phase (Lowe et al. 2018). However, T1 seeds continuously expressing Nos:ZmWUS2 showed poor germination. While replacing the Nos promoter with a Z. mays auxin-inducible promoter (ZmAxig1) and co-transformation of ZmPLTP:ZmBBM and ZmAxig1:ZmWUS2 stimulated somatic embryo formation and obtained phenotypically normal transgenic plants without excision ZmWUS2 and ZmBBM expression cassettes (Lowe et al. 2018). The callus-free transformation approach has been successfully tested in seven different Z. mays inbred lines (Lowe et al. 2018). Interestingly, a recent study showed that the ZmPLTP:ZmWUS2 alone was sufficient to promote rapid somatic embryo formation from Z. mays immature embryos in a noncell autonomous manner. When transforming Z. mays with two Agrobacterium strains, one containing ZmPLTP:ZmWUS2 and the other containing selectable and visual marker cassettes, the transformed Z. mays T0 plants expressed the selectable marker gene but without the integration of ZmWUS2 (Hoerster et al. 2020). This result suggests that transformed cells expressing ZmWUS2 could stimulate somatic embryogenesis of their neighboring cells. ZmPLTP:ZmWUS2 also significantly shortened the tissue culture time in S. bicolor by inducing direct somatic embryo formation and regeneration, and also bypassed genotype-dependent callus formation (Che et al. 2022). Similarly, using two strains with one containing ZmPLTP:ZmWUS2 and ZmPLTP:ZmBBM expression cassettes, and the other harboring a selectable marker expression cassette to transform S. bicolor, the transformed S. bicolor T0 plants expressed the selectable marker gene but without the integration of ZmWUS2 and ZmBBM (Aregawi et al. 2022). This strategy increases transformation efficiency and expands amenable genotypes of different monocot species. A recent study showed that Nos:ZmWUS2 and 3xENH–Ubi:ZmBBM (three consecutive viral enhancers including Figwart mosaic virus, Peanut chlorotic streak virus, and Mirabilis mosaic virus) were used to improve leaf transformation efficiency and obtain plants with Cas9-mediated gene dropouts and insertion in Z. mays and S. bicolor (Wang et al. 2023). Moreover, regenerated plants were successfully obtained by using Nos:ZmWUS2 and 3xEnh–Ubi:ZmBBM in Eragrostis tef, Panicum virgatum, Cenchrus americanus, Setaria italica, Secale cereale, Hordeum vulgare and O. sativa (Wang et al. 2023). These results suggest that this may be a universal method for genetic transformation and genome editing of the Poaceae. In addition, recent studies showed that using Nos:ZmWUS2, Ubi:IPT or Ubi:AtSTM enhanced organogenesis in aseptic seedling leaves of Arabidopsis, Nicotiana benthamiana, and Solanum lycopersicum, and in mature plants of N. benthamiana, Solanum tuberosum and Vitis vinifera (Cody et al. 2023; Maher et al. 2020). When Nos:ZmWUS2, Ubi:AtSTM or Ubi:IPT were co-transformed with Cas9/gRNA plasmids, gene-edited shoots were obtained without tissue culture. The tissue culture-free method has great potential to accelerate the breeding process for many plant species (Cody et al. 2023; Maher et al. 2020).
In contrast to the adverse effects of ectopic expression of ZmWUS2 and ZmBBM, overexpression of transcription factor encoding genes Growth-regulating factor (GRF) and/or its cofactor GRF-interacting factor1 (GIF) does not cause aberrant phenotypes in transgenic plants. In callus induction and plant regeneration, the GRF-GIF recruits SWITCH2/SUCROSE NONFERMENTING 2 chromatin remodeling complexes to confer the meristematic potential of the proliferative tissue during organogenesis. Accordingly, overexpression of AtGRF5 or GRF5 orthologs enhanced transformation efficiency in Beta vulgaris, B. napus, G. max, Helianthus annuusl and Z. mays (Kong et al. 2020). Furthermore, a fused GRF4-GIF1 chimeric protein increases transformation efficiency and accelerates the speed of regeneration in T. aestivum, O. sativa, and citrus (Debernardi et al. 2020). Compared with the control, the transformation efficiency with the chimeric GRF4-GIF1 protein expression was increased by 7.8-, 2.1- and 4.7- fold in T. aestivum, O. sativa, and citrus, respectively (Debernardi et al. 2020). Similarly, overexpression of GRF5, or GRF4 and GIF1 also achieved high transformation efficiency in Citrullus lanatus. AtGRF5, or ClGRF4 and ClGIF1 factors also facilitate efficient transformation and increase CRISPR/Cas9-based genome editing efficiency in C. lanatus (Feng et al. 2021; Pan et al. 2022b) (Table 1).
Nanoparticle uptake and translocation in plant cells
Agrobacterium-mediated method is the most frequently used tool for gene delivery in plant transformation. However, this method usually requires regeneration from tissue culture and infects only some plant species. Furthermore, it is hard to use Agrobacterium for chloroplast or mitochondrion transformation. Nanoparticles (NPs), natural or manufactured ultradisperse objects ranging from 1 to 100 nm, are promising materials for exogenous biomolecule delivery because of their ability to traverse the plant cell without external force and their broad host applicability. The application of nanotechnology to plant cells requires understanding the interaction between NPs and plant cells, including the uptake and translocation of NPs.
Nanoparticle uptake in plant cells
In plant science, NPs can be applied to roots and above-ground plant tissues especially leaves. Shoot surfaces are usually covered with a cuticle, which acts as a lipophilic barrier to protect primary organs of above-ground plants. NPs can enter the cell wall through natural openings, such as stomata pores (Eichert et al. 2008). Damages and wounds may also be feasible pathways for NP internalization in both aerial and hypogeal parts of plants (Al-Salim et al. 2011) (Fig. 5). In addition, delivery methods affect NP uptake efficiency in plants. A recent study showed that compared with the NP drop-cast method, the aerosol application help to improve NP uptake in C. lanatus (Raliya et al. 2016).
Nanoparticle translocation in plant cells
Once penetrate the outer protective layers of plants, mobilization of NPs in plants through apoplastic and symplastic paths. Apoplastic transport takes place outside the plasma membrane through the cell wall and extracellular spaces, while symplastic transport occurs between the cytoplasm of adjacent cells connected by plasmodesmata and sieve plate pores with the movement of water and solutes. Apoplastic transport has been demonstrated to facilitate the radial movement of NPs (Gonzalez-Melendi et al. 2008; Larue et al. 2014; Sun et al. 2014). However, the longitudinal Casparian strip composed of lignin-like structures prevents this radial movement in the root endodermis (Lv et al. 2015; Sun et al. 2014), and the symplastic path could bypass this barrier (Schwab et al. 2016) (Fig. 5). The cell wall is a multi-layered structure of pore diameter ranging from 5 to 20 nm (Fleischer et al. 1999; Fujino and Itoh 1998; Zemke-White et al. 2000). Recent studies demonstrated that different types of NPs with a mean diameter between 3 and 50 nm could easily pass through Arabidopsis and citrus cell walls (Etxeberria et al. 2016; Torney et al. 2007). When NPs penetrate the cell wall and reach the plasma membrane, they can enter cells through endocytosis. In addition, NPs can also cross the plasma membrane directly (Chang et al. 2013). Once NPs enter the cytoplasm, plasmodesmata promote the cell-to-cell movement of NPs. The transport of NPs of various sizes through plasmodesmata has been demonstrated in some plant species (Geisler-Lee et al. 2013; Lin et al. 2009; Zhai et al. 2014).
Application of nanoparticles in plant transformation
Over the past decade, NPs have been applied for plant delivery. Early studies showed NP-mediated plasmid DNA and protein delivery into plant cells with external force. For instance: (1) Gold-functionalized mesoporous silica nanoparticles (Au-MSNs)-mediated delivery of DNA (Torney et al. 2007) and proteins (Martin-Ortigosa et al. 2012, 2014) through the biolistic method. (2) Combined utilization of polyethylene glycol (PEG)-mediated transformation and polymeric dimethylaminoethyl metacrylate (DMAEM)-based polymers effectively deliver plasmid DNA into Ceratodon purpureus protoplasts and obtain stable transformants (Finiuk et al. 2017). (3) Polyethylenimine (PEI) nanoparticles deliver DNA into suspended cells of Crocus sativus through ultrasound, resulting in improved transfection efficiency (Firoozi et al. 2018). (4) Combined peptide-displaying micelle complexes (MCs) and cell wall-loosening zwitterionic liquid (ZIL) carry DNA into specific plant organelles through the vacuum/compression method (Miyamoto et al. 2022). Of these methods, cell-penetrating peptide-displaying MCs (CPP-MCs) was used to deliver DNA into nuclei while combined CPP-MCs and chloroplast-targeting peptide-displaying MCs (CPP/CTP-MCs) could be used for delivering DNA into chloroplasts (Table 2).
However, other studies have demonstrated that NPs can pass through plant cell walls without external force: (1) MSNs-mediated foreign DNA delivery into intact Arabidopsis roots without mechanical force (Chang et al. 2013). (2) Application of single-walled carbon nanotubes (SWNTs) for the delivery of small interfering RNA (siRNA) and plasmid DNA into a variety of plant species (Demirer et al. 2020, 2019a, b; Kwak et al. 2019). In addition, chitosan-complexed single-walled carbon nanotubes (CS-SWNTs) could deliver plasmid DNA into chloroplasts of mature Eruca sativa, Nasturtium officinale, Spinacia oleracea, tobacco plants and isolated Arabidopsis mesophyll protoplasts (Kwak et al. 2019). (3) Using PEI functionalized carbon dots (CDs) to efficiently deliver plasmid DNA or siRNA into intact plants (Schwartz et al. 2020; Wang et al. 2020). (4) DNA nanostructures and PEI functionalized gold nanoclusters (PEI-AuNCs) internalize into plant mature cells and deliver a siRNA to silence green fluorescent protein (GFP) expression in transgenic N. benthamiana plants (Zhang et al. 2021a; Zhang et al. 2019). Moreover, a recent study has reported that the double-stranded RNA (dsRNA) can be coupled to layered double hydroxides (LDH) nanoparticles, inducing gene silencing through injection into S. lycopersicum flower pedicel (Molesini et al. 2022). Another recent study used polymer-functionalized graphene oxide nanoparticles (GONs) to deliver siRNAs into intact N. benthamiana cells (Li et al. 2022). These successful applications indicate that NPs have great potential for plant delivery (Fig. 6, Table 2).
To fully leverage NPs for plant genetic engineering, it is essential to achieve stable transformation enabling the generation of transgenic plants. Chitosan nanoparticles can deliver a thionin gene with antimicrobial properties into Allium cepa and Paulownia tomentosa cells, producing transgenic A. cepa and P. tomentosa resistance to black rot diseases and bacterial infection, respectively (Hussien 2020; Hussien et al. 2022). A groundbreaking study showed that stable genetic transformation had been successfully achieved in G. hirsutum plants using magnetic nanoparticles (MNPs) technology (Zhao et al. 2017). In this system, the BTΔα-CPTI gene-MNPs complex is delivered into G. hirsutum pollen under a magnetic field. Pollen magnetofection not only perfectly protects foreign DNA integrity, but also maintains pollen viability. Insect-resistant transformed plants are successfully generated through magnetofected pollen pollination. The exogenous gene was successfully integrated into the genome, effectively transcribed, and stably inherited into the offspring (Zhao et al. 2017). Y18 and SU12, two previously difficult-to-transform G. hirsutum varieties, are successfully transformed using this system. In addition, genetically modified C. annuum and Cucurbita moschata plants have also been successfully created (Zhao et al. 2017). A recent study reported that the MNPs system was also used to deliver exogenous genes to different Z. mays inbred lines and successfully obtained transgenic plants (Wang et al. 2022b). Further investigation found that transfection with a cool temperature pretreatment of pollen to open the germination aperture can improve the efficiency of DNA entry and maintain pollen viability (Wang et al. 2022b). As this method is genotype-independent, culture-free, and easy to handle, it has great potential to transform recalcitrant and genotype-dependent crops and thus accelerate the breeding process (Table 2).
Conclusions and perspectives
Many developmental regulatory genes have been shown to work effectively both in dicots and monocots (Table 1), and manipulation of these genes has great potential for developing genotype-independent genetic transformation methods in various crops. However, constitutive expression of developmental regulatory genes, such as ZmWUS2 and ZmBBM often interferes with normal plant development and leads to negative pleiotropic effects. So fine-tuning the expression of these genes is essential for applying them to plant transformation (Hoerster et al. 2020; Lowe et al. 2016, 2018; Mookkan et al. 2018, 2017). Overexpression of GRF and/or GIF can improve the transformation efficiency in a variety of crops but did not cause abnormal phenotypes in transgenic plants (Debernardi et al. 2020; Kong et al. 2020). This may be due to the post-transcriptional down-regulation of GRF by endougenous miRNA396 in T0 plants, which provides a built-in mechanism for alleviating pleiotropic problems (Debernardi et al. 2020; Li et al. 2021). There are many genes, such as ABI3 and LBDs, affecting plant regeneration have not been used for plant transformation. It is worth investigating whether fine-tuning the expression of these genes could facilitate the improvement of plant transformation. A recent study has established a versatile CRISPR-Combo platform for simultaneous genome editing and gene activation in plants (Pan et al. 2022a). This system can be applied to achieve plant regeneration by simultaneously activating BBM1 and editing the genome at Grain weight2 (GW2) and Grain number 1a (GN1a) loci without exogenous hormone application in O. sativa (Pan et al. 2022a). This system has promising application prospects in crop breeding.
Over the past decade, NPs have been widely used to deliver genes and proteins into plant cells (Demirer et al. 2019a; Kwak et al. 2019; Martin-Ortigosa et al. 2014). However, most of them are transient transformations of foreign genes. To fully leverage NPs for plant genetic engineering, transgenes have to be stably inherited to the next generation. Currently, MNPs have successfully achieved stable genetic transformation in G. hirsutum, C. annuum, C. moschata, and Z. mays (Wang et al. 2022b; Zhao et al. 2017). However, a recent study reported that the transfection of Lilium brownii, S. bicolor, and Z. mays pollens by MNPs was unsuccessful (Vejlupkova et al. 2020), possibly due to the structure of the single aperture on the pollen wall and the entry of exogenous DNA is blocked when the aperture is covered by wall material or the operculum. Indeed, promoting aperture open by pretreating maize pollens at cool temperatures facilitates exogenous DNA entry and expression (Wang et al. 2022b), which opens a window for applying NP-mediated plant transformation in troublesome plant species. Overall, either manipulation of developmental regulatory genes or nanotechnology facilitates genotype-independent plant genetic transformation and further promotes functional genome research and crop breeding.
Data availability
This manuscript is a review, no data was used for the research described in the article.
Abbreviations
- ABI:
-
Abscisic acid insensitive
- AGL:
-
Agamous-like
- ARF:
-
Auxin response factor
- ARR:
-
Arabidopsis response regulator
- ATP:
-
Adenosine triphosphate
- ATXR:
-
Arabidopsis trithorax-related
- Au-MSN:
-
Gold-functionalized mesoporous silica nanoparticle
- AuNC:
-
Gold nanocluster
- AuxRE:
-
Auxin response element
- BBM:
-
Baby boom
- CD:
-
Carbon dot
- CIM:
-
Callus-inducing medium
- CPP:
-
Cell-penetrating peptide
- CTP:
-
Chloroplast-targeting peptide
- CUC:
-
Cup-shaped cotyledon
- CYCD:
-
Cyclin D
- DMAEM:
-
Dimethylaminoethyl metacrylate
- DRN:
-
Dornröschen
- dsRNA:
-
Double-stranded RNA
- ESR:
-
Enhancer of shoot regeneration
- FUS:
-
FUSCA
- GFP:
-
Green fluorescent protein
- GIF:
-
GRF-interacting factor
- GN:
-
Grain number
- GON:
-
Graphene oxide nanoparticle
- GRF:
-
Growth-regulating factor
- GW:
-
Grain weight
- HDAC:
-
Histone deacetylases
- H3K27me3:
-
Histone H3 lysine 27 trimethylation
- H3K36me3:
-
Histone H3 lysine 36 trimethylation
- iPB:
-
in planta Particle bombardment
- IPT:
-
Isopentenyl transferase
- JMJ:
-
JUMONJI C domain-containing protein
- LBD:
-
Lateral organ boundaries domain
- LDH:
-
Layered double hydroxide
- LEC:
-
Leafy cotyledon
- LRR:
-
Leu-rich repeat
- MC:
-
Micelle complex
- MET:
-
Methyltransferase
- MNP:
-
Magnetic nanoparticle
- MP:
-
Monopteros
- NM:
-
Nanomaterial
- NP:
-
Nanoparticle
- NTH:
-
Nicotiana tabacum Homeobox
- PEG:
-
Polyethylene glycol
- PEI:
-
Polyethylenimine
- PIN:
-
PIN-PORMED
- PLK:
-
Receptor-like kinase
- PLT:
-
PLETHORA
- PRC:
-
POLYCOMB REPRESSIVE COMPLEX
- RIM:
-
Root-inducing medium
- SAM:
-
Shoot apical meristem
- SERK:
-
Somatic embryogenesis receptor-like kinase
- SIM:
-
Shoot-inducing medium
- siRNA:
-
Small interfering RNA
- STM:
-
Shoot meristemless
- SWNT:
-
Single-walled carbon nanotube
- TSA:
-
Trichostatin A
- Vir:
-
Virulence
- WIND:
-
Wound-induced dedifferentiation
- WOX:
-
Wuschel related homeobox
- WUS:
-
WUSCHEL
- YUC:
-
YUCCA
- ZIL:
-
Zwitterionic liquid
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This work was supported by the National Key Research and Development Program of China (2022YFF1003500 and 2022YFF1002400), the National Natural Science Foundation of China (31900610 and 31871702) and the Beijing Nova Program (Z201100006820114).
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QH and XWan conceived and designed the review. TY, XWei and AP contributed to collecting and analyzing the literature of original studies. TY and YQ contributed to figure preparation. TY and QH wrote the manuscript. SW, XA and XWan revised the manuscript. All authors read and approved the final manuscript.
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Yan, T., Hou, Q., Wei, X. et al. Promoting genotype-independent plant transformation by manipulating developmental regulatory genes and/or using nanoparticles. Plant Cell Rep 42, 1395–1417 (2023). https://doi.org/10.1007/s00299-023-03037-2
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DOI: https://doi.org/10.1007/s00299-023-03037-2