Plant actin depolymerizing factor: actin microfilament disassembly and more

As described above, angiosperms have acquired an expanded number of ADF genes, which is hypothesized to have derived from a single ADF in P. patens (Augustine et al. 2008; Roy-Zokan et al. 2015). These plant ADFs share protein structure with yeast and mammalian ADF/cofilin (Bowman et al. 2000, Fig. 1). Residues required for ADF activity and regulation, such as those for actin binding and phosphorylation (see below), have also been conserved in plant ADFs (Fig. 1).

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The functional divergence and specialization resulting from this expansion of ADF genes are clearly manifested in differences in tissue- and organ-specific gene expression patterns. For example, among 11 members of A. thaliana ADFs, AtADF1, −2, −3, and −4, which are classified into subclass I, are expressed throughout the plants at relatively high levels, whereas AtADF7 and AtADF10, which belong to subclass IIa, are expressed only in flowers, particularly in pollens. Another subclass of ADFs, AtADF8 and AtADF11 in subclass IIb, showed specific expression in root epidermal cells. Although both subclass III and subclass IV showed expression in a wide variety of tissues, the restricted expression of subclass III AtADF5 and AtADF9 in root apical meristem is not seen with subclass IV AtADF6 (Ruzicka et al. 2007). The distinct expression patterns of AtADF1 (subclass I), AtADF5 (subclass III) and AtADF6 (subclass IV) were also observed by Dong et al. (2001a), in which the restricted expression of AtADF5 in root apical meristem was clearly noted. In rice, OsADF2, −4, and −5 are expressed throughout the plant, whereas OsADF9 and −10 show specific expression in spikelets, and OsADF1 and −8 show high expressions in spikelets and are also expressed in other organs. OsADF3 and −11 are expressed throughout plants, except for roots. Promoter-GUS analysis also revealed the vascular specific expression of OsADF1 and −3 (Huang et al. 2012).

In addition to variations in expression patterns, biochemical activity also varies among ADFs. Particularly, it has been noted that pollen ADFs have structural and biochemical characters different than vegetative ADFs. The antibody raised against pollen-specific ADF did not cross-react with vegetative ADFs (Allwood et al. 2002; Smertenko et al. 2001). Pollen-specific LlADF1 exhibited much lower activity in actin depolymerization than maize ZmADF3, which is expressed in vegetative organs (Smertenko et al. 2001). Accordingly, pollen-specific AtADF7 is less efficient at disassembling F-actin than vegetative AtADF1 (Zheng et al. 2013). Although ADFs are commonly regulated by phosphorylation, as described later, pollen-specific LlADF1 seems to be exceptional (Allwood et al. 2002). Further differences have been seen in microscope images of the intracellular localization of pollen-specific ADFs. Vegetative ADFs exhibit nucleoplasmic localization in addition to co-localization with F-actin (Dong et al. 2013; Inada et al. 2016; Ruzicka et al. 2007; Tholl et al. 2011; Tian et al. 2009), whereas both immunostaining analysis and expression of fluorescent protein-tagged ADFs have shown the absence of pollen-specific ADFs in the nucleus (Allwood et al. 2002; Smertenko et al. 2001).

The differentiation of physiological function has also been reported for ADFs. Purified AtADF9 shows strong F-actin bundling activity, whereas AtADF1 exhibits classical ADF activity in F-actin destabilization (Tholl et al. 2011). The loss of AtADF9 expression causes early flowering phenotypes, which are not complemented with the constitutive expression of distant AtADF4 or AtADF8 (Burgos-Rivera et al. 2008). Transient expression of AtADF1, −5, −6, −7, and −10 (referred as AtADF12 in the paper), but not that of AtADF2, −3, −4, and −9, inhibits the resistance of barley (Hordeum vulgare) against powdery mildew fungus Blumeria graminis f. sp. hordei (Miklis et al. 2007). Overexpression of AtADF6, but not that of AtADF5, inhibits the transport of RPW8.2-YFP, a resistant protein for powdery mildew fungi, to the membrane surrounding specialized infection hyphae, haustoria (Wang et al. 2009b). These differences in cellular function could be caused by differences in biochemical activity or regulatory mechanisms of ADFs, however, the underlying mechanisms remain unknown.

Characterized angiosperm ADFs show well conserved gene structures, comprising three exons, including a very short 1st exon. As represented by the gene structure of A. thaliana 11 ADF members (Fig. 2), ADFs of angiosperms, including petunia (Petunia hybrid) (Mun et al. 2002) and rice (Huang et al. 2012), possess a very short 1st exon that contains only start codons, which is followed by a long 1st intron in most cases. Notably, mammalian ADF/cofilin sequences also have a short 1st exon (Maciver and Hussey 2002; Thirion et al. 2001), whereas P. patens ADF do not possess introns (Augustine et al. 2008).

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The long 1st intron (1659 bp) of petunia ADF (PhADF1) functions in enhancing expression of PhADF1 (Mun et al. 2002). When the GUS gene was fused to the 1.7 kb upstream region of PhADF1 and expressed in A. thaliana, GUS expression was only seen in the vascular area, whereas a construct containing PhADF1 1.7 kb promoter-1st intron-GUS showed strong GUS activity throughout the plant. Notably, when the PhADF1 genomic region from the 1.7-kb native promoter to the 2nd intron was fused upstream of GUS, the transgenic plant showed much lower expression levels than plants expressing PhADF1 promoter-1st intron-GUS, suggesting that PhADF1 introns function differently in the regulation of gene expression (Mun et al. 2002). The enhancement of gene expression by the 1st intron is conserved in another member of petunia ADF, PhADF2, as well as in AtADF1 (Jeong et al. 2007). In addition, inserting the PhADF1 1st intron can alter both expression level and pattern of other genes. A. thaliana profilin 5 (PRF5) normally expresses only in reproductive organs. Insertion of the PhADF1 1st intron between the 1st exon of PRF5 and GUS gene results in PRF5 expression throughout the plant. Owing to the high A/T composition, no meaningful conserved sequences were found in these ADF 1st intron sequences (Jeong et al. 2007); thus, the regulatory mechanisms remain unknown.

The structure of the promoter region has been examined in petunia and rice. For petunia PhADF1, several potential transcription factor-binding sites and hormone response domains were found in the upstream region of the gene body (Mun et al. 2002). Huang et al. (2012) performed comprehensive analyses on the promoter structure and expression pattern of all the 11 rice ADFs and found the presence of stress-related cis-acting elements, including ABA-responsive element, dehydration-responsive element/C-repeat, and low-temperature responsive element in the 1-kb promoter regions. Accordingly, the expression of some OsADFs is induced by stresses such as low temperature, drought, ABA, and salt (Huang et al. 2012).

The alternative splicing of ADF/cofilin that produces variations in both the ADF/cofilin sequence and function has been reported in human (Thirion et al. 2001) and Caenorhabditis elegans (McKim et al. 1994; Ono and Benian 1998; Ono et al. 2008). The A. thaliana database (TAIR, http://www.arabidopsis.org/) indicated that AtADF1, −3, −4, and −5 have splicing variants. For AtADF1 (At3g46010), which has a 139 amino acid long At3g46010.1 variant and 150 amino acid long At3g46010.2 variant, the sequence of At3g46010.1 has been identified in the A. thaliana EST database (Dong et al. 2001a), and its biochemical activity has been analyzed (Dong and Hong 2013; Dong et al. 2013). However, At3g46010.2, which has an additional 11 residues following the start codon, has not been characterized and it is not known whether the two variants differ in expression pattern or activity in F-actin depolymerization.

The activity of ADF/cofilin in animal models is post-transcriptionally regulated by many factors, including environmental pH and phosphorylation. Interactions with 14-3-3 protein, phosphatidylinositol 4,5-bisphosphate (PIP₂), and actin-interacting protein (AIP) also affect the activity of ADF/cofilin (Bernstein and Bamburg 2010).

These regulatory factors are well conserved in plants. Regarding the pH dependency of ADF activity, plant ADFs, such as those in wheat (TaADF) (Ouellet et al. 2001), tobacco (Nicotiana tabacum, NtADF1) (Chen et al. 2002), lily (LlADF1), and maize (ZmADF3) (Allwood et al. 2002), show high activity in binding to F-actin at pH 6.5, whereas they bind to G-actin more efficiently at pH 8.0, similarly to ADF/cofilin in animal models. This pH-dependent change in ADF/cofilin activity is possibly caused by the pH-dependent conformational changes of actin (Blondin et al. 2002).

Other factors known to regulate activities of plant ADFs are summarized below.

Phosphorylation of serine (Ser) at the N-terminus is a conserved regulatory mechanism of ADF activity in F-actin disassembly. Upon phosphorylation, ADF becomes inactivated and loses its F-actin-binding ability (Blanchoin et al. 2000; Ressad et al. 1998). In animals, this serine is located at the 3rd amino acid of ADF/cofilin, whereas many plant ADFs have the 6th serine (S6) phosphorylated (Fig. 1).

This S6 phosphorylation of plant ADFs was first shown with ZmADF3. A phosphomimetic mutation at S6 made ZmADF3 lose its ability to bind F- or G-actin (Smertenko et al. 1998). Microscopic observation also confirmed the loss of the F-actin-binding ability of plant ADFs by phosphorylation. Porter et al. (2012) produced A. thaliana plants stably overexpressing a coding sequence of AtADF4 conjugated with green fluorescent protein (GFP) and found that the co-localization of AtADF4-GFP with F-actin was disrupted when a phosphomimetic mutation was incorporated at S6 of AtADF4 (Porter et al. 2012). Similarly, phosphomimetic AtADF1 that was conjugated to GFP and transiently expressed in onion peels lost its filamentous localization pattern (Dong and Hong 2013). However, this reduction in co-localization with F-actin by the incorporation of a phosphomimetic mutation was not reproduced in another study that used transgenic plants stably expressing the genomic region of AtADF4 containing a 1.5-kb native promoter, exons, introns, and 3′ UTR (Inada et al. 2016). Biochemical analysis needs to be performed using those plants expressing the mutant form of ADFs to conclusively determine the relationship between the phosphostatus of ADF and its intracellular localization.

In animal systems, both kinases and phosphatases regulating the phosphostatus of ADF/cofilin were identified and well characterized (Bernstein and Bamburg 2010; Mizuno 2013). In plants, several candidate ADF kinases have been reported. Calcium-dependent protein kinase (CDPK) possibly phosphorylates ZmADF3 (Smertenko et al. 2001) and was partially purified (Allwood et al. 2001). However, chelating Ca²⁺ by EGTA does not abolish ZmADF3 phosphorylation, thus other factor(s) can also function in ZmADF3 phosphorylation (Smertenko et al. 1998). An in vitro assay using purified proteins showed that AtCDPK6 phosphorylates AtADF1 (At3g46010.1) at S6. Induced expression of AtCDPK6 increased F-actin bundling in planta, a phenotype similar to that of Atadf1, indicating the function of AtCDPK6 in the suppression of ADF activity (Dong and Hong 2013). Meanwhile, a 52-kD kinase that requires Mn²⁺ for its activity, which is a property of plant receptor-like protein kinases, was identified to phosphorylate wheat TaADF (Ouellet et al. 2001). Recently, A. thaliana CASEIN KINASE1-LIKE PROTEIN2 (CKL2) was identified to regulate activities of subclass I AtADFs (AtADF1, −2, −3, and −4) and stomatal closure upon ABA treatment or drought (Zhao et al. 2016). Knockout mutant ckl2 is unable to close stomata under ABA treatment or drought stress, and this phenotype is partially suppressed by Atadf4. CKL2 physically interacts with and phosphorylates subclass I AtADFs. It will be of interest to determine whether CKL2 regulates the functions of AtADF in other pathways, such as pathogen responses (Inada et al. 2016; Porter et al. 2012, see below).

Although phosphorylation is an important regulatory mechanism of ADF activity in F-actin disassembly, its importance in ADF function may vary depending on the variants or physiological events that ADF is involved in. In P. patens, which has a single ADF in the genome, phosphoregulation of ADF is essential for cell growth, because both phosphodeficient and phosphomimetic mutants of PpADF expression only partially complement the effect caused by the loss of PpADF expression (Augustine et al. 2008). Similarly, neither phosphodeficient nor phosphomimetic mutants of AtADF4 complement the enhanced resistance against powdery mildew disease in Atadf4 (Inada et al. 2016, see below). On the other hand, the phosphomimetic mutant of AtADF4 did complement the Atadf4 susceptible phenotype against bacterial pathogens (Porter et al. 2012). Furthermore, the F-actin-binding activity of ZmADF3 was inhibited by the incorporation of a phosphomimetic mutation, whereas its activity on F-actin disassembly was not (Smertenko et al. 1998).

In addition to S6, tyrosine 68 (T68) is also a residue that is commonly phosphorylated in mammalian, chicken (Gallus gallus), and Xenopus cofilin, but is not present in mammalian or chicken ADF (Bernstein and Bamburg 2010). Upon phosphorylation of T68, ubiquitination and degradation of cofilin is increased; therefore regulating the level of cofilin protein (Yoo et al. 2010). This tyrosine residue is conserved in some plant ADFs (Fig. 1), although there have been no reports to date showing the phosphorylation of ADF tyrosine residue or ubiquitination of plant ADFs.

Phosphatidylinositol 4,5-bisphosphate (PIP₂) is an established regulator of mammalian ADF/cofilin, and upon the binding of PIP₂, the ADF/cofilin activity is inhibited (Bernstein and Bamburg 2010). The only example of PIP₂ regulation on plant ADF is shown with ZmADF3. Biochemical analysis showed that the activity of recombinant ZmADF3 on F-actin depolymerization was inhibited by both PIP₂ and phosphatidylinositol 4-monophosphate (PIP) (Gungabissoon et al. 1998).

ADF/cofilin interacts with PIP₂ through a large, positively charged surface, consisting of lysine (K) and arginine (R) (Zhao et al. 2010). These K–R clusters are conserved in plant ADFs (Fig. 1), indicating the conservation of the PIP₂ regulation of plant ADFs.

14-3-3 proteins, which were named after their particular elution and migration patterns on two-dimensional DEAE cellulose chromatography and starch gel electrophoresis, are present in all eukaryotic organisms including plants. 14-3-3 proteins act as phosphosensors, monitoring the phosphostatus of a specific site, and translating the information into a change in the activity of the target protein. In plants, 14-3-3 proteins are involved in various aspects of plant physiology including biotic responses (Lozano-Duran and Robatzek 2015). In mammals, 14-3-3ζ binds and stabilizes phosphorylated ADF/cofilin, thus negatively regulating the ADF/cofilin activity of severing and depolymerizing F-actin (Gohla and Bokoch 2002).

Arabidopsis thaliana 14-3-3λ interacts with AtADF1 and regulates F-actin organization in vivo (Zhao et al. 2015). However, contrary to what is expected from animal 14-3-3 that stabilizes phosphorylated ADF/cofilin thus suppresses F-actin depolymerizing activity of ADF/cofilin, a knockout mutant of 14-3-3λ exhibited an elongated hypocotyl phenotype, similarly to Atadf1 and Atadf4. Authors also observed that a 14-3-3λ loss-of-mutant increased the phosphorylation level of AtADF1 thus hindered the proper localization of AtADF1 to F-actin (Zhao et al. 2015). Therefore, the regulatory mechanism of ADF by 14-3-3 may differ between animals and plants. As ADF phosphorylation is an important component of the regulation by 14-3-3, it is necessary to understand the entire mechanism, in which both kinase and 14-3-3 are involved, to reveal the regulatory mechanisms of ADF function.

Actin-interacting protein (AIP) is a conserved WD-repeat protein, which is required for efficient disassembly of F-actin by ADF/cofilin (Ono et al. 2004). Recently, it was demonstrated that AIP1 severs F-actin that is fully decorated with ADF/cofilin, possibly by competing with ADF/cofilin in F-actin binding, thus lowering the concentration of ADF/cofilin, which promotes F-actin severing by ADF/cofilin (Chen et al. 2015; Gressin et al. 2015).

Several papers have described a conserved role of plant AIP in promoting ADF-mediated F-actin disassembly. Allwood et al. (2002) identified interaction between A. thaliana AIP1 and lily LlADF1 using the yeast two hybrid assay and co-immunostaining analysis. They also performed an in vitro assay and demonstrated that A. thaliana AIP1 promotes F-actin depolymerization by LlADF1 (Allwood et al. 2002). Two AIP1 genes are encoded in the A. thaliana genome, and suppression of AIP1 expression impairs the growth and development of plants and induces increased bundling of F-actin, which is a phenotype seen in adf mutants (Ketelaar et al. 2004). Overexpression of AtAIP1 reduces F-actin bundling and induces swollen root hairs (Ketelaar et al. 2007). Knockout of P. patens AIP1, which is encoded by a single gene in the genome, causes severe defects in the tip growth, which is partially rescued by PpADF expression. F-actin in the P. patens aip1 mutant was more static and slower in remodeling than that in wild type moss, thus providing support that moss AIP functions in F-actin regulation through ADF (Augustine et al. 2011).

Shi et al. (2013) showed that rice AIP1 (OsAIP1) could promote ADF activity in severing and depolymerizing F-actin by an in vitro assay. In vivo, a knockdown of OsAIP1 promotes, whereas its overexpression inhibits, F-actin assembly. Co-sedimentation analysis showed the enhancement of F-actin disassembly by OsAIP1 only in the presence of ADF. The increase in frequency of in vivo F-actin severing by OsAIP1 in the presence of ADF was also confirmed by observation with total internal reflection fluorescence microscopy (TIRFM), by which the organization and movement of F-actin at the cell surface can be visualized at high resolution, thus confirming the role of OsAIP in regulating F-actin dynamics (Shi et al. 2013).

ADF controls cell elongation via the regulation of F-actin organization, thus contributes to plant growth. The knockdown of PpADF suppresses the tip growth of moss (Augustine et al. 2008), whereas the reduction of single ADF expression in angiosperms often exhibits cell elongation. Cotton (Gossypium hirsutum) ADF1 (GhADF1) expresses abundantly in fiber cells, and GhADF1 downregulation alters the cell wall morphology and elongates length of fiber cells (Wang et al. 2009a). Knockdown of AtADF1 significantly elongates organ length, such as that of cotyledons, hypocotyls, roots, and stems, whereas over-expression significantly shortens their lengths (Dong et al. 2001b). The effect of AtADF1 overexpression on the elongation of dark-grown hypocotyl is suppressed by the introduction of mutations in the actin-binding domain of AtADF1 (Dong et al. 2013). The loss of AtADF4 expression also causes hypocotyl elongation when grown in the dark (Henty et al. 2011), but shortens the root hairs in the standard growth condition with light (Inada et al. 2016). Therefore, ADF regulates cell elongation differently depending on tissues.

Organ morphology is also affected by altered ADF expression. AtADF1 overexpression causes wavy hypocotyls (Dong et al. 2001b), and Atadf4 exhibits wavy and flattened mature leaves, which is not observed in Atadf1 or Atadf3 (Inada et al. 2016). However, as this phenotype in leaf shape was more strongly manifested in plants in which expressions of all of subclass I AtADFs were suppressed, other members of subclass I AtADFs, AtADF1, −2, and −3, possibly contribute to the regulation of leaf shape redundantly (Inada et al. 2016). The alteration in leaf shape is also reported with induced AtADF2 knockdown plants (Clement et al. 2009). Ethanol-inducible AtADF2 RNAi plants exhibited more serration of leaves at the circumference. In addition, ectopic appearance of lateral roots, and small, shrunken, and bent siliques that contained less fertile seeds were observed (Clement et al. 2009). Although leaf serration and phenotypes of lateral root and silique were not observed in subclass I AtADFs knockdown lines (Inada et al. 2016), this difference in phenotypes could be due to difference in the level of AtADF2 expression suppression.

The role of ADF in regulating flowering timing has been indicated in two reports. The downregulation of AtADF1 expression significantly delayed the timing of flowering, whereas plants overexpressing AtADF1 flowered with timing similar to that of the wild type (Dong et al. 2001b). AtADF9 expresses at relatively low levels in seedlings and mature tissues, but at very high level in the callus (Ruzicka et al. 2007). The knockout mutant Atadf9 shows delayed growth and early flowering (Burgos-Rivera et al. 2008). This early flowering phenotype is correlated with a lower expression of FLC and higher expression of other flowering-related genes such as CO and LFY in Atadf9 (Burgos-Rivera et al. 2008). As mentioned above, this early flowering phenotype of Atadf9 was not complemented with AtADF4 or AtADF8 expression, which is correlated with the results that Atadf4 showed no changes in flowering timing (Inada et al. 2016). Thus, AtADFs functionally differentiate regarding the regulation of flowering timing.

The acquisition of multiple ADF genes in angiosperm lineages has made it possible for plant ADFs to obtain a role in responses to both abiotic and biotic stresses, as emphasized in recent studies.

Many papers reported increased protein accumulation or gene expression of ADF, particularly ADFs of grasses, when plants are subjected to various abiotic stresses.

Drought stress induced accumulation of OsADF in leaves of rice seedlings (cv. CT9993 and IR62266) (Salekdeh et al. 2002) and accumulation of OsADF2 expression in the rice variety Azucena (Yang et al. 2003). OsADF3 accumulates in the sheath of the cultivars Nipponbare and Zhonghua 8 during drought and osmotic stresses, but not during cold or salt stresses (Ali and Komatsu 2006; Huang et al. 2012). On the contrary, in roots, salt stress induces OsADF3 accumulation in Nipponbare (Huang et al. 2012; Yan et al. 2005), indicating a tissue-specific function of OsADF3. In a cDNA library of smooth cordgrass (Spartina alterniflora), which is a halophyte that is capable of tolerating salinity as high as double that of sea water, the gene expression of ADF is induced when plants are subjected to salinity stress (Baisakh et al. 2008).

ADF could also be involved in the tolerance to both high- and low-temperature stresses. Smooth cordgrass ADF was induced under heat stress (Baisakh and Subudhi 2009). The expression level of OsADF3 in anthers is higher in heat-tolerant cultivars than less tolerant ones (Gonzalez-Schain et al. 2016). However, wheat ADF (TaADF) has been identified as a gene of which expression is rapidly and strongly upregulated during low temperatures (Danyluk et al. 1996). TaADF accumulates at higher levels when wheat plants are subjected to low temperatures. The accumulation of TaADF is much higher in freezing-tolerant cultivars than less tolerant ones, thus suggesting its role in cold acclimation (Ouellet et al. 2001).

The exogenous application of the plant hormone, abscisic acid (ABA), induces swelling, root hair formation, and initiation of lateral root primordia in tips of young seminal rice roots. Proteomic analysis revealed that two ADFs of rice (Taichung native 1), called as ADF-1 and -2 in the paper, accumulate in response to ABA application. These OsADFs exhibit the same amino acid sequences; thus, are possibly the same protein of phosphorylated or dephosphorylated form (Chen et al. 2006). This ABA-induced OsADF was later identified as OsADF3 (Huang et al. 2012). ABA, but not salicylic acid, jasmonic acid, and ethylene, induces TaADF3 expression. The induction of TaADF3 expression was also seen during drought and cold stresses, but not salt stress or wounding (Tang et al. 2015).

The only example for the functional indication of ADFs during abiotic stresses is from a study of OsADF3 overexpressed in A. thaliana. OsADF3 overexpressing A. thaliana plants became more tolerant against both drought and osmotic stresses (Huang et al. 2012). Further genetic studies are necessary to clarify the role of ADF in abiotic stresses in the future.

The role of plant ADFs in interactions with pathogenic microbes, including nematodes, bacteria, viruses, and fungi, in both compatible (results in pathogen growth and proliferation) and incompatible (results in arrest of pathogen growth and often in plant cell death) interactions, has been recently highlighted in many reports. Generally, ADF positively regulates plant susceptibility in compatible interactions and plant resistance in incompatible interactions, although there are exceptions.

In a compatible interaction with nematodes, A. thaliana ADF2 acts as a positive regulator to establish the interaction, i.e., helps the nematode infecting the host plant. The root knot nematode Meloidogyne incognita forms giant cells in infected host roots, where the dynamic reorganization of host F-actin is observed (de Almeida Engler et al. 2004). Clement et al. (2009) found that AtADF2 gene expression is increased in cells containing giant cells. Transgenic plants with reduced AtADF2 expression exhibit severely delayed maturation of giant cells and significantly reduced egg production, which are correlated with increased bundling of F-actin in giant cells in AtADF2 knockdown plants (Clement et al. 2009).

In an incompatible interaction with the bacterial pathogen, Pseudomonas syringae pv. tomato (Pst) DC3000 harboring the avirulent protein AvrPphB, A. thaliana ADF4 plays a role in host resistance. The knockout mutant of AtADF4 shows increased susceptibility against Pst DC3000 AvrPphB, but not against lines carrying AvrRps2 or AvrB (Tian et al. 2009). This increased susceptibility is correlated with reduced RPS5 expression, a gene responsible for resistance against Pst DC3000 AvrPphB (Porter et al. 2012).

Soybean mosaic virus (SMV) establishes a compatible interaction with the soybean (Glycine max), and SMV P3, a protein with unknown function, interacts with soybean ADF2. This P3-GmADF2 interaction was shown in a yeast two hybrid assay and bimolecular fluorescent complementation assay. As SMV P3 possibly functions in virus replication, systemic infection, pathogenicity, overcoming resistance, and cell-to-cell movement, the authors suggested that the interaction between P3 and GmADF2 could facilitate the cell-to-cell movement of P3 (Lu et al. 2015).

The functions of ADFs in both compatible and incompatible interactions with fungi are highlighted in many reports. In an incompatible interaction with stem rust Puccinia graminis f. sp. tritici race QCCJ, barley rpg4-mediated resistance locus 1 (RMRL1) mediates a resistance against this fungus. This locus contains HvRga1, Rpg5, and HvAdf3, although suppression of HvAdf3 expression alone did not induce resistance against P. graminis (Wang et al. 2013). In an incompatible interaction with P. striiformis f. sp. tritici CYR23, the ADF7 expression of the wheat genotype Suwon 11 (TaADF7) was sharply elevated, whereas an infection by compatible CYR31 caused much smaller changes in TaADF7 expression. Reduced expression of TaADF7 caused increased susceptibility to CYR23 (Fu et al. 2014). On the other hand, TaADF3 functions in an opposite manner in interactions with P. striiformis f. sp. tritici. The expression of TaADF3 is downregulated by incompatible CYR23, but upregulated by compatible CYR31. The suppression of TaADF3 expression enhances resistance to both incompatible CYR23 and compatible CYR31, and impedes both fungal entry and haustoria formation of CYR31 (Tang et al. 2015).

In addition, we recently reported a function of A. thaliana subclass I ADFs, particularly AtADF4, in a contribution to the susceptibility against compatible powdery mildew fungus, Golovinomyces orontii (Inada et al. 2016). We found that the knockout mutant of Atadf4 shows significantly enhanced resistance against G. orontii. The altered susceptibility is not observed in Atadf1, whereas Atadf3 shows enhanced yellowing, which is a sign of enhanced immune response, at later infection stages. Transgenic plants in which the expression of all of four subclass I ADFs is suppressed (ADF1-4Ri) exhibit even more enhanced resistance against G. orontii and no visually noticeable mycelium formation at 2 weeks post inoculation, indicating the functional redundancy among subclass I ADFs in response to G. orontii. This increased resistance against G. orontii in Atadf4 and ADF1-4Ri is correlated with the infected cell-specific accumulation of reactive oxygen species and cell death, which are mediated by both salicylic acid and jasmonic acid. From this prominently enhanced resistance of Atadf4 and ADF1-4Ri, significant reorganization of F-actin in those mutants and transgenic plants was expected. However, we observed no changes in F-actin organization in uninfected Atadf4 and ADF1-4Ri, and only a transient increase in F-actin density in infected ADF1-4Ri cells at a very early infection stage. These unexpected results prompted us to examine another function of ADF in the nucleus. An expression of a construct containing an AtADF4 genomic sequence fused to GFP and a nuclear exporting signal revealed the importance of nuclear localization of AtADF4 in the A. thaliana–G. orontii interaction, suggesting an unconventional role of AtADF4 (Inada et al. 2016, further discussed below).

As summarized above, ADF is involved in many aspects of plant physiology. Particularly, as plant ADFs can function in resistance to various abiotic and biotic stresses, the achievements obtained from plant ADF research could be translated into applications, such as a production of stress-tolerant plants.

For future plant ADF research, I would like to propose two major issues that need to be resolved.

In summary, further studies on plant ADFs will not only contribute to understanding of plant physiology, but also greatly contribute to basic cell biology.