WHI-2 Regulates Intercellular Communication via a MAP Kinase Signaling Complex

ORIGINAL RESEARCH published: 22 January 2020 doi: 10.3389/fmicb.2019.03162 Frontiers in Microbiology | www.frontiersin.org 1January 2020 | Volume 10 | Article 3162 Edited by: Monika Schmoll, Austrian Institute of Technology (AIT), Austria Reviewed by: Jesus Aguirre, National Autonomous University of Mexico, Mexico Jinkui Yang, Yunnan University, China *Correspondence: N. Louise Glass [email protected] †Present address: A. Pedro Gonçalves, Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan Specialty section: This article was submitted to Fungi and Their Interactions, a section of the journal Frontiers in Microbiology Received: 15 November 2019 Accepted: 31 December 2019 Published: 22 January 2020 Citation: Gonçalves AP, Chow KM, Cea-Sánchez S and Glass NL (2020) WHI-2 Regulates Intercellular Communication via a MAP Kinase Signaling Complex. Front. Microbiol. 10:3162. doi: 10.3389/fmicb.2019.03162 WHI-2 Regulates Intercellular Communication via a MAP Kinase Signaling Complex A. Pedro Gonçalves1†, Karen M. Chow1, Sara Cea-Sánchez2and N. Louise Glass1,3* 1Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA, United States, 2Departamento de Genética, Universidad de Sevilla, Sevilla, Spain, 3Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, United States The formation of the fungal mycelial network is facilitated by somatic cell fusion of germinating asexual spores (or germlings). Neurospora crassa germlings in close proximity display chemotropic growth that is dependent upon an intracellular network of mitogen-activated protein kinase (MAPK) signaling cascades. Approximately 80 genes involved in intercellular communication and fusion have been identified, including three mutants with similar morphological phenotypes: 1whi-2, 1csp-6, and 1amph-1. Here we show that WHI-2 localizes to the cell periphery and regulates endocytosis, mitochondrial organization, sporulation, and cell fusion. WHI-2 was required to transduce signals through a conserved MAPK pathway (NRC-1/MEK-2/MAK-2) and target transcription factors (PP-1/ADV-1). The amph-1 locus encodes a Bin/Amphiphysin/Rvs domain-containing protein and mis-expression of whi-2 compensated for the cell fusion and endocytosis deficiencies of a 1amph-1 mutant. The csp-6 locus encodes a haloacid dehalogenase phosphatase whose activity was essential for cell fusion. Although fusion-deficient with themselves, cells that lacked whi-2,csp-6, or amph-1 showed a low frequency of chemotropic interactions with wild type cells. We hypothesize that WHI-2 could be important for signal perception during chemotropic interactions via a role in endocytosis. Keywords: cell fusion, WHI-2, CSP-6, AMPH-1, endocytosis, MAPK INTRODUCTION Fungi can sense their surroundings, receive environmental cues, interpret them, and respond accordingly. During asexual growth, germinated asexual spores (germlings) and hyphae of the ascomycete fungus Neurospora crassa display social behaviors that trigger the process of cell-cell communication and somatic cell fusion. Cell fusion creates a mycelial network that allows the circulation of nutrients, water and cellular elements including genetic material throughout an interconnected colony (Leeder et al., 2011; Fischer and Glass, 2019). Somatic cell fusion in N. crassa operates in an analogous way to somatic cell fusion events in mammalian systems, including during muscle, placenta, and bone tissue development (Hernández and Podbilewicz, 2017). In N. crassa, somatic cell fusion of germlings is initiated when two cells (which can be genetically identical) undergo chemotropic interactions via the exchange of yet-to-be discovered signals by forming polarized cellular protrusions called conidial anastomosis tubes (CATs) (Gabriela Roca et al., 2005). After CATs from germlings come into contact, a switch from cell growth to cell Gonçalves et al. WHI-2 Function in Cell Fusion wall dissolution is initiated (Gonçalves et al., 2019), followed by plasma membrane merger and cytoplasmic continuity; nuclear fusion is not a consequence of somatic cell fusion (Leeder et al., 2011). The combination of polar growth, hyphal branching, and cell fusion events is vital for the formation of the interconnected multicellular hyphal network that is the hallmark growth habit of filamentous fungi (Glass et al., 2004). The availability of a well-annotated genome (Galagan et al., 2003; Borkovich et al., 2004) and a near full genome deletion strain collection (Colot et al., 2006) have enabled screening of deletion mutants for cell fusion phenotypes in N. crassa (Fu et al., 2011). Deletion strains affected in cell communication and fusion often show a reduction in aerial hyphae extension and flat-like growth and approximately 80 genes have been found to play a role in these processes in N. crassa. The functions of these genes have been partially characterized and range from intracellular signaling, calcium modulation, membrane merger, production of reactive oxygen species, actin regulation, vesicle trafficking and transcriptional control (Glass et al., 2004; Leeder et al., 2011; Fischer and Glass, 2019). Two conserved mitogenactivated protein kinase (MAPK) modules form the core of the intracellular signal transduction network that is activated during cell fusion: the SOFT (SO)/MIK-1/MEK-1/MAK-1 cascade—that is part of the cell wall integrity pathway—and the STE-50/STE- 20/HAM-5/NRC-1/MEK-2/MAK-2 module (Fischer and Glass, 2019). During chemotropic growth that precedes cell fusion, components of both of these pathways are recruited to the tip of germling CATs and to the tips of fusion hyphae (Fleissner et al., 2009b; Dettmann et al., 2012, 2014; Jonkers et al., 2014). The tip recruitment and displacement of the MAK-2 signaling module to a single fusion tip occurs every ∼8–10 min and alternates at CAT and fusion tips of chemotropic partners in a perfectly out of phase manner with localization of SO, resembling a pingpong mechanism of signal sending and receiving (Fleissner et al., 2009b; Leeder et al., 2011; Serrano et al., 2018). These two pathways are required for the activation of the transcription factors PP-1 and ADV-1 that function as master regulators of cell fusion genes (Fischer et al., 2018). Despite recent advances, the function of many cell fusion genes remains unclear. In particular, whi-2, the N. crassa ortholog of the Saccharomyces cerevisiae gene WHISKEY2 (WHI2), has been shown to be required for cell fusion (Fu et al., 2014). The S. cerevisiae Whi2 was initially identified as a central player in the coordination between cell proliferation and nutrient availability. Loss-of-function mutations in WHI2 result in cells that cannot properly sense the extracellular nutritional status and fail to shift from exponential to stationary growth (Saul and Sudbery, 1985), leading to cells that are smaller than normal due to cell division without sustained cell growth. Yeast whi2 mutants also show actin cytoskeleton disorganization, increased cell death, aberrant mitochondrial morphology and defects in executing endocytosis (Binley et al., 1999; Care et al., 2004; Leadsham et al., 2009). Additionally, whi2 mutants show an increase in the activity of the Ras/cAMP/PKA pathway, permitting the downstream general stress response transcription factor Msn2/4 to remain phosphorylated and outside of the nucleus, where it is unable to activate the expression of cell cycle arrest genes (Radcliffe et al., 1997a; Leadsham et al., 2009; Sadeh et al., 2011). Overexpression of WHI2 results in filamentous growth that is dependent on Ste11 and partially dependent on Ste7, Ste20 and Ste12 (Radcliffe et al., 1997b). These proteins are orthologs of N. crassa NRC-1 (Ste11), MEK-2 (Ste7), STE-20 (Ste20), and PP-1 (Ste12), components of a MAPK signaling complex and its target transcription factor that are required for somatic cell fusion in a number of filamentous fungi (Fischer and Glass, 2019). The S. cerevisiae WHI2 gene also seems to be a hot spot for adaptive mutations, indicating a central role for the respective protein in fungal development and environmental responses (Cheng et al., 2008; Gresham et al., 2008; Kvitek and Sherlock, 2013; Lang et al., 2013; Teng et al., 2013; Szamecz et al., 2014; Treusch et al., 2015; Payen et al., 2016; Comyn et al., 2017). In this study, we examined the role of the N. crassa WHI-2 during fungal development. Our findings indicate that WHI-2 localized to the cell periphery, affected endocytosis and mitochondrial morphology, and functioned upstream of the NRC-1/MEK-2/MAK-2/PP-1/ADV-1 signaling pathway to activate cell-cell communication. Additionally, we discuss two other cell fusion proteins, CSP-6 and AMPH-1, whose functions are related to WHI-2. CSP-6 showed a localization pattern similar to WHI-2 and its deletion phenocopied the morphological and cell fusion defects of a 1whi-2 strain. AMPH-1 is an endocytosis regulator whose absence was compensated for by the mis-expression of WHI-2. This work provides new details on genes/proteins that function upstream of a key MAPK signaling module. MATERIALS AND METHODS Strains and Culture Media Standard procedures for the handling of N. crassa cells were employed. Cells were grown in Vogel’s minimal medium (VMM) plus 2% (w/v) sucrose and 1.5% (w/v) agar (Vogel, 1956). Crosses were performed on synthetic cross medium (Westergaard and Mitchell, 1947). Wild type and deletion strains are available from the Fungal Genetics Stock Center (FGSC) (McCluskey et al., 2010) and were constructed as part of the Neurospora Genome Project (Colot et al., 2006). Strains used in this study are listed in Table S1. For all the experiments, the indicated strains were grown for ∼7 days in VMM-containing slant tubes and a conidial suspension was obtained by adding sterile ddH2O into tubes, vortexing and passing the mixture through cheesecloth to remove hyphal fragments. Hygromycin B (Thermo Fisher Scientific, Waltham, MA, USA) was used at a final concentration of 200 µg/ml. Strain Construction The whi-2,csp-6, and amph-1 genes were amplified from genomic DNA of the FGSC2489 wild type strain using primers ACCTCTAGAATGGCTGCCGCGGGAGGAG and CAG TTAATTAAACGCAGTCCAATCACACTCATCTCC for whi-2 (creating XbaI/PacI restriction sites), primers TTTTACTAGT ATGAGCAACTCGAACCCG and TTTTTTAATTAAAAGA GTGACGTCCAGAACCAG for csp-6 (creating SpeI/PacI restriction sites) and primers TTTTTTAATTAAAAGAGTGA Frontiers in Microbiology | www.frontiersin.org 2January 2020 | Volume 10 | Article 3162 Gonçalves et al. WHI-2 Function in Cell Fusion CGTCCAGAACCAG and CGGTTAATTAAAACAGTTCC GCTGATACTC for amph-1 (creating XbaI/PacI restriction sites). The resulting PCR products were cloned into pCR-Blunt II-TOPO, excised using the respective combination of restriction enzymes and inserted into pMF272 (GenBank accession number: AY598428.1) (Freitag et al., 2004). In pMF272, whi-2,csp-6 and amph-1 were placed downstream of a ccg-1 promoter and upstream of sgfp and a ccg-1 terminator. For construction of the CSP-6D284A strain, site-directed mutagenesis using primers ccttgttctaGCTttggatgaaa and tttcatccaaAGCtagaacaagg were used. These primers were used in a Pfu-based PCR using the pMF272 vector carrying the wild type csp-6 (described above) as the DNA template that was followed by treatment with the DpnI restriction enzyme. The resulting vectors were transformed into 1whi-2;his-3,1csp-6;his-3 and 1amph-1;his-3 conidia, respectively, using a Gene Pulser electroporator (Bio-Rad, Hercules, CA, USA) at 1.5 kV, 25 µF, 600 Ω. Homokaryotic strains expressing the indicated gfp-tagged genes were obtained by backcrosses. Sanger sequencing to confirm that there were no irregularities in the constructs was performed at the UC Berkeley DNA Sequencing Facility. Microscopy Conidia were diluted to a concentration of 1.5 ×107cells/ml. For the evaluation of conidial morphology, 10 µl were pipetted onto a glass slide and covered with a coverslip. To examine communication frequency, 80 µl of conidial suspension was spread onto 5 cm VMM agar plates. In co-culture experiments two strains were mixed in a 1:1 proportion before plating. Staining with FM4-64 (N-(3-triethylammoniumpropyl)-4-(4- diethylaminophenylhexatrienyl) pyridinium dibromide; Thermo Fisher Scientific, Waltham, MA, USA) was carried out by incubating 2 µM FM4-64 in a 1.5 ×107cells/ml conidial suspension in a total volume of 500 µl for 15 min in the dark; the cells were then washed twice with ddH2O and resuspended in 500 µl to reestablish the initial spore concentration. The plates were briefly dried in a fume hood and incubated at 30◦C, in the dark for 3.5–4 h or 16–20 h to analyze cells at the germling or hyphal stage, respectively. Squares of ∼1 cm were excised and observed. For the analysis of the accumulation of endocytic intermediates, 15 µl of 4 µM FM4-64 was added to the agar slice immediately before imaging. Conidial morphology and cell communication were assessed using a Zeiss Axioskop 2 using a 40x Plan-Neofluor oil immersion objective lens. The percentage of cell communication was determined by counting the relative frequency of cell pairs that displayed a chemotropic behavior when germinated conidia were within ∼15 µm of each other. For the FM4-64 microscopy assay, as well as WHI-2, CSP-6, AMPH-1, ARG-4, MAK-2 and SO localization studies, a Leica SD6000 confocal microscope equipped with a Yokogawa CSU- X1 spinning disk head, 488 nm and 561 nm lasers and a 100 × 1.4 N.A. oil-immersion objective lens controlled by Metamorph (Molecular Devices, LLC, San Jose, CA, USA) was used. Images were analyzed using ImageJ (Schneider et al., 2012). Multiple cells were analyzed per experiment and representative examples are shown. Flow Cytometry In order to examine if plasma membrane material was being appropriately guided to the vacuoles by endocytosis, we adapted a previously published method (Zheng et al., 1998). Conidia at a concentration of 106/ml were inoculated into glass tubes containing 1.5 ml VMM without agar and grown at 30◦C, 200 rpm, for a total duration of 4 hrs; 2 µM FM4-64 and 10 µM 7-amino-4-chloromethylcoumarin (CMAC Blue; Thermo Fisher Scientific, Waltham, MA, USA) were added to the cultures for the last 45 and 15 min, respectively. The conidia were harvested by centrifugation (5,000 rpm, 5 min, 4◦C) and washed twice with cold 1x PBS before being resuspended in cold 1x PBS and at least 10,000 events acquired on a BD LSRFortessa X-20 flow cytometer (BD Biosciences, Franklin Lakes, NJ, USA). The fluorescence of FM4-64 was recorded using a 488 nm laser and 685LP (710/50 nm) filter; the fluorescence of CMAC Blue was recorded using a 355 nm laser and (515/30 nm) filter. FlowJo (FlowJo, LLC, Ashland, OR, USA) was used for analyses. Bioinformatics and Statistical Analysis The presence of conserved domains was assessed using InterProScan 5 (Jones et al., 2014). The WHI-2/Whi2p amino acid alignment was edited using BoxShade (https:// embnet.vital-it.ch/software/BOX_form.html). The percentage of identity and similarity was calculated using the Sequence Manipulation Suite (http://www.bioinformatics.org/sms2/ident_ sim.html). Statistical significance was tested by ANOVA followed by a Tukey post-hoc test using Prism (GraphPad Software, San Diego, CA, USA). At least three independent experiments were performed for all data shown in this paper. The schematic model of the function of WHI-2, CSP-6, and AMPH-1 was built using BioRender (app.biorender.com). RESULTS WHI-2 Is Epistatic to the NRC-1/MEK-2/MAK-2 Signaling Pathway The N. crassa WHI-2 (NCU10518) is a 297 amino acid protein that harbors two BTB (Broad-complex, Tramtrack, and Bric-à-brac)/POZ (POx virus and Zinc finger) conserved domains (Figure S1). These domains have been shown to be involved in protein-protein interactions during multiple cellular processes ranging from ion channel assembly and gating, actin dynamics, transcriptional regulation to chromatin remodeling (Perez-Torrado et al., 2006). A recent report suggested that whi-2 homologs might be distant relatives of members of the human disease-related potassium channel tetramerization domain (KCTD) protein family (Teng et al., 2018). N. crassa WHI-2 shows 24% identity and 33.5% similarity to S. cerevisiae Whi2p, but is substantially shorter (297 aa compared to 486 aa) (Figure S1). Previous deletion strain screenings in N. crassa identified multiple genes, including whi-2, as being required for germling fusion (Chinnici et al., 2014; Fu et al., 2014). In addition to the germling fusion defect (Figures 1A,B), the 1whi- 2deletion strain displayed additional morphological defects (Fu et al., 2014), such as an impairment in the formation of aerial hyphae (Figure S2), production of unseparated proconidial Frontiers in Microbiology | www.frontiersin.org 3January 2020 | Volume 10 | Article 3162 Gonçalves et al. WHI-2 Function in Cell Fusion FIGURE 1 | Cell fusion and conidiogenesis defects observed in a 1whi-2 mutant can be partially rescued by the introduction of a constitutively active allele of nrc-1.(A,B) Cell-cell communication was analyzed by observing brightfield microscopy (A) of closely positioned germlings 4 h post-inoculation. Red and blue arrows indicate conidial anastomosis tubes (CATs) and cell communication/fusion events, respectively. The relative frequency of cell-cell communication is shown in (B). Error bars represent the standard deviation. *p-value <0.0001 vs. wild type; #p-value <0.001 vs. 1whi-2. (C) Conidial morphology was assessed in WT and whi-2 strains using brightfield microscopy. Note the presence of proconidial chains in the 1whi-2 strain. (D) Hyphal fusion was evaluated 16 h post-inoculation. Blue arrows point to hyphal fusion events. (E,F) Radial growth (E) and sporulation (F) were analyzed in wild type and 1whi-2 colonies 24 h or 7 days after inoculation on Petri dishes, respectively. chains (Figure 1C) and lack of hyphal fusion (Figure 1D). The introduction of an epitope-tagged whi-2 allele (whi-2-gfp) in the 1whi-2 mutant complemented the germling and hyphal fusion (Figures 1A,B,D), conidial separation (Figure 1C) and aerial hyphae (Figure S2) developmental defects. The 1whi- 2mutant grew slower than the wild type strain (Figure 1E) and produced profuse spores across a Petri plate, as compared to the wild type strain that sporulated mainly around the perimeter of the plate (Figure 1F). The 1whi-2 strain also did not produce protoperithecia when grown on synthetic cross medium, as shown in a previous deletion collection screening (Fu et al., 2014). Fertility was restored in 1whi-2;whi-2-gfp cells and this strain was used as a female in crosses in subsequent experiments (Table S1). Existing data suggests that 1whi-2 cells can communicate with wild type partner cells at a low frequency (Fu et al., 2014), a phenotype that we confirmed in 1whi-2/wild type germling pairs (Figure 2A). When MAK-2-GFP or SO-GFP were expressed in the 1whi-2 mutant, recruitment of both proteins to the CATs of 1whi-2 cells undergoing chemotropic interactions with the wild type cells was observed (Figure 2B). Thus, the absence of WHI-2 did not directly affect the ability to form CATs nor the recruitment of MAK-2 and SO to communicating cell tips in wild type +1whi-2 pairings. Phosphorylation of the MAP kinases MAK-1 and MAK- 2 is reduced in 1whi-2 germlings (Fu et al., 2014). To further explore the relationship between the MAK-2 pathway and WHI-2, we utilized a gain-of-function mutation nrc- 1allele (proline to serine mutation at position 451 of NRC-1). Strains containing this allele show a ∼12-fold increase in MAK-2 phosphorylation (Dettmann et al., 2012). When the nrc-1P451Sallele was introduced into the 1whi-2 mutant, the formation of proconidial chains was suppressed and cell fusion-associated chemotropism was restored to levels similar to an nrc-1P451Sstrain (Figures 1A–C). At the macroscopic level, aerial hyphae development was also partially restored in the 1whi-2 mutant expressing nrc-1P451S (Figure S2). These data place WHI-2 upstream of the STE- 50/STE-20/HAM-5/NRC-1/MEK-2/MAK-2/PP-1/ADV-1 signal transduction pathway. Deletion of whi-2 Results in Cells That Accumulate Endocytic Intermediates and Possess a Defective Mitochondrial Network In S. cerevisiae, the deletion of WHI2 causes a defect in endocytosis (Care et al., 2004). Here we employed the lipophilic styryl dye FM4-64 to track the accumulation of endocytic intermediates in N. crassa germlings. FM4-64 is unable to freely cross membranes; instead it is anchored on the outer leaflet of the plasma membrane bilayer. When endocytic membranous structures are formed, the dye becomes incorporated intracellularly into the endosomes and Golgi, and subsequently into the vacuoles (Fischer-Parton et al., 2000); it has been shown that endocytosis mutants show delayed or fragmented staining of intracellular vesicles (Gachet and Hyams, 2005; Martin et al., 2005). N. crassa wild type germlings readily Frontiers in Microbiology | www.frontiersin.org 4January 2020 | Volume 10 | Article 3162 Gonçalves et al. WHI-2 Function in Cell Fusion FIGURE 2 | Cells lacking whi-2 are capable of establishing chemotropic interactions with the wild type cells and show recruitment of MAK-2 and SO to CATs. (A) Cytoplasmic GFP-expressing wild type cells were mixed with FM4-64-stained 1whi-2 cells and observed by microscopy after germination. (B) MAK-2-GFP-expressing (upper panel) or SO-GFP-expressing (lower panel) 1whi-2 cells were mixed, respectively, with SO-dsRed-expressing or MAK-2-mCherry-expressing wild type cells and observed by microscopy after germination. Note the formation of CATs (red arrows). showed plasma membrane and intracellular staining and round membranous structures were observed in the cytoplasm as early as at ∼9.5 min after the addition of FM4-64 (Video 1 and Figure 3A). After 30 min of incubation with FM4-64, wild type cells displayed large FM4-64-positive membranous structures (Figure 3B). In contrast, the intracellular accumulation of FM4- 64 in 1whi-2 cells was delayed and appeared as small elements, typical of fungal mutants with endocytosis defects (Gachet and Hyams, 2005; Martin et al., 2005) (Video 1 and Figures 3A,B). S. cerevisiae whi2 mutants show highly fragmented mitochondria or agglomeration of mitochondria in balllike structures, depending on the growth phase (Leadsham et al., 2009; Mendl et al., 2011). We used a strain harboring a gfp-tagged arg-4 (encoding the mitochondrial acetylornithineglutamate acetyltransferase) (Bowman et al., 2009) to image the mitochondrial network in N. crassa germlings. In wild type germlings, mitochondria were abundant and formed a tubularshaped network (Figure 3C). During cell communication and germling fusion, the shape of the mitochondrial network remained unchanged, although organelles were excluded from the tip of CATs until fusion and cytoplasmic continuity were attained (Figure 3D and Video 2). In contrast to the mitochondrial organization in wild type cells, 1whi-2 germlings displayed aberrant mitochondria that appeared to be fragmented and clustered into “masses” (Figure 3C). These observations indicated that WHI-2 was required for normal endocytosis and mitochondrial morphology in N. crassa. CSP-6 and AMPH-1 Are Two Fusion Proteins Whose Function Is Related to WHI-2 In a previous deletion strain screening, csp-6 and amph-1 were also found to be required for cell fusion in N. crassa (Fu et al., 2011, 2014; Chinnici et al., 2014). In addition, 1csp-6 and 1amph-1 cells also have a defect in conidial separation (Figure 4A and Figure S2), phenotypically similar to proconidial chains in 1whi-2 mutants (Figure 1C) (Fu et al., 2014; Ghosh et al., 2014). CSP-6 (NCU08380) is a Haloacid Dehalogenase (HAD) family Ser/Thr phosphatase and the ortholog of Psr1/2 from S. cerevisiae. In yeast and in N. crassa, WHI-2 and CSP-6 have been shown to directly interact (Kaida et al., 2002; Zhou et al., 2018). AMPH-1 (NCU01069) harbors an Arfaptin Homology/Bin-Amphiphysin-Rvs (AH/BAR) domain; AMPH-1 homologs in S. cerevisiae (Rvs161p and Rvs167p) regulate the actin cytoskeleton, endocytosis and mating, while in neurons AMPH-1 plays a role in clathrin-mediated endocytosis (Takei et al., 1999; Friesen et al., 2006). Although phenotypically similar, the growth of the 1amph-1 mutant was more affected than growth of the 1whi-2 or 1csp-6 mutants (Figure S2). We confirmed that cell communication in populations of 1csp-6 germlings was absent, while a low frequency of CAT formation was observed in self-pairings of 1amph-1 germlings (Figures 4B,C). The introduction of a gfp-tagged csp-6 or amph-1 allele partially compensated for the developmental defects observed in 1csp-6 and 1amph-1 mutants, respectively (Figures 4A–C and Figure S2). Since the complementation of amph-1 with the gfp-tagged amph-1 allele was modest (Figure 4C), we conducted a co-segregation analysis by crossing the wild type and 1amph-1 deletion strains and analyzing the resistance of the progeny to hygromycin B; all strains that displayed wild type-like growth were sensitive to hygromycin B whereas all strains with flat-like growth were resistant to it (Figure S3). The 1csp-6 and 1amph-1 mutants communicated with wild type germlings, although at low frequency (Figure 4D); this observation had been previously suggested for 1amph-1 (Fu et al., 2014). Frontiers in Microbiology | www.frontiersin.org 5January 2020 | Volume 10 | Article 3162 Gonçalves et al. WHI-2 Function in Cell Fusion FIGURE 3 | Strains lacking whi-2 are defective in the accumulation of FM4-64-positive membranous structures and show defects in mitochondrial dynamics. (A,B) The uptake of FM4-64 via plasma membrane-derived structures was followed over time in wild type and 1whi-2 germlings. A time course experiment is shown in (A). Note the formation of large FM4-64-positive membranous structures in the wild type strain (arrows). Representative images after 30 min of incubation are shown in (B). These panels are complemented by Video 1.(C) The organization of the mitochondrial network was examined using an ARG-4-GFP construct (Bowman et al., 2009). Note the appearance of fragmented (“frag”) and clusters (“cluster”) of mitochondria in 1whi-2 cells. (D) Mitochondrial dynamics during cell fusion were evaluated by producing time-lapse videos of interacting wild type germlings. Note the absence of mitochondria at the fusion spot during the first minutes after contact (arrow). This panel is complemented by Video 2. To explore how the predicted phosphatase activity of CSP-6 plays a role during cell fusion and asexual development in N. crassa, we constructed a mutated allele of CSP-6 predicted to abolish activity. In S. cerevisiae, a point mutation in the predicted catalytic aspartic acid residue of the hhhDxDx(T/V) motif— where “h” is a hydrophobic residue and “x” is any residue— abolished phosphatase activity (Rebay, 2015). This aspartic acid residue belongs to the HAD domain and is conserved in N. crassa. A 1csp-6 mutant that carried a phosphatasedead, Pccg-1-driven csp-6D284A allele showed the same defects as the 1csp-6 deletion strain, namely the lack of aerial hyphae (Figure S2) and inability to form CATs and undergo cell fusion (Figures 4B,C). To assess the relationship between whi-2,amph-1, and csp-6, we placed an extra copy of whi-2 under the control of a constitutive promoter (Pccg-1) in the 1amph-1 and 1csp-6 strains. The 1amph-1;Pccg-1-whi-2 strain showed suppression of the conidial separation defect of the 1amph- 1mutant (Figure 4A), restoration of CAT formation and chemotropic interactions (Figures 4B,C), and normal aerial hyphae development (Figure 4E). In contrast, over-expression of whi-2 did not complement the morphological (Figure S2) or communication defects of the 1csp-6 mutant (Figures 4A–C). These data showed that the deletion of whi-2,csp-6, and amph- 1leads to similar cellular phenotypes and that the mis-expression of whi-2 compensated for the absence of amph-1, indicating that AMPH-1 functions upstream of WHI-2. In order to examine if the deletion of amph-1 results in an endocytic defect, as predicted from S. cerevisiae literature (Munn et al., 1995; Kaksonen et al., 2005), and whether the mis-expression of whi-2 also compensated for an endocytosis defect, we employed a flow cytometry-based methodology. The combined labeling of endocytic intermediates and vacuolar lumens (with FM4-64 and carboxydichlorofluorescein diacetate (CDCFDA), respectively) has been previously used to isolate S. cerevisiae mutants unable to properly execute endocytosis and transport plasma membrane material to the vacuole (Zheng et al., 1998). Such mutants display a shift in FM4-64/CDCFDA fluorescence as compared to wild type cells. We adopted a similar strategy, but utilized CMAC Blue to stain the lumen of the vacuoles instead of CDCFDA. The deletion of whi-2 or amph- 1resulted in a shift in FM4-64/CMAC Blue fluorescence profile as compared to wild type cells (Figure 5). However, the 1whi-2 and 1amph-1 strains carrying Pccg-1-whi-2-gfp showed a profile more similar to wild type cells (Figure 5). These data suggest that endocytosis defect was at least partially compensated for by the mis-expression of whi-2-gfp in 1amph-1 cells. Additionally, the FM4-64/CMAC Blue fluorescence shift in 1whi-2 cells was also partially recovered by the mis-expression of nrc-1P451S (Figure 5), consistent with suppression of cell fusion defects in 1whi-2 cells (Figure 1). Frontiers in Microbiology | www.frontiersin.org 6January 2020 | Volume 10 | Article 3162 Gonçalves et al. WHI-2 Function in Cell Fusion FIGURE 4 | The mis-expression of whi-2 in cells lacking amph-1 but not csp-6 compensates for germling communication and asexual defects. (A) Conidial morphology of indicated strains was analyzed by brightfield microscopy. (B) Cell-cell communication between cells from single strains (genetically identical) were evaluated between closely positioned germlings (B, 4 h post-inoculation). In (B), red and blue arrows indicate conidial anastomosis tubes (CATs) and communication/fusion events, respectively. Note the presence of CATs in the 1amph-1 strain (lower micrograph, red arrows). The relative frequency of cell-cell communication of strains shown in (B) is shown in (C). Error bars represent the standard deviation.*p-value <0.0001 vs. wild type; #p-value <0.0001 vs. 1csp-6; and, p-value <0.0001 vs. 1amph-1. (D) Cytoplasmic GFP-expressing wild type cells were mixed with FM4-64-stained 1csp-6 or 1amph-1 cells and observed by microscopy after germination. Note the formation of CATs (red arrows). (E) The production of aerial hyphae and sporulation was evaluated after 7 days of growth for the indicated strains. WHI-2 and CSP-6 Localize Mainly to the Cell Periphery While AMPH-1 Is Present in Cortical Patches and Puncta Previous reports showed that WHI-2 localized by immunofluorescence to the cytoplasm, small vesicles or vacuoles and by subcellular fractionation to the cytoplasmic and nuclear fractions; AMPH-1 immunolocalization studies showed a punctate pattern suggestive of small vesicles and by subcellular fractionation CSP-6 was present in the cytoplasmic and nuclear fractions (Fu et al., 2014; Zhou et al., 2018). However, the AMPH- 1-RFP construct only marginally complemented the fusion defect of 1amph-1 (Fu et al., 2014), the immunofluorescence for WHI-2 was not very resolved (Fu et al., 2014) and the subcellular fractionation for WHI-2 and CSP-6 showed that both proteins were in all fractions tested (Zhou et al., 2018). Therefore, we sought to determine the localization of these proteins using confocal microscopy by tagging them with GFP, under the control of the constitutive Pccg-1 promoter, and introducing them into their respective deletion strains (Figures 1,4). In dormant conidia, WHI-2-GFP was distributed across the cytoplasm while CSP-6-GFP was predominantly present in the cell periphery (Figure 6A). AMPH-1 was mainly localized in cortical patches although some cytoplasmic staining was observed (Figure 6A). In germlings, WHI-2 and CSP-6 were present mainly in the cell periphery and occasionally in intracellular puncta (Figure 6A); AMPH-1 was present in cytoplasmic puncta. In mature hyphae, the localization of WHI-2 and CSP-6 was mainly at the cell periphery and at septa (Figure 6A). For WHI-2, we also observed cytoplasmic localization and in the membrane of round intracellular vesicles (Figure 6A). In hyphae, AMPH-1 was present in puncta or small Frontiers in Microbiology | www.frontiersin.org 7January 2020 | Volume 10 | Article 3162 Gonçalves et al. WHI-2 Function in Cell Fusion FIGURE 5 | The mis-expression of nrc-1P451Sand whi-2-gfp compensates for the endocytosis defect of 1whi-2 and 1amph-1 cells, respectively. The wild type (red) and other indicated strains (blue) were stained with FM4-64 and CMAC Blue to label endocytic intermediates and vacuolar lumens, respectively. Note that while the wild type shows an overlap of FM4-64 and CMAC Blue, indicating that plasma membrane-derived endocytic intermediates are guided to the vacuoles, cells lacking whi-2 and amph-1 displayed a shift in red/blue fluorescence. n=4. Shown is a representative set of experiments. intracellular vesicles that tended to accumulate at the hyphal tip (Figure 6C). A1amph-1;whi-2-gfp strain was able to communicate and fuse (Figures 4B,C), but a 1csp-6;whi-2-gfp strain displayed the same morphological defects as its parental deletion mutant (Figures 4B,C). We therefore assessed whether localization of WHI-2-GFP was affected in the 1amph-1 mutant relative to the 1csp-6 mutant and wild type cells. In the 1amph-1 mutant, WHI-2 displayed a cell periphery localization, consistent with what was observed in a 1whi-2;whi-2-gfp strain (Figure 6A). However, in the 1csp-6 mutant, WHI-2-GFP was no longer present in the cell periphery, but accumulated in cytoplasmic patches and puncta (Figure 6B). These data suggest that CSP- 6 is required for localization of WHI-2, consistent with reports of physical interaction of these two proteins in N. crassa and S. cerevisiae (Kaida et al., 2002; Zhou et al., 2018). DISCUSSION Germinated asexual spores of N. crassa cooperate during the formation of the somatic mycelial network by undergoing regulated cell fusion. Our study highlights the importance of WHI-2, an ortholog of the S. cerevisiae Whi2p, which binds to Psr1p (HAD family of protein phosphatases; CSP-6 ortholog) and regulates the response to nutritional stress by affecting both TORC1 and the Ras-cAMP-PKA pathway (Sudbery et al., 1980; Kaida et al., 2002; Müller and Reichert, 2011; Chen et al., 2018). The deletion of whi-2 in N. crassa resulted in a panoply of morphological phenotypes, including defects in conidial separation, an inability to undergo chemotropic interactions and cell fusion, aerial hyphae formation, growth rate and female fertility. Our data showed that the lack of whi- 2also caused an accumulation of FM4-64-positive membranous structures that likely correspond to endocytic intermediates and the destabilization of the mitochondrial organization. Using a constitutive nrc-1 allele, we showed that WHI-2 plays an active role during cell-cell communication in N. crassa by transducing signals to the NRC-1/MEK-2/MAK-2 pathway. In support of this conclusion, the deletion of whi-2,csp-6 or amph-1 abolishes activation of prm-1 (Fischer et al., 2019), which encodes a protein involved in plasma membrane merger during cell fusion (Fleissner et al., 2009a). The prm-1 gene is directly regulated by the transcription factors PP-1 and ADV-1, which sit downstream Frontiers in Microbiology | www.frontiersin.org 8January 2020 | Volume 10 | Article 3162 Gonçalves et al. WHI-2 Function in Cell Fusion FIGURE 6 | Localization of WHI-2, CSP-6 and AMPH-1 at different asexual stages. (A) The localization of WHI-2 (upper panel), CSP-6 (middle) and AMPH-1 (lower) was examined in the deletion strains carrying a GFP-tagged construct of the respective protein. Panels from left to right indicate conidia, germlings and mature hyphae. ves, intracellular vesicle membrane; sep, septum. (B) Localization of WHI-2 in 1amph-1 and 1csp-6 mutant background. (C) Schematic model of the role of WHI-2, CSP-6, and AMPH-1 in signal reception during cell-cell communication of N. crassa germlings. Sensing of a gradient of the chemotropic signal(s) may occur via endocytosis of the chemotropic signal or via internalization of a receptor. WHI-2 and CSP-6 interact and sit at the cell periphery. AMPH-1 could be involved in vesicle scission during endocytosis and is epistatic to WHI-2. WHI-2 may also play a role in one or more steps of endocytosis, potentially via AMPH-1. WHI-2 functions upstream of the NRC-1/MEK-2/MAK-2 signaling pathway. Previous western blot data (Fu et al., 2014) indicated that WHI-2 could also affect signaling through another MAPK pathway composed of a MIK-1/MEK-1/MAK-1 module. These two MAPK cascades are involved in the activation of the transcription factors PP-1 and ADV-1, which directly regulate the expression of genes involved in cell communication and fusion. WHI-2 also controls the organization of the intracellular mitochondrial network. For simplicity, a number of signaling components and phosphorylation events have been left out (Please see Fischer and Glass, 2019, for an extended review). of the NRC-1/MEK-2/MAK-2 pathway (Fischer et al., 2018). These data suggest that WHI-2 functions upstream in the sequence of signal transduction events that lead to chemotropism and cell fusion (Figure 6C). In yeast, Whi2p is a nutrient sensor (Müller and Reichert, 2011; Chen et al., 2018), and in mammalian models a specific form of endocytosis is regulated by nutrient availability (Pang et al., 2014). In N. crassa, the 1whi-2 mutant was phenotypically similar when grown under various carbon and nitrogen sources, indicating further biochemical and genetic analyses are required to assess whether WHI-2 affects nutrient sensing. It will be also interesting to examine the range of phenotypes controlled by the WHI-2/MAPK axis by taking the advantage of the 1whi-2;nrc-1P451Sstrain. Although endocytosis is required for proper morphogenesis and apical growth in filamentous fungi (Riquelme et al., 2018), it has been suggested that these organisms might not undergo clathrin-dependent endocytosis (Schultzhaus et al., 2017). An alternative form of endocytosis termed fluid-phase endocytosis or pinocytosis, cells internalize small molecules present in the extracellular fluid through invaginations of the plasma membrane, forming intracellular vesicles (Epp et al., 2013) and a role for Whi2p during pinocytosis has been suggested as a way to sense cell density in yeast (Care et al., 2004). Additionally, this form of endocytosis has been proposed to mediate cell-cell communication between animal alveolar macrophages (Schneider et al., 2017). Pinocytosis could function as a mechanism to survey the extracellular space for gradients of certain peptides or metabolites and whenever the concentration is above a defined threshold, as when cells that produce a communication signal are in close proximity, the activation of the cell-cell fusion machinery would ensue. Evidence from various organisms support the hypothesis that endocytosis could play a role in cell-cell communication in N. crassa (Figure 6C). In animals, fusogens are internalized via RAB-5 and DYNAMIN-1 GTPases-dependent clathrin-mediated endocytosis (Shin et al., 2014; Smurova and Podbilewicz, 2016). In the filamentous fungus Ustilago maydis, the pheromone receptor Pra1 cycles between the early endosomes and the plasma membrane in endocytic vesicles, triggering cell communication-associated MAPK signaling pathways when the mating pheromone is perceived. Mutations that impair endocytosis cause Pra1 to be depleted from the plasma Frontiers in Microbiology | www.frontiersin.org 9January 2020 | Volume 10 | Article 3162