In the filamentous fungus Aspergillus nidulans, both microtubules and actin filaments are important for polarized growth at the hyphal tip. Less clear is how different microtubule-based and actin-based motors work together to support this growth. Here we examined the role of myosin-V (MYOV) in hyphal growth. MYOV-depleted cells form elongated hyphae, but the rate of hyphal elongation is significantly reduced. In addition, although wild type cells without microtubules still undergo polarized growth, microtubule disassembly abolishes polarized growth in MYOV-depleted cells. Thus, MYOV is essential for polarized growth in the absence of microtubules. Moreover, while a triple kinesin null mutant lacking kinesin-1 (KINA) and two kinesin-3s (UNCA and UNCB) undergoes hyphal elongation and forms a colony, depleting MYOV in this triple mutant results in lethality due to a severe defect in polarized growth. These results argue that MYOV, through its ability to transport secretory cargo, can support a significant amount of polarized hyphal tip growth in the absence of any microtubule-based transport. Finally, our genetic analyses also indicate that KINA (kinesin-1) rather than UNCA (kinesin-3) is the major kinesin motor that supports polarized growth in the absence of MYOV.
Citation: Zhang J, Tan K, Wu X, Chen G, Sun J, Reck-Peterson SL, et al. (2011) Aspergillus Myosin-V Supports Polarized Growth in the Absence of Microtubule-Based Transport. PLoS ONE 6(12): e28575. doi:10.1371/journal.pone.0028575
Editor: Gustavo Henrique Goldman, Universidade de Sao Paulo, Brazil
Received: June 24, 2011; Accepted: November 10, 2011; Published: December 14, 2011
This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Funding: This work was supported by National Institutes of the Health grants (5RO1GM069527 and 1RO1GM097580-01 to X. X. and 1 DP2 OD004268-01 to S. R.-P.) and a Uniformed Services University of the Health Sciences intramural grant (R071JD to X. X.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Type V myosins have been implicated in organelle transport in numerous organisms . In the budding yeast Saccharomyces cerevisiae, where cellular transport of vesicles depends solely on the actin cytoskeleton, class V myosins transport most if not all of the cell's organelles, including late Golgi elements, post-Golgi secretory vesicles, peroxisomes, mitochondria, and the endoplasmic reticulum –. In higher eukaryotic cells, where both microtubules and the actin cytoskeleton participate in the intracellular transport of organelles and vesicles, microtubules are used for long-distance transport, while actin filaments are used for short-range transport in the cell periphery –. For example, melanosomes in mouse melanocytes are first transported along microtubules out the cells dendrites, where they are then captured by myosin-V at dendritic tips . Similarly, in mouse cerebellar Purkinje neurons, the endoplasmic reticulum (ER) is first distributed throughout dendrites by microtubule motors, and then transported into dendritic spines by myosin-Va . That said, the extent to which myosin-V acts as a cargo transporter as opposed to a dynamic tether to simply grab cargo following its transport to the microtubule plus end by kinesins, remains a point of intense debate , . While the recent characterization of myosin Va-dependent ER transport in Purkinje neurons provided strong support for the idea that myosin-V functions as a point-to-point cargo transporter , , the extent to which this is true in other cellular contexts remains to be seen.
Filamentous fungi, in contrast to budding yeast, use both microtubules and actin filaments for the transport of cargo that supports polarized growth at the hyphal tip –. Thus, filamentous fungi are well suited for studying how microtubule- and actin-based transport systems are coordinated. Here we used the filamentous fungus Aspergillus nidulans, a major fungal model organism , to study the function of myosin-V and to ask whether coordination between actin and microtubule tracks is a necessary component of myosin-V-based transport. Our current results indicate that myosin-V in A. nidulans is able to support polarized growth on its own, i.e. in the absence of microtubule-based transport, which supports the idea that myosin-V is able to function as a cargo transporter. In addition, we show that in the absence of myosin-V, the kinesin-1 KINA is more important than the kinesin-3 UNCA in supporting hyphal tip growth.
Construction of the conditional null mutant of MYOV
The genome of A. nidulans contains only one myosin-V heavy chain homolog, which is encoded by the gene An8862 (called “myoV” here) . This myoV gene was identified via blast search against the A. nidulans database using the amino acid sequence of the mouse myosin-Va heavy chain (the product of the dilute locus) as a query. As expected, A. nidulans MYOV shows significant sequence similarity throughout its N-terminal motor domain with myosin-Vs from other species (data not shown). More importantly, its C-terminal cargo-binding domain is clearly homologous to that of Myo2p in budding yeast , myo5 in U. maydis  and myosin-Va in mouse  (Figure S1), confirming that MYOV is a true myosin-V ortholog.
We constructed alcA-GFP-myoV, a conditional null mutant of myoV, in which the myoV gene is replaced by a GFP-myoV fusion gene driven by the regulatable alcA promoter. Homologous integration of the GFP-tagged myoV sequence present in plasmid palcA-GFP-myoV into the genomic myoV locus generates two copies of myoV, a truncated myoV gene with its own promoter, and a full-length GFP-tagged myoV fusion gene under the control of the alcA promoter (Figure 1A). The homologous integration event was confirmed by a Southern blot analysis (Figure 1B). Moreover, the GFP-MYOV fusion protein is detectable by western blotting using anti-GFP antibody when the alcA-GFP-myoV cells are grown on glycerol, but not when glucose is used as a carbon source (Figure 1C). Shutting off myoV expression using glucose-containing YUU rich medium (called “MYOV depletion”) caused a noticeable reduction in colony size, with the diameter of alcA-GFP-myoV colonies being ~50% that of wild type (Figure 1D). On non-repressive glycerol medium, the alcA-GFP-myoV strain grew as well as the wild-type strain (Figure 1D). This observation argues that the GFP-MYOV fusion protein is functional and that the phenotype on glucose-containing YUU medium is due to the depletion of MYOV rather than any dominant negative effect caused by the expression of the N-terminal portion of MYOV from the native promoter. Therefore, we used glucose-containing medium to examine the effect of MYOV depletion, and glycerol-containing medium to observe myosin-V localization in A. nidulans.
(A) A diagram showing the homologous integration of the palcA-GFP-myoV plasmid into the genome (see Materials and Methods for details). (B) A Southern blot confirming the homologous integration event. (C) A Western blot showing that the GFP-MYOV fusion protein can be detected in extracts of cells grown on glycerol but not on glucose. A protein extract from a wild type strain grown on glycerol was use as a negative control for the anti-GFP antibody. PONCEAU S staining of the same blot is shown as a loading control. (D) Growth phenotypes of the alcA-GFP-myoV strain grown on glucose (YUU) and glycerol (MM+glycerol) plates at 37°C for 2 days. The strains were point inoculated on different plates. Note that on YUU, the growth of the mutant is significantly reduced, but on MM+glycerol, the mutant colony is almost identical to a wild type colony.
GFP-MYOV localizes near the hyphal apex and septum
Fluorescence microscopy revealed that GFP-MYOV was highly concentrated at the hyphal apex (Figure 2A). Given that exocytosis in A. nidulans most likely occurs at the hyphal apex , the concentration of MYOV in this region is consistent with it playing a key role in delivering secretory vesicles to support hyphal tip growth, as is the case for Myo2 in S. cerevisiae . GFP-MYOV was also observed on both sides of the septum (Figure 2B), reminiscent of the localization of the Woronin body that plugs the septal pore . The significance of this localization will be studied in the future. The accumulation of GFP-MYOV at the hyphal tip depends on the actin cytoskeleton, as short-term treatment with the actin-depolymerizing drug latrunculin A diminished the accumulation (Figure 2C). Interestingly, GFP-MYOV signals near septa were not affected by latrunculin A treatment (Figure 2C). While it is possible that the GFP-MYOV is not tethered at septa by the actin cytoskeleton, it is hard to rule out the possibility that some actin filaments at septa are resistant to latrunculin treatment.
(A) GFP-MYOV localizes to the hyphal tip. (B) GFP-MYOV localizes on two sides of the septum. (C) The effect of latrunculin A on GFP-MYOV localization. Cells were treated with 12 µM latrunculin A for 20 minutes. Arrowheads point to hyphal tips where the GFP-MYOV signals are diminished. Arrows point to GFP-MYOV signals near septa, which persist after treatments with latrunculin A. Bars, 5 µm.
MYOV depletion inhibits hyphal elongation but not septation
While MYOV depletion in A. nidulans did not completely inhibit polarized growth, it did reduce the rate of hyphal growth significantly. Specifically, the size of alcA-GFP-myoV colonies on glucose-containing medium was ~50% that of wild type cells (Figure 1D). During the course of this work, the Oakley lab made a deletion mutant of myoV. The colony size exhibited by their deletion mutant is almost identical to that of the alcA-based mutant described here (Dr. Berl Oakley, personal communication), confirming that A. nidulans myoV is indeed not essential. We performed a quantitative analysis on hyphal elongation rate and hyphal width for the alcA-myoV mutant. After incubation in glucose medium for 12 hours, the alcA-myoV mutant exhibited a dramatic difference in hyphal length relative to wild type cells (Figure 3A, B). Specifically, hyphae in the mutant were ~3 times shorter that those in wild type cells (Figure 3B). Interestingly, myoV mutant hyphae were also ~2 times wider than wild type hyphae (Figure 3A, C). Importantly, similar changes in morphology were also observed in the myosin-V deletion mutant (Dr. Berl Oakley, personal communication). Together, these results suggest that polarized growth at the hyphal tip is partially replaced by non-polarized cell expansion when MYOV is missing.
(A) Morphology of the alcA-myoV mutant 8 hours after germinating on repressive YUU medium at 37°C. A wild type cell is shown for comparison. Septa are indicated by arrow heads. (B, C and D) Quantitative analyses of hyphal length (B), hyphal width (C), and septum distribution (D) in wild type and the alcA-myoV mutant. Means and standard deviations are shown in the graphs. For hyphal length measurements, only those hyphae whose entire length could be seen through whole z-stacks (10–20 µm) were measured (n = 75 for the mutant; n = 70 for the wild type control). For hyphal width measurements, values were taken from hyphal regions where the hyphal width is uniform (n = 37 for both the mutant and the wild type control). For measurements of septum distribution, the lengths of the hyphal segments between adjacent septa were measured (n = 172 for the mutant; n = 147 for the wild type control). The differences between the mutant and the wild type controls are significant for hyphal length, hyphal width, and the length of hyphal segments (p<0.01 in all three cases). Bar, 5 µm.
Septation was not abolished in the myoV mutant. Instead, septa in the mutant were spaced more closely as compared to wild type cells (Figure 3A, D). Specifically, the average length of hyphal segments, as defined by the distance between adjacent septa, was 17.8 µm in wild type cells, versus 10.7 µm in the myoV mutant (Figure 3D). Thus, although MYOV may transport certain components to the septum, as demonstrated by studies in Schizosaccharomyces pombe , this role is not essential for septum formation in A. nidulans. This result is consistent with an earlier observation made in U. maydis , indicating that myosin-V is not essential for septum formation in filamentous hyphae.
MYOV supports significant polarized hyphal tip growth in the absence of microtubule-based transport
We tested whether MYOV is essential for polarized hyphal growth in the absence of microtubules. After overnight treatment with benomyl to disassemble microtubules, wild type cells were still able to form short germ tubes (Figure 4A) . Under the same conditions, MYOV depletion abolished polarized growth (Figure 4B). Thus, in the absence of microtubules, MYOV becomes essential for polarized growth. This result, together with similar results in U. maydis , strengthen the idea that efficient polarized growth in filamentous fungi requires a class V myosin and microtubule-based transport. That said, the data in Figure 4 does not rigorously exclude the possibility that MYOV only supports polarized growth in the absence of microtubules when cells are very short, since benomyl-treated cells fail to undergo long-distance hyphal tip extension , , .
Cells were grown overnight at 32°C in YUU medium and in the presence of 2.4 µg/ml benomyl. Shown are a wild type strain (A) and the alcA-myoV mutant (B). The control in Panel C shows that the alcA-myoV mutant undergoes polarized growth when grown on glycerol medium in the presence of benomyl. All panels shown are at the same magnification. Bar, 5 µm.
To address the functional relationship between MYOV and microtubule-based transport in long hyphae where microtubules are distributed normally, we examined the effect of MYOV depletion in cells lacking kinesin-based transport. In most eukaryotic organisms, kinesin-1, kinesin-2 and kinesin-3 proteins transport membranous cargoes along microtubules to support a variety of cellular functions, including polarized secretion –. While kinesin-1 and kinesin-3 are both present in fungal genomes, kinesin-2 is not , . In A. nidulans, one kinesin-1 gene, kinA , and two kinesin-3 genes, uncA and uncB , , have been identified. KINA is required for the microtubule-plus-end accumulation of cytoplasmic dynein and for hyphal growth , , . UNCA is important for transporting vesicles towards the microtubule plus end , a function very similar to that of kinesin-3 in U. maydis, which powers early endosome transport towards the microtubule plus end , . While the deletion mutant of uncB forms a normal colony, the deletion mutants of uncA and kinA produce small colonies , . However, while the colony size of the ΔuncA/ΔuncB double mutant is similar to that of the ΔuncA mutant, the colony size of the ΔuncA/ΔkinA double mutant is similar to that of the ΔkinA single mutant (which is slightly smaller than the ΔuncA mutant) . In this study, we constructed the triple kinesin null mutant ΔkinA/ΔuncA/ΔuncB. The growth of this triple kinesin null mutant is very similar to that of the ΔkinA single mutant, except that conidiation (asexual spore formation) in the triple mutant is slightly less robust than in the ΔkinA single mutant (Figure 5A, 6B).
(A) The quadruple mutant failed to grow on a YUU plate. (B) In YUU liquid culture, the quadruple mutant failed to undergo polarized hyphal growth after an eight-hour incubation at 37°C. An arrow head points to a spore that had not undergone germination, thus indicating that mutant cells had undergone isotropic growth. (C) After an overnight incubation at 32°C, cells were highly abnormal in shape, and leakage of cell contents could be seen (arrows). An image of DAPI staining is included to demonstrate the presence of multiple nuclei. All panels shown are at the same magnification. Bar, 5 µm.
(A) Polarized growth occurs in both the ΔuncA/alcA-myoV and ΔkinA/alcA-myoV mutants. All strains were grown in YUU liquid medium for 6.5 hours at 37°C. All panels shown are at the same magnification. Bar, 5 µm. (B) After a 2-day incubation on a YUU plate at 37°C, the ΔkinA/alcA-myoV double mutant grew dramatically more slowly than either single mutant, while the growth of ΔuncA/alcA-myoV double mutant was only mildly worse than that of the alcA-myoV mutant.
To determine whether polarized growth still occurs when these three kinesins and MYOV are missing, we crossed the triple kinesin null mutant (containing the ΔkinA, ΔuncA and ΔuncB alleles) to the alcA-myoV mutant to obtain a quadruple mutant possessing all four mutant alleles. Importantly, while the quadruple mutant was able to grow and form colonies on glycerol medium, which allows expression of myoV, it was not able to grow on the glucose-containing medium, which represses myoV expression (Figure 5A). In terms of the terminal phenotype of the quadruple mutant grown in glucose medium, we found that it exhibited a severe polarity defect (Figure 5B, C). Specifically, after 8 hours of growth at 37°C, by which time wild type cells had formed elongated hyphae, the quadruple mutant exhibited a round morphology (Figure 5B). These mutant cells had clearly undergone isotropic growth since they were much larger in diameter than spores (Figure 5B, arrow head). After overnight incubation at 32°C, mutant cells exhibited dramatic defects in cell morphology (Figure 5C). This phenotype was also accompanied by leakage of cell contents, suggesting a cell wall abnormality (arrows in Figure 5C). While such a cell lysis phenotype is also exhibited by the A. nidulans slaB mutant, which is defective in endocytosis , the polarity defect exhibited by our quadruple mutant is much more severe. Indeed, many quadruple mutant cells were dead, as evidenced by a complete failure to undergo hyphal growth more than 15 hours after the cells had been shifted to glycerol medium. The lethality is almost certainly caused by the failure in polarized growth rather than a defect in mitosis, since the abnormally-shaped mutant cells did contain multiple nuclei (see insert in Figure 5C). Together, these results argue that MYOV is required in the triple-kinesin null mutant background to support the delivery of vesicular cargo needed for growth at the hyphal tip.
KINA is crucial in supporting hyphal growth in MYOV-depleted cells
Unlike the quadruple mutant described above, introducing single mutant alleles of either KINA or UNCA into MYOV-depleted cells did not eliminate polarized growth (Figure 6A). However, colony growth of the ΔkinA/alcA-myoV double mutant on plates was dramatically slower than that of either single mutant (Figure 6B). In contrast, the growth of the ΔuncA/alcA-myoV double mutant was only mildly more attenuated than that of either single mutant (Figure 6B). Thus, loss of both UNCA and MYOV does not produce a much more dramatic growth defect than that caused by loss of MYOV or UNCA alone. These genetic results suggest that while MYOV and KINA function independently to a large extent in supporting hyphal growth, MYOV and UNCA may function in the same pathway to support hyphal growth, although it is not known whether UNCA and MYOV transport the same cargoes. That said, the functions of UNCA and MYOV are clearly not identical to each other, as MYOV is much more important than UNCA for supporting hyphal growth in the ΔkinA background. This conclusion is evident from the fact that the ΔkinA/alcA-myoV double mutant described in our current study is much sicker on plates than the ΔkinA/ΔuncA double mutant described previously, which looks very much like the ΔkinA single mutant .
In this study, we analyzed the function of myosin-V in the filamentous fungus A. nidulans, where both microtubules and the actin cytoskeleton contribute to the transport of organelles and vesicles required for polarized growth at the hyphal tip , , –. The results of our study indicate that MYOV is able to support significant hyphal elongation without microtubule-based transport. Importantly, our study also shows that plus-end-directed kinesin motors are able to support significant hyphal elongation without the aid of MYOV. Together, these observations, which mirror in part results obtained using U. maydis , , support the idea that myosin-V and plus-end-directed kinesin motors function in parallel to support fungal hyphal growth. The A. nidulans genome contains 11 kinesin-like genes . Our current results demonstrate that, in the absence of MYOV, the loss of just three kinesin genes kinA (kinesin-1), uncA (kinesin-3) and uncB (kinesin-3) is sufficient to abolish polarized hyphal tip growth. Thus, none of the other plus-end-directed kinesins are able to transport the materials required for polarized growth at the hyphal tip in the quadruple mutant. Interestingly, both the ΔkinA/alcA-myoV and ΔuncA/alcA-myoV double mutants are able to undergo polarized growth initially, suggesting that kinesin-1 and kinesin-3 proteins compensate for each other in the absence of myosin-V. That said, the ΔkinA/alcA-myoV double mutant is much sicker on plates than the ΔuncA/alcA-myoV double mutant although the colony size of ΔkinA is similar or only slightly smaller than that of ΔuncA. Thus, KINA is more critical than UNCA for supporting hyphal growth in the absence of MYOV.
There are five myosin genes in A. nidulans, one coding for myosin-I , , one for myosin-II, one for myosin-V, and two for the Csm proteins in which a chitin synthase domain is fused to a myosin motor domain (myosin-17) , . How these motors function together in hyphal tip growth and cytokinesis requires further study. While the exact cargoes of MYOV still need to be identified in A. nidulans, the results of this current study clearly demonstrate that MYOV is the main actin motor supporting hyphal tip growth. Moreover, our results show that this role becomes essential when microtubules and/or the plus-end-directed cargo-transporting kinesins are absent. Thus, while other myosin motors, such as the chitin-synthase-containing myosin, myosin-17, play a role in hyphal growth , , their functions must be either MYOV-dependent or microtubule-dependent since they fail to support hyphal growth in the absence of MYOV and microtubule motors. This idea is consistent with recent results demonstrating that myosin-17 in U. maydis is transported to the hyphal tip by myosin-V (myosin-5) and kinesin-1 along separate actin and microtubule tracks , .
In higher eukaryotic cells, myosin-V has been implicated in capturing cargoes at the periphery of the cell following their long-range, microtubule-dependent delivery –, , . Moreover, a direct physical interaction between myosin-V and kinesin  may serve to facilitate the switching of organelle movement from microtubules to actin tracks, as well as to enhance each motor's processivity . Our current study does not exclude the possibility of microtubule-to-actin track switching as a transport mode for some cargoes when both the microtubule-based and the actin-based transport systems are functioning normally. However, in the absence of the microtubule motors implicated in transporting cargoes, myosin-V is clearly able to support some hyphal growth on its own. Thus, myosin-V appears able to transport cargoes in vivo in the absence of kinesin-mediated delivery of these cargoes to the microtubule plus end. This idea is consistent with the recent findings in U. maydis, Dictyostelium, and Purkinje neurons, that myosin-V can function in vivo as a point-to-point organelle transporter rather than simply as a cargo tether acting near the microtubule plus end , , .
The identity of the vesicular cargo(es) transported by myosin-V in A. nidulans is unknown. While the hyphal-tip localization of myosin-V and its importance in hyphal elongation are consistent with its function in transporting secretory vesicles as in S. cerevisiae and Schizosaccharomyces pombe , , , , the localization is also consistent with potential roles for the myosin in organizing the spitzenkörper, a vesicle-supply center –, and/or in endocytosis at the hyphal tip region , –. In this study, we found that A. nidulans MYOV also localizes near septa. Indeed, the possibility that MYOV may play a role in secretion near septa cannot be excluded, since the hyphal tip may not be the only place where secretion occurs , . Interestingly, the localization of MYOV near septa is confined to two spots on each side of the septum, which is almost identical to the localization of Woronin bodies , . The Woronin body is a peroxisome-derived fungal organelle that plugs the septal pores to prevent the leakage of hyphal materials into a damaged hyphal segment –. Whether myosin-V is involved in Woronin body function will need to be determined in the future.
Materials and Methods
A. nidulans strains, growth conditions, and techniques
The strains used in this study are listed in Table 1. Aspergillus nidulans growth media, such as YAG, YUU, or MM+glycerol+supplements, growth conditions, DAPI staining of the nuclei, and A. nidulans molecular genetic methods were prepared or performed as described previously . To repress myosin-V expression from the alcA promoter, the glucose-containing rich medium YUU was used. For benomyl treatment of cells, a final concentration of 2.4 µg/ml was used. For latrunculin A treatment of cells, a final concentration of 12 µM was used. Southern and western blot analyses were done as described previously . The GFP antibody used in this study was from Covance.
Construction of the alcA-GFP-myoV strain
We made a conditional null mutant of myosin-V, alcA-GFP-myoV, wherein the only functional copy of the A. nidulans myoV gene is under the control of the alcA promoter, which can be turned off by glucose and derepressed in glycerol medium. The strain was constructed as follows. Two oligonucleotides: myo5′Not1 (TCATGTGCGGCCGCTGGCGCATAATTATGAGGTCGGGACGAGGGCCTGG) and myos3′Sma1 (ACGACCCGGGCTTGTCGTCGAACATTATCTCAATGTACTTTCC), were used as primers to amplify from genomic DNA a fragment corresponding to the 5′ 935 bp of the myoV coding sequence. This PCR product was digested with NotI and SmaI and ligated into NotI/SmaI-digested pLB01  creating plasmid palcA-GFP-myoV in which the alcA promoter and the coding sequence for GFP are placed in frame immediately 5′ of the myoV heavy chain coding sequence. palcA-GFP-myoV was transformed into the A. nidulans strain GR5, transformants with similar growth defects were selected, and their genomic DNAs were subjected to a Southern blot analysis.
Construction of the ΔkinA/ΔuncA/ΔuncB triple kinesin null mutant
The single kinesin null mutant was made using standard A. nidulans molecular genetic techniques. The coding sequences of kinA, uncA and uncB was replaced by the A. fumigatus pyroA gene, the A. fumigatus pyrG gene, and the glufosinate resistance gene (bar) of Streptomyces hygroscopicus, respectively , . These gene replacement strategies were used in strains lacking nkuA . The genotype of each kinesin null mutant was confirmed by PCR and Southern blot analyses. Genetic crosses were performed to create the triple kinesin null mutant. The genotype of the triple kinesin null was then confirmed by PCR.
Introducing the kinesin null alleles into the alcA-myoV background
Genetic crosses were performed to create the ΔkinA/alcA-myoV and ΔuncA/alcA-myoV double mutants and the ΔkinA/ΔuncA/ΔuncB/alcA-myoV quadruple mutants. To obtain the double mutants, we selected progeny whose colony morphology resembled that of the ΔkinA or ΔuncA single mutants on glycerol plates, and then verified the presence of the alcA-myoV allele (which is actually alcA-GFP-myoV) by observing the hyphal tip accumulation of GFP-MYOV in cells grown on glycerol. To obtain the quadruple mutant, we selected the progeny whose colony morphology resembled that of the triple kinesin-null mutant on glycerol plates (which are similar in size to the ΔkinA single mutant) and that also contained the alcA-myoV allele, as evidenced by the hyphal-tip accumulation of GFP-MYOV in cells grown on glycerol. We then performed a genotyping analysis on 11 selected strains by PCR of the genomic DNA, and all five strains that were not viable on YUU were shown to contain the three kinesin-null alleles. This analysis confirmed the genotype of the quadruple mutants, and it also demonstrated that knocking out these three kinesins does not negatively affect the hyphal tip localization of GFP-MYOV.
Image acquisition and analyses
Cells were grown in ΔTC3 culture dishes (Bioptechs, Butler, PA) containing 1.5 ml of MM medium containing glycerol (or glucose) and supplements. Images were captured as described previously  using an IX70 inverted fluorescence microscope (Olympus, Tokyo, Japan) (with a 100× objective) coupled to a 5-MHz MicroMax cooled charge-coupled device camera (Princeton Scientific Instruments, Monmouth Junction, NJ). IPLab software was used for image acquisition and analysis. For quantitative measurements of hyphal length, hyphal width, and septum distribution, we used a Zeiss confocal LSM510-meta with a 40× objective.
Sequence comparisons among myosin V proteins from mouse and three fungal species. Upper: Sequence alignments of the C-terminal cargo-binding domains of myosin-V proteins from A. nidulans (AmyoV), U. maydis (UmyoV), S. cerevisiae (Myo2p) and mouse (MmyoV). Bottom: A phylogenetic tree of four myosin V proteins from the above-mentioned species. The alignment and phylogenetic tree were made using the MegAlign tool of the DNA Star program.
We thank Reinhard Fischer and Nadine Zekert for sending us ΔkinA and ΔuncA mutant strains, and Berl Oakley for sharing unpublished data on Aspergillus nidulans myosin-V. We also thank Gregory Jedd and Michelle Momany for discussions on Woronin bodies.
Conceived and designed the experiments: JZ KT XW SR-P JH XX. Performed the experiments: JZ KT XW GC JS JH XX. Analyzed the data: JZ KT XW GC JS JH XX. Wrote the paper: XX SR-P JH.
- 1. Akhmanova A, Hammer JA (2010) Linking molecular motors to membrane cargo. Curr Opin Cell Biol 22: 479–487.
- 2. Estrada P, Kim J, Coleman J, Walker L, Dunn B, et al. (2003) Myo4p and She3p are required for cortical ER inheritance in Saccharomyces cerevisiae. J Cell Biol 163: 1255–1266.
- 3. Pashkova N, Jin Y, Ramaswamy S, Weisman LS (2006) Structural basis for myosin V discrimination between distinct cargoes. Embo J 25: 693–700.
- 4. Altmann K, Frank M, Neumann D, Jakobs S, Westermann B (2008) The class V myosin motor protein, Myo2, plays a major role in mitochondrial motility in Saccharomyces cerevisiae. J Cell Biol 181: 119–130.
- 5. Lipatova Z, Tokarev AA, Jin Y, Mulholland J, Weisman LS, et al. (2008) Direct interaction between a myosin V motor and the Rab GTPases Ypt31/32 is required for polarized secretion. Mol Biol Cell 19: 4177–4187.
- 6. Fagarasanu A, Mast FD, Knoblach B, Jin Y, Brunner MJ, et al. (2009) Myosin-driven peroxisome partitioning in S. cerevisiae. J Cell Biol 186: 541–554.
- 7. Chang W, Zaarour RF, Reck-Peterson S, Rinn J, Singer RH, et al. (2008) Myo2p, a class V myosin in budding yeast, associates with a large ribonucleic acid-protein complex that contains mRNAs and subunits of the RNA-processing body. RNA 14: 491–502.
- 8. Wu X, Bowers B, Rao K, Wei Q, Hammer JA (1998) Visualization of melanosome dynamics within wild-type and dilute melanocytes suggests a paradigm for myosin V function In vivo. J Cell Biol 143: 1899–1918.
- 9. Wagner W, Brenowitz SD, Hammer JA (2011) Myosin-Va transports the endoplasmic reticulum into the dendritic spines of Purkinje neurons. Nat Cell Biol 13: 40–48.
- 10. Langford GM (2002) Myosin-V, a versatile motor for short-range vesicle transport. Traffic 3: 859–865.
- 11. Loubery S, Coudrier E (2008) Myosins in the secretory pathway: tethers or transporters? Cell Mol Life Sci 65: 2790–2800.
- 12. Stiess M, Bradke F (2011) Neuronal transport: myosins pull the ER. Nat Cell Biol 13: 10–11.
- 13. Horio T, Oakley BR (2005) The role of microtubules in rapid hyphal tip growth of Aspergillus nidulans. Mol Biol Cell 16: 918–926.
- 14. Fuchs U, Manns I, Steinberg G (2005) Microtubules are dispensable for the initial pathogenic development but required for long-distance hyphal growth in the corn smut fungus Ustilago maydis. Mol Biol Cell 16: 2746–2758.
- 15. Konzack S, Rischitor PE, Enke C, Fischer R (2005) The role of the kinesin motor KipA in microtubule organization and polarized growth of Aspergillus nidulans. Mol Biol Cell 16: 497–506.
- 16. Schuchardt I, Assmann D, Thines E, Schuberth C, Steinberg G (2005) Myosin-V, Kinesin-1, and Kinesin-3 cooperate in hyphal growth of the fungus Ustilago maydis. Mol Biol Cell 16: 5191–5201.
- 17. Fischer R, Zekert N, Takeshita N (2008) Polarized growth in fungi–interplay between the cytoskeleton, positional markers and membrane domains. Mol Microbiol 68: 813–826.
- 18. Harris SD (2010) Hyphal growth and polarity. In: Borkovich K, Ebbole D, editors. Cellular and Molecular Biology of Filamentous Fungi. Washington DC: American Society for Microbiology. pp. 238–259.
- 19. Goldman GH, Osmani SA (2008) The Aspergilli: Genomics, Medical Aspects, Biotechnology, and Research Methods. CRC press. 551 p.
- 20. Galagan JE, Calvo SE, Cuomo C, Ma LJ, Wortman JR, et al. (2005) Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzae. Nature 438: 1105–1115.
- 21. Reck-Peterson SL, Novick PJ, Mooseker MS (1999) The tail of a yeast class V myosin, myo2p, functions as a localization domain. Mol Biol Cell 10: 1001–1017.
- 22. Mercer JA, Seperack PK, Strobel MC, Copeland NG, Jenkins NA (1991) Novel myosin heavy chain encoded by murine dilute coat colour locus. Nature 349: 709–713.
- 23. Taheri-Talesh N, Horio T, Araujo-Bazan L, Dou X, Espeso EA, et al. (2008) The Tip Growth Apparatus of Aspergillus nidulans. Mol Biol Cell 19: 1439–1449.
- 24. Govindan B, Bowser R, Novick P (1995) The role of Myo2, a yeast class V myosin, in vesicular transport. J Cell Biol 128: 1055–1068.
- 25. Zekert N, Veith D, Fischer R (2010) Interaction of the Aspergillus nidulans microtubule-organizing center (MTOC) component ApsB with gamma-tubulin and evidence for a role of a subclass of peroxisomes in the formation of septal MTOCs. Eukaryot Cell 9: 795–805.
- 26. Mulvihill DP, Edwards SR, Hyams JS (2006) A critical role for the type V myosin, Myo52, in septum deposition and cell fission during cytokinesis in Schizosaccharomyces pombe. Cell Motil Cytoskeleton 63: 149–161.
- 27. Weber I, Gruber C, Steinberg G (2003) A class-V myosin required for mating, hyphal growth, and pathogenicity in the dimorphic plant pathogen Ustilago maydis. Plant Cell 15: 2826–2842.
- 28. Oakley BR, Morris NR (1980) Nuclear movement is beta–tubulin-dependent in Aspergillus nidulans. Cell 19: 255–262.
- 29. Vale RD (2003) The molecular motor toolbox for intracellular transport. Cell 112: 467–480.
- 30. Lawrence CJ, Dawe RK, Christie KR, Cleveland DW, Dawson SC, et al. (2004) A standardized kinesin nomenclature. J Cell Biol 167: 19–22.
- 31. Soldati T, Schliwa M (2006) Powering membrane traffic in endocytosis and recycling. Nat Rev Mol Cell Biol 7: 897–908.
- 32. Rischitor PE, Konzack S, Fischer R (2004) The Kip3-like kinesin KipB moves along microtubules and determines spindle position during synchronized mitoses in Aspergillus nidulans hyphae. Eukaryot Cell 3: 632–645.
- 33. Schoch CL, Aist JR, Yoder OC, Turgeon G (2003) A complete inventory of fungal kinesins in representative filamentous ascomycetes. Fungal Genet Biol 39: 1–15.
- 34. Requena N, Alberti-Segui C, Winzenburg E, Horn C, Schliwa M, et al. (2001) Genetic evidence for a microtubule-destabilizing effect of conventional kinesin and analysis of its consequences for the control of nuclear distribution in Aspergillus nidulans. Mol Microbiol 42: 121–132.
- 35. Zekert N, Fischer R (2009) The Aspergillus nidulans kinesin-3 UncA motor moves vesicles along a subpopulation of microtubules. Mol Biol Cell 20: 673–684.
- 36. Zhang J, Li S, Fischer R, Xiang X (2003) Accumulation of cytoplasmic dynein and dynactin at microtubule plus ends in Aspergillus nidulans is kinesin dependent. Mol Biol Cell 14: 1479–1488.
- 37. Lenz JH, Schuchardt I, Straube A, Steinberg G (2006) A dynein loading zone for retrograde endosome motility at microtubule plus-ends. Embo J 25: 2275–2286.
- 38. Wedlich-Soldner R, Straube A, Friedrich MW, Steinberg G (2002) A balance of KIF1A-like kinesin and dynein organizes early endosomes in the fungus Ustilago maydis. Embo J 21: 2946–2957.
- 39. Hervas-Aguilar A, Peñalva MA (2010) Endocytic machinery protein SlaB is dispensable for polarity establishment but necessary for polarity maintenance in hyphal tip cells of Aspergillus nidulans. Eukaryot Cell 9: 1504–1518.
- 40. Virag A, Lee MP, Si H, Harris SD (2007) Regulation of hyphal morphogenesis by cdc42 and rac1 homologues in Aspergillus nidulans. Mol Microbiol 66: 1579–1596.
- 41. Schuster M, Treitschke S, Kilaru S, Molloy J, Harmer NJ, et al. (2011) Myosin-5, kinesin-1 and myosin-17 cooperate in secretion of fungal chitin synthase. Embo J. In press.
- 42. Steinberg G (2011) “Motors in fungal morphogenesis: cooperation versus competition.” Curr Opin Microbiol. In press.
- 43. McGoldrick CA, Gruver C, May GS (1995) myoA of Aspergillus nidulans encodes an essential myosin I required for secretion and polarized growth. J Cell Biol 128: 577–587.
- 44. Yamashita RA, May GS (1998) Constitutive activation of endocytosis by mutation of myoA, the myosin I gene of Aspergillus nidulans. J Biol Chem 273: 14644–14648.
- 45. Fujiwara M, Horiuchi H, Ohta A, Takagi M (1997) A novel fungal gene encoding chitin synthase with a myosin motor-like domain. Biochem Biophys Res Commun 236: 75–78.
- 46. Takeshita N, Yamashita S, Ohta A, Horiuchi H (2006) Aspergillus nidulans class V and VI chitin synthases CsmA and CsmB, each with a myosin motor-like domain, perform compensatory functions that are essential for hyphal tip growth. Mol Microbiol 59: 1380–1394.
- 47. Wu XS, Tsan GL, Hammer JA (2005) Melanophilin and myosin Va track the microtubule plus end on EB1. J Cell Biol 171: 201–207.
- 48. Wu X, Xiang X, Hammer JA (2006) Motor proteins at the microtubule plus-end. Trends Cell Biol 16: 135–143.
- 49. Huang JD, Brady ST, Richards BW, Stenolen D, Resau JH, et al. (1999) Direct interaction of microtubule- and actin-based transport motors. Nature 397: 267–270.
- 50. Ali MY, Lu H, Bookwalter CS, Warshaw DM, Trybus KM (2008) Myosin V and Kinesin act as tethers to enhance each others' processivity. Proc Natl Acad Sci U S A 105: 4691–4696.
- 51. Jung G, Titus MA, Hammer JA (2009) The Dictyostelium type V myosin MyoJ is responsible for the cortical association and motility of contractile vacuole membranes. J Cell Biol 186: 555–570.
- 52. Motegi F, Arai R, Mabuchi I (2001) Identification of two type V myosins in fission yeast, one of which functions in polarized cell growth and moves rapidly in the cell. Mol Biol Cell 12: 1367–1380.
- 53. Win TZ, Gachet Y, Mulvihill DP, May KM, Hyams JS (2001) Two type V myosins with non-overlapping functions in the fission yeast Schizosaccharomyces pombe: Myo52 is concerned with growth polarity and cytokinesis, Myo51 is a component of the cytokinetic actin ring. J Cell Sci 114: 69–79.
- 54. Riquelme M, Reynaga-Pena CG, Gierz G, Bartnicki-Garcia S (1998) What determines growth direction in fungal hyphae? Fungal Genet Biol 24: 101–109.
- 55. Harris SD, Read ND, Roberson RW, Shaw B, Seiler S, et al. (2005) Polarisome meets spitzenkörper: microscopy, genetics, and genomics converge. Eukaryot Cell 4: 225–229.
- 56. Steinberg G (2007) Hyphal growth: a tale of motors, lipids, and the Spitzenkörper. Eukaryot Cell 6: 351–360.
- 57. Araujo-Bazan L, Peñalva MA, Espeso EA (2008) Preferential localization of the endocytic internalization machinery to hyphal tips underlies polarization of the actin cytoskeleton in Aspergillus nidulans. Mol Microbiol 67: 891–905.
- 58. Upadhyay S, Shaw BD (2008) The role of actin, fimbrin and endocytosis in growth of hyphae in Aspergillus nidulans. Mol Microbiol 68: 690–705.
- 59. Peñalva MA (2010) Endocytosis in filamentous fungi: Cinderella gets her reward. Curr Opin Microbiol 13: 684–692.
- 60. Hayakawa Y, Ishikawa E, Shoji JY, Nakano H, Kitamoto K (2011) Septum-directed secretion in the filamentous fungus Aspergillus oryzae. Mol Microbiol 81: 40–55.
- 61. Read ND (2011) Exocytosis and growth do not occur only at hyphal tips. Mol Microbiol 81: 4–7.
- 62. Peraza-Reyes L, Espagne E, Arnaise S, Berteaux-Lecellier V (2010) Peroxisomes in filamentous fungi. In: Borkovich K, Ebbole D, editors. Cellular and Molecular Biology of Filamentous Fungi. Washington DC: American Society for Microbiology. pp. 191–206.
- 63. Jedd G (2011) Fungal evo-devo: organelles and multicellular complexity. Trends Cell Biol 21: 12–19.
- 64. Momany M, Richardson EA, Van Sickle C, Jedd G (2002) Mapping Woronin body position in Aspergillus nidulans. Mycologia 94: 260–266.
- 65. Xiang X, Osmani AH, Osmani SA, Xin M, Morris NR (1995) NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration. Mol Biol Cell 6: 297–310.
- 66. Liu B, Morris NR (2000) A spindle pole body-associated protein, SNAD, affects septation and conidiation in Aspergillus nidulans. Mol Gen Genet 263: 375–387.
- 67. Nayak T, Szewczyk E, Oakley CE, Osmani A, Ukil L, et al. (2006) A versatile and efficient gene-targeting system for Aspergillus nidulans. Genetics 172: 1557–1566.
- 68. Straubinger B, Straubinger E, Wirsel S, Turgeon G, Yoder O (1992) Versatile fungal transformation vectors carrying the selectable bar gene of Streptomyces hygroscopicus. Fungal Genet Newsl 39: 82–83.