- Research article
- Open Access
Association of six YFP-myosin XI-tail fusions with mobile plant cell organelles
© Reisen and Hanson; licensee BioMed Central Ltd. 2007
- Received: 29 July 2006
- Accepted: 09 February 2007
- Published: 09 February 2007
Myosins are molecular motors that carry cargo on actin filaments in eukaryotic cells. Seventeen myosin genes have been identified in the nuclear genome of Arabidopsis. The myosin genes can be divided into two plant-specific subfamilies, class VIII with four members and class XI with 13 members. Class XI myosins are related to animal and fungal myosin class V that are responsible for movement of particular vesicles and organelles. Organelle localization of only one of the 13 Arabidopsis myosin XI (myosin XI-6; At MYA2), which is found on peroxisomes, has so far been reported. Little information is available concerning the remaining 12 class XI myosins.
We investigated 6 of the 13 class XI Arabidopsis myosins. cDNAs corresponding to the tail region of 6 myosin genes were generated and incorporated into a vector to encode YFP-myosin tail fusion proteins lacking the motor domain. Chimeric genes incorporating tail regions of myosin XI-5 (At MYA1), myosin XI-6 (At MYA2), myosin XI-8 (At XI-B), myosin XI-15 (At XI-I), myosin XI-16 (At XI-J) and myosin XI-17 (At XI-K) were expressed transiently. All YFP-myosin-tail fusion proteins were targeted to small organelles ranging in size from 0.5 to 3.0 μm. Despite the absence of a motor domain, the fluorescently-labeled organelles were motile in most cells. Tail cropping experiments demonstrated that the coiled-coil region was required for specific localization and shorter tail regions were inadequate for targeting. Myosin XI-6 (At MYA2), previously reported to localize to peroxisomes by immunofluorescence, labeled both peroxisomes and vesicles when expressed as a YFP-tail fusion. None of the 6 YFP-myosin tail fusions interacted with chloroplasts, and only one YFP-tail fusion appeared to sometimes co-localize with fluorescent proteins targeted to Golgi and mitochondria.
6 myosin XI tails, extending from the coiled-coil region to the C-terminus, label specific vesicles and/or organelles when transiently expressed as YFP fusions in plant cells. Although comparable constructs lacking the motor domain result in a dominant negative effect on organelle motility in animal systems, the plant organelles remained motile. YFP-myosin tail fusions provide specific labeling for vesicles of unknown composition, whose identity can be investigated in future studies.
- Yellow Fluorescent Protein
- Motor Domain
- Golgi Body
- Golgi Stack
- Peroxisomal Target Signal
Intracellular motility of organelles and transport vesicles is critical for optimization of photosynthesis and metabolism. The dynamic nature of mitochondria [1, 2], chloroplasts , non-green plastids , peroxisomes [5, 6], and Golgi bodies  has been documented through chlorophyll or fluorescent protein labeling of the organelles. Though inhibitor studies [5, 6, 8–10] indicate that the actin cytoskeleton is important for motility of all of these organelles, little information is available on the motor proteins responsible for movement of particular cargoes in plants.
Myosins are molecular motors carrying cargoes on actin filaments in eukaryotic cells [11–13]. Myosins have three common domains: a highly conserved motor domain located at the N-terminus which interacts with actin and hydrolyses ATP; an IQ domain which binds calmodulin or calmodulin-related proteins; a tail which varies by length and structure and which contains a coiled-coil domain consisting of alpha-helices for protein dimerization . When the Arabidopsis genome sequence became available, a total of 17 myosin-like genes were identified [15–17]. They fall into 2 classes: myosin class VIII containing 4 genes and myosin class XI containing 13 members . In the complete rice genome sequence, 2 class VI and 12 class XI myosins were detected . Class VIII myosins were predicted to be involved in new cell wall formation and transport in the plasmodesmata , while class XI myosins, which are closely related to animal and fungal myosin class V , were considered likely to be involved in vesicle and organelle movement.
There may actually be more than 13 myosin XIs present in the Arabidopsis cell, as myosin genes are quite large, with many exons and introns that might undergo alternative splicing. In animals, alternative splicing allows the same gene to encode different myosins that have different cargo-binding capabilities . In plants, myosin transcript data is still quite limited even in plant systems with abundant genomic resources. That alternative splicing does occur in plant myosin transcripts has recently been shown by the sequencing of two cDNAs corresponding to alternatively spliced transcripts of a single rice myosin XI gene .
In order to investigate whether members of the myosin XI gene family in plants localize to specific cargoes, we made expression constructs in which the motor domain of the myosin was replaced by yellow fluorescent protein (YFP). We have examined the localization of 6 different YFP-myosin tail fusions expressed transiently, each encoded by a different myosin XI gene. We have determined how much of the tail region is required for specific labeling of organelles and have evaluated the motility of the labeled organelles. We have investigated whether any organelles labeled with the YFP-tails co-localize with mitochondria, plastids, peroxisomes, or Golgi.
Fluorescent protein markers for transient expression
YFP-class XI myosin-tail constructs label small plant cell organelles
To obtain myosin tail sequences, cDNA for myosin XI-5 (At MYA1), myosin XI-6 (At MYA2), myosin XI-8 (At XI-B), myosin XI-15 (At XI-I), myosin XI-16 (At XI-J) and myosin XI-17 (At XI-K) was obtained from Arabidopsis thaliana Columbia leaves by RT-PCR. Sequencing of two cDNAs for each gene confirmed that the gene model in Genbank was correct (data not shown). A few cDNAs exhibited minor nucleotide alterations, likely PCR errors, that did not affect the amino acid sequence. We did not detect any alternative splicing; however, more thorough studies using transcripts from a variety of tissues will be needed to determine whether these genes' transcripts exist in multiple forms.
Motility of compartments labeled with YFP-tail fusions
The labeled vesicles were observed to be motile in most cells examined [see Additional files 3, 4, 5, 6]. In other systems, expression of defective myosins lacking a functional motor domain results in cessation of movement of the normal cargo carried by the particular myosin, a dominant negative phenotype . Evidently the abnormal YFP-tail myosin is not able to affect the function of a motor that can operate on the fluorescent organelle. If the fusion protein is unable to dimerize with an endogenous myosin and thereby destroy its function, then motility would be expected. Perhaps, unexpectedly, the fusion protein cannot dimerize with its homologous wild-type myosin through the coiled-coil domain but is still able to bind a cargo. The number of molecules of YFP-myosin present through transient expression may not be high enough to dimerize with most wild-type myosins to create a dominant-negative effect. Alternatively, the YFP-truncated myosin may be interacting with subcellular structures to which the wild-type myosin does not normally adhere. Another explanation is that that more than one class XI myosin is responsible for moving the same cargo. A further possible reason for the continued movement of the unidentified vesicles is that other motors move the same vesicle on microtubules; use of both the microfilaments and microtubules for motility has been reported for both Golgi stacks  and chloroplasts . In animals, melanosomes are moved by both microtubule and actin motors . However, the mobility of plant peroxisomes is prevented by actin and myosin inhibitors [5, 6], so the continued movement of these organelles cannot be explained by use of microtubule motors.
Determining class XI myosin domains and tail lengths sufficient for targeting
Comparison of the labeled compartments to Golgi, mitochondria, and peroxisomes
For Myosin XI-6, the "nocoil" construct was expressed rather than the full tail region, because for unknown reasons, the shorter construct produced more consistent labeling. YFP::Myosin XI-6-nocoil (Figure 7B) co-localized with the peroxisomal catalase::DsRed2 marker but not with the mitochondrial or Golgi body marker. The YFP::Myosin XI-5-tail (Figure 7A), YFP::Myosin XI-8-tail (Figure 8A) and YFP::Myosin XI-15-tail (Figure 8B) do not co-localize with any of the markers. YFP::Myosin XI-16-tail did not co-localize with the peroxisome marker, but slight overlaps were observed with the mitochondrial and Golgi markers (Figure 9A). We did not detect any conclusive co-localization with any marker for YFP::Myosin XI-17-tail (Figure 9B), though occasionally there were a few slight overlaps with Golgi stacks.
The co-localization of YPF::myosin XI-6-nocoil confirms the finding that this myosin interacts with peroxisomes, as previously reported in studies using anti-MYA2 (XI-6) antibodies in transgenic Arabidopsis plants expressing a GFP-tagged peroxisomal targeting signal peptide . None of the other five myosin constructs tested co-localized with this peroxisome marker. The overlap of the signal of YFP::myosin XI-16-tail with the Golgi and mitochondrial markers is suggestive but not entirely conclusive, because YFP and GFP are difficult to separate due to overlapping excitation peaks. Further studies with additional control fluorescent protein fusions need to be undertaken in order to verify whether YFP::myosin XI-16 interacts with Golgi bodies and mitochondria. Nevertheless, our experiments do show that motile vesicles are reproducibly labeled with myosin YFP-tail fusions. The identity of these vesicles can be further probed in the future through co-localization with proteins and dyes known to label various compartments involved in vesicular transport processes.
Occasional labeling of linear structures
Not all linear structures appeared similar to microfilaments. Sometimes we observed short linear structures (Figure 10B, 10D) that appeared more similar to microtubules than microfilaments . Usually a myosin would not be expected to react with microtubules. However, there is evidence that motors sometimes link the actin and tubulin cytoskeleton. The Drosophila myosin VI interacts with a microtubule plus-end-binding protein [35, 36]. Even though peroxisomes move on microfilaments , the plant peroxisomal multifunctional protein was shown to bind cortical microtubules in vitro, and peroxisomes and microtubules were observed to interact . In CHO cells, peroxisome association with microtubules was also described . Thus, for unknown reasons, perhaps the myosin XI YFP-tail constructs can sometimes interact with microtubules.
Six different fluorescent myosin XI-tail fusion proteins can label small vesicular structures. Of the 6 fusion proteins analyzed, only YFP::myosin XI-6 evidently interacts with peroxisomes. Most of the C-terminus past the motor domain and IQ repeats was necessary for the myosin to be targeted to an organelle. N-terminal deletions past the coiled-coil region results resulted in loss of specific labeling of vesicles. Unlike in animal systems, the defective myosins did not disrupt motility of the labeled organelles. Either the YFP-myosins can bind to organelles not usually mobilized by the corresponding normal myosins, were not present in adequate concentrate to saturate the normal myosin subunits, or there is redundancy in the motor machinery that is responsible for intracellular trafficking.
RNA extraction, RT-PCR, plasmid construction
Arabidopsis thaliana cv Columbia leaf RNA extraction was performed using RNeasy Plant Mini Kit (Quiagen) followed by reverse transcription using Omniscript reverse transcriptase (Qiagen) with an oligo-dT17 primer. Myosin XI tails were amplified by PCR using the Taq PCR Master Mix Kit (Quiagen) with the following primer pairs:
For Myosin XI-5 (At MYA1; AT1g17580): Myo5fwd 5'GCTTAGAATGCTGAAAATGGCTGC3' and Myo5rev 5'GGATCTGACCTTTCCAACAAGAAC3';
For Myosin XI-6 (At MYA2; AT5g43900): Myo6fwd 5'GCTTAAGATGGCTGCTAGAG3'and Myo6rev 5'AGTGCAAGAATACAAATGCTGG3';
For Myosin XI-8 (At XIB; AT1g04160): Myo8fwd 5'CTTAAGATGGCTGCTCGAG3'and Myo8rev 5'AGTGCAAGAATACGAATTC3';
For Myosin XI-15 (At XI-I; AT4g33200): Myo15fwd 5'CTTAAACAGGTTGCTAATGAAGC3' and Myo15rev 5'TCAAATGATCTGCTTTGAGGTTG3';
For Myosin XI-16 (At XIJ; AT3g58160): Myo16fwd 5'TCAAAGCAGGCTGACAGAA3' and Myo16rev 5'TCAAAAGTAATCTTCGAAGCCC3';
For Myosin XI-17 (At XIK; AT5g20490): Myo17fwd 5'CGCACGAGACACAGGAGCCCTTA3' and Myo17 rev 5'GGCGATGTACTGCCTTCTTTACG3'.
Primers for GATEWAY directional cloning
Myosin XI-5 (At MYA1)
Myosin XI-17 (At XI-K)
Myosin XI-6 (At MYA2)
Myosin XI-15 (At XI-I)
Myosin XI-8 (At XI-B)
Myosin XI-16 (At XI-J)
At Catalase 2 cDNA (At4g35090) was obtained by RT-PCR using the following primer pairs: 5'ATGGATCCTTACAAGTATCGTC3' and 5'CTAGATGCTTGGCCTCACG3'. The PCR product was cloned into a pCR2.1-TOPO T/A vector (Invitogen), and sequenced. The gene was then amplified with the following primers for allowing a directional cloning into the pENTR/D TOPO vector (Invitrogen): 5'CACCGATCCTTACAAGTATCGTC3' and 5'TTAGATGCTTGGTCTCACG3'. The gene was fused to YFP in the pEarleyGate104  by LR reaction (Invitrogen). The catalase cDNA was also fused downstream of DsRed2 in the binary pGDR vector  by using the KpnI restriction site. Primers containing KpnI restriction sites (bold) were used: 5'GGGGTACCATGGATCCTTACA3' and 5'GGGGTACCTAGATGCTTGGTC3'. The purified PCR product was digested by KpnI and cloned into the KpnI linearized and dephosphorylated pGDR vector using T4 ligase (Invitrogen). Positive clones were screened by digestion profile and confirmed by sequencing.
Sequence alignment and cladogram for myosin tails
Myosin tail sequences were aligned by using MultAlign , and edited with GeneDoc . Coiled-coil regions were predicted with COILS  in the SMART module [45, 46] and "dilute" domains were identified with Pfam . Amino acid similarity tree (cladogram) was made in Megalign (DNAStar) with the Clustal W method.
Onion cells or Arabidopsis thaliana leaves were bombarded with plasmid-coated tungsten particles using a Model PDS 1000/He Biolistic Particle Delivery System™ (BioRad, Hercules, CA, USA) according to manufacturer's instructions. Plasmid DNA (2 μg for each shot) was precipitated on tungsten particles, and onion or A. thaliana epidermal cells were bombarded twice. The expression was observed 24 h after bombardment.
Agrobacterium-mediated transient expression was performed as previously described . Briefly, the binary GATEWAY-plasmid vectors were transformed by electroporation into A. tumefaciens strain C58C1 carrying the virulence helper plasmid pCH32 . The transformants were inoculated into 5 ml LB medium supplemented with 50 μg ml-1 kanamycin and 5 μg ml-1 tetracycline and grown at 28°C overnight. Cells were precipitated and resuspended to an OD of 0.5 in solution containing 10 mm MgCl2, 10 mm MES pH 5.6 and 150 μm acetosyringone. The cells were left at room temperature on the bench for 2 h before infiltration into N. bentamiana leaves. Observation was done 48 h after infiltration.
Confocal laser scanning microscopy
Confocal microscopy was performed on a Leica DMRE-7 (SDK) microscope equipped with a TCS-SP2 confocal scanning head (Leica Microsystems Inc., Bannockburn, IL, USA). Images were collected with a Leica 63 × HCX PL APO water immersion objective (NA = 1.20). YFP was excited at 514 nm with an ArKr laser, and emission was detected between 525 and 625 nm. Chlorophyll was excited at 488 nm with an ArKr laser and emission was detected between 640 and 715 nm. DsRed was excited at 514 with an ArKr laser or at 543 nm with a GreNe laser and emission was detected between 563 and 660 nm. GFP was excited at 488 with an ArKr laser and emission was detected between 498 and 515 nm. For co-localization experiments, images were sequentially collected in order to minimize cross-talk of GFP and YFP. For time lapse series YFP and chlorophyll were both excited at 488 nm and pictures were collected without frame averages. Organelle motility was measured with the ImarisTrack module from the Image Analyzing Software Imaris 5.0 (Bitplane AG, Zurich, Switzerland). Labeled organelles were detected with the spot function and tracks were analyzed by using the autoregressive motion algorithm. Brownian movement was tracked with the Brownian motion algorithm.
This research was supported by DOE Energy Biosciences grant 89-ER14030 to MRH. Chris Hawes kindly provided the ERD2::GFP construct. We thank Alex Wong for assisting with sequence comparisons and Elizabeth Takacs for participating in the agroinfiltration experiments.
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