Myosins are a large superfamily of motor proteins which, in association with actin, are involved in intra- cellular motile processes. In addition to the conventional myosins involved in muscle contractility, there is, in animal cells, a wide range of unconventional myosins implicated in membrane-associated processes, such as vesicle transport and membrane dynamics. In plant cells, however, very little is known about myosins. We have raised an antibody to the recombinant tail region of Arabidopsis thaliana myosin 1 (a class VIII myosin) and used it in immunofluorescence and EM studies on root cells from cress and maize. The plant myosin VIII is found to be concentrated at newly formed cross walls at the stage in which the phragmoplast cytoskeleton has depolymerized and the new cell plate is beginning to mature. These walls are rich in plasmodesmata and we show that they are the regions where the longitudinal actin cables appear to attach. Myosin VIII appears to be localized in these plasmodesmata and we suggest that this protein is involved in maturation of the cell plate and the re-establishment of cytoplasmic actin cables at sites of intercellular communication.
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The myosins are a large superfamily of molecular motors which generate movement and mechanical force in ATP-dependent interactions with actin filaments. On the basis of their conserved head or motor domain sequences, i.e. the highly conserved region containing the ATPase and actin binding sites, the myosins can be divided into at least 14 classes (designated I to XIV) ( Cope et al. 1996 ; Mermall et al. 1998 ). In addition, each class of myosin contains tail domains which are characteristic for each myosin and are believed to be responsible for the specific subcellular localization and function of these motors.
In unicellular systems and mammalian cells the involvement of the conventional two-headed, filament-forming myosins (myosin IIs) is well established in muscular contraction and cytoplasmic contractile events such as cytokinesis. In addition, the so-called unconventional myosins of class I, V and VI are now relatively well described; several of them have recently been shown to be involved in various actin-based and membrane-associated functions, which include vesicle transport, cytokinesis and such specialized functions as auditory perception (for recent reviews see Bähler 1996; Fath & Burgess 1994; Hammer 1994; Hasson & Mooseker 1995; Mermall et al. 1998 ; Mooseker & Cheney 1995; Titus 1993).
The first myosin gene to be cloned and sequenced from a plant, Arabidopsis thaliana myosin 1 (ATM1) ( Knight & Kendrick-Jones 1993), was placed by phylogenetic analysis of its motor domain sequence into a new class of myosins (class VIII). Since then a further 10 plant myosin genes (from Arabidopsis, Helianthus, Acetabularia and Chlamydomonas) have been cloned and sequenced ( Kinkema & Schiefelbein 1994; Kinkema et al. 1994 ; La Claire et al. 1995 ; Vugrek and Menzel, personal communication) and, on the basis of their conserved motor domain sequences, have been placed into three new classes (classes VIII, XI and XIII) ( Cope et al. 1996 ) by phylogenetic analysis. Further analysis of their highly divergent C-terminal tail sequences confirms this classification. None of the plant myosins identified thus far belong to class I or II. The plant myosins in class XI are closely related to the animal myosin Vs but are sufficiently different to be grouped into a separate class ( Cope et al. 1996 ). Furthermore, PCR screens and the Arabidopsis genome sequencing project indicate the existence of additional myosins in classes VIII, XI and XIII ( Kinkema et al. 1994 ; La Claire et al. 1995 ; Moepps et al. 1993 ; Plazinski et al. 1997 ; Vugrek and Menzel, personal communication).
The important point to emerge from this analysis is that all the myosin genes identified from plants belong to unique classes which do not contain animal or protozoan myosins. The motile processes in higher plants and animals may be specifically different and, in order to investigate the plant-specific localization and function, we generated an antibody against a recombinant tail region of myosin ATM1. The immunolabelling patterns in root cells from Lepidium sativum (cress) and Zea mays (maize) indicate that this myosin VIII is predominantly localized at the cell periphery where it is preferentially associated with those plasma membrane regions involved in the assembly of new cell walls. The immunogold and immunofluorescence images reveal that this myosin is also associated with cell-to-cell contact areas in root cells and appears to accumulate specifically in plasmodesmata. These results suggest the intriguing possibility that in plant cells actomyosin-based forces are involved in the selective ‘gating’ of plasmodesmata.
Immunological studies of myosin VIII in root tissue preparations
To raise antibodies specifically against the Arabidopsis thaliana myosin (ATM1), a class VIII plant myosin, we expressed and purified its tail region and used it as the immunogen. This tail region appears to be unique and consists of a short stretch of predicted α-helical coiled-coil (amino acids 950–1019 containing about 10 heptad repeats) and a unique C-terminal region (residues 1020–1166) ( Knight & Kendrick-Jones 1993) which has no apparent homologies or recognisable motifs. The only noticeable features are two clusters of serine residues and a cluster of basic residues at its very C-terminus. For expression, a vector of the pGEX series was modified so that fusion proteins with GST (Glutathione-S-transferase) on their N-termini and a stretch of six histidine residues on their C-termini could be expressed. This vector is especially useful when, as in this case, proteolytic degradation of the expressed protein is a problem. Using the modified vector with two affinity labels, intact fusion protein could be prepared for antibody production.
For our immunological studies, we used root tissue from Arabidopsis thaliana, cress (Lepidium sativum) and maize (Zea mays) and coleoptile tissue from maize for Western blots. Since cress and Arabidopsis belong to the same dicot family (Brassicaceae), antibodies raised against the Arabidopsis thaliana myosin 1 (ATM1) were expected to cross-react with a myosin of the same class in cress and this appears to be the case. We also found that we could obtain the same immunofluorescence pattern in maize roots.
To check the specificity of the affinity-purified polyclonal anti-ATM1 antibody, immmunoblot analyses were carried out on subcellular fractions from cress root and maize coleoptiles ( Fig. 1). In both cress roots ( Fig. 1A,a) and maize coleoptiles ( Fig. 1B,b), the antibody cross-reacts with a 130 kDa band in the microsomal membrane fraction ( Fig. 1). This subcellular distribution indicates that the intact 130 kDa myosin VIII is associated with the membrane fraction, reminiscent of the membrane localization of the myr 4 myosin in rat brain fractions ( Bähler et al. 1994 ). In our experience, many of the unconventional myosins in animal tissues and tissue culture cells are preferentially bound to cytoskeletal-membrane fractions. In cress roots there is also a faint cross-reacting band at 170 kDa ( Fig. 1a) which may be the product of one of the class XI myosin genes recently identified by Kinkema & Schiefelbein (1994). When protein extracts were rapidly prepared from cress roots in the presence of a wide spectrum of protease inhibitors and MgATP and subjected to immunoprecipitation with the anti-ATM1 antibody, a single band of approximately 130 kDa was detected on Western blots ( Fig. 1c). The size of the immunoprecipitated protein is in good agreement with the predicted molecular weight of the ATM1 protein (131.2 kDa) ( Knight & Kendrick-Jones 1993). There was no corresponding Coomassie-stained band on the SDS-PAGE gel ( Fig. 1C) indicating that the amount of myosin VIII in these tissues is likely to be very low. Purified myosin VIII tail fusion protein when mixed with anti-myosin antibody specifically blocked the Western blot and immunofluorescent staining patterns.
Immunolocalization of myosin VIII along the transverse cell walls in root tissue
For the immunolocalization studies, we used root tissue from Arabidopsis, cress and maize seedlings. Root tissues were preferred because they are more convenient to handle and their simple architecture allows one to consistently identify the various cell types undergoing different developmental programmes. Virtually identical antibody labelling patterns were obtained with root tissues from all three plants (images from Arabidopsis are not shown). Cress and maize roots were preferred: cress because it is closely related to Arabidopsis and its roots are more robust, and maize because its cytoskeleton has been comprehensively studied (e.g. Baluska et al. 1992 ; Blancaflor & Hasenstein 1995).
The anti-ATM1 antibody strongly labelled the peripheral region underlying the transverse cell walls in the roots of all three plants ( Figs 2b,d and 3b). In contrast and acting as an internal control, the longitudinal walls in these cells exhibited rather punctate myosin VIII labelling ( Fig. 2d,h). The labelling was most prominent in the region containing meristematic and early post-mitotic cells which were undergoing cell division. The strongest labelling was found along newly formed cell walls which were in the process of maturation.
Controls using either pre-immune serum or secondary antibody alone or antibody to vertebrate non-muscle myosin II ( Drenckhahn et al. 1983 ) did not show any staining in root cells (data not shown).
Myosin VIII localisation during mitosis
The distribution of myosin VIII, actin and microtubules during stages in the cell cycle in root meristems in higher plants are shown in Figs 2 and 3 and are summarised in the schematic drawings in Fig. 6. At the onset of mitosis (prophase), actin is localised as dense irregular networks surrounding the enlarged, round nucleus ( Figs 2a, 3a and 6a). At this stage, myosin VIII labelling is concentrated along the transverse cell walls and is sparsely distributed along the longitudinal cell walls ( Fig. 2b). At the beginning of metaphase, when the nuclear envelope disintegrates, actin staining is concentrated along the two opposing transverse cell walls with a few actin filaments reaching towards the centre of the cell ( Figs 2g and 6b). Myosin VIII labelling is more intense than in prophase and is concentrated at the opposing transverse cell walls, co-localizing with the actin filaments ( Figs 2h and 6b).
The different stages in the cell cycle can be readily assigned by following the distribution of microtubules and mitotic chromosomes. At metaphase, when the chromosomes are aligned midway between the spindle poles, dense bundles of kinetochore microtubules connect the chromosomes to the poles (see SP in Figs 3g and 6d). During telophase, in the early phragmoplast (P) region where the new cell wall forms between the separating daughter nuclei, intense anti-tubulin staining is seen as a broad phragmoplast band in the centre of the newly forming cell plate ( Figs 3d and 6e). In late cytokinesis, the phragmoplast P* forms a ring-like structure surrounding the newly developing cell plate ( Figs 3d,g and 6f). Myosin VIII staining does not occur in the callose-rich cell plate region in the early (P) or in the developing late phragmoplast (P*) ( Figs 3c,f and 6f) but is confined entirely to the opposing transverse cell walls which are strongly stained ( Fig. 3c,f,h). The DAPI-stained chromatin in these cell stages is still slightly condensed ( Fig. 3e,i), and the shape and small size of the nuclei reveal that these cells are in a late phase of cell division. Later, in G1-phase (G in Fig. 3), shortly after disintegration of the phragmoplast microtubules ( Fig. 3d,g), extensive labelling of the myosin VIII was detected in this area ( Figs 3c,f,h and 6g). In these cells the chromatin in the nuclei is uncondensed ( Fig. 3e,i), and the phragmoplast microtubules have become integrated into the cortical microtubule network ( Figs 3g and 6h). At this late G1 stage, anti-ATM1 staining is thus very strongly concentrated along or in the newly formed cell wall ( Fig. 3b,f,h) and the actin filaments are arranged in a regular network reaching from the cell walls to the nucleus ( Figs 2c,e, 3a and 6c). It should be noted that during all these stages the transverse cell walls are always highly labelled with anti-ATM1 antibody whereas the longitudinal walls show only punctate labelling ( Figs 2b,d,h and 3b).
In interphase cells, after completion of cell division, the transverse cell walls are stained with anti-ATM1 antibody, but less brightly than during mitosis ( Fig. 2d,f). Actin staining of the same region shows a very prominent F-actin array, with characteristically arranged actin filament bundles ( Figs 2c,e and 6i). The actin co-localizes with the myosin VIII labelling along the transverse cell walls and extends into the cell centre where the bundles appear to separate into several finer filaments surrounding the nucleus. These finer central actin bundles are not labelled with myosin VIII.
Association of myosin VIII with the plasma membrane and plasmodesmata
1. Confocal microscopy. Optical sections through cress root tips labelled with the anti-ATM1 antibody confirmed that the myosin VIII was localized along the whole transverse cell wall, whereas the longitudinal walls show only punctate labelling. An overlay of a phase-contrast image and the fluorescent myosin-staining is shown in pseudo-colour ( Fig. 4a). The myosin VIII labelling pattern is densely punctate, with the highest density of label in new cell walls in early G1, shortly after phragmoplast disintegration. An overlay of optical sections ( Fig. 4b) reveals that the punctate labelling pattern passed through the whole cell wall area. Along the longitudinal cell walls a less dense distribution of myosin VIII in distinct patches can also be observed. In Fig. 4(c), the myosin VIII labelling in G1-phase cells is shown at a higher magnification, revealing intense myosin VIII labelling of the plasma membrane associated with the newly formed cell wall.
2. Immunogold electron microscopy. To confirm these immunofluorescence images, we prepared ultra-thin frozen sections of cress roots and subjected them to indirect immunogold labelling with our anti-ATM1 antibody. In the electron microscope, labelling was detected along the newly formed cell wall between two cells (arrows indicate the 10 nm immunogold particles in Fig. 5a,b). This cell wall shows the features of a young cell wall after the disintegration of the phragmoplast and before it loses its ‘wavy’ appearance, characteristic of the final stages in the maturation of the cell wall. The anti-ATM1/immunogold labelling (10 nm particles) occurred in association with the plasma membrane and at thin membranous structures going through the cell wall which are thought to be plasmodesmata. Other regions of the sections were virtually free of any immunogold labelling.
For a more detailed localisation of the myosin in the cell walls, we used ultra-thin sections of maize roots embedded in LR White Resin which preserves the membrane ultrastructure better than cryo-fixation. Transverse as well as longitudinal cell walls possessing primary and secondary plasmodesmata showed characteristic anti-ATM1/immunogold labelling ( Fig. 5c,d,e). In young transverse cell walls, plasmodesmata were seen decorated with strings of gold particles ( Fig. 5c) and in longitudinal cell walls, where secondary plasmodesmata were mostly arranged in large pit fields, the immunogold particles were especially enriched in this area ( Fig. 5d,e). The cytoplasm and other cell structures were very rarely labelled when compared with the pit fields.
We have performed the first cytological characterization of an unconventional myosin in higher plants using an antibody specifically raised against a recombinant tail region of the first plant myosin gene to be cloned and sequenced. This gene (ATM1) was isolated from a dicot plant Arabidopsis thaliana (Knight & Kendrick-Jones 1993). The predicted molecular weight of ATM1 is 131 kDa, and it contains a motor domain (head), four IQ-motifs predicted to bind calmodulin or light chains and a tail domain with a predicted short coiled-coil region which implies its dimerisation into a double-headed molecule. The whole tail region of this myosin was expressed and used as an immunogen to generate specific antibodies. Immunoblot analysis using these anti-ATM1 antibodies identified an approximately 130 kDa band which is highly enriched in the membrane fraction in cress and maize tissues. These results suggest that the myosin VIII is membrane-bound, possibly by its C-terminal globular region. In this connection it is interesting that the animal myosin Is and myosin Vs are known to be bound to membranes ( Mooseker & Cheney 1995).
Immunofluorescence and immunoelectron microscopy of cress and maize root tissues using the anti-ATM1 antibody showed that the myosin VIII is concentrated along the plasma membranes at transverse cell walls both in meristematic cells and in the post-mitotically growing root cells. Cells in G1 phase are extensively stained along their young transverse cell walls, whereas there is only punctate staining along longitudinal cell walls. The immunolocalization patterns show that myosin VIII is concentrated along the transverse walls where F-actin is attached perpendicularly. This suggests that myosin VIII may have some role in the formation of new cell walls as it has a less dense distribution along established side walls. One key feature of the new end walls is that they are a specialized zone of concentrated cell–cell contact where plasmodesmata are formed at cell division. It is significant, therefore, that immunogold studies show myosin to be located at these intercellular plant cell junctions.
In previous studies, myosin-like proteins from plants have been characterized either with cross-reacting antibodies or by stimulation of their ATPase activity by F-actin (for review see Asada & Collings 1997; Kendrick-Jones & Reichelt 1999). Such studies have revealed a variety of proteins, perhaps reflecting the diverse classes of myosins. One 240 kDa protein has been isolated from Chara that moves muscle F-actin at 60 μm sec–1 in in vitro motility assays which strongly suggests that this protein is the motor responsible for cytoplasmic streaming. This myosin when viewed in the electron microscope after rotary shadowing ( Yamamoto et al. 1995 ) has similar characteristics to a myosin V, i.e. it is a dimer of two 210–220 kDa heavy chains with pear-shaped heads (motor domains) and a slightly curled globular tail about 80 nm long. Thus far it has not been possible to clone and sequence the gene for this Chara myosin. The predicted molecular weights of class VIII myosins is about 130 kDa and for class XI myosins about 170 kDa. In higher plants, a 170 kDa myosin has been biochemically isolated from lily pollen tubes ( Yokota & Shimmen 1994) and an antibody to this protein recognizes 170 kDa polypeptides in tobacco, Tradescantia and Arabidopsis tissue ( Yokota et al. 1995 ). When heterologous anti-myosin antibodies have been used to stain plant cells, they have mostly produced punctate staining patterns throughout the cell which is indicative of the labelling of organelles and vesicles involved in membrane transport ( Grolig et al. 1988 ; Miller et al. 1995 ; Qiao et al. 1989 ). It can be concluded that homologues of the myosin superfamily exist in higher plants and are involved in a variety of membrane associated processes. However, it is clear that the anti-myosin VIII localization reported here has distinct differences from these previous studies. One of the striking features of myosin VIII localization is that it becomes concentrated in newly deposited cross-walls in contrast to its sparse occurrence along side walls. This suggests that it may be involved, not so much in the process of vesicle transport and fusion which bring cell plate precursors to the mid-line of the phragmoplast, but in those processes of cell plate maturation. Indeed, myosin VIII labelling is found most strongly when the actin and microtubules of the phragmoplast have depolymerized, and it is important to examine the stage-specific processes in which myosin VIII may be implicated.
Several studies show that cell wall formation occurs in two separate stages. For instance, caffeine is known not to effect the formation of the phragmoplast cytoskeleton nor the actual deposition of the central cell plate, but the later stage of fusion with the mother wall and the conversion of the callose-rich plate into a less flexible wall ( Hepler & Bonsignore 1990; Valster & Hepler 1997). Mineyuki & Gunning (1990) have reviewed these later stages of cell division and concluded that insertion and maturation factors interact with the cell plate or pass into it from the cortical division site. Callose (a major component of the cell plate) is removed from cell plates soon after they attach ( Northcote 1989) and pectic polysaccharides are inserted ( Moore & Staehelin 1988; Samuels et al. 1995 ). The appearance of myosin VIII coincides therefore with the onset of these wall-consolidating processes. The protein could bring the islands of membrane plate material together or it could trigger the exocytosis of new cell wall material. High concentrations of calcium–calmodulin are found near the phragmoplast/cell plate ( Hepler 1994) and it is possible that changes in the calcium levels at the transition between plate deposition/maturation affect the localisation and activity of myosin VIII. In Chara, a polyclonal antibody raised against smooth and skeletal myosin has been shown to label plasmodesmata ( Radford & White 1998)–a localisation pattern which agrees with our previous results ( Reichelt et al. 1997 ) and this paper.
In the early post-mitotic root cells of cress and maize the transverse walls are intensely labelled with the anti-myosin VIII and actin antibodies. This myosin antibody does not decorate F-actin cables involved in cytoplasmic streaming but it is interesting that myosin VIII is concentrated along those walls to which the longitudinal actin cables are directed and attached. The cytoplasmic actin cables largely depolymerize in cell division but streaming is restored along the interphase array during early postcytokinesis. Another possible role for myosin VIII (which is detected in the membrane fraction) is that it may be part of the system for anchoring or directing the cytoplasmic F-actin cables. Since F-actin goes to (or through) plasmodesmata ( White et al. 1994 ), it has been suggested to be involved in the intercellular movement of certain viruses ( McLean et al. 1995 ), proteins and mRNA ( Lucas et al. 1996 ). Such particle movement is most likely to be an exaggerated form of normal directed cell transport. It is interesting therefore that the density of plasmodesmata is far greater in the transverse end walls than in the longitudinal side walls ( Juniper & Barlow 1969). The movement of virus particles ( McLean et al. 1995 ; Waigmann & Zambryski 1995; Zambryski 1995), and the fact that cytochalasin D enlarges the plasmodesmatal neck ( White et al. 1994 ), indicates that there is a gating mechanism which controls the size of the pore and that this is likely to be under contractile regulation ( Ding et al. 1996 ; Overall et al. 1982 ; White et al. 1994 ). The present study has shown that myosin VIII is localized at plasmodesmata and, particularly since it is an actin-interacting protein, is a strong candidate for being part of any intercellular gating complex.
Analytical grade reagents were obtained from BDH Chemicals Ltd (Poole, UK), Bethesda Research Laboratories Inc. (Gaithersburg, MD, USA) and Sigma Chemical Co. Ltd (Poole, UK). Enzymes supplied by New England BioLabs (Hertfordshire, UK) and Promega Corporation (Madison, WI, USA) were used according to the manufacturer’s standard assay conditions. Radiochemicals were supplied by Amersham International (Amersham, UK). Oligonucleotides were synthesized on an Applied Biosystems 390B automated synthesizer (Applied Biosystems Inc., Foster City, CA, USA) by Terry Smith (Laboratory of Molecular Biology, Cambridge, UK).
Expression of recombinant ATM1 and antibody preparation
The vector pGEX-H6 used for the expression of the tail region of Arabidopsis thaliana myosin VIII (ATM1) is based on pGEX4T-3 (Pharmacia) with the addition of a C-terminal string of six histidine residues. This allows the intact expressed protein to be purified using two specific affinity tags by the so-called ‘affinity-sandwich’ protocol ( Binder et al. 1994 ). The vector was constructed by inserting a double-stranded oligonucleotide consisting of: 5′-GGC CGC CAC CAT CAC CAT CAC CAT –3′ and 5′-GGC CAT GGT GAT GGT GAT GGT GGC –3′ into the NotI site of pGEX4T-3. This oligonucleotide introduces the 6 His (H6) sequence C-terminal to a regenerated NotI site such that if the insert is correctly engineered this His-tag should remain in frame with both upstream sequences and the downstream stop codon.
The ATM1 insert was produced by PCR using the intact ATM1 cDNA clone (3.851Kb) ( Knight & Kendrick-Jones 1993) as template and the following oligonucleotides: 5′-CGA ATT CCC GGG TCG GAG GTG CCA AGA CAA ATG AGT TAG GTG AG –3′ and 5′-GCC ACG ATG CGG CCG CTA TAC CTG GTG CTA TTT CTC CTT CCC CAC CA –3′ as primers which also introduce NotI and XmaI restriction sites (underlined). The PCR product (2952–3632 in the ATM1 cDNA) containing the whole tail-region of ATM1 including the coiled-coil and the C-terminal globular regions (amino acid residues 938–1166) was first blunt-end cloned into puc18, digested with HincII and transformed into E. coli JM101 cells. Positive clones were recognized by blue/white selection and PCR screening and were sequenced. Clones which contained the correct inserts were digested with NotI and XmaI and ligated into the dephosphorylated expression vector pGEX-H6. The ATM1-pGEX-H6 construct was expressed in E. coli BL21 (DE3) cells ( Studier & Moffat 1986). Freshly transformed colonies were inoculated into 2XTY medium containing 100 mg ml–1 ampicillin, grown overnight at 37°C and then induced with 0.6 m m IPTG and grown for a further 3 h at 37°C. The cells were harvested by centrifugation at 5000 g and resuspended in PBS containing 1% TritonX-100 and a battery of protease inhibitors (see section on immunoprecipitation and Western blot analysis). The cells were lysed in a French Press and the supernatant collected by centrifugation at 12 000 g. The ATM1 was expressed as a soluble fusion protein, GST-ATM1-H6, with a molecular weight of 54 kDa. The supernatant was filtered through a 0.45 μm filter and applied to a Glutathione(GT)-Sepharose 4B column and purified according to the manufacturer’s instructions (Pharmacia P-L Biochemicals Inc.). After application of the expressed protein, the GT-Sepharose column was washed with at least four volumes (volume of supernatant applied) of PBS containing 1% Triton X-100 and the protease inhibitor cocktail and the bound fusion protein eluted with 10 m m glutathione, 50 m m Tris–HCl, pH 8.0. Further purification of the fusion protein using the His-tag by Ni-affinity chromatography was performed under non-denaturing conditions according to the manufacturer’s instructions (Novagen, Inc.).
The ATM1-GST fusion protein was further purified by SDS-PAGE on a 10% acrylamide maxi-gel and the major band cut out and electroeluted. Three 100 μg aliquots of this fusion protein were used for antibody production in rabbits, as described by Harlow & Lane (1988). The resulting polyclonal serum was affinity-purified for the localization and Western blotting studies in two steps; first using a glutathione-S-transferase (GST)-agarose affinity column to remove any anti-GST antibodies and then using the recombinant ATM1 protein on immunoblots to purify the anti-ATM1 antibodies. For these immunoblots the recombinant protein purified on a GT-Sepharose column was separated on an SDS-Page gel and transferred to nitrocellulose. The nitrocellulose blot was stained with Ponceau red and the strips containing the recombinant ATM1 were cut out, blocked with 5% non-fat dry milk in TBS (Tris buffered saline) for 1 h and then incubated with the undiluted polyclonal serum overnight at 4°C on a rotating wheel. The nitrocellulose strips were washed repeatedly with TBS containing 0.05% Tween 20 and the bound ATM1-antibodies eluted by vortexing the strips for 30 sec in 0.2 m Glycine, pH 2.2, and then quickly neutralizing with 1 m Tris–HCl, pH 7.6. The specificity of these purified antibodies was checked on blots; they strongly cross-reacted against GST-ATM1 fusion protein and thrombin cleaved 28 kDa fragment (see below) but gave no reactivity against GST even at low dilution. These antibodies weakly cross-react with the tail regions of purified chicken skeletal and brush border cytoplasmic myosin IIs. To check the identity of the expressed GST-ATM1 fusion protein it was cleaved with thrombin to yield 26 kDa and 28 kDa fragments. N-terminal sequencing of the 28 kDa fragment confirmed that it was the tail region of ATM1 and the commercially available anti-GST antibody (Pharmacia P-L Biochemicals Inc.) identified the 26 kDa fragment as GST.
For competitive blocking of the anti-ATM1 antibodies, soluble myosin VIII tail fusion protein was expressed and purified using Ni2+-NTA-Agarose chromatography (Qiagen Ltd) in PBS.
Immunoprecipitation, subcellular fractionation and Western blot analysis
To detect the ATM1 protein in cells by immunoprecipitation, fresh 2-day-old cress roots were homogenized in an ice-cold solution containing 0.2 m KCl, 15 m m Tris–HCl, ph 7.2, 1 m m EDTA, 5 m m DTT, 0.1% Triton X-100, and a broad range of protease inhibitors (10 μg ml–1 aprotinin, 10 μg ml–1 chick ovalbumin trypsin inhibitor, 10 μg ml–1 N-benzoyl- l-arginine ethyl ester hydrochloride (BAEE), 10 μg ml–1 tosyl- l-arginine methyl ester (TAME), 0.1 m m phenyl-methylsulphonyl fluoride (PMSF), 10 μg ml–1 pepstatin, 10 μg ml–1 leupeptin (all obtained from Sigma) and 0.5 m m Pefabloc SC (AEBSF) 4-(2-Aminoethyl)-benzenesulphonyl fluoride (Boehringer, Mannheim, Germany). The roots were first homogenized in a Polytron Omnimixer (Kinematica, Luzern, Switzerland), then in a Dounce homogenizer and the cell debris removed by filtration through one layer of nylon mesh. ATP and MgCl2 were added to the preparation to a final concentration of 5 m m and 10 m m, respectively, and the cells lysed in a French press under high pressure. A further aliquot of 5 m m MgATP was added, and the preparation immediately centrifuged at 50 000 g for 30 min. Two millilitres of the supernatant was incubated with 100 μl anti-ATM1 antibody for 1 h at 4°C and then 50 μl of Protein-A-Sepharose CL-4B (Sigma, P-3391) (swollen in PBS) was added and incubated for a further 1 h at 4°C. The immunocomplexes bound to the protein-A-beads were washed three times with 2 ml of PBS and then finally drained with a syringe inserted directly into the beads to completely remove the PBS. For SDS-PAGE ( Matsudeira & Burgess 1978), 50 μl of sample buffer (2%SDS, 10% glycerol, 100mMDTT, 60mMTris–HCl, pH 6.8 and 0.001% bromphenol blue) was added to the beads, heated to 85°C for 5 min, centrifuged and the supernatant loaded onto a gel.
The protein samples were run on SDS-PAGE 5–20% acrylamide gradient gels using the method of Matsudeira & Burgess (1978 ) and electrophoretically transferred to 0.1 μm nitrocellulose (Schleicher & Schuell, Dassel, Germany) according to the method of Burnette (1981). The nitrocellulose was blocked with 10% (w/v) Marvel (non-fat dry milk) in PBS containing 0.3% Tween-20 (blocking buffer) before incubating with the anti-ATM1 antibody diluted 1 : 500 in blocking buffer. The secondary antibody was biotinylated goat anti-rabbit IgG(H + l) Vectastain, diluted 1 : 200 and the blot developed using the Vectastain ABC Peroxidase kit (PK-4001, Vector Laboratories, Peterborough, UK). Developing solution was 0.9 mg ml–1 DAB, 0.4 mg ml–1 NiCl2, 0.01%H2O2 in 100 m m Tris, pH 7.5.
To prepare fractions containing the membrane bound proteins, plant material (cell cultures from Arabidopsis, cress roots and maize coleoptiles) was homogenized (10 min in a mortar) in an ice-cold solution of 250 m m Tris–HCl (pH 8.0), 25 m m EDTA, 330 m m sucrose, 5 m m DTT, 5 m m ascorbic acid and 1 m m phenyl-methylsulphonyl fluoride (PMSF) followed by filtration through one layer of nylon mesh. All subsequent steps were carried out at 4°C. The post-mitochondrial supernatant (15 min, 4000 g; Biofuge 22R-Heraeus, Offenbach, Germany) was centrifuged for 50 min at 13 800 g (Biofuge 22R-Heraeus). The resulting pellet was used as the membrane bound protein fraction. For Bradford analysis the latter sample was resuspended in 200 μl of a solution containing 10 m m MES/bis-tris-phosphate (BTP) pH 7.5, 5 m m EDTA and 20% glycerol.
SDS-PAGE was performed on these samples diluted in sample buffer containing 3% SDS, 6% sucrose, 100 m m DTT, 60mMTris–HCl, pH 6.8, and 0.001% bromphenol blue. The samples were heated to 80°C for 10 min, centrifuged and the supernatant loaded onto 8% gels. After protein separation, the gels were stained with Coomassie blue or electrophoretically transferred to nitrocellulose using a transblot cell (Bio-Rad, München, Germany). For immunostaining (at room temperature) the nitrocellulose membrane was pre-incubated with 4% BSA in TBS for 30 min, washed for 30 min (three times for 10 min) in TTBS (TBS buffer containing 0.05% Tween-20) and incubated with anti-ATM1 antibody (diluted 1: 1000 in TTBS; control in TTBS). After washing in TTBS the membrane was incubated for 1 h in TTBS containing the secondary antibody (goat anti-rabbit IgG, whole molecule) conjugated to alkaline phosphatase (Sigma A-9919; dilution 1: 100 000). Washing in TTBS was followed by alkaline phosphatase detection using the fast-red staining protocol described by Druguet & Pepys (1977).
Immunofluorescence and immunogold localization of ATM1
The specimens for immunofluorescence microscopy were prepared by the method of Baluska et al. (1992) . Briefly, 2-day-old cress and maize roots were cut and fixed in 4% formaldehyde in MTSB (Microtuble Stabilizing Buffer) containing 50 m m PIPES, 5 m m MgSO4 and 5 m m EGTA, pH 6.9 for 1 h at room temperature. The roots were dehydrated in a graded ethanol series (30% to 97% ethanol in PBS) (PBS contained 0.14 m NaCl, 2.7 m m KCl, 6.5 m m Na2HPO4, 1.5mMK2HPO4, 3 m m NaN3, pH 7.3) then incubated in wax:ethanol (1 : 2, 1 : 1 and 2 : 1 steps) and finally infiltrated in 100% Steedman’s wax (PEG-400 distearate and 1-hexadecanol, 9 : 1(w/w)) at 37°C. The infiltrated roots were then embedded by allowing the wax to polymerize at room temperature. Longitudinal sections 4 μm thick were cut with a microtome (Jung, Heidelberg, Germany) and mounted on slides coated with glycerol-albumen (Serva). The sections were dewaxed in 100% ethanol, rehydrated in an ethanol series (97% to 30% ethanol in PBS), washed with PBS and then finally with MTSB. If sections were subjected to immunostaining with anti-actin antibody, incubation in methanol at –20°C for 10 min was required after the ethanol series ( Vitha et al. 1997 ). After methanol, the sections were washed with PBS and then MTBS. For immunostaining the sections were incubated with the affinity-purified anti-ATM1 antibody (diluted 1 : 200 in PBS with 0.1% BSA) or monoclonal anti-actin (ICN, anti-actin, clone C4, cat. no. 69–100) or anti a-tubulin antibody (Amersham, N356) (both diluted 1 : 200 in PBS-BSA) for 60 min at room temperature. After washing with MTSB, the sections were incubated with fluorescein isothiocyanate (FITC) conjugated anti-rabbit IgG raised in goat (Sigma Chemical Co, St. Louis, MO, USA, F-6005) or rhodamine-conjugated anti-mouse IgG raised in goat (Sigma, T-5393), both diluted 1 : 200 in PBS-BSA, for 1 h at room temperature. Controls included incubating with secondary antibody only, mouse pre-immune serum and monoclonal anti-thymus-myosin II antibody which cross-reacts against a wide spectrum of cytoplasmic myosin IIs in animal cells ( Drenckhahn et al. 1983 ). DNA was labelled by incubating with DAPI (10 μg ml–1) for 5 min at room temperature. Specimens were examined in a Zeiss Axiovert using a Zeiss Planachromat or Neofluar 40× or 100×. Micrographs were taken using Kodak Ektachrome 400 ASA film. The labelled sections were also viewed in a confocal laser scanning microscope (Bio-Rad MRC 600) equipped with argon/krypton lasers and dual excitation/emission filter sets for both TRITC and FITC for the double-labelled specimens.
For immunoelectron microscopy 2-day-old cress roots were cut and fixed in 8% formaldehyde and 0.1% glutaraldehyde in PBS for 1 h at room temperature, embedded in a drop of 3.2 m sucrose and frozen on metal holders in liquid nitrogen. Ultra-thin sections were cut on an cryo-ultramicrotome (Ultracut UCT, Leica/Reichert-Jung, Germany) fitted with cryodevice FC-S and transferred onto nickel grids. The sections were blocked against non-specific labelling by incubating in 0.02 m glycine in PBS for 10 min, 2% gelatin in PBS for 5 min and 0.1% BSA (typeV, Sigma) +5% FCS in PBS for 10 min. For immunolabelling the sections were incubated at room temperature for 30 min with the primary antibody, affinity-purified anti-ATM1 (diluted 1 : 50 in PBS/BSA). They were washed with PBS/BSA and then incubated with secondary antibody goat antirabbit IgG-10 nm gold conjugate (BioCell, Cardiff, U.K) diluted 1 : 50 in PBS/BSA. The sections were washed with PBS and the reaction stabilized with 1% glutaraldehyde in PBS. After washing in distilled water, sections were contrasted with ice-cold 0.4% uranyl acetate in 1.8% methylcellulose. Labelled sections were examined in a Philips EM301 electron microscope at 80 kV.
For the immunolocalisation studies on plasmodesmata ( Fig. 5c,d,e) a similar protocol was used. Two-day-old maize roots were cut and fixed in 4% paraformaldehyde in MTSB buffer for 90 min at room temperature. After washing in MTSB and PBS, and dehydration in a graded ethanol series, the tissue was embedded in LR White Resin (Hard grade, Biocell, Cardiff, UK) and left to polymerise at 36°C. Ultra-thin sections were cut on an ultramicrotome and transferred onto formvar coated nickel grids. The sections were blocked with 50 m m glycine, 5% BSA and 5% normal goat serum in PBS for 30 min and washed with wash buffer (WB) (PBS containing 1% BSA and 0.1% gelatin). They were incubated first with anti-ATM1 (diluted 1 : 50 with WB) at room temperature for 90 min, washed with WB and incubated with the second antibody, goat anti-rabbit IgG-10 nm gold conjugate (diluted 1 : 50 in WB) for 90 min. The sections were washed with WB and PBS, post-fixed with 3% glutaraldehyde for 15 min, washed extensively with distilled water and contrasted with ice-cold 2% aqueous uranyl acetate and 1% osmium tetroxide (to enhance plasmodesmata visualization). The labelled sections were examined in a Zeiss EM 10 electron microscope at 60 kV.
We wish to thank Drs Paul Luzio and Nick Bright (Department of Clinical Biochemistry, University of Cambridge) for the use of their facilities and for advice and assistance with the immunoelectron microscopy; Pat Edwards and Dr Brad Amos for their help with the confocal microscopy; Dr Jamie Cope for his advice on the molecular biological aspects of this work; and Monika Polsakiewicz for excellent technical assistance. This work was supported by fellowships to S.R. from Graduiertenförderung des Landes Nordrhein-Westfalen, Deutscher Akademische Austauschdienst (DAAD) and Boehringer Ingelheim Fonds. Financial support to AGRAVIS (Bonn) by the Deutsche Agentur für Raumfahrtangelegenheiten (DARA, Bonn) and the Ministerium für Wissenschaft und Forschung (MWF, Düsseldorf) is gratefully acknowledged.