- Research article
- Open Access
Bazooka mediates secondary axon morphology in Drosophila brain lineages
© Spindler and Hartenstein; licensee BioMed Central Ltd. 2011
- Received: 2 December 2010
- Accepted: 27 April 2011
- Published: 27 April 2011
In the Drosophila brain, neural lineages project bundled axon tracts into a central neuropile. Each lineage exhibits a stereotypical branching pattern and trajectory, which distinguish it from other lineages. In this study, we used a multilineage approach to explore the neural function of the Par-complex member Par3/Bazooka in vivo. Drosophila bazooka is expressed in post-mitotic neurons of the larval brain and localizes within neurons in a lineage-dependent manner. The fact that multiple GAL4 drivers have been mapped to several lineages of the Drosophila brain enables investigation of the role of Bazooka from larval to adult stages Bazooka loss-of-function (LOF) clones had abnormal morphologies, including aberrant pathway choice of ventral projection neurons in the BAla1 lineage, ectopic branching in the DALv2 and BAmv1 lineages, and excess BLD5 lineage axon projections in the optic medulla. Exogenous expression of Bazooka protein in BAla1 neurons rescued defective guidance, supporting an intrinsic requirement for Bazooka in the post-mitotic neuron. Elimination of the Par-complex member Par6 recapitulated Bazooka phenotypes in some but not all lineages, suggesting that the Par complex functions in a lineage-dependent manner, and that Bazooka may act independently in some lineages. Importantly, this study highlights the potential of using a multilineage approach when studying gene function during neural development in Drosophila.
- Green Fluorescent Protein
- Mushroom Body
- Antennal Lobe
- BAla1 Lineage
- Control Clone
Neurons of the Drosophila brain are grouped into individual units, termed lineages. All neurons belonging to a single lineage are derived from a common neuroblast. Neurons born in the embryo and larva compose the primary and secondary lineages, respectively. Each group of secondary neurons emits a secondary axon tract (SAT) into the central neuropile along the existing primary axon tracts (PATs). As early as embryonic development, lineages begin to acquire a unique morphology that is retained into the larval stages [1–3]. During pupation, approximately 40% of embryonic-born primary neurons are lost, and the secondary neurons begin to generate an intricate network of arbors in the pupal neuropile compartments . SATs are the primary scaffolding and functional units of the adult brain, therefore in the context of using Drosophila as a model to understand circuit formation, it is important to elucidate the mechanisms that underlie stereotypical lineage morphologies.
Key aspects of neuron growth that dictate morphology include axon guidance, branch formation and axon versus dendrite specification. Previous reports indicate a role for the Par-complex proteins (Par3, Par6 and atypical protein kinase (aPK)C) during the latter. Cultured mammalian hippocampal neurons initially send out numerous processes, which all have equal potential to become dendrites or axons. The neurite that becomes the axon retains high levels of Par proteins at its tip. Ectopic expression of Par3 or Par6 or inhibition of aPKC results in neurons which lack a single specified axon [4, 5]. There are two possible mechanisms by which the Par complex affects axon selection from a pool of neurites. On the one hand, the Par complex may segregate additional axon-specific proteins into a single neurite, whereas on the other hand, growth-cone accumulation of Par-complex members could enable one neurite to competitively outgrow other neurites to win axon fate. The axon-specific machinery affected by ectopic expression of Par-complex members is currently unknown.
Elimination of the Par complex from the Drosophila mushroom body does not disrupt the formation of dendrites and axons . This suggests that either 1) Drosophila brains use a separate mechanism for axon and dendrite specification because of the unique organization of the neuron; 2) in vitro mammalian studies do not reflect the actual cellular events which take place in vivo; or 3) the Par complex controls a cellular process (such as axon guidance or branching) that may differ between neurons in the Drosophila brain. We suspect the third possibility to be correct, and localization of Par3 to the tip of the extending axon in cultured hippocampal cells makes it tempting to speculate a role for the Par complex in the growth cone during neurite growth and guidance.
Par-complex proteins have a rich history in invertebrate models. These polarity proteins were originally identified in Caenorhabditis. elegans as factors establishing the first asymmetric divisions that produce the anterior and posterior cells . During Drosophila embryonic development, the Par complex has a well-described role in epithelial polarity [9–13]. Bazooka, the Drosophila homolog of Par3, is present at the apical basal boundary in adherens junctions even before the arrival of Drosophila E-cadherin . Null mutations in bazooka result in embryonic lethality, in which large holes form in the cuticle (hence the name bazooka) and embryos fail to undergo dorsal closure .
In the Drosophila brain, the Par complex is traditionally associated with asymmetric division of the neuroblast  and spindle orientation during neuroblast division . Whereas Bazooka is actively sequestered from the daughter ganglion mother cell (GMC) during neuroblast division, it is re-expressed in the post-mitotic neurons of at least the mushroom body . However, it has not been reported whether Bazooka is globally re-expressed in the transient GMC or post-mitotic neurons throughout the Drosophila brain.
In addition to regulating cellular polarity and asymmetric divisions, the polarity proteins have also been studied in the context of directional guidance. In vitro, aPKC and Par3 localize to the leading edge of scraped Madin-Darby canine kidney (MDCK)11 cells under the control of PATJ (protein associated with Lin 7 (PALS)1-associated tight junction) during wound closure . Par3 and T-cell lymphoma invasion and metastasis (Tiam)1 are required at the leading edge of freely migrating polarized keratinocytes for directional guidance . Finally, phosphorylated Par3 protein modulates front-rear polarity from the leading edge of migrating Hela cells . In vivo, perturbation of the Par complex affects directional orientation of the leading process in rhombic lip-cell migration in the developing chicken cerebellum , and it is required for border-cell migration in Drosophila embryos .
The establishment of apical-basal polarity, spindle orientation and directional migration all require strict control of the cytoskeletal machinery. This array of functions controlled by the Par complex can potentially be explained by its ability to associate with cytoskeletal regulators, such as Rac1, a common denominator in many cellular events [22, 23]. We speculate that ectopic Par-complex expression in cultured mammalian neurons disrupts the cytoskeletal machinery used during neurite outgrowth, therefore inhibiting axon-dendrite formation. Whether polarity proteins are required for growth-cone movement or guidance, as suggested by their localization to the growth cone in culture conditions, has yet to be reported.
What in vivo role does the Par complex command during axon outgrowth? Drosophila neural lineages present an advantageous model to address this question. Lineages are relatively large, and have stereotyped morphologies that can be followed throughout development. At third instar, SATs have an unbranched trajectory into the central neuropile, which can be identified according to established nomenclature . During pupal stages, each lineage expands and elaborates via pathfinding, branching and pruning to produce the final lineage morphologies of the adult brain.
To investigate the in vivo role of Par-complex proteins during neural growth and guidance, we generated bazooka LOF clones with the help of mosaic analysis with a repressible cell marker (MARCM) and lineage-specific drivers . We found that Bazooka is re-expressed in post-mitotic neurons, accumulates within the larval growth cone, and mediates directional guidance, branching and axon projection number in a lineage-dependent manner. We observe similar phenotypes upon manipulation of an additional Par-complex member, Par6. Based on this evidence, we propose a model in which Bazooka is utilized during axon growth to control diverse aspects of neural morphology, such as axon pathfinding and branching, depending on the shape each neuron must acquire.
Markers and stocks
The larval secondary neurons and axon tracts were labeled with an antibody against neurotactin (BP106; Developmental Studies Hybridoma Bank, University of Iowa, IO, USA) and adult axon tracts were labeled with an antibody against neuroglian (BP104; Developmental Studies Hybridoma Bank). An antibody against Drosophila N-cadherin (DN-Ex#7, Developmental Studies Hybridoma Bank) was used to mark the neuropile in both larva and adult. The fly stocks used in this study were: UAS-Baz:GFP (with an upstream activator sequence (UAS) and a green fluorescent protein (GFP) tag; a gift from Dr Prokop) , UAS-Baz (a gift from Dr Doe) , UAS-mcd8:GFP (#5137; Bloomington Drosophila Stock Center, University of Indiana, IN, USA), baz 4 /FM7a (#3295l; Bloomington Drosophila Stock Center). To generate MARCM clones, we used the following stocks: FRT19A,hsFLP,tubGAL80;pins/Cyo (#5133; Bloomington Drosophila Stock Center), period-GAL4,UAS-GFP  and atonal-GAL4,UAS-GFP . The following Flippase recognition target (FRT) lines were gifts from the Doe lab: FRT19A, FRT19A, baz4/FM7C and FRT19A, par6Δ226/FM7C .
Immunohistochemistry and histology
The following antibodies and dilutions were used: anti-neurotactin 1:10 (BP106), anti-DN-Cadherin 1:20 (DN-Ex#7) (both Developmental Studies Hybridoma Bank); anti-Bazooka rabbit 1:500 (a gift from Dr Wodarz); Alexa 546-conjugated anti-rat Ig 1:500 (A11081), Alexa 546-conjugated anti-mouse Ig 1:500 (A11030) (both Molecular Probes, Eugene, OR, USA); and Cy5-conjugated anti-rat Ig 1:100 (112-175-102), FITC-conjugated anti-mouse 1:200 (115-095-100), Cy3-conjugated anti-rabbit Ig 1:200 (711-165-152) and Cy5-conjugated anti-mouse Ig 1:100 (115-175-166) (all Jackson ImmunoResearch, West Grove, PA, USA). For antibody labeling, standard procedures were followed . In brief, brains were dissected in 1× phosphate-buffered saline (PBS) pH 7.4 and fixed in 4% formaldehyde 30 minutes at room temperature or overnight at 4°C. Fixed brains were washed with 1× PBS at least 30 minutes, and either stored in methanol at -20°C or further processed. After at least three washes of 15 minutes each in 1× PBS with Triton X-100 0.1 to 0.3% (PBT), brains were incubated in 10% normal goat serum (GS0500; Capralogics Inc., Hardwick, MA, USA) for at least 1 hour at room temperature, followed by primary antibody incubation overnight at 4°C. Brains were then washed at least 30 minutes in 1× PBT three times, incubated again in 10% normal goat serum for at least 1 hour, and left in secondary antibody for 2 hours at room temperature or overnight at 4°C. Finally, brains were washed at least four times for 15 minutes each in 1× PBT, and mounted on glass slides in mounting medium (Vectashield; H-1000; Vector Laboratories, Burlingame, CA, USA). Brains were viewed under a confocal microscope (20× or 40× objective; MRC 1024ES microscope with Radiance 2000 and Laser Sharp 2000, version 5.2 build 824 software; all Bio-Rad, Hercules, CA, USA). Confocal sections were taken at 2 μm intervals for all preparations. We used Imagej1.41d software (National Institutes for Health, Bethesda, MD, USA) for image analysis and for generation of merged confocal sections. In cases where confocal stacks contained overlapping SATs along the Z-axis, Imagej4.1 was used to mask non-target lineages before generating a merged stack.
To visualize individual SATs in the adult brain, we generated MARCM clones  and visualized clones with lineage-specific driver lines period (per)-GAL4 and atonal (ato)-GAL4. To visualize clones in period- and atonal-expressing lineages, we generated flies with the following genotypes:
FRT19A,hsFLP,GAL80ts; per- GAL4,UASGFP/CyO
FRT19A,hsFLP,GAL80ts; per- GAL4,UASGFP/Cyo; UAS-Baz/TM3; FRT19A,hsFLP,GAL80ts; ato- GAL4,UASGFP/CyO.
For controls, we crossed FRT19A virgin females with males of each of the above lines. For mutant clones, we crossed FRT19A, baz4/FM7C or FRT19A, par6D226/FM7C virgin females to males of the above lines. Only female progeny were used in our analysis.
Embryos were collected overnight on standard agar plates with yeast paste. Within 24 hours of hatching, first instar larvae were hand-picked, placed on standard fly food plates, and heat shocked for 1 to 2 hours at 37°C. After heat shock, the larvae were transferred to bottles with standard fly food and left at room temperature until eclosion. Female adult brains were dissected within 10 days of eclosion.
Counting cell number in MARCM clones
In clones visualized with atonal- GAL4, cell numbers were counted in two ways: first, the volume of the clustered neurons was measured using Labelfield, SurfaceGen and Volume modules of Amira software (version 3.1.1; Mercury Computer Systems, Inc., Chelmsford, MA, USA). The total number was divided by 125 μm3, the measured volume of a single cell body. To verify the accuracy of the volume method, another set of atonal- GAL4 clones was generated and labeled with SYTOX blue (Invitrogen, Carlsbad, CA, USA) to manually count the cell body number with ImageJ1.41d. Both methods produced a similar number of cell bodies for their respective genotypes (data not shown).
Bazooka is expressed in neuroblasts, GMCs and post-mitotic neurons in third instar larvae
Lineage-specific Bazooka:GFP localization
Developmental profile of wild-type BAla1, DALv2 and BAmv1
Srahna and colleagues previously reported a developmental series for the BLD5 lineage . The presence of a distinct point of proximal branches sequestered from distal arbors distinguishes BLD5 as a PD-type lineage. In this study, we established the developmental profile for the period- GAL4 expressing lineages BAla1, BAmv1 and DALv2.
The BAla1 lineage contains the multiglomerular projection neurons of the antennal lobe (AL) . In the third instar stage, cell bodies form a cluster in the anterior cortex, ventrally adjacent to the basal anterior (BA) compartment. The BAla1 SAT projected dorsoposteriorly through the middle antennal cerebral tract (mACT) in the larval brain, ultimately terminating in the centroposterior lateral (CPL) compartment. A small tuft of filopodia marked the location of future branches on the proximal SAT (see Additional file 1, Figure S1A). In pupal stages, proximal neurites branched into the presumptive AL, and the terminal SAT grew into the lateral horn (see Additional file 1, Figure S1B). By eclosion, the BAla1 SAT projected widespread dendritic arborizations into the AL. In the posterior direction, the SAT continued as an unbranched lateral bundle in the mACT, and terminated in the lateral horn (see Additional file 1, Figure S1C). Because BAla1 has proximal branches in the AL and distal branches in the lateral horn, it is a PD-type lineage.
Neurons of the DALv2 lineage innervate most of the ellipsoid body. At third instar, the DALv2 SAT projected dorsomedially into the centroposterior medial (CPM) compartment  (see Additional file 1, Figure S1D). During pupation, the SAT emitted proximal branches into the glomeruli of the developing lateral bulb (the major input domain of the ellipsoid body), and distal branches into the midline of the brain at the position of the presumptive ellipsoid body (see Additional file 1, Figure S1E). At eclosion, this lineage had full proximal branches that stretched dorsally into the inferior-medial protocerebrum (IMP), ventrally into the lateral accessory lobe (LAL) and additionally into the lateral bulb (LB). Finally, the terminal arbors branched throughout multiple layers of the ellipsoid body (see Additional file 1, Figure S1F). Because the DALv2 lineage has a large domain of branches along the SAT projecting into the LB, IMP and LAL, we consider it a C-type lineage.
The BAmv1 lineages contribute to the adult fan-shaped body and LAL. Initially, the larval BAmv1 SAT projected ventrally into the neuropile and twisted dorsoposteriorly into the longitudinal basomedial fascicle (loBM) . Like the BAla1 SAT, small tufts of filopodia marked points of future branching (see Additional file 1, Figure S1G). During pupal stages, distal branches began to form the fan-shaped body at the midline (see Additional file 1, Figure S1H), which was complete in the adult brain (see Additional file 1, Figure S1I), and a set of finer continuous branches were projected into the LAL and inferior protocerebrum. The continuous branch pattern along approximately half of the BAmv1 adult SAT is indicative of a C-type lineage.
Bazooka elimination disrupts SAT morphology
In the process of screening through hundreds of brains, we found only one clone in the BAmv1 lineage and two clones in the DALv2 lineages, suggesting that bazooka loss of function in these particular lineages inhibits period-GAL4-controlled GFP expression, or that these lineages require Bazooka for growth and maintenance. Although only a small number of clones were obtained, it is noteworthy that both the C-type BAmv1 and DALv2 SATs displayed a large amount of branching along the length of the tract (Figure 4F,D). Control clones in these lineages never exhibited such branching patterns. In control DALv2 clones, all branching in the proximal DALv2 SAT had normal morphology (Figure 4C, arrow). By contrast, the ectopic branches in the bazooka LOF DALv2 clones had a bulbous morphology resembling axonal terminals (Figure 4D).
We next examined BLD5 SAT morphology in control and bazooka LOF clones. The BLD5 lineage consists of approximately 40 neurons, also known as dorsal cluster neurons . It has been shown previously that in the adult, BLD5 neurons project proximal arbors into the lobula of the ipsilateral optic lobe and a stereotypical set of axon projections into the contralateral optic medulla. At mid-pupa, the distal axon projections into the medulla number approximately 30, whereas only 11 axons remain in the medulla by eclosion . Similar to these previous reports, our control clones averaged 11 axon projections into the medulla (Figure 4G', n = 23). However, bazooka LOF clones averaged approximately 17 distal axons (Figure 4H', n = 14), suggesting that either too many axons are initially projected or that too few axons are retracted from the medulla during pupal development. In addition to ectopic terminal projections, we also saw an increase in the number of proximal projections (Figure 4G,H). We never found more than one extension into the ipsilateral medulla in the control clones, whereas two or more proximal projections into the medulla were seen in the bazooka LOF clones (Figure 4H).
The last lineage we analyzed was BAla1. In control BAla1 clones, 100% of the clones remained bundled as a single fascicle in the mACT (Figure 4A). By contrast, 91% (n = 11) of the bazooka LOF clones reached the lateral horn by way of the inner (i)ACT, a tract system normally taken by the dorsal and lateral projection neurons that form part of three other (period- negative) lineages  (Figure 4B). Finally, the bazooka LOF clones regularly contained three to five neurons, whereas control clones contained 20 or more cells. The visualization of a few neurons per clone is most likely due to misregulation of the period- GAL4 driver rather than to general defects in division or neuron survival, because a small clone size was seen only in bazooka LOF clones visualized with period- GAL4, but not with atonal- GAL4 (Figure 4H) or elav- GAL4 drivers (data not shown). However, we cannot exclude that bazooka affects cell proliferation/survival in the specific subset of lineages that are visualized with period-GAL4.
In summary, the C-type lineages had ectopic branching patterns whereas the two PD-type lineages had ectopic axon guidance/retraction phenotypes in bazooka LOF clones.
Bazooka is not required for establishment of dendrite versus axon in the BAla1 lineage
We next investigated whether the dendrites targeted appropriately. The wild-type proximal arbors of the BAla1 lineage were multiglomerular in the AL, but some glomeruli were innervated more densely than others. Many of the VA1d and DP1m glomeruli were extensively filled with BAla1 proximal branches, whereas most of the VL1 and VL2a glomeruli were only sparsely filled (Figure 5C,E,G). Even with fewer neurons visualized, the bazooka LOF clones continued to project into the same glomeruli as control clones, but more densely than controls (Figure 5D,F,H; see Additional file 2, FigureS2), suggesting that not only are dendrites specified, but they also retain their same character. We did observe a few glomeruli that were innervated more often in the bazooka LOF clones than in the controls. The DM1, DP1l and VL2a glomeruli contained dense arborizations in at least 20% of the bazooka LOF clones, whereas the DA4, DL5, VA1lm, VL2p, VM7, VP1-3 and SOG glomeruli had increased arbors in approximately 10% of the bazooka LOF clones (see Additional file 2, Figure S2). However, it was difficult to determine if this innervation pattern is obscured in the wild types by the multiglomerular projections more common to control clones.
In the distal SAT, terminal arbors of the mutant BAla1 lineage branched into the correct vicinity of the lateral horn compared with control clones (Figure 5I,J), even though branches into the dorsal lateral horn derived from axons that traveled into the iACT. In the BLD5 lineage, both proximal and distal projections in bazooka LOF clones obeyed medullar boundaries similar to the control clones (see Figure 4G-H). Taken together, the data suggest that neurites with dendritic and axonal morphology are generated at their normal positions in BAla1 and BLD5 bazooka LOF clones. By contrast, the DALv2 clones obtained had ectopic proximal projections with bulbous morphology, resembling axonal endings (Figure 4D, arrow). It is noteworthy that both BAla1 and BLD5 lineages are PD-type, whereas the DALv2 lineage is C-type. Therefore, we cannot eliminate the possibility that bazooka is required differently by different lineage types in the establishment of dendrite versus axon.
Baz is required intrinsically for axon guidance of the BAla1 SAT
Par6 is required for BLD5 and DALv2 morphology, but not BAla1 or BAmv1
In both bazooka and par6 LOF BLD5 clones, the cell number was slightly larger than that of control clones. To verify that an increase in neuron number was not the basis for the increased number of projections, we plotted the cell number of each clone against the number of axons in the medulla. Although we did find an overall increase in clone size, comparing clones of only the same number (around 40 cells) still showed an increase in the number of distal extensions (see Additional file 3, Figure S3). Furthermore, if projection number into the medulla were directly proportional to cell number, we would expect the control clone containing approximately 60 cells to have an increased number of projections into the medulla, which it did not.
To determine if the increased number of distal extensions in the bazooka and par6 LOF clones was significant, we compared clones with a similar clone size (between 30 and 50 neurons) using a paired Student's t-test. The increased number of axons projecting into the medulla was significant for both the bazooka (P = 0.0018) and par6 (P = 0.0114) LOF clones.
In this study, we investigated the in vivo function of the Par-complex proteins, Par3/Baz and Par6, during neural development. Using MARCM and lineage-specific visualization, we investigated BAla1, BAmv1, DALV2 and BLD5 lineage morphologies in the absence of Bazooka and Par6 proteins. Our main method was to use a multilineage approach to explore the in vivo role of Par-complex proteins during axon growth and guidance. The mushroom body lineages have traditionally served as 'test' lineages when studying gene function in the Drosophila brain; however, the multilineage approach used in this study highlights the diverse functions of a protein complex between individual lineages.
Bazooka lineage-dependent localization and function
Par3/Bazooka is a highly conserved gene found in both vertebrate and invertebrate species. In epithelial cells and neuroblasts, Par3/Bazooka localizes to the apical membrane, where it mediates spindle orientation, thereby establishing cellular polarity and assisting asymmetric cell division [9–13]. In post-mitotic hippocampal neurons, a cell type that no longer requires maintenance of asymmetric division, mammalian Par3 specifically localizes to the axon in vitro [4, 5]. The dual use of a protein in polarized mitotic cells and in post-mitotic environments is an interesting area of exploration; however, little is known about the expression, localization or function of neuronal Par3 in vivo.
In the present study, we used both PD-type (BAla1 and BLD5) and C-type branching lineages (BAmv1 and DALv2) to study Bazooka localization and function. We found that the localization pattern of Baz:GFP in individual neural lineages correlated with bazooka LOF phenotypes. For example, larval BAla1 SATs localized Bazooka to the growth cone and exhibited axon-guidance defects in mutant bazooka clones. By contrast, BAmv1 and DALv2 SATs showed uniform distribution of ectopic Bazooka and subsequently had diffuse branching and neurite morphology defects along the length of the SAT upon Bazooka elimination.
It is important to note that we used single-copy Baz:GFP analysis when studying the localization of Bazooka in individual lineages. Subsequent experiments showed that two copies of UAS-Baz were required to induce morphologic changes in the BAla1 and DALv2 lineages (Figure 7). Therefore, it is likely that the gross morphology of the lineage was not disturbed while Bazooka localization was investigated. Taken together, our data suggest that Bazooka is used in a lineage-dependent manner depending on the ultimate morphology each lineage develops.
Autonomous versus non-autonomous Bazooka function in neurons
The similarity between Bazooka localization to the growth cone of the BAla1 SAT and that of Par3 localization to the axon tip in cultured hippocampal cells is intriguing. Therefore, we focused on the BAla1 lineage to study the in vivo function of bazooka in neurons. Given that bazooka is expressed in neuroblasts and most, if not all, neurons (including the GMC precursors), the role of this gene in BAla1 SAT guidance has the potential to be either cell-autonomous or non-autonomous in the neuron. Based on the autonomous role of Bazooka during cultured hippocampal neuron development and its known functions during in vitro cell migration, we hypothesized that bazooka would also play an autonomous role in vivo. Several lines of evidence suggested that Bazooka is an autonomous factor regulating neural morphology. First, re-expression of Bazooka in the post-mitotic BAla1 neurons significantly restored BAla1 SAT guidance in mutant clones. Second, overexpression of Bazooka in only post-mitotic BAla1 neurons resulted in additional misguidance phenotypes, suggesting that tightly controlled balance of bazooka expression is required within the neuron. Third, bazooka was expressed within the post-mitotic neurons, and ectopic Bazooka:GFP entered the axon and accumulated at the growth cone, suggesting the presence of cell-autonomous machinery that actively shuttles Bazooka to specific sites in the BAla1 neurons.
Bazooka regulates directional axon extension
The idea that polarity proteins can affect directional migration of the growth cone in vivo is consistent with cell migration studies in vitro. Par-complex members are required at the leading edge of cultured MDCK11, keratinoctyes and HeLa cells to regulate directional migration [17–19]. It is tempting to speculate that bazooka has a role in regulating cytoskeletal scaffolding during directional growth-cone guidance in Drosophila BAla1 neurons. In cultured rat hippocampal neurons, LIMK1, the kinase that phosphorylates the actin binding protein Cofilin, directs Par3 and Par6 to the growth cone and accelerates axon formation . Furthermore, mammalian Par3 associates with LIMK2 during epithelial tight-junction formation . Rac1 offers a tempting link between the Par complex, LIMK signaling and cytoskeletal rearrangement. Rac1 serves as an accessory to the Par complex [34–36], and can stimulate LIMK activity to regulate cytoskeletal rearrangement .
In contrast to cytoskeletal rearrangement, bazooka may instead function during signal transduction within the BAla1 neurons. Shrana and colleagues found that a balance between Wnt and fibroblast growth factor signaling controls axon retraction from the optic medulla in BLD5 neurons. The Wnt signal transducer Disheveled promotes axon differentiation in cultured hippocampal neurons by regulating aPKC, the binding partner for Par3 and Par6 . Whether bazooka regulates the cellular machinery that allows for cytoskeletal rearrangement or serves as a mediator in signal transduction is an interesting area for further investigation.
The Par complex acts in a lineage-dependent manner
Regardless of the mode of action of bazooka, its function does not seem to be equal in all lineages. The localization of ectopic Bazooka protein is not uniform across lineages, and bazooka null mutations generate SAT-dependent phenotypes, suggesting a differential requirement for Bazooka between individual SATs. Previous work  concluded that Par-complex proteins, including Baz, are not involved in establishing neuronal polarity, that is, distinction of dendritic versus axonal domains, in the lineages of the mushroom body. Our findings support this conclusion, as bazooka and par6 mutant clones still had discrete dendritic and axonal arborizations. The fact that loss of Baz and other Par-complex members apparently caused no structural abnormalities in the mushroom body suggests that these lineages do not require the Par complex for normal morphogenesis, which is not unexpected, given the differential requirement in other lineages analyzed in this study.
We found that par6 null mutations affected some SATs more severely than others, suggesting that the Par complex itself may act in a lineage-dependent manner. Because Bazooka has the ability to localize in some cells independently of the Par complex , it is possible that Bazooka has different modes of action depending on the morphologic needs of the neuron. We speculate that Bazooka acts independently from the Par complex during guidance of the BAla1 and BAmv1 SATs, where par6 LOF seems to have no effect; however, the similarity between bazooka and par6 LOF phenotypes in the DALv2 and BLD5 lineages points to the possibility that these neurons utilize the polarity proteins as a complex. Preliminary analysis of clones mutant for aPKC, randomly induced by the pan-neuronal driver elav-Gal4, yielded structural abnormalities in a number of lineages (SS and VH, unpublished data). The involvement of this and other Par-complex members in lineage morphogenesis awaits further study.
We have shown that Bazooka is expressed throughout the larval post-mitotic neurons, is transported to particular domains of the axon in a lineage-specific manner, and is required for branching regulation and axon guidance in correlation with its lineage-dependent localization patterns. BAla1 SAT guidance abnormalities in bazooka LOF clones could be rescued by post-mitotic specific re-expression of Bazooka protein, whereas overexpression of Bazooka in post-mitotic BAla1 neurons resulted in additional guidance phenotypes. Finally, we found that par6 LOF clones phenocopied bazooka LOF phenotypes in some, but not all lineages, suggesting a lineage-dependent use of the polarity proteins as a functioning complex.
Based on all the data, we speculate that bazooka acts in a cell-autonomous, lineage-dependent manner to control overall SAT morphology by mediating axon branching dynamics (in C-type lineages) or by steering axons into appropriate tract systems (in PD-type lineages) as they respond to targeting signals in the brain.
We are grateful to Drs C. Doe and A. Prokop for providing us with fly stocks and to Dr A. Wodarz for giving us antibodies. This work was supported by NIH Grant RO1 NS29357-15 to VH and the Ruth L. Kirschstein National Research Service Award GM007185 to SS.
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