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Curr Biol. Author manuscript; available in PMC 2009 May 20. Published in final edited form as: Published online 2008 May 8. doi: 10.1016/j.cub.2008.04.033. | PMCID: PMC2474551 NIHMSID: NIHMS52283 |
Spatial regulation of nanos is required for its function in dendrite morphogenesis Jillian L. Brechbiel and Elizabeth R. Gavis* Department of Molecular Biology, Princeton University, Princeton, NJ 08544 Spatial control of mRNA translation is a well established mechanism for generating cellular asymmetries and for functional specialization of polarized cells like neurons. A requirement for the translational repressor Nanos (Nos) in the Drosophila larval peripheral nervous system (PNS) implicates translational control in dendrite morphogenesis [ 1]. Nos was first identified by its requirement in the posterior of the early embryo for abdomen formation [ 2]. Nos synthesis is targeted to the posterior pole of the oocyte and early embryo through translational repression of unlocalized nos mRNA coupled with translational activation of nos mRNA localized at the posterior pole [ 3, 4]. Mutations that abolish nos localization prevent abdominal development whereas de-repression of unlocalized nos mRNA suppresses head/thorax development, indicating that spatial regulation of nos is essential for anterior-posterior patterning [ 3, 5]. The observation that both loss and overexpression of Nos affect dendrite branching complexity in class IV dendritic arborization (da) neurons suggests that nos might also be regulated in these larval sensory neurons [ 1]. Here we show that localization and translational control of nos mRNA are essential for late stages of da neuron morphogenesis. RNA-protein interactions that regulate nos translation in the oocyte and early embryo also regulate nos in the PNS. Live imaging of nos mRNA shows that the cis-acting signal responsible for posterior localization in the oocyte/embryo mediates localization to the processes of class IV da neurons, but suggests a different transport mechanism. The need to target nos mRNA to the processes of da neurons may reflect a requirement for Nos protein in controlling translation locally within dendrites. Nos is Required in Da Neurons to Maintain Dendrite Complexity Da neurons, which innervate the larval epidermis, can be divided into four classes based on the complexity of their dendritic arbors, with class IV being the most highly branched [ 6]. These neurons elaborate primary and secondary branches during the first instar stage of larval development. By the second instar stage, higher order branches extend to completely cover the larval body wall [ 7]. Complete, nonredundant coverage or “tiling” of the epidermis by class IV da neurons is maintained throughout larval development [ 8]. Mutation of nos results in a reduction in the number of higher order branches of class IV da neurons without affecting the morphology of the main branches [ 1]. This decreased branching complexity could reflect an early role for nos in the initial elaboration of the dendritic branches or a later role in maintaining coverage of the receptive field during larval growth. To distinguish between these possibilities, we examined the morphology of nos mutant class IV da neurons at different larval stages. In these, and all subsequent experiments, class IV da neurons are marked by mCD8:GFP, expressed using the GAL4477 driver [ 9]. Branching complexity was monitored by quantitation of branch termini (see Supplemental Experimental Procedures and legend). From the first larval instar through the early third instar stage, da neurons in wild-type larvae, nos mutant larvae, and nos mutant larvae carrying a genomic nos transgene, gnos [ 3], show no significant difference in branching complexity ( and data not shown). Morphological defects are first detected at the late third instar stage, when a significant reduction of higher order branching is observed in nos mutant da neurons as compared to wild-type neurons (). Whereas terminal branch density decreases slightly as body size increases from early to late third instar stages in wild-type larvae, the density of terminal branches decreases dramatically in nos mutant larvae (). Wild-type branching is restored in nos mutant larvae by addition of gnos, which includes native transcriptional regulatory sequences required for nos expression and rescues all nos mutant embryonic phenotypes [ 3, 10] (). These results indicate that Nos is not required for the initial elaboration of dendritic branches but instead plays a role at later stages of development, possibly by maintaining existing branches or promoting new branch extension during larval growth. nos is Localized to the Processes of Da Neurons Localized translation of nos required for embryonic patterning is achieved through a combination of mRNA localization and translational control. To determine if nos is spatially regulated in da neurons, we analyzed the distribution of nos mRNA by modifying a fluorescent labeling method previously used to investigate the mechanism of nos mRNA localization during oogenesis [ 4]. In this method, a fusion between bacteriophage MS2 coat protein (MCP) and either GFP or RFP is tethered to nos mRNA bearing 6 stem-loop binding sites for MCP [ nos-(ms2)6]. Here, we have improved detection of nos by introducing 18 MCP-binding stem-loops [ nos-(ms2)18]. The nos-(ms2)18 transgene behaves indistinguishably from gnos and the previously described nos-(ms2)6 transgenes in the oocyte and early embryo (K. Forrest and E.R.G., unpublished). To label nos-(ms2)18 RNA specifically in da neurons, we expressed MCP-RFP under UAS control using GAL4477 in larvae carrying the nos-(ms2)18 transgene. In neurons from control larvae that express MCP-RFP without nos-(ms2)18 mRNA, RFP fluorescence is largely confined to the nucleus due to a nuclear localization signal engineered in MCP-RFP that targets unbound MCP-RFP to the nucleus (). By contrast, RFP-labeled nos-(ms2)18 mRNA ( nos* RFP) can be detected in the cell body and in particles that are distributed along the dendrites and axons of class IV da neurons (). Analysis of nos* RFP throughout larval development showed that localization of nos to the processes of da neurons can first be detected early at the third instar stage (data not shown). We have not been able to confirm localization of native nos mRNA in da neurons by in situ hybridization methods, most likely due to a combination of low transcript abundance and high background from the underlying muscle tissue. However, we have previously shown that fluorescently labeled nos mRNA is a valid proxy for native nos mRNA in the oocyte and embryo [ 4]. Moreover, the correlation between dendritic localization of nos* RFP and its ability to rescue the nos mutant dendritic branching defect, described below, gives us confidence that it recapitulates the distribution of native nos in these neurons. The nos 3′UTR is Required for Efficient nos Localization in the PNS Posterior localization of nos in the oocyte and early embryo is mediated by a complex cis-acting localization signal in the nos 3′ untranslated region (3′UTR) comprising multiple, partially functional localization elements [ 11]. To test whether the same sequences direct dendritic localization of nos in da neurons, we analyzed the distribution of RFP-labeled nos–(ms2)18 RNAs bearing 3′UTR deletions ( Figure S1A). Deletion of the entire localization signal ( nosΔ LS) or three of the four localization elements ( nos+ 1), respectively, abolishes or severely reduces posterior localization of nos in the oocyte and embryo [ 11]. Both deletions also compromise localization to the processes of da neurons ( and data not shown). Quantitation of nos* RFP particles shows reduced accumulation in dendrites of larvae expressing nos+ 1-(ms2)18 mRNA relative to larvae expressing nos-(ms2)18 mRNA, whereas no significant difference is detected within the cell body (). In contrast, the distribution of RFP-labeled nos+ 2- (ms2)18 mRNA is similar to that of nos-(ms2)18mRNA (). This RNA lacks two of the four localization elements but retains the nos +2 element, which confers near wild-type localization in the embryo [ 11]. The nos+ 1-(ms2)18 and nos+ 2-(ms2)18 transcripts are present at comparable levels in da neurons as determined by RT-PCR ( Figure S2) and similar results were obtained for two independent lines of each transgene (data not shown), indicating that the observed difference in localization to neuronal processes is not likely due to a difference in expression or stability. Thus, the same sequences that mediate posterior localization of nos at earlier developmental stages target nos to the processes of class IV da neurons. This result suggests that one or more factors that recognize this localization signal to mediate localization during oogenesis may be used again for dendritic localization. Localization of nos is Required for its Function in the PNS Since posterior localization of nos is essential for its function in embryonic development, we investigated whether dendritic localization of nos is also required for its function in the larval PNS. The nos-(ms2)18, nos+1-(ms2)18 and nos+2-(ms2)18 transgenes were introduced into nos mutant larvae and assayed for their ability to rescue the nos mutant dendritic defect. All three transgenes include sequences required for nos translational regulation (see below) and none of these transgenes on its own affects dendrite branching complexity (data not shown). Class IV da neurons in nos mutant larvae carrying either the nos-(ms2)18 or nos+2-(ms2)18 transgene exhibit nearly wild-type dendritic branching, indicating that both transgenes are able to rescue the nos mutant phenotype (). In contrast, the nos+1-(ms2)18 transgene fails to rescue, as larvae show reduced branching complexity (). These results indicate that the localization of nos to class IV da neurons is required for nos function in dendrite morphogenesis. Because currently available anti-Nos antibodies are not adequate to detect Nos protein in da neurons (our data, also see Ref. [ 1]), we cannot show definitively that nos mRNA localization leads to local production of Nos protein. However, the correlation between the localization to neuronal processes and the ability to rescue the nos mutant branching defect revealed by the nos+ 1-(ms2)18 and nos+ 2-(ms2)18 mRNAs provides strong evidence that nos mRNA localization plays a critical role by targeting synthesis of Nos to dendrites. Live imaging of nos mRNA Particle Movement in Da Neurons Although most mRNAs are thought to be transported as particles along cytoskeletal elements by motor proteins, nos accumulates at the posterior of the oocyte by a passive diffusion and entrapment mechanism [ 4]. As a first step toward investigating the mechanism of nos localization in da neurons, we performed time lapse imaging of nos* RFP in da neurons of intact larvae at high magnification and time resolution. Control neurons expressing only MCP-RFP contain few RFP-labeled particles outside of the cell body and these particles rarely exhibit movement ( Movie S1). In contrast, in neurons expressing nos* RFP, dynamic particles are readily detected in the cell body and processes ( and Movie S2). Photobleaching of RFP that occurs at the requisite high image capture rates and the potential for tissue damage limits our time sequences to ≤90 sec. During these short periods, we observe particles traveling with linear trajectories, in both anterograde and retrograde directions along the neuronal processes, and in some cases, individual particles exhibit bi-directional movement (; Movie S2). By analyzing sustained particle runs in a single direction (average run distance = 4.1 μm; see Supplemental Experimental Procedures) within the dendrites of five neurons from three independent larvae, we calculated a mean average dendritic particle velocity of 0.56 μm/sec (range=0.21–0.97 μm/sec, n=40). This value is similar to those we have observed, using the same labeling method, for dynein-dependent transport of bicoid ( bcd) mRNA in the Drosophila oocyte [ 12] and similar rates have been observed for microtubule-dependent transport of ribonucleoprotein particles in the dendrites of cultured hippocampal neurons [ 13– 16]. Like nos, these dendritic RNA-containing particles exhibit bi-directional movement. The generation of brighter and more photostable MCP fusion proteins that permit visualization of particles over longer time periods and in various mutant backgrounds will enable us to determine how these complex particle dynamics lead to accumulation of RNA in dendrites. Whereas localization of nos during oogenesis occurs by diffusion and entrapment [ 4], the trajectories and velocities exhibited by dendritic nos particles are characteristic of cytoskeletal-based transport. Analysis of microtubule polarity in da neurons indicates that the majority of microtubules are oriented with their minus ends distal to the cell body [ 17]. Although individual da neuron subclasses were not distinguished in this study, the observations suggest that transport of nos mRNA particles into dendrites utilizes dynein. nos RNA injected into blastoderm embryos exhibits microtubule-dependent apical localization characteristic of pair-rule transcripts, whose transport is dynein-mediated [ 18, 19]. Since endogenous nos mRNA is not apically localized, the significance of such transport has been unclear. Our results suggest that the ability of nos to engage dynein-dependent transport machinery is indeed relevant to its role in the PNS. Regulation of Dendrite Morphogenesis by Glo and Smg Translational activation of nos at the posterior pole is tightly coupled to translational repression of unlocalized nos mRNA to prevent accumulation of Nos in the anterior of the embryo, where Nos suppresses anterior development [ 5]. Since nos localization during oogenesis is inefficient, this linkage is essential to silence nos mRNA that remains distributed throughout the bulk cytoplasm [ 20]. Translational repression of nos mRNA is mediated by a structural motif, the translational control element (TCE), within the nos 3′UTR [ 21– 23] ( Figure S1B). TCE function requires the formation of two stem-loops, designated as II and III, that have temporally distinct activities [ 24, 25]. Whereas stem-loop III mediates repression of nos during oogenesis, through its interaction with Glorund (Glo), stem-loop II is responsible for repression of nos in the early embryo, through its interaction with a different repressor, Smaug (Smg) [ 26– 28]. Replacement of the nos 3′UTR by α-tubulin 3′UTR sequences ( nos-tub3′ UTR) abolishes nos localization and translational repression, leading to unrestricted synthesis of Nos and defects in anterior development [ 5]. GAL4 mediated overexpression of a UAS-nos-tub3′ UTR transgene in class IV da neurons is also deleterious, causing decreased branching complexity. This overexpression phenotype is ameliorated by reinsertion of the nos TCE [ 1]. The observation that both loss and overexpression of nos cause similar defects indicates that although nos is required for dendrite morphogenesis, the level of Nos protein must be carefully modulated in da neurons. Moreover, the ability of the TCE to suppress the toxicity of nos mRNA overexpression in da neurons suggests that it may normally function to control Nos levels in the PNS. We therefore sought to determine whether endogenous nos is regulated by the TCE in da neurons. Ectopic expression studies have identified several additional somatic cell types where the TCE can repress translation, including neuroendocrine cells and the dorsal pouch epithelium [ 29, 30]. However, TCE function in the dorsal pouch does not depend on the Glo or Smg binding sites, but requires a distinct sequence motif with homology to the Bearded (Brd) box [ 29]. Mutation of the Brd box-like motif does not abrogate the ability of the TCE to suppress excess nos activity in da neurons (data not shown). Consequently, to determine whether endogenous nos mRNA might be regulated by the TCE, we first analyzed da neurons in glo and smg mutant larvae. Larvae mutant for glo or smg survive until third instar stage, permitting us to examine the effect of eliminating either repressor on dendrite morphology of da neurons. Compared to wild-type class IV da neurons, glo mutant larvae show a significant decrease in the number of higher order dendritic branches as reflected by a decreased number of terminal dendritic processes (). Because glo mutant larvae exhibit additional defects (J.L.B. and E.R.G., unpublished), we disrupted glo function specifically in class IV da neurons either by using GAL4477 to express a UAS-gloRNAi transgene or by using the MARCM method [ 31] to generate mosaic animals. In both cases, glo mutant da neurons show decreased branching complexity (). Mutation of smg or GAL4477-mediated overexpression of a UAS-smg transgene also causes loss of high order branches (). Larvae doubly mutant for glo and smg do not show a more severe phenotype than larvae mutant for either gene alone (), suggesting that each repressor contributes independently. Thus, defects due to loss or overexpression of the repressors are consistent with defects caused by loss or overexpression of nos. Due to the aforementioned inadequacy of anti-Nos antibodies, we have not been able to monitor changes in Nos protein levels in glo and smg mutant da neurons. However, when combined with the analysis of Glo and Smg binding site mutations presented below, these results strongly support a role for glo and smg in regulation of nos for dendrite morphogenesis. TCE-dependent Translational Regulation of nos is Required for Dendrite Development In the oocyte, Glo binds specifically to the distal double-stranded helix of TCE stem-loop III (the Glo Recognition Helix or GRH; Figure S1B) [ 27]. In the embryo, Smg interacts with nos TCE stem-loop II, via nucleotides within the loop designated as the Smg Recognition Element (SRE; Figure S1B) [ 22, 24]. A second SRE located downstream of the TCE in the nos 3′UTR appears to act redundantly [ 22, 23]. To determine whether the defects observed in glo and smg mutant da neurons are due to loss of TCE-mediated repression, we tested whether mutation of the nos GRH or SREs produces a similar phenotype. Mutations that disrupt both SREs (SREs −), the binding site for Glo (GRH −), or the SREs and GRH (SREs −GRH −) together ( Figure S1B) were introduced into the gnos transgene. The resulting gnosSREs−, gnosGRH−, a nd gnosSREs−GRH− transgenes all produce mRNAs that show wild-type localization in the early embryo but whose translation is not restricted to the posterior pole (Ref [ 10]; E.R.G., unpublished). When compared to larvae expressing the wild-type gnos transgene , branching complexity is significantly reduced in da neurons of larvae expressing gnosSREs−, gnosGRH−, a nd gnosSREs−GRH− transgenes (). Moreover, each of these transgenes behaves similarly to the gnos-tub3′ UTR transgene, which lacks the entire nos 3′UTR, indicating that mutation of the GRH and/or SREs is sufficient to disrupt nos regulation in the PNS. Together, these results show that TCE-mediated regulation of nos in da neurons is essential for dendrite morphogenesis. Furthermore, the finding that the same phenotype is produced by either eliminating the repressors or mutating their binding sites provides strong evidence that this regulation is mediated by Glo and Smg. In many cell types, protein synthesis is spatially regulated through the transport of translationally silent mRNAs and activation of these mRNAs at the target destination. Linkage of translation and localization serves not only to prevent premature accumulation of nos during transit to the oocyte posterior, but to silence the large pool of nos that remains unlocalized due to inefficient posterior localization [ 20]. We cannot yet distinguish whether localization of nos in da neurons is similarly inefficient or whether translational repression of nos serves primarily to repress translation during transport. However, the deleterious effect on dendrite morphogenesis caused by mutations that disrupt TCE function show that, as for maternally synthesized nos mRNA, localization alone is not sufficient to modulate its activity. nos plays an important role in dendrite morphogenesis and we show that nos function in da neurons requires spatial regulation of nos mRNA. Cis-acting sequences and two cognate factors that control nos mRNA localization and/or translation in the oocyte and early embryo are redeployed during larval stages to regulate localization and translation of nos in da neurons. Localization of nos mRNA to the processes of class IV da neurons is essential for dendritic branching. For the first time, we observe movement of RNA particles in neurons of intact animals and analysis of nos mRNA particle movement suggests that nos localization occurs by different mechanisms depending on cellular context. Taken together, our results support a role for Nos as a local regulator of translation in the PNS. In the early embryo, Nos functions in a complex with the RNA-binding protein Pumilio (Pum) to repress hunchback mRNA translation, thereby promoting abdominal development [ 32, 33]. Whereas Pum is produced throughout the embryo [ 33, 34], restriction of Nos synthesis to the posterior limits the spatial domain of the repressor complex. Mutations in nos and pum produce similar defects in dendrite morphogenesis, suggesting that Nos and Pum also act together to repress translation in da neurons [ 1]. Thus, spatial regulation of nos may serve a similar function in the PNS as it does in the early embryo, by restricting the activity of the Nos/Pum repressor complex to dendrites. We are grateful to K. Forrest for initiating this project by generating and characterizing the nos-(ms2)18 and UAS-MCP-RFP transgenic lines, T. Weil for assistance with particle movement analysis and preparation of the Supplemental Movies, A. Becalska for generation of nos+2-(ms2)18 transgenic lines, and N. Jeurkar for generation of UASp-smg transgenic lines. We also thank Y.N. Jan and R. Wharton for fly stocks, B. Ye, U. Mayor, and W. Grueber for technical advice, J. Goodhouse (Princeton) and A. Sossick (Gurdon Institute) for microscopy assistance, and B. Ye, T. Weil, and I. Clark for comments on the manuscript. E.R.G. thanks her sabbatical host A. Brand and members of the Brand lab for hospitality during this work. 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