Synaptic transmission from Drosophila photoreceptors to lamina neurons requires recycling of histamine neurotransmitter. Synaptic histamine is cleared by uptake into glia and conversion into carcinine, which functions as transport metabolite. How carcinine is transported from glia to photoreceptor neurons remains unclear. In a targeted RNAi screen for genes involved in this pathway, we identified carT, which encodes a member of the SLC22A transporter family. CarT expression in photoreceptors is necessary and sufficient for fly vision and behavior. Carcinine accumulates in the lamina of carT flies. Wild-type levels are restored by photoreceptor-specific expression of CarT, and endogenous tagging suggests CarT localizes to synaptic endings. Heterologous expression of CarT in S2 cells is sufficient for carcinine uptake, demonstrating the ability of CarT to utilize carcinine as a transport substrate. Together, our results demonstrate that CarT transports the histamine metabolite carcinine into photoreceptor neurons, thus contributing an essential step to the histamine–carcinine cycle.https://doi.org/10.7554/eLife.10972.001
Photoreceptors are light-sensitive neurons in the eyes of the fruit fly Drosophila that form connections with other neurons in the fly’s brain. At these connections, which are called synapses, the photoreceptors continuously release a chemical called histamine.
Photoreceptors will release more or less histamine depending on changes in light intensity, but always tend to release more histamine than they can produce themselves from scratch. This means that the visual system in Drosophila relies on a pathway that recycles histamine. That is to say, glial cells (which support the activity of the neurons) remove the chemical from synapses and return it to the photoreceptor neurons in a slightly modified form called “carcinine”. The photoreceptors then quickly convert the chemical back into histamine, ready to be released.
Stenesen et al. set out to identify the proteins that support this recycling pathway, and started by screening around 130 genes that encode transporter proteins for potential roles in histamine recycling. This screen identified a gene encoding a protein that was named CarT. This protein transports carcinine, the modified version of the histamine neurotransmitter.
Stenesen et al. show that the photoreceptor neurons make the CarT protein and need this protein to take up the carcinine released by the supporting glial cells. Without CarT, photoreceptor neurons cannot transmit visual information, and so mutant flies in which the gene for CarT is deleted are blind. Follow-up studies related to this work could involve identifying the transporters that move histamine and carcinine in and out of the glia cells, and exploring what other neurons and behaviors in fruit flies rely on CarT’s activity.https://doi.org/10.7554/eLife.10972.002
Histaminergic neurotransmission plays an important role in a variety of mammalian and invertebrate behavioral processes and contributes to the regulation of arousal, sleep and circadian rhythms (Nall and Sehgal, 2014; Panula and Nuutinen, 2013). Defects in histaminergic signaling are linked to multiple neurodegenerative diseases, depression and Tourette’s syndrome (Panula and Nuutinen, 2013; Shan et al., 2015; Castellan Baldan et al., 2014). Synaptic clearance and recycling of monoamine neurotransmitters, including serotonin and dopamine, depend on transporters that promote uptake into the presynaptic terminals or the surrounding glia (Torres and Amara, 2007). For histamine, such transporter activities have been documented in mammalian and invertebrate glia (Yoshikawa et al., 2013; Edwards and Meinertzhagen, 2010). In the Drosophila visual system, histidine decarboxylase (Hdc) generates histamine in photoreceptor neurons (Burg et al., 1993). Light-induced depolarization of these neurons (Wang and Montell, 2007) promotes synaptic release of histamine, which opens histamine-gated chloride channels on postsynaptic L1 and L2 lamina neurons, triggering their hyperpolarization (Pantazis et al., 2008). These postsynaptic voltage changes can be followed with electroretinograms (ERGs) that reveal ON and OFF transient peaks coinciding with initiation and cessation of the light source (Alawi and Pak, 1971; Heisenberg, 1971). In addition to identifying mutants that interfere with presynaptic release (Kim et al., 2012), this phenotype has also contributed to the genetic dissection of histamine recycling (Edwards and Meinertzhagen, 2010). Synaptic histamine is taken up into epithelial glia that completely envelope photoreceptor synapses (Meinertzhagen and O'Neil, 1991). Within these glia, histamine is modified by the Ebony-catalyzed condensation with β-alanine (Richardt et al., 2002; Borycz et al., 2002; Hartwig et al., 2014; Richardt et al., 2003). The reaction product carcinine is transferred to photoreceptors, which recover histamine by Tan-catalyzed hydrolysis (Borycz et al., 2002; True et al., 2005; Wagner et al., 2007). This histamine–carcinine cycle (see below: Figure 4—figure supplement 1), reminiscent of the glutamate–glutamine cycle in the mammalian brain (Bröer and Brookes, 2001), is necessary to maintain visual neurotransmission (Borycz et al., 2005) and depends on the compartmentalization of glial Ebony and neuronal Tan (Stuart et al., 2007). Mutants for ebony or tan lack ON and OFF transients (Heisenberg, 1971; Hotta and Benzer, 1969; Chaturvedi et al., 2014), indicating that neither histamine synthesis in photoreceptor neurons by Hdc nor a putative direct re-uptake mechanism is sufficient to sustain neurotransmitter release at photoreceptor synapses (Ziegler et al., 2013). The identity of the transporters that facilitate glial uptake of histamine from the synaptic cleft and transport of its metabolite, carcinine, out of glia and into photoreceptor neurons remains a long-standing mystery, (Edwards and Meinertzhagen, 2010; Stuart et al., 2007; Romero-Calderón et al., 2007; 2008). Here, we show that the previously uncharacterized CG9317 gene, that we named carT, encodes a transporter responsible for uptake of carcinine into photoreceptor neurons. We demonstrate that CarT activity is a prerequisite for visual neurotransduction.
The Drosophila genome is estimated to contain 603 transmembrane transporters (Ren et al., 2007; Featherstone, 2011). To concentrate on those transporters with a higher probability of participating in histamine neurotransmitter recycling, we focused on families that contain individual members previously associated with neurotransmitter transport. This includes known serotonin, dopamine, gamma-aminobutyric acid, and glutamate neurotransmitter transporters in the solute-linked carrier (SLC) families SLC1 and SLC6, and other transporters in the SLC17, SLC18 and SLC22A families (César-Razquin et al., 2015). In addition, ATP-binding cassette transporters have been implicated in altered neurotransmitter distribution (Borycz et al., 2008). In Drosophila, these transporter families contain 137 members that we considered as candidates potentially involved in the histamine–carcinine cycle. To test their possible roles in photoreceptor neurons, we knocked down each candidate gene individually using Glass Multiple Response element (GMR)-Gal4 to drive double-stranded RNA expression in photoreceptors and evaluated visual signal transduction by ERG recordings.
The screen yielded a single transporter gene, CG9317, whose knockdown caused severely reduced ON and OFF transients (Figure 1A). To test the consistency of this result in multiple genetic backgrounds and confirm its specific requirement in photoreceptor neurons, we expressed the CG9317 RNAi transgene with two additional photoreceptor-specific Gal4 lines, longGMR-Gal4 (Wernet et al., 2003) and otd1.6-Gal4 (McDonald et al., 2010) and the pan-glial driver, repo-Gal4 (Sepp et al., 2001). ERG recordings indicated that CG9317 is necessary in photoreceptor neurons, but not glia, for proper histaminergic transduction in the visual system (Figure 1A–C). Of note, compared with wild type, none of these genotypes displayed significantly reduced sustained negative potentials ( Figure 1D), indicating that CG9317 knockdown did not affect overall photoreceptor health (Williamson et al., 2010). Based on these results and the findings presented below, we will refer to CG9317 as carcinine transporter, abbreviated carT.
To test whether carT is the causal gene, the knockdown of which is responsible for loss of ERG ON and OFF transient components, we generated null alleles by clustered regularly-interspaced short palindromic repeats (CRISPR)/Cas9-mediated mutagenesis (Gratz et al., 2013; Bassett et al., 2013; Yu et al., 2013). We isolated three individual CRISPR-induced deletions: 11 bp for carT16A, 26 bp for carT16B and 56 bp for carT43 (Figure 2A). Each of these mutations resulted in a frameshift within the first transmembrane domain (Figure 2B) followed by a premature stop codon within 17, 19 and 1 bp, respectively. All three carT alleles were homozygous viable and fertile, but lacked the ON and OFF transients, indicating that carT is required for visual signal transduction (Figure 2C,D). For further analysis, we focused on the allele with the largest deletion, carT43. To prove that loss of CarT function causes the ERG-phenotype in carT43 mutants, we tested whether it could be rescued by cell type-specific expression of the CarT transcript. When driven in carT43 mutant photoreceptor neurons by longGMR-Gal4, CarT restored ON and OFF transient components of ERG recordings (Figure 2C,D). By contrast, glial-specific expression of CarT failed to rescue ON and OFF transient defects (Figure 2C,D). To further probe CarT function, we generated a Myc-CarT transgene. This N-terminally tagged transporter was fully functional, as its expression in carT43 also rescued defects in ON and OFF transients (Figure 2C,D). Taken together, these data indicate that expression of CarT in photoreceptor neurons is necessary and sufficient for visual signal transduction.
To examine whether the disruption of visual neurotransmission in carT mutants alters visual behavior, we used a phototaxis assay (Benzer, 1967). Wild-type flies were naturally phototactic (Figure 2E). However, flies with defects in the synthesis of histamine (HdcMB07212) or its recycling (ebony1 or tan1) were randomly distributed between the lit and dark arms of a T-maze, consistent with a lack of phototactic preference due to their inability to detect light (Figure 2E). Similarly, phototactic behavior was severely reduced in carT43 flies (Figure 2E). Light preference of carT43 flies was restored by expression of wild-type CarT in photoreceptor neurons under control of longGMR-Gal4 (Figure 2F). Together, these results indicate that CarT expression in photoreceptor neurons is necessary and sufficient for behavioral aspects of normal vision and electrophysiological properties of visual transduction.
Interference with aspects of the histamine–carcinine cycle by different mutations causes distinct changes in the distribution of these two metabolites in the retina and lamina, although overall architecture of these tissues is not altered in carT, ebony, tan and Hdc mutants (Figure 3A–D) and references (Chaturvedi et al., 2014; Borycz et al., 2008). Consistent with their function in the histamine–carcinine cycle, characteristic increases in the levels of histamine in ebony1 (Figure 3C) and carcinine in tan1 heads (Figure 3D) were detected by antibody staining (Chaturvedi et al., 2014). When compared with wild type, carT43 heads displayed no discernable alterations in histamine staining intensity or distribution (Figure 3C). However, carcinine levels were elevated in carT43 lamina (Figure 3D, arrow) and medulla (arrowhead). Staining for carcinine in carT43 lamina partially localized to the glia visualized by repo-Gal4 driven UAS-mCD8::RFP (Figure 3E) suggested a build up of carcinine in the glia and the extracellular space in the lamina, consistent with a requirement of CarT in carcinine transport into photoreceptors. Notably, carcinine accumulation in carT43 brains was restored to wild-type levels by photoreceptor-specific expression of a Myc-CarT transgene (Figure 3D).
Within photoreceptors, the longGMR-driven Myc-CarT transporter was enriched in their axonal endings in the lamina (arrow in Figure 3B) and the distal retina (arrowhead in Figure 3B) indicating CarT may function near synaptic terminals and in neuronal cell bodies to facilitate perisynaptic and long-distance recycling, two pathways previously suggested (Chaturvedi et al., 2014; Borycz et al., 2012; Rahman et al., 2012). Endogenous CarT RNA expression is highly enriched in the eye (http://flybase.org/reports/FBlc0000157.html). To further examine endogenous CarT expression, we utilized CRISPR-induced deletions coupled with homology-directed repair to incorporate an in-frame insertion of tdTomato N-terminally to the CarT coding sequence (Figure 2B). ERG analysis of flies harboring one copy of this tdTomato-CarT over the nonfunctional carT43 allele displayed normal ON and OFF transient responses, indicating that the endogenous tdTomato-tagged CarT was fully functional (Figure 2C,D). This endogenous tdTomato-CarT was highly enriched within photoreceptor projections in the lamina and medulla (Figure 3F). Co-labeling with the glial Ebony (Figure 3G), or synaptic Bruchpilot and a 3xPax3-eGFP, which labels photoreceptor neurons (Figure 3H), indicates that CarT is present in photoreceptors near synaptic terminals (Figure 3H).
To determine whether the CarT transporter utilizes carcinine as a substrate, we developed an immunofluorescence-based carcinine transport assay. Full-length or internally truncated Myc-CarT were expressed in S2 cells that were probed by antibody staining for carcinine uptake. When cultured in standard Schneider’s medium, transfected S2 cells displayed no appreciable carcinine staining, indicating a lack of endogenous carcinine and sufficient specificity of the carcinine antibody in this context (Figure 4A and A’; quantified in D). When culture media was supplemented with carcinine (0.5 mM), cells expressing full-length Myc-CarT stained positively for carcinine, indicating its uptake in these cells. Importantly, neighboring untransfected cells (negative for the Myc epitope) lacked carcinine staining, despite being maintained in the same carcinine-supplemented medium as Myc-CarT positive cells (Figure 4B and B’). Furthermore, an internal deletion of 10 of the 12 transmembrane domains within CarT abolished carcinine uptake (Figure 4C and C’; quantified in D). Taken together, these data demonstrate CarT functions as a carcinine transporter.
Sequence comparison indicates that CarT is a member of the SLC22 family of transporters (Eraly et al., 2004) and together with other CarT-like transporters in invertebrates constitutes a distinct subfamily (Figure 2—figure supplement 1). Interestingly, OCT2 and OCT3, members of the closely related organic cation subfamily of SLC22A transporters, have been implicated in histamine uptake into human astrocytes (Yoshikawa et al., 2013) and the transport of histamine receptor antagonists (Koepsell, 2013). Many of the biochemically characterized members of the extended SLC22 family that are involved in the transport of neurotransmitters, exhibit overlapping substrate specificity providing transport redundancies (Koepsell, 2013). However, our data argue against such redundancy as carT null alleles efficiently blocks synaptic transmission dependent on the histamine–carcinine cycle (Figure 4—figure supplement 1). A role in this process has previously been suggested for the putative Na/Cl– dependent neurotransmitter/osmolyte transporter Inebriated (Stuart et al., 2007), possibly by directly transporting carcinine into photoreceptors (Gavin et al., 2007). No direct evidence for such a function has been reported, however, suggesting that Inebriated may indirectly support the histamine–carcinine cycle by promoting the long-distance recycling of β-alanine from photoreceptors to glia (Stuart et al., 2007; Chaturvedi et al., 2014; Borycz et al., 2012). An indirect role of Inebriated is also more consistent with its role in water homeostasis in the hindgut (Luan et al., 2015).
Here, we presented several lines of evidence that CG9317, which is highly expressed in heads, but not bodies (Eraly et al., 2004), encodes the carcinine transporter CarT. Heterologous expression of CarT in cultured cells was sufficient to facilitate carcinine uptake. This biochemical activity and the accumulation of carcinine in CarT lamina could be consistent with CarT facilitating export of carcinine from glia, or its import into photoreceptors. Strong support for the second possibility is provided by genetic experiments that reveal a requirement of CarT in photoreceptors, but not glia and the accumulation of carcinine in the lamina. CarT expression in photoreceptors is necessary and sufficient to sustain visual transduction, as indicated by ON and OFF transients as signatures of synaptic activity and by visual behavior. Together, these findings support a role of CarT as the transmembrane transporter responsible for the uptake of carcinine into photoreceptor neurons, a critical step in the histamine–carcinine cycle.
Histamine, similar to its impact on multiple behaviors in the mammalian brain (Nall and Sehgal, 2014; Panula and Nuutinen, 2013; Shan et al., 2015; Castellan Baldan et al., 2014), has been implicated in several circuits in the insect brain as well, including those controlling sleep, circadian rhythms and thermosensation (Nall and Sehgal, 2014; Buchner et al., 1993; Oh et al., 2013; Hong et al., 2006; Suh and Jackson, 2007). The identification of CarT’s role in the histamine–carcinine cycle will provide additional tools to further address the role of histaminergic circuits in these different behaviors.
Flies were maintained using standard conditions. Fly lines GMR-Gal4 (BL1104), longGMR-Gal4 (BL8121), repo-Gal4 (BL7415), ebony1 (BL1658), tan1(BL130), HdcMB07212(BL25260), UAS-mCD8::RFP (BL32218) were provided by the Bloomington Drosophila Stock Center. The otd1.6-Gal4 line (McDonald et al., 2010) was a gift from T. Cook (Cincinnati Children’s, Cincinnati, OH). The UAS-CG9317.RNAi line (VDRC KK101145) was obtained from the Vienna Drosophila Resource Center (VDRC). Other UAS-RNAi lines used for screening were obtained from either the VDRC or the Transgenic RNAi Project. CRISPR-mediated mutagenesis was performed via tools and protocols available from the O’Connor-Giles, Wildonger, and Harrison laboratories (www.flycrispr.wisc.edu). A germline mutation rate of 76.1% of injected flies was detected by polychromase chain reaction (PCR) amplification of the target region, slow ramp speed re-annealing, T7 endonuclease treatment, and polyacrylamide gel electrophoresis analysis of potential cleavage products (Gratz et al., 2013; Bassett et al., 2013; Yu et al., 2013). Exact lesions were characterized by sequencing of PCR products. Identified mutations were homozygous viable and crossed into a w+ background prior to ERG recordings and behavioral assays. To generate UAS-CarT transgenic flies, a CarT complementary DNA was obtained form the Berkeley Drosophila Genome Project, cloned into a modified pUASt vector, sequence verified, and injected into embryos (Rainbow Transgenics, Camarillo, CA) using standard methods. Endogenous tdTomato was tagged by dual-cut CRISPR-mediated excision of 532 base pairs, including the CarT start site, and introduction of a donor plasmid containing an in-frame tdTomato sequence with roughly 1 kb homology arms (Gratz et al., 2014). Homology-directed repair resulting in the td-Tomato insertion was detected by PCR amplification of the tdTomato insert, and proper in-frame insertion was verified by sequencing.
ERGs were recorded as previously described (Williamson et al., 2010). In brief, voltage measurements of immobilized female flies were recorded with electrodes containing 2M NaCl placed on the corneal surface and inserted into the thorax. Measurements were filtered through an electrometer (IE-210; Warner Instruments, Hamden, CT), digitized with a Digidata 1440A and MiniDigi 1B system, and recorded using Clampex 10.2 and quantified with Clampfit software (Molecular Devices, Sunnyvale, CA). Light pulses (1 s) were computer controlled (MC1500; Schott, Mainz, Germany).
For light-choice assays (Benzer, 1967), male flies were collected within 12 hr of eclosion and aged for 3–4 d. Flies were anesthetized briefly with CO2, transferred to empty culture tubes, and left to recover for 1 hr. For testing, a group of 20 flies was introduced into a T-maze apparatus and allowed to distribute for 20 s between a dark tube and a tube exposed to incandescent light. Each group was tested in triplicate. A light preference index was calculated using the equation, PI = (#Light- #Dark) / #total. For all genotypes, at least 100 flies were tested.
Fly heads were dissected in HL3 hemolymph-like solution (Stewart et al., 1994) to remove the proboscis and posterior cuticle, fixed for 4 hr in ice cold 4% 1-ethyl-3-(-3-dimethylaminopropyl) carbodiimide (wt/vol, Sigma, St Louis, MO) in 0.1 M phosphate buffer solution, washed overnight in 25% (wt/vol) sucrose in phosphate buffer (pH 7.4), embedded in optimal cutting temperature compound, frozen in dry ice, and sectioned at 20 μm thickness on a cryostat microtome (Hacker-Bright, Winnsboro, SC). Sections were incubated overnight with antibodies to histamine (1:1000, Sigma, St Louis, MO, cat# H7403 preabsorbed with 200 µM carcinine) or carcinine (1:1000, Immunostar, Hudson, WI, cat# 22939 preabsorbed with 200 µM histamine [Chaturvedi et al., 2014]). Other antibodies used include anti-Ebony (gift from Bernhard Hovemann [Richardt et al., 2002]), anti-Bruchpilot (nc82, Hybridoma Bank, Iowa City), anti-Myc (9E10, BAbCO, Richmond, CA), and anti-RFP (Rockland, Limerick, PA, cat# 600-401-379). Secondary antibodies were labeled with Alexa488 (1:500, Molecular Probes, Pittsburg, PA, cat# A-11008), Alexa568 (1:500, Molecular Probes, cat# A-11011), or Alexa647 (1:250, Molecular Probes, cat#A-21235). Where indicated, Topro-3 Iodide (Molecular Probes, T3605) was used to stain DNA. Images were captured with 20× NA 0.75 or 63× NA 1.4 lenses on an inverted confocal microscope (LSM510 Meta; Carl Zeiss, Oberkochen, Germany) at 21°C–23°C.
Because radioactive carcinine is not commercially available, we developed an immunofluorescence-based transport assay. Drosophila S2 cells were cultured using standard methods and transfected with plasmids containing Myc-tagged constructs as noted using the TransIT-2020 manufacturer’s protocol (Mirus, Madison, WI). Transfected cells were incubated with 0.5 mM carcinine for 24 hr prior to a 1 hr fixation in ice cold 4% 1-ethyl-3-(-3-dimethylaminopropyl) carbodiimide (wt/vol, Sigma) in 0.1 M phosphate buffer solution. Cells were then permeabilized in phosphate-buffered saline containing 0.3% Saponin, blocked in 5% normal goat serum, and incubated overnight with carcinine and Myc antibodies. Quantification was performed in ImageJ by normalizing the integrated density of the carcinine signal by that of the Myc signal.
CarT was identified as a SLC22 family member using BLASTpsi alignments against the NCBI non-redundant protein sequence database. Drosophila SLC22-related family members were identified from existing annotations on FlyBase and by running a BLASTp search with the CarT Isoform C peptide sequence against only Drosophila melanogaster (taxid:7227). Searches for individual organisms were performed using the following taxa identifiers on NCBI BLASTp suite: Homo sapiens (taxid:9606), Mus musculus (taxid:10090), Apis mellifera (taxid:7460). Additionally, previously identified mammalian SLC22 transporters were included (Koepsell, 2013; Zhu et al., 2015; Martin and Krantz, 2014). For preparation of multiple alignments, CLUSTAL Omega was used (http://www.ebi.ac.uk/Tools/msa/clustalo/) with default parameters (Sievers et al., 2011). Multiple sequence alignments were entered into Clustal W2 and phylogenies were generated using the Neighbor-joining clustering method with default parameters (Larkin et al., 2007). The resulting phylogenies were analyzed using Interactive Tree of Life (iToL; http://itol.embl.de), an online phylogeny tree viewer and editor (Letunic and Bork, 2011).
Statistical significance was determined using one-way analysis of variance (ANOVA) followed by Tukey’s or Bonferroni’s multiple comparisons using GraphPad Prism 6.
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Hugo J BellenReviewing Editor; Howard Hughes Medical Institute, Baylor College of Medicine, United States
eLife posts the editorial decision letter and author response on a selection of the published articles (subject to the approval of the authors). An edited version of the letter sent to the authors after peer review is shown, indicating the substantive concerns or comments; minor concerns are not usually shown. Reviewers have the opportunity to discuss the decision before the letter is sent (see review process). Similarly, the author response typically shows only responses to the major concerns raised by the reviewers.
Thank you for submitting your work entitled "The carcinine transporter CarT is required in Drosophila photoreceptor neurons to sustain histamine recycling" for peer review at eLife. Your submission has been favorably evaluated by K VijayRaghavan (Senior editor), Hugo Bellen (Reviewing editor), and two reviewers, one of whom David Krantz, has agreed to reveal his identity.
The reviewers have discussed the reviews with one another and the Reviewing editor has drafted this decision to help you prepare a revised submission.
The authors first performed an RNAi screen to knock down 132 transporter candidates and found that one – CG9317 – which they rename carT, disrupts ERGs a standard measure of signaling in the visual system. They determined that expression was required in photoreceptors but not glia, then confirm their findings using CRISPR/CAS-9 mutants in carT and genetic rescue with a cart transgenes. They back up their electrophysiological results with both behavioral assays demonstrating phototactic deficits and carcinine build-up in carT mutants, both rescued with a carT transgene. Finally they prove that carT transports carcinine into S2 cells as predicted. The paper by Stenesen et al. very convincingly shows that the CarT transporter is required for carcinine uptake, which in turn is a reaction product of histamine modification in glia cells that take up histamine from the synaptic cleft. With this discovery, the circle for release and reuptake of this neurotransmitter has been closed for the first time.
Minor points that we would like to see addressed:
Minor concerns include some difficulty in visualizing the label for carcinine and histamine in Figure 3. It seems likely that this could result from the relatively low resolution of the PDF. Nonetheless, the authors should ensure that the images will be easily interpreted in the final version on the manuscript.
The authors should also comment on the overall distribution of endogenous carT, and whether or not this is known. The model in Figure 4 indicates that carT localizes to photoreceptors but not glia and this is clearly supported by their RNAi data. However, it seems possible that carT could be expressed in other neurons in the CNs and perhaps play a role in other organs.
Additional, small changes that might improve the paper for the interested reader include a list of the genes that were probed in their RNAi screen, and a brief note about the phylogeny of SLC22A family in the fly. The authors state: "[…] our data argue against such redundancy for CarT as it efficiently blocks the histamine-carcinine cycle." Nonetheless, it would be nice to know if there are any similar fly orthologs with the potential to compensate for loss of carT.
I think it would be reasonable to ask the authors to provide better colocalization data for CarT in the synaptic region of the lamina to support their core argument. Ideally one would like to know whether CarT resides at the capitate projections, invaginations of glia into the photoreceptor terminals, but an immuno-EM study of this is beyond the scope of the present work. However, colocalization analysis with glia markers, active zone markers and pre- and postsynaptic cell markers at high resolution would be helpful.
Similarly, it would be helpful to see carcinine accumulations in the mutant indeed occurring the glia cells, as predicted by the model, to support the core argument. Again, this would only require higher resolution and more detailed immunohistochemical analysis.https://doi.org/10.7554/eLife.10972.010
- Helmut Krämer
- Drew Stenesen
- Andrew T Moehlman
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We would like to thank Drs. Hong-Sheng Li and Tao Wang for communicating results before publication, and Drs. Aylin Rodan, Anna Ziegler and Bernhard Hovemann and the Krämer lab for helpful comments and the Bloomington Stock Center for fly stocks, the Berkeley Drosophila Genome Project for producing DNA clones, the Drosophila Genomics Resource Center for their distribution. FlyBase provided important information used in this work. This work was supported by grants from the NIH (EY010199 and EY021922) to H. K., NIH training grant (5T32DA007290) to D.S., NSF Graduate Research Fellowship (1000176311) to A.T.M., and by core grant EY020799.
- Hugo J Bellen, Reviewing Editor, Howard Hughes Medical Institute, Baylor College of Medicine, United States
© 2015, Stenesen et al.
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