Drosophila gustatory projections are segregated by taste modality and connectivity
Peer review process
This article was accepted for publication as part of eLife's original publishing model.
History
- Version of Record published
- Accepted Manuscript published
- Accepted
- Received
- Preprint posted
Decision letter
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Marta ZlaticReviewing Editor; MRC Laboratory of Molecular Biology, United Kingdom
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K VijayRaghavanSenior Editor; National Centre for Biological Sciences, Tata Institute of Fundamental Research, India
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Stefanie HampelReviewer; University of Puerto Rico Medical Sciences Campus, Puerto Rico
Our editorial process produces two outputs: i) public reviews designed to be posted alongside the preprint for the benefit of readers; ii) feedback on the manuscript for the authors, including requests for revisions, shown below. We also include an acceptance summary that explains what the editors found interesting or important about the work.
Decision letter after peer review:
Thank you for submitting your article "Drosophila gustatory projections are segregated by taste modality and connectivity" for consideration by eLife. Your article has been reviewed by 2 peer reviewers, and the evaluation has been overseen by a Reviewing Editor and K VijayRaghavan as the Senior Editor. The following individual involved in the review of your submission has agreed to reveal their identity: Stefanie Hampel (Reviewer #1).
The reviewers have discussed their reviews with one another, and the Reviewing Editor has drafted this to help you prepare a revised submission.
The Reviewers agree that the paper provides new insight into morphologically distinct labellar gustatory projection subtypes and their connectivity on a synaptic level in Drosophila. The conclusions are well supported by data and rigorous analysis.
We would like to suggest the following revisions to improve the clarity and accessibility of the results to a general audience:
1) Improve the presentation of the results to make them visually more informative and striking. For example, an expansion of Figure 4 would be helpful whereby the dry connectivity map and diagram are integrated with a topographical/ "organotypic" and functional map. Can the projections in the SEZ (Figure 2) be correlated with the location of the sensory neurons in the labellum (based on light microscopy data), with respect to their molecular/modality/receptors?
2) Given that the authors did not reconstruct the entire GRN population it should be discussed that an additional unknown GRN class could have been missed.
Reviewer #2 (Recommendations for the authors):
My suggestions focus on the presentation of their data, and not any technical aspects per se. I think they could do a bit more to make their results more accessible and visually more informative and striking to others, both those working closely in the field as well as those working in more different areas. What I would love to see is an expansion of Figure 4 (either here or in a later figure as a summary) whereby the dry connectivity map and diagram are integrated with a topographical/ "organotypic" and functional map. For example, can the projections in the SEZ (Figure 2) be correlated with the location of the sensory neurons in the labellum (based on light microscopy data), with respect to their molecular/modality/receptors?
https://doi.org/10.7554/eLife.78110.sa1Author response
We would like to suggest the following revisions to improve the clarity and accessibility of the results to a general audience:
1) Improve the presentation of the results to make them visually more informative and striking. For example, an expansion of Figure 4 would be helpful whereby the dry connectivity map and diagram are integrated with a topographical/ "organotypic" and functional map. Can the projections in the SEZ (Figure 2) be correlated with the location of the sensory neurons in the labellum (based on light microscopy data), with respect to their molecular/modality/receptors?
We have updated figure 4 with clearer labels to make it more informative and accessible. Unfortunately, it is not possible to correlate projections with location on the labellum. The only single neuron projection analysis that I am aware of does not map the fibers by location on the proboscis labellum (Nayak and Singh, 1985). In addition, as each chemosensory bristle contains multiple GRNs, it would be necessary to label molecularly-defined single GRNs from each bristle in order to generate such a map. Instead, we now include additional discussion on the possibility that there may be GRN subgroups based on location in the labellum or bristle subtype that further divide the groups that we categorized (ln 310-330).
2) Given that the authors did not reconstruct the entire GRN population it should be discussed that an additional unknown GRN class could have been missed.
We now include discussion that additional GRN classes or subclasses may exist (ln 307-310).
Reviewer #2 (Recommendations for the authors):
My suggestions focus on the presentation of their data, and not any technical aspects per se. I think they could do a bit more to make their results more accessible and visually more informative and striking to others, both those working closely in the field as well as those working in more different areas. What I would love to see is an expansion of Figure 4 (either here or in a later figure as a summary) whereby the dry connectivity map and diagram are integrated with a topographical/ "organotypic" and functional map. For example, can the projections in the SEZ (Figure 2) be correlated with the location of the sensory neurons in the labellum (based on light microscopy data), with respect to their molecular/modality/receptors?
We appreciate this comment and have added additional information on the connectivity in figure 4 and additional labeling of the groups (by modality) to make the figure more accessible. Unfortunately, it is not possible to correlate the projections in Figure 2 based on the location in the labellum. The only single neuron projection analysis that I am aware of does not map the fibers by location on the proboscis labellum (Nayak and Singh, 1985). In addition, as each chemosensory bristle contains multiple GRNs, it would be necessary to label molecularly-defined single GRNs from each bristle in order to generate such a map. However, we have included additional discussion on the possibility that there may be GRN subgroups based on location in the labellum or bristle subtype that further divide the groups that we have categorized based on modality (ln 309-329).
https://doi.org/10.7554/eLife.78110.sa2