3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Classifying Drosophila Olfactory Projection Neuron Subtypes by Single-cell RNA Sequencing

      research-article

      Read this article at

      ScienceOpenPublisherPMC
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          The definition of neuronal type and how this relates to the transcriptome are open questions. Drosophila olfactory projection neurons (PNs) are among the best-characterized neuronal types: different PN classes target dendrites to distinct olfactory glomeruli, while PNs of the same class exhibit indistinguishable anatomical and physiological properties. Using single-cell RNA-sequencing, we comprehensively characterized the transcriptomes of most PN classes and unequivocally mapped transcriptomes to specific olfactory function for 6 classes. Transcriptomes of closely related PN classes exhibit the largest differences during circuit assembly but become indistinguishable in adults, suggesting that neuronal subtype diversity peaks during development. Transcription factors and cell-surface molecules are the most differentially expressed genes between classes and are highly informative in encoding cell identity, enabling us to identify a new lineage-specific transcription factor that instructs PN dendrite targeting. These findings establish that neuronal transcriptomic identity corresponds with anatomical and physiological identity defined by connectivity and function.

          Related collections

          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          27 July 2018
          16 November 2017
          16 November 2018
          : 171
          : 5
          : 1206-1220.e22
          Affiliations
          [1 ]Department of Biology and Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA
          [2 ]Biophysics Graduate Program, Stanford University, Stanford, CA 94305, USA
          [3 ]Neurosciences Graduate Program, Stanford University, Stanford, CA 94305, USA
          [4 ]Departments of Bioengineering and Applied Physics, Stanford University, Stanford, CA 94305, USA
          [5 ]Chan Zuckerberg Biohub, Stanford, CA 94305, USA
          [6 ]Corresponding authors: lluo@ 123456stanford.edu (L.L.); quake@ 123456stanford.edu (S.R.Q.)
          [7 ]Lead Contact.
          Author notes

          Author Contributions

          H.L., F.H., and L.L. designed experiments with support from S.R.Q. F.H. and H.L established the single-cell RNA-seq protocol. H.L. performed all fly experiments with help from B.W., Q.X., J.L., T.L., and D.J.L., and prepared sequencing libraries. F.H. performed cell sorting, designed the ICIM algorithm, and analyzed data with input from H.L., L.L., and S.R.Q. H.L., F.H., S.R.Q., and L.L. wrote the paper.

          Article
          PMC6095479 PMC6095479 6095479 nihpa982283
          10.1016/j.cell.2017.10.019
          6095479
          29149607
          29a2fca9-47c7-4957-8fe7-0026e9fb4ab4
          History
          Categories
          Article

          Comments

          Comment on this article

          Related Documents Log