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Integration of temporal and spatial patterning generates neural diversity

Author

Listed:
  • Ted Erclik

    (New York University
    University of Toronto at Mississauga)

  • Xin Li

    (New York University
    †Present address: Department of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.)

  • Maximilien Courgeon

    (New York University)

  • Claire Bertet

    (New York University)

  • Zhenqing Chen

    (New York University)

  • Ryan Baumert

    (New York University)

  • June Ng

    (New York University)

  • Clara Koo

    (New York University)

  • Urfa Arain

    (University of Toronto at Mississauga)

  • Rudy Behnia

    (New York University)

  • Alberto Del Valle Rodriguez

    (Center for Genomics and Systems Biology, New York University Abu Dhabi)

  • Lionel Senderowicz

    (University of Chicago)

  • Nicolas Negre

    (University of Chicago)

  • Kevin P. White

    (University of Chicago)

  • Claude Desplan

    (New York University
    Center for Genomics and Systems Biology, New York University Abu Dhabi)

Abstract

In the Drosophila optic lobes, 800 retinotopically organized columns in the medulla act as functional units for processing visual information. The medulla contains over 80 types of neuron, which belong to two classes: uni-columnar neurons have a stoichiometry of one per column, while multi-columnar neurons contact multiple columns. Here we show that combinatorial inputs from temporal and spatial axes generate this neuronal diversity: all neuroblasts switch fates over time to produce different neurons; the neuroepithelium that generates neuroblasts is also subdivided into six compartments by the expression of specific factors. Uni-columnar neurons are produced in all spatial compartments independently of spatial input; they innervate the neuropil where they are generated. Multi-columnar neurons are generated in smaller numbers in restricted compartments and require spatial input; the majority of their cell bodies subsequently move to cover the entire medulla. The selective integration of spatial inputs by a fixed temporal neuroblast cascade thus acts as a powerful mechanism for generating neural diversity, regulating stoichiometry and the formation of retinotopy.

Suggested Citation

  • Ted Erclik & Xin Li & Maximilien Courgeon & Claire Bertet & Zhenqing Chen & Ryan Baumert & June Ng & Clara Koo & Urfa Arain & Rudy Behnia & Alberto Del Valle Rodriguez & Lionel Senderowicz & Nicolas N, 2017. "Integration of temporal and spatial patterning generates neural diversity," Nature, Nature, vol. 541(7637), pages 365-370, January.
  • Handle: RePEc:nat:nature:v:541:y:2017:i:7637:d:10.1038_nature20794
    DOI: 10.1038/nature20794
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    Cited by:

    1. Hailun Zhu & Sihai Dave Zhao & Alokananda Ray & Yu Zhang & Xin Li, 2022. "A comprehensive temporal patterning gene network in Drosophila medulla neuroblasts revealed by single-cell RNA sequencing," Nature Communications, Nature, vol. 13(1), pages 1-19, December.

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