4.8 Article

Ig Superfamily Ligand and Receptor Pairs Expressed in Synaptic Partners in Drosophila

Journal

CELL
Volume 163, Issue 7, Pages 1756-1769

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2015.11.021

Keywords

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Funding

  1. China Scholarship Council (CSC)
  2. University of California, Los Angeles (UCLA) Philip Whitcome Training Program
  3. Canadian Institute of Health Research Fellowship
  4. Jane Coffin Childs Memorial Fund for Medical Research
  5. Robert A. and Renee E. Belfer Family Foundation
  6. Target A.L.S.
  7. Human Frontiers Science Program
  8. National Institute of Health [R01GM067858, R01NS62821, R01NS28182]
  9. Ramon y Cajal contract [RYC-2011-09479]
  10. Ministerio de Economia y Competitividad grant [BFU2012-32282]

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Information processing relies on precise patterns of synapses between neurons. The cellular recognition mechanisms regulating this specificity are poorly understood. In the medulla of the Drosophila visual system, different neurons form synaptic connections in different layers. Here, we sought to identify candidate cell recognition molecules underlying this specificity. Using RNA sequencing (RNA-seq), we show that neurons with different synaptic specificities express unique combinations of mRNAs encoding hundreds of cell surface and secreted proteins. Using RNA-seq and protein tagging, we demonstrate that 21 paralogs of the Dpr family, a subclass of immunoglobulin (Ig)-domain containing proteins, are expressed in unique combinations in homologous neurons with different layer-specific synaptic connections. Dpr interacting proteins (DIPs), comprising nine paralogs of another subclass of Ig-containing proteins, are expressed in a complementary layer-specific fashion in a subset of synaptic partners. We propose that pairs of Dpr/DIP paralogs contribute to layer-specific patterns of synaptic connectivity.

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