4.3 Article

CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila

Journal

G3-GENES GENOMES GENETICS
Volume 8, Issue 9, Pages 2979-2990

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1534/g3.118.200572

Keywords

Fussel/SKOR; dILP2; Drifter; pars intercerebralis; lifespan extension

Funding

  1. NIH [GM099650, NS072128, OD024794, OD023691]
  2. US-Israel Binational Science Foundation [2013380]

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CORL proteins (known as SKOR in mice, Fussel in humans and fussel in Flybase) are a family of CNS specific proteins related to Sno/Ski oncogenes. Their developmental and adult roles are largely unknown. A Drosophila CORL (dCORL) reporter gene is expressed in all Drosophila insulin-like peptide 2 (dILP2) neurons of the pars intercerebralis (PI) of the larval and adult brain. The transcription factor Drifter is also expressed in the PI in a subset of dCORL and dILP2 expressing neurons and in several non-dILP2 neurons. dCORL mutant virgin adult brains are missing all dILP2 neurons that do not also express Drifter. This phenotype is also seen when expressing dCORL-RNAi in neurosecretory cells of the Pl. dCORL mutant virgin adults of both sexes have a significantly shorter lifespan than their parental strain. This longevity defect is completely reversed by mating (lifespan increases over 50% for males and females). Analyses of dCORL mutant mated adult brains revealed a complete rescue of dILP2 neurons without Drifter. Taken together, the data suggest that dCORL participates in a neural network connecting the insulin signaling pathway, longevity and mating. The conserved sequence and CNS specificity of all CORL proteins imply that this network may be operating in mammals.

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