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      Neuromodulatory Regulation of Behavioral Individuality in Zebrafish

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          Summary

          Inter-individual behavioral variation is thought to increase fitness and aid adaptation to environmental change, but the underlying mechanisms are poorly understood. We find that variation between individuals in neuromodulatory input contributes to individuality in short-term habituation of the zebrafish ( Danio Rerio) acoustic startle response (ASR). ASR habituation varies greatly between individuals, but differences are stable over days and are heritable. Acoustic stimuli that activate ASR-command Mauthner cells also activate dorsal raphe nucleus (DRN) serotonergic neurons, which project to the vicinity of the Mauthner cells and their inputs. DRN neuron activity decreases during habituation in proportion to habituation and a genetic manipulation that reduces serotonin content in DRN neurons increases habituation, whereas serotonergic agonism or DRN activation with ChR2 reduces habituation. Finally, level of rundown of DRN activity co-segregates with extent of behavioral habituation across generations. Thus, variation between individuals in neuromodulatory input contributes to individuality in a core adaptive behavior.

          eToc

          The mechanisms of vertebrate behavioral individuality are poorly understood. Pantoja et al. find that differences between individuals in sensory-evoked neuromodulatory input modulate behavior and co-segregate with behavioral differences in a sensory-evoked adaptive behavior. Thus, variation between individuals in neuromodulation contributes to behavioral individuality.

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          Author and article information

          Journal
          8809320
          1600
          Neuron
          Neuron
          Neuron
          0896-6273
          1097-4199
          13 July 2016
          7 July 2016
          3 August 2016
          03 August 2017
          : 91
          : 3
          : 587-601
          Affiliations
          [1 ]Department of Molecular and Cell Biology, University of California Berkeley, Berkeley, California, USA 94720
          [2 ]Helen Wills Neuroscience Institute, University of California Berkeley, Berkeley, California, USA 94720
          [3 ]Physical Bioscience Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA 94720
          Author notes
          [* ]To whom correspondence should be addressed: ehud@ 123456berkeley.edu
          Article
          PMC4976045 PMC4976045 4976045 nihpa796102
          10.1016/j.neuron.2016.06.016
          4976045
          27397519
          acadd54b-c6ca-47a1-acb3-e048689597e2
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