It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Animals must slow or halt locomotion to integrate sensory inputs or to change direction. In Caenorhabditis elegans, the GABAergic and peptidergic neuron RIS mediates developmentally timed quiescence. Here, we show RIS functions additionally as a locomotion stop neuron. RIS optogenetic stimulation caused acute and persistent inhibition of locomotion and pharyngeal pumping, phenotypes requiring FLP-11 neuropeptides and GABA. RIS photoactivation allows the animal to maintain its body posture by sustaining muscle tone, yet inactivating motor neuron oscillatory activity. During locomotion, RIS axonal Ca2+ signals revealed functional compartmentalization: Activity in the nerve ring process correlated with locomotion stop, while activity in a branch correlated with induced reversals. GABA was required to induce, and FLP-11 neuropeptides were required to sustain locomotion stop. RIS attenuates neuronal activity and inhibits movement, possibly enabling sensory integration and decision making, and exemplifies dual use of one cell across development in a compact nervous system.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details





1 Buchmann Institute for Molecular Life Sciences (BMLS), Goethe University, Frankfurt, Germany; Institute for Biophysical Chemistry, Goethe University, Frankfurt, Germany
2 Buchmann Institute for Molecular Life Sciences (BMLS), Goethe University, Frankfurt, Germany; Institute for Biophysical Chemistry, Goethe University, Frankfurt, Germany; Functional Genomics and Proteomics Group, Department of Biology, KU Leuven, Leuven, Belgium
3 Buchmann Institute for Molecular Life Sciences (BMLS), Goethe University, Frankfurt, Germany; Institute for Biophysical Chemistry, Goethe University, Frankfurt, Germany; Max-Planck-Institute for Brain Research, Frankfurt, Germany
4 Buchmann Institute for Molecular Life Sciences (BMLS), Goethe University, Frankfurt, Germany; Institute for Biophysical Chemistry, Goethe University, Frankfurt, Germany; od green GmbH, Schärding am Inn, Austria
5 Max Planck Institute for Biophysical Chemistry, Göttingen, Germany
6 Max Planck Institute for Biophysical Chemistry, Göttingen, Germany; Department of Biology, University of Marburg, Marburg, Germany
7 Functional Genomics and Proteomics Group, Department of Biology, KU Leuven, Leuven, Belgium
8 Buchmann Institute for Molecular Life Sciences (BMLS), Goethe University, Frankfurt, Germany; Institute of Cell Biology and Neuroscience, Goethe University, Frankfurt, Germany
9 Buchmann Institute for Molecular Life Sciences (BMLS), Goethe University, Frankfurt, Germany; Institute of Cell Biology and Neuroscience, Goethe University, Frankfurt, Germany; Center for Computational and Theoretical Biology (CCTB), University of Würzburg, Würzburg, Germany