کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2035544 | 1072193 | 2014 | 13 صفحه PDF | دانلود رایگان |

• Activation or ablation of subsets of PI neurons degrades rest:activity rhythms
• Molecular oscillations in clock cells are unaffected by PI cell manipulations
• GRASP analysis delineates a circuit connecting pacemaker neurons to PI output cells
• The CRF homolog, DH44, is a circadian output molecule expressed by PI cells
SummaryThough much is known about the cellular and molecular components of the circadian clock, output pathways that couple clock cells to overt behaviors have not been identified. We conducted a screen for circadian-relevant neurons in the Drosophila brain and report here that cells of the pars intercerebralis (PI), a functional homolog of the mammalian hypothalamus, comprise an important component of the circadian output pathway for rest:activity rhythms. GFP reconstitution across synaptic partners (GRASP) analysis demonstrates that PI cells are connected to the clock through a polysynaptic circuit extending from pacemaker cells to PI neurons. Molecular profiling of relevant PI cells identified the corticotropin-releasing factor (CRF) homolog, DH44, as a circadian output molecule that is specifically expressed by PI neurons and is required for normal rest:activity rhythms. Notably, selective activation or ablation of just six DH44+ PI cells causes arrhythmicity. These findings delineate a circuit through which clock cells can modulate locomotor rhythms.
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Journal: - Volume 157, Issue 3, 24 April 2014, Pages 689–701