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Wegner, S, Belle, MDC, Hughes, ATL, Diekman, CO and Piggins, HD (2017) Delayed Cryptochrome Degradation Asymmetrically Alters the Daily Rhythm in Suprachiasmatic Clock Neuron Excitability. Journal of Neuroscience, 37 (33). pp. 7824-7836. ISSN 0270-6474
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Wegner et al (2017) Delayed Cry degradation asymetrically alters rhythm in SCN excitability.pdf - Published Version Available under License Creative Commons Attribution. Download (3MB) | Preview |
Abstract
Suprachiasmatic nuclei (SCN) neurons contain an intracellular molecular circadian clock and the Cryptochromes (CRY1/2), key transcriptional repressors of this molecular apparatus, are subject to post-translational modification through ubiquitination and targeting for proteosomal degradation by the ubiquitin E3 ligase complex. Loss-of-function point mutations in a component of this ligase complex, Fbxl3, delay CRY1/2 degradation, reduce circadian rhythm strength, and lengthen the circadian period by ∼2.5 h. The molecular clock drives circadian changes in the membrane properties of SCN neurons, but it is unclear how alterations in CRY1/2 stability affect SCN neurophysiology. Here we use male and femaleAfterhoursmice which carry the circadian period lengthening loss-of-functionFbxl3Afhmutation and perform patch-clamp recordings from SCN brain slices across the projected day/night cycle. We find that the daily rhythm in membrane excitability in the ventral SCN (vSCN) was enhanced in amplitude and delayed in timing inFbxl3Afh/Afhmice. At night, vSCN cells fromFbxl3Afh/Afhmice were more hyperpolarized, receiving more GABAergic input than theirFbxl3+/+counterparts. Unexpectedly, the progression to daytime hyperexcited states was slowed byAfhmutation, whereas the decline to hypoexcited states was accelerated. In long-term bioluminescence recordings, GABAAreceptor blockade desynchronized theFbxl3+/+but not theFbxl3Afh/AfhvSCN neuronal network. Further, a neurochemical mimic of the light input pathway evoked larger shifts in molecular clock rhythms inFbxl3Afh/Afhcompared withFbxl3+/+SCN slices. These results reveal unanticipated consequences of delaying CRY degradation, indicating that theAfhmutation prolongs nighttime hyperpolarized states of vSCN cells through increased GABAergic synaptic transmission.SIGNIFICANCE STATEMENTThe intracellular molecular clock drives changes in SCN neuronal excitability, but it is unclear how mutations affecting post-translational modification of molecular clock proteins influence the temporal expression of SCN neuronal state or intercellular communication within the SCN network. Here we show for the first time, that a mutation that prolongs the stability of key components of the intracellular clock, the cryptochrome proteins, unexpectedly increases in the expression of hypoexcited neuronal state in the ventral SCN at night and enhances hyperpolarization of ventral SCN neurons at this time. This is accompanied by increased GABAergic signaling and by enhanced responsiveness to a neurochemical mimic of the light input pathway to the SCN. Therefore, post-translational modification shapes SCN neuronal state and network properties.
| Item Type: | Article |
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| Uncontrolled Keywords: | 11 Medical And Health Sciences, 17 Psychology And Cognitive Sciences |
| Subjects: | B Philosophy. Psychology. Religion > BF Psychology Q Science > QH Natural history > QH301 Biology |
| Divisions: | Natural Sciences & Psychology (closed 31 Aug 19) |
| Publisher: | Society for Neuroscience |
| Related URLs: | |
| Date Deposited: | 05 Apr 2018 10:45 |
| Last Modified: | 04 Sep 2021 02:47 |
| DOI or ID number: | 10.1523/JNEUROSCI.0691-17.2017 |
| URI: | https://researchonline.ljmu.ac.uk/id/eprint/8418 |
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