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Circadian Regulation of GluA2 mRNA Processing in the Rat Suprachiasmatic Nucleus and Other Brain Structures
H. Míková, V. Kuchtiak, I. Svobodová, V. Spišská, D. Pačesová, A. Balík, Z. Bendová
Language English Country United States
Document type Journal Article
Grant support
19-17037S
Grantová Agentura České Republiky
1030217
Grantová Agentura, Univerzita Karlova
CZ.CZ.02.1.01/0.0/0.0/16_025/0007444
European Regional Development Fund
67985823
Research Project of the AS CR RVO
CZ.1.05/1.1.00/02.0109
National Sustainability Program II
NLK
ProQuest Central
from 1997-02-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2010-02-01 to 1 year ago
Health & Medicine (ProQuest)
from 1997-02-01 to 1 year ago
Psychology Database (ProQuest)
from 1997-02-01 to 1 year ago
- MeSH
- Receptors, AMPA genetics metabolism MeSH
- Circadian Rhythm genetics MeSH
- RNA Editing genetics MeSH
- Exons genetics MeSH
- RNA, Messenger genetics metabolism MeSH
- Suprachiasmatic Nucleus metabolism MeSH
- RNA Processing, Post-Transcriptional genetics MeSH
- Rats, Wistar MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
The mammalian circadian system consists of a major circadian pacemaker located in the suprachiasmatic nucleus (SCN) of the hypothalamus and peripheral clocks in the body, including brain structures. The SCN depends on glutamatergic neurotransmission for transmitting signals from the retina, and it exhibits spontaneous 24-h rhythmicity in neural activity. The aim of this work was to evaluate the degree and circadian rhythmicity of AMPA receptor GluA2 subunit R/G editing and alternative flip/flop splicing in the SCN and other brain structures in Wistar rats. Our data show that the circadian rhythmicity in the SCN's GluA2 mRNA level was highest at dawn, while the circadian rhythm in R/G editing peaked at CT10 and the rhythmic flip varied with the acrophase at the late subjective night. The circadian rhythmicity was confirmed for R/G editing and splicing in the CA3 hippocampal area, and rhythmic variation of the flip isoform was also measured in the olfactory bulbs and cerebellum. The correlations between the R/G editing and alternative flip/flop splicing revealed a structure-dependent direction. In the hippocampus, the edited (G)-form level was positively correlated with the flip variant abundance, in accord with published data; by contrast, in the SCN, the flip variant was in associated more with the unedited (R) form. The edited (G) form and flop isoform also predominated in the retina and cerebellum.
References provided by Crossref.org
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