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Central and peripheral circadian clock genes, their statistical analysis for rhythms, and relationship to health and disease
Sothern R. B., Yamamoto T, Cornélissen G, Takumi T, Halberg F.
Jazyk angličtina Země Česko
Typ dokumentu grafy a diagramy, tabulky
NLK
Masaryk University Scholarly Journals
od 2000 do 2010
- MeSH
- biologické hodiny fyziologie genetika MeSH
- chronická nemoc MeSH
- chronobiologické poruchy genetika MeSH
- cykly aktivity fyziologie genetika MeSH
- flavoproteiny farmakokinetika MeSH
- modely u zvířat MeSH
- myši MeSH
- proteiny buněčného cyklu genetika MeSH
- transportní proteiny genetika MeSH
- Check Tag
- myši MeSH
- Publikační typ
- grafy a diagramy MeSH
- tabulky MeSH
Molecular clocks present in organs and individual cells throughout the body are central for the temporal coordination of rhythms in internal biological processes among themselves and with external environmental cycles; altered function of specific clock gene (CG) components can have significant impact relevant to health and disease. We herein review current knowledge pertaining to the presence and robustness of circadian rhythms in CGs in the suprachiasmatic nucleus and peripheral organs, and the importance of CGs to general health and the diagnosis and treatment of human disorders and disease. Also discussed are developmental aspects of rhythms in some CGs and tissues, time of day vs. circadian stage, using synchronized vs. constant conditions to monitor a rhythm, and subjective vs. objective interpretations of rhythms. To emphasize the latter, chronobiological statistics (ANOVA, single cosinor) are applied to published circadian CG mRNA expression data (which had been described subjectively) as an example of objectively determining rhythm probability and obtaining estimates for circadian amplitudes and acrophases. The data base consisted of 14 CGs (mPer1,2,3, mCry1,2, mBmal1, mCK1?,?, mClock, mDbp, mNpas2, mRev-erb?,ß, mTim) in each of 7 mouse organs harvested every 4h for 24h from male Balb/c mice on day 3 in continuous darkness. Excluding the usually non–24h-rhythmic testis and CG mTim, rhythms significant at p?0.05 were found in 81% (63/78) of CGs and when including borderline significant at p?0.10, in 97% (76/78) of CGs. A statisticallydetermined circadian amplitude and acrophase for each CG in each tissue can be useful in making objective comparisons of rhythm parameters in CGs between various peripheral organs, species, and/or studies of different conditions (e.g., photoperiods, feeding schedules, aging, disease). Use of these parameters adds new endpoints for diagnoses and approaches for therapeutic interventions in conditions where disturbance of circadian CG expression is an important cause of morbidity associated with chronic illnesses and diseases with a strong circadian component, including cardiovascular disease, epilepsy, cancer, metabolic syndrome, and sleep-related disorders, among others, also reviewed herein.
Lit.: 161
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- $a Molecular clocks present in organs and individual cells throughout the body are central for the temporal coordination of rhythms in internal biological processes among themselves and with external environmental cycles; altered function of specific clock gene (CG) components can have significant impact relevant to health and disease. We herein review current knowledge pertaining to the presence and robustness of circadian rhythms in CGs in the suprachiasmatic nucleus and peripheral organs, and the importance of CGs to general health and the diagnosis and treatment of human disorders and disease. Also discussed are developmental aspects of rhythms in some CGs and tissues, time of day vs. circadian stage, using synchronized vs. constant conditions to monitor a rhythm, and subjective vs. objective interpretations of rhythms. To emphasize the latter, chronobiological statistics (ANOVA, single cosinor) are applied to published circadian CG mRNA expression data (which had been described subjectively) as an example of objectively determining rhythm probability and obtaining estimates for circadian amplitudes and acrophases. The data base consisted of 14 CGs (mPer1,2,3, mCry1,2, mBmal1, mCK1?,?, mClock, mDbp, mNpas2, mRev-erb?,ß, mTim) in each of 7 mouse organs harvested every 4h for 24h from male Balb/c mice on day 3 in continuous darkness. Excluding the usually non–24h-rhythmic testis and CG mTim, rhythms significant at p?0.05 were found in 81% (63/78) of CGs and when including borderline significant at p?0.10, in 97% (76/78) of CGs. A statisticallydetermined circadian amplitude and acrophase for each CG in each tissue can be useful in making objective comparisons of rhythm parameters in CGs between various peripheral organs, species, and/or studies of different conditions (e.g., photoperiods, feeding schedules, aging, disease). Use of these parameters adds new endpoints for diagnoses and approaches for therapeutic interventions in conditions where disturbance of circadian CG expression is an important cause of morbidity associated with chronic illnesses and diseases with a strong circadian component, including cardiovascular disease, epilepsy, cancer, metabolic syndrome, and sleep-related disorders, among others, also reviewed herein.
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