| Literature DB >> 23624321 |
Yoshiko Yamada1, Shin-Ya Nishide, Yoshihiro Nakajima, Toshiyuki Watanabe, Yoshihiro Ohmiya, Ken-Ichi Honma, Sato Honma.
Abstract
A firefly luciferase reporter enabled us to monitor promoter activity in vivo as well as ex vivo; however, this requires a sufficient supply of the substrate luciferin and specific monitoring devices. To overcome these disadvantages, we developed transgenic rats carrying a secreted enzyme Cypridina luciferase (CLuc) reporter under the promoter of clock gene Per2 (Per2-CLuc). Per2-CLuc activity in serially sampled blood from freely moving rats exhibited robust circadian rhythms with a peak at early morning. The Per2-CLuc bioluminescence could be quantified even with approximately 100pl of plasma. Plasma Per2-CLuc rhythms were phase reversed, and the level was reduced by restricting food access for 2h during the light phase, suggesting that the plasma Per2-CLuc rhythms reflect the phase of peripheral clocks entrained to feeding cues as well as fuel metabolism. Fasting for 2days did not alter the circadian Per2-CLuc rhythms in rats, suggesting that feeding per se did not affect the circadian Per2-CLuc rhythms. Tissue-specific Per2-CLuc rhythms were observed in culture medium of peripheral tissues. The Per2-CLuc reporter is a powerful tool to access gene expression in vivo as well as ex vivo with ordinary laboratory equipment.Entities:
Keywords: Circadian rhythm; Clock gene; In vivo recording; Secreted luciferase reporter; Transgenic rats
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Year: 2013 PMID: 23624321 DOI: 10.1016/j.ab.2013.04.019
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365