PT  - JOURNAL ARTICLE
AU  - Kentarou Ushijima
AU  - Satoru Koyanagi
AU  - Yuuki Sato
AU  - Takamitsu Ogata
AU  - Naoya Matsunaga
AU  - Akio Fujimura
AU  - Shigehiro Ohdo
TI  - Role of Activating Transcription Factor-4 in 24-Hour Rhythm of Serotonin Transporter Expression in the Mouse Midbrain
AID  - 10.1124/mol.112.079079
DP  - 2012 Aug 01
TA  - Molecular Pharmacology
PG  - 264--270
VI  - 82
IP  - 2
4099  - http://molpharm.aspetjournals.org/content/82/2/264.short
4100  - http://molpharm.aspetjournals.org/content/82/2/264.full
SO  - Mol Pharmacol2012 Aug 01; 82
AB  - Serotonin (5-HT) transporter (5-HTT) plays a key role in the control of 5-HT neuronal activity by reuptaking extracellular 5-HT from the synapse cleft. We have previously demonstrated that 5-HTT mRNA expression levels and its uptake activity in the mouse midbrain are significantly higher in the dark phase than those in the light phase. However, the molecular mechanisms of time-dependent expression of 5-HTT have not been clarified. In this study, expression of 5-HTT mRNA in the mouse midbrain showed a significant 24-h rhythm and was higher in the dark phase. Although such an oscillation was eliminated by a Clock gene mutation, CLOCK and BMAL1 did not activate 5-HTT transcription in the luciferase reporter assay. Activating transcription factor-4 (ATF4), a member of the ATF/cAMP response element (CRE)-binding protein family, is a component responsible for sustaining circadian oscillations of CRE-mediated gene expression. ATF4 significantly activated 5-HTT transcription in vitro and time dependently bound to the CRE site in the 5-HTT promoter in the mouse midbrain. In addition, mutation of the Clock gene disrupted temporal binding of ATF4 to the CRE site in the 5-HTT promoter. These results indicated that the circuit of circadian-basis molecular regulation between the clockwork system and mouse 5-HTT gene was connected by the ATF4 signaling pathway.