A noncanonical E-box enhancer drives mouse Period2 circadian oscillations in vivo

被引:246
作者
Yoo, SH
Ko, CH
Lowrey, PL
Buhr, ED
Song, EJ
Chang, SW
Yoo, OJ
Yamazaki, S
Lee, C
Takahashi, JS
机构
[1] Northwestern Univ, Dept Neurobiol & Physiol, Evanston, IL 60208 USA
[2] Northwestern Univ, Howard Hughes Med Inst, Evanston, IL 60208 USA
[3] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[4] Univ Toronto, Dept Psychol, Toronto, ON M5S 3G3, Canada
[5] Florida State Univ, Coll Med, Dept Biol Sci, Tallahassee, FL 32306 USA
[6] Vanderbilt Univ, Dept Biol Sci, Nashville, TN 37235 USA
关键词
Bmal1; gene; circadian clock; clock gene; luciferase; Period2; locus;
D O I
10.1073/pnas.0409763102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mouse Period2 (mPer2) locus is an essential negative-feedback element of the mammalian circadian-clock mechanism. Recent work has shown that mPer2 circadian gene expression persists in both central and peripheral tissues. Here, we analyze the mouse mPer2 promoter and identify a circadian enhancer (E2) with a noncanonical 5'-CACGTT-3' E-box located 20 bp upstream of the mPer2 transcription start site. The E2 enhancer accounts for most circadian transcriptional drive of the mPer2 locus by CLOCK:BMAL1, is a major site of DNasel hypersensitivity in this region, and is constitutively bound by a transcriptional complex containing the CLOCK protein. Importantly, the E2 enhancer is sufficient to drive self-sustained circadian rhythms of luciferase activity in central and peripheral tissues from mPer2-E2::Luciferase transgenic mice with tissue-specific phase and period characteristics. Last, genetic analysis with mutations in Clock and Bmal1 shows that the E2 enhancer is a target of CLOCK and BMAL1 in vivo.
引用
收藏
页码:2608 / 2613
页数:6
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