TY - JOUR
T1 - Involvement of CLOCK:BMALI heterodimer in serum-responsive mPerl induction
AU - Jung, Hosung
AU - Choe, Youngshik
AU - Kim, Hyunjung
AU - Park, Noheon
AU - Son, Gi Hoon
AU - Khang, Inkoo
AU - Kim, Kyungjin
PY - 2003/1/20
Y1 - 2003/1/20
N2 - A rapid induction of mouse periodl (mPerl) gene expression is supposed to be critical in the clock gene regulation, especially in the phase resetting of the clock, but its molecular mechanism is poorly understood. Based on the previous finding that the process does not involve de novo synthesis of proteins, we postulated the involvement of CLOCK:BMALI heterodimer, a positive regulator of circadian oscillator, in the rapid induction of mPerl transcription. To test this hypothesis, we utilized CLOCKδ19, a dominant-negative mutant, to suppress the function of CLOCK:BMALI in vitro. Serum-evoked rapid increases of mPerl mRNA expression and promoter activity were significantly blunted when CLOCK:BMALI function was interfered with. Furthermore, DNA binding activity of CLOCK:BMALI heterodimer to five E-boxes of mPerl promoter markedly increased shortly after serum shock. Taken together, these results suggest that CLOCK:BMALI heterodimer is not only a core component of negative feedback loop driving circadian oscillator, but also involved in the rapid induction of mPerl during phase resetting of the clock.
AB - A rapid induction of mouse periodl (mPerl) gene expression is supposed to be critical in the clock gene regulation, especially in the phase resetting of the clock, but its molecular mechanism is poorly understood. Based on the previous finding that the process does not involve de novo synthesis of proteins, we postulated the involvement of CLOCK:BMALI heterodimer, a positive regulator of circadian oscillator, in the rapid induction of mPerl transcription. To test this hypothesis, we utilized CLOCKδ19, a dominant-negative mutant, to suppress the function of CLOCK:BMALI in vitro. Serum-evoked rapid increases of mPerl mRNA expression and promoter activity were significantly blunted when CLOCK:BMALI function was interfered with. Furthermore, DNA binding activity of CLOCK:BMALI heterodimer to five E-boxes of mPerl promoter markedly increased shortly after serum shock. Taken together, these results suggest that CLOCK:BMALI heterodimer is not only a core component of negative feedback loop driving circadian oscillator, but also involved in the rapid induction of mPerl during phase resetting of the clock.
KW - Bmall
KW - Clock
KW - Mouse period I (mPerl)
KW - NIH-3T3 mouse fibroblast cells
KW - Serum shock
KW - Transcriptional regulation
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U2 - 10.1097/00001756-200301200-00003
DO - 10.1097/00001756-200301200-00003
M3 - Article
C2 - 12544823
AN - SCOPUS:0037454474
SN - 0959-4965
VL - 14
SP - 15
EP - 19
JO - NeuroReport
JF - NeuroReport
IS - 1
ER -