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NPAS2: An Analog of Clock Operative in the Mammalian Forebrain
Martin Reick,1Joseph A. Garcia,2Carol Dudley,1Steven L. McKnight1*
Neuronal PAS domain protein 2 (NPAS2) is a transcription
factor expressed primarily in the mammalian forebrain. NPAS2 is highlyrelated in primary amino acid sequence to Clock, a transcriptionfactor
expressed in the suprachiasmatic nucleus that heterodimerizeswith
BMAL1 and regulates circadian rhythm. To investigate thebiological
role of NPAS2, we prepared a neuroblastoma cell linecapable of
conditional induction of the NPAS2:BMAL1 heterodimerand identified
putative target genes by representational differenceanalysis, DNA
microarrays, and Northern blotting. Coinductionof NPAS2 and BMAL1
activated transcription of the endogenous Per1,Per2, and Cry1 genes, which encode negatively
activating componentsof the circadian regulatory apparatus, and
repressed transcriptionof the endogenous BMAL1 gene.
Analysis of the frontal cortex ofwild-type mice kept in a 24-hour
light-dark cycle revealed thatPer1, Per2, and
Cry1 mRNA levels were elevated during darknessand reduced
during light, whereas BMAL1 mRNA displayed the oppositepattern. In situ hybridization assays of mice kept in constantdarkness
revealed that Per2 mRNA abundance did not oscillate asa
function of the circadian cycle in NPAS2-deficient mice. Thus,NPAS2
likely functions as part of a molecular clock operativein the
mammalian forebrain.
1 Department of Biochemistry,
2 Department of Internal Medicine, University of
Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas,
TX 75390, USA.
*
To whom correspondence should be addressed. E-mail:
smckni{at}biochem.swmed.edu
The editors suggest the following Related Resources on Science sites:
In Science Magazine
REPORTS
Jared Rutter, Martin Reick, Leeju C. Wu, and Steven L. McKnight (20 July 2001) Science293 (5529), 510.
[DOI: 10.1126/science.1060698] |Abstract »|Full Text »|PDF »|Supplemental Data »
PERSPECTIVES
Ueli Schibler, Juergen A. Ripperger, and Steven A. Brown (20 July 2001) Science293 (5529), 437.
[DOI: 10.1126/science.1063296] |Summary »|Full Text »
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