Affiliation:
1. Department of Biochemistry,
2. Department of Internal Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
Abstract
Neuronal PAS domain protein 2 (NPAS2) is a transcription factor expressed primarily in the mammalian forebrain. NPAS2 is highly related in primary amino acid sequence to Clock, a transcription factor expressed in the suprachiasmatic nucleus that heterodimerizes with BMAL1 and regulates circadian rhythm. To investigate the biological role of NPAS2, we prepared a neuroblastoma cell line capable of conditional induction of the NPAS2:BMAL1 heterodimer and identified putative target genes by representational difference analysis, DNA microarrays, and Northern blotting. Coinduction of NPAS2 and BMAL1 activated transcription of the endogenous
Per1
,
Per2
, and
Cry1
genes, which encode negatively activating components of the circadian regulatory apparatus, and repressed transcription of the endogenous
BMAL1
gene. Analysis of the frontal cortex of wild-type mice kept in a 24-hour light-dark cycle revealed that
Per1
,
Per2
, and
Cry1
mRNA levels were elevated during darkness and reduced during light, whereas
BMAL1
mRNA displayed the opposite pattern. In situ hybridization assays of mice kept in constant darkness revealed that
Per2
mRNA abundance did not oscillate as a function of the circadian cycle in NPAS2-deficient mice. Thus, NPAS2 likely functions as part of a molecular clock operative in the mammalian forebrain.
Publisher
American Association for the Advancement of Science (AAAS)
Cited by
475 articles.
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