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An Error has occurred retrieving Wikidata item for infobox Neuronal PAS domain protein 2 (NPAS2, also known as MOP4) is a protein in mammals encoded by the Npas2 gene. ^{[1] [2]} NPAS2 is paralogous to CLOCK, a key protein involved in the maintenance of circadian rhythms in mammals, and its role in the brain is thought to be as a generator and maintainer of mammalian circadian rhythms. More specifically, NPAS2 is an activator of transcription and translation of core clock and clock-controlled genes through its role in a negative feedback loop in the suprachiasmatic nucleus (SCN), the brain region responsible for the control of circadian rhythms. ^[3]

Discovery

The mammalian NPAS2 gene was first sequenced and characterized in 1997 by Yu-Dong Zhou et al. ^[4] The gene’s cDNAs encoding mouse and human forms of NPAS2 were isolated and sequenced. RNA blotting assays were used to demonstrate the selective presence of the gene in brain and spinal cord tissues of mice.

Structure

In Humans

The NPAS2 gene resides on chromosome 2 at the band q11.2 ^[5]. The gene is 176,679 bases long and contains 25 exons ^[6].

In Mice

The Npas2 gene has been found to reside on chromosome 1 at 17.98 centimorgans and is 169,505 bases long ^[7].

Function

In The Brain

The NPAS2 protein is a member of the basic helix-loop-helix (bHLH)-PAS transcription factor family and is expressed in the SCN. Proteins like NPAS2 bind to other proteins via their PAS domain, a protein-protein binding domain. Like its paralogue, CLOCK (another PAS domain-containing protein), the NPAS2 protein can dimerize with the BMAL1 protein and engage in a transcription/translation negative feedback loop (TTFL) to activate transcription of the mammalian Per and Cry core clock genes. ^[3] NPAS2 has been shown to form a heterodimer with BMAL1 in both the brain and in cell lines, suggesting its similarity in function to the CLOCK protein in this TTFL.

Redundancy is a key feature of TTFLs that regulate circadian rhythms. BMAL1 is redundant for CLOCK in the sense that if CLOCK is absent, BMAL1 will take over to maintain the mammalian circadian rhythms. NPAS2 has been shown to be analogous to the function of CLOCK in CLOCK-deficient mice. ^[3] Npas2-mutant mice which do not express functional NPAS2 protein still maintain robust circadian rhythms in locomotion. However, like CLOCK-deficient mice in the CLOCK/BMAL1 TTFL, Npas2- mutant mice (in the NPAS2/BMAL1 TTFL) still have small defects in their circadian rhythms such as a shortened circadian period and an altered response to changes in the typical light-dark cycle. ^[3] In addition, Npas2 knockout mice show sleep disturbances and have decreased expression of mPer2 in their forebrains. ^[8] Mice without functional alleles of both Clock and Npas2 became arrhythmic once placed in constant darkness, suggesting that both genes have overlapping roles in maintaining circadian rhythms. In both wild-type and Clock knockout mice, Npas2 expression is observed at the same levels, confirming that Npas2 plays a role in maintaining these rhythms in the absence of Clock. ^[3]

In Other Body Tissues

Npas2 is expressed also in liver tissues, and its mRNA is upregulated in Clock-mutant mice. However, studies have shown that Npas2 alone is unable to maintain circadian rhythms in peripheral tissues in the absence of CLOCK protein, unlike in the SCN. ^[3] One theory to explain this observation is that neurons in the brain are characterized by intercellular coupling and can thus respond to deficiencies in key clock proteins in nearby neurons to maintain rhythms. In peripheral tissues such as the liver and lung, however, the lack of intercellular coupling does not allow for this compensatory mechanism to occur. A second theory as to why NPAS2 can maintain rhythms in CLOCK-deficient SCNs but not in CLOCK-deficient peripheral tissues is that there exists an additional unknown factor in the SCN that is not present in peripheral tissues. ^[3]

Non-Circadian Function

NPAS2 deficient mice have been shown to have long term memory deficits, suggesting that the protein may play a key role in the acquisition of such memories. This was tested by inserting a reporter gene (lacZ) that resulted in the production of an NPAS2 lacking the bHLH domain. These mice were then given several tests, including the cued and contextual fear task, and showed long-term memory deficits in both tasks ^[9].

Interactions

NPAS2 has been shown to interact with:

• ARNTL (also known as BMAL1). Like Clock, Npas2 mRNA cycles with a similar phase to that of Bmal1, with both peaking 8 hours before Per2. This is consistent with the observation that NPAS2 forms a heterodimer with BMAL1 to drive Per2 expression. ^{[10] [11]}
• EP300. NPAS2 and EP300 interact in a time-dependent, synchronized manner. EP300 is recruited to NPAS2 as a coactivator of clock gene expression. ^[12]
• Retinoic acid receptor alpha (RARα) and retinoid X receptor alpha (RXRα). In peripheral clocks, RARα and RXRα interact with NPAS2 by inhibiting the NPAS2:BMAL1 heterodimer-mediated expression of clock genes. This interaction depends upon humoral signaling by retinoic acid and serves to phase-shift the clock. ^[10]
• Small heterodimer partner (SHP). In the liver circadian clock, NPAS2 and SHP engage in a TTFL: NPAS2 controls the circadian rhythms of SHP by rhythmically binding to its promoter, while SHP inhibits transcription of Npas2 when present. ^[13]

Clinical significance

Npas2 genotypes can be determined through tissue samples from which genomic DNA is extracted and assayed. The assay is performed under PCR conditions and can be used to determine specific mutations and polymorphisms. ^[14]

Polymorphisms and tumorigenesis

Mounting evidence suggests that the NPAS2 protein and other circadian genes are involved in tumorigenesis and tumor growth, possibly through their control of cancer-related biologic pathways. A missense polymorphism in NPAS2 (Ala394Thr) has been shown to be associated with risk of human tumors including breast cancer. ^[15] These findings provide evidence suggesting a possible role for the circadian Npas2 gene in cancer prognosis. These results have been confirmed in both breast and colorectal cancers. ^[16]

NPAS2 and mood disorders

Current research has revealed an association between seasonal affective disorder (SAD) and general mood disorder related to NPAS2, ARNTL, and CLOCK polymorphisms. These genes may influence seasonal variations through metabolic factors such as body weight and appetite. ^{[17] [18]}

See also

• Clock (gene)
• Bmal1/Arntl (gene)
• Suprachiasmatic nucleus (SCN)
• Per (gene)

References

External links

• NPAS2+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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