MOP-3, also known as BMAL1, is a critical component of the circadian clock, a complex time-keeping system that governs the rhythmic expression of genes throughout the body. As an integral transcription factor within this biological clock, MOP-3 forms a heterodimer with CLOCK, another core clock protein, to drive the expression of various genes, including those responsible for regulating cycles of sleep and wakefulness, hormone release, and metabolic processes. The expression of MOP-3 is not static; it oscillates in a 24-hour cycle and is subject to modulation by a variety of environmental and internal cues. The precise calibration of MOP-3 expression is crucial for the maintenance of circadian rhythms, and its dysregulation can lead to disruptions in these rhythms, which are foundational to numerous physiological processes.
Understanding the factors that can induce the expression of MOP-3 is of scientific interest as it provides insights into how circadian rhythms are entrained and maintained. Certain chemicals have been identified that can potentially stimulate the production of MOP-3. For instance, retinoic acid, a metabolite of vitamin A, is thought to enhance MOP-3 expression by engaging with nuclear receptors that can bind to DNA elements within circadian genes. Similarly, forskolin, which increases cellular cAMP levels, may lead to the activation of protein kinases that phosphorylate transcription factors involved in the expression of MOP-3. Another example is melatonin, a hormone known for its role in regulating sleep patterns, which may act through its receptors to synchronize the circadian clock by inducing MOP-3. Compounds like lithium chloride and resveratrol also play a role in the intricate signaling pathways that can lead to the upregulation of MOP-3, with lithium chloride acting through the inhibition of enzymes like GSK-3β, while resveratrol may exert its effect by activating sirtuins, thereby influencing the clock machinery. These and other compounds, such as sodium butyrate, valproic acid, and sulforaphane, interact with the epigenetic landscape or antioxidant response pathways, suggesting that the regulation of MOP-3 expression extends beyond simple transcriptional activation to encompass a broader regulatory network, which includes chromatin remodeling and cellular defense mechanisms. The study of these chemicals grants researchers a more profound understanding of the temporal orchestration of physiological functions and the molecular underpinnings of the circadian system.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid may upregulate MOP-3 expression through its interaction with retinoic acid receptors that bind to retinoic acid response elements associated with the transcriptional control of circadian genes. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin could stimulate MOP-3 expression by elevating intracellular cAMP, which activates protein kinase A (PKA) and could lead to the phosphorylation and activation of transcription factors that govern the expression of the MOP-3 gene. | ||||||
Melatonin | 73-31-4 | sc-207848 sc-207848A sc-207848B sc-207848C sc-207848D sc-207848E | 1 g 5 g 25 g 100 g 250 g 1 kg | $64.00 $72.00 $214.00 $683.00 $1173.00 $3504.00 | 16 | |
Melatonin might induce MOP-3 expression by acting as a synchronizer of the circadian clock, possibly through melatonin receptors that trigger signaling pathways directly tied to the homeostasis of clock gene expression. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride can upregulate MOP-3 expression by inhibiting glycogen synthase kinase-3 beta (GSK-3β), which plays a role in the phosphorylation state and function of various proteins linked to circadian rhythm maintenance, including components of the clock gene feedback loop. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol is thought to increase MOP-3 expression by activating sirtuin 1 (SIRT1), which may lead to the deacetylation of BMAL1 and thus affect the circadian clock's regulation at a transcriptional level. | ||||||
Caffeine | 58-08-2 | sc-202514 sc-202514A sc-202514B sc-202514C sc-202514D | 5 g 100 g 250 g 1 kg 5 kg | $32.00 $66.00 $95.00 $188.00 $760.00 | 13 | |
Caffeine might stimulate MOP-3 expression through antagonism of adenosine receptors, leading to a cascade of intracellular events that culminate in the heightened transcriptional activity of genes involved in maintaining circadian rhythms. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
Dexamethasone, a synthetic glucocorticoid, has been shown to upregulate MOP-3 expression in a time-dependent manner, suggesting that glucocorticoid signaling plays a role in synchronizing peripheral clocks by directly stimulating clock gene expression. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
Sodium butyrate could stimulate MOP-3 transcription by inhibiting histone deacetylases, leading to a relaxed chromatin structure at the MOP-3 promoter region, which makes the gene more accessible for transcriptional machinery. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Valproic acid may induce BMAL1 expression through its histone deacetylase inhibitory activity, which could result in hyperacetylation of histones near the BMAL1 gene, thereby promoting transcriptional activation. | ||||||
Docosa-4Z,7Z,10Z,13Z,16Z,19Z-hexaenoic Acid (22:6, n-3) | 6217-54-5 | sc-200768 sc-200768A sc-200768B sc-200768C sc-200768D | 100 mg 1 g 10 g 50 g 100 g | $92.00 $206.00 $1744.00 $7864.00 $16330.00 | 11 | |
Docosahexaenoic acid, an omega-3 fatty acid, may upregulate MOP-3 expression by altering cellular membrane composition and fluidity, which can influence a variety of signaling pathways and transcription factors involved in the expression of circadian genes. | ||||||