The DUX family of proteins, typified by their homeobox domains, are pivotal in the orchestration of early embryonic development processes. These proteins, especially those such as DUX4 and DUX5, are key in zygotic genome activation, a critical phase where the embryonic genome begins to express and assume control over the development process post-fertilization. The DUX proteins are also closely studied for their roles in chromatin structure regulation, influencing the accessibility of DNA for transcription. Although the mechanisms that control the expression of DUX proteins are complex and not yet fully elucidated, research has revealed that certain chemical compounds are capable of modulating their expression levels. These compounds act through diverse cellular pathways, affecting the chromatin landscape, DNA methylation patterns, and various signaling cascades, ultimately leading to changes in DUX gene transcription.
An array of chemical activators has been identified that can potentially induce the expression of DUX proteins, each operating through distinct molecular mechanisms. For instance, compounds such as histone deacetylase inhibitors, including Trichostatin A and Valproic acid, can increase histone acetylation, leading to a more relaxed and transcriptionally active chromatin state around the DUX gene loci. Other activators work by intervening in the cellular signaling pathways; for example, Forskolin raises intracellular cAMP levels, which can activate protein kinase A and downstream transcription factors that stimulate DUX gene transcription. Additionally, agents like 5-Azacytidine can induce DNA demethylation, thereby removing repressive epigenetic marks and enhancing gene expression. Similarly, retinoids such as Retinoic acid and Isotretinoin interact with nuclear receptors, with downstream effects that include the upregulation of genes like those in the DUX family. Each of these compounds suggests the intricate network of biological interactions that govern gene expression, demonstrating the sophisticated regulatory systems that cells employ to manage the expression of developmentally important genes such as DUX.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
This cytidine analog could demethylate DNA by inhibiting DNA methyltransferases, thereby potentially upregulating the transcription of the DUX gene through epigenetic remodeling. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A could directly stimulate the transcription of the DUX gene by preventing deacetylation of histones, thus keeping the chromatin in an open state conducive to gene expression. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Valproic acid may increase acetylation levels of histones associated with the DUX gene locus, leading to enhanced transcriptional activity of the gene. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride may disrupt the activity of GSK-3, a kinase involved in numerous signaling pathways, which could lead to the stimulation of DUX gene transcription by altering downstream signaling. | ||||||
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 elevate intracellular cAMP, which may subsequently activate PKA and CREB, leading to the induction of the DUX gene transcription. | ||||||
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 might bind to its nuclear receptors, which then bind to retinoic acid response elements in the genome, potentially increasing transcription of the DUX gene. | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $62.00 $178.00 | 8 | |
β-Estradiol may stimulate the transcription of the DUX gene by engaging estrogen receptors that interact with estrogen response elements in the gene's promoter region. | ||||||
Calcium dibutyryladenosine cyclophosphate | 362-74-3 | sc-482205 | 25 mg | $147.00 | ||
As a synthetic analog of cAMP, Calcium dibutyryladenosine cyclophosphate could activate PKA, leading to an upregulation of transcription factors that promote the expression of the DUX gene. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
Epigallocatechin Gallate could promote the transcription of the DUX gene by altering the methylation patterns of DNA and modifying histone acetylation, thus changing the chromatin landscape at the gene locus. | ||||||
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 may trigger an increase in histone acetylation at the DUX gene promoter, thereby stimulating transcriptional activation of the gene. | ||||||