CBP146, a protein encoded by the BAZ1A gene in mice, plays a pivotal role in the intricate machinery of chromatin remodeling and transcription regulation within the cell. This protein acts as a scaffold for the assembly of various protein complexes that modify the structure of chromatin, thereby controlling the accessibility of DNA for transcription. The precise expression of cbp146 is critical for normal cellular function and development, as it is involved in pathways that maintain genomic stability and modulate gene expression in response to internal and external cues. Understanding how to upregulate cbp146 expression is an area of significant interest within the field of molecular biology, as it offers insights into the mechanisms that control gene activity and the maintenance of cellular homeostasis.
Several chemicals have been identified that may serve as potential activators of cbp146 expression by targeting different molecular pathways. For instance, epigenetic modifiers such as 5-Aza-2'-deoxycytidine and Trichostatin A could enhance cbp146 expression by altering DNA methylation and histone acetylation patterns, leading to a more relaxed chromatin structure that promotes gene transcription. Compounds like Forskolin, which elevate cAMP levels, could activate protein kinase A, potentially resulting in the phosphorylation of transcription factors that stimulate the expression of cbp146. Furthermore, signaling molecules such as beta-estradiol may engage estrogen receptors that interact with specific DNA sequences to upregulate the expression of adjacent genes, including cbp146. Lithium chloride, on the other hand, may indirectly upregulate cbp146 by inhibiting GSK-3 and affecting the stability of transcription factors. Additionally, naturally occurring compounds like Resveratrol are implicated in the activation of sirtuins, which might lead to the deacetylation of transcription factors and coactivators, thereby enhancing the transcription of genes like cbp146. These compounds, among others, provide a diverse set of tools for research into the regulation of gene expression and the complex interplay between chromatin architecture and cellular function.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
5-Aza-2′-Deoxycytidine could demethylate the promoter region of cbp146, leading to the recruitment of transcription machinery and subsequent upregulation of gene transcription. | ||||||
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 can elevate acetylation levels of histones near the cbp146 locus, thereby unwinding chromatin and permitting transcription factors to stimulate cbp146 transcription. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
By inhibiting histone deacetylation, Valproic acid may promote an open chromatin state at the cbp146 gene, facilitating transcription initiation and upsurge in gene expression. | ||||||
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, through its interaction with retinoic acid receptors, could initiate a cascade of events leading to the recruitment of transcriptional coactivators to the cbp146 gene, boosting its expression. | ||||||
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 | |
By raising intracellular cAMP, Forskolin can activate protein kinase A, which may phosphorylate transcription factors that directly bind and stimulate cbp146 promoter activity. | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $62.00 $178.00 | 8 | |
Estrogen receptor activation by β-Estradiol can stimulate the transcriptional activity of estrogen-responsive elements associated with the cbp146 gene, leading to increased gene expression. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin may upregulate the expression of cbp146 by inhibiting histone acetyltransferase, which could result in a more transcriptionally active chromatin configuration around the gene. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride can inhibit GSK-3, potentially leading to the stabilization and activation of transcription factors that target the cbp146 promoter to stimulate its 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 | 18 | |
Sodium butyrate, as an HDAC inhibitor, may cause hyperacetylation of histones at the cbp146 gene, resulting in an upsurge in the recruitment of transcriptional machinery to the gene. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol can stimulate sirtuin activity which, in turn, may deacetylate specific transcription factors or coactivators leading to enhanced transcriptional activity of the cbp146 gene. |