GIOT-2, officially recognized as zinc finger protein 44 (ZNF44), is a gene whose expression is critical in the complex tapestry of human genetic regulation. Located within the vast expanse of the human genome, ZNF44 encodes a protein that belongs to the zinc finger protein family, known for their role in binding to DNA and influencing the transcriptional fate of genes. The GIOT-2 protein is predicted to play a pivotal role in the regulation of transcription by RNA polymerase II, a process central to the expression of many genes within human cells. This protein's activity is hypothesized to occur within the nucleus, where it may interact with DNA in a sequence-specific manner, guiding the transcriptional machinery to specific genomic loci and thus affecting gene expression patterns. The ubiquitous expression of GIOT-2 across various tissues, including the thyroid and kidney, underscores its potential importance in maintaining the proper function of diverse biological systems.
The expression of GIOT-2, like that of many genes, can be influenced by a myriad of chemical compounds that can act as activators. Compounds such as Trichostatin A and 5-Aza-2'-deoxycytidine are known to induce changes in chromatin structure and DNA methylation, respectively, potentially leading to an upsurge in GIOT-2 expression. Trichostatin A, a potent histone deacetylase inhibitor, can result in a more transcriptionally active chromatin state, which may favor the binding of transcriptional machinery to the GIOT-2 promoter. On the other hand, 5-Aza-2'-deoxycytidine can induce DNA demethylation, a process that often correlates with gene activation and could conceivably increase the transcription of GIOT-2. Beta-estradiol and Retinoic Acid, by interacting with their respective nuclear hormone receptors, can initiate transcriptional cascades that include the upregulation of genes like GIOT-2. Additionally, small molecule activators such as Forskolin, which raises intracellular cAMP levels, could activate a signaling cascade that results in the enhanced transcription of genes including GIOT-2. These chemicals represent just a fraction of the potential activators that could exert an influence on the expression of this gene by targeting various biological pathways and molecular mechanisms within the cell. Each activator operates through distinct pathways, yet all converge on the central dogma of molecular biology, potentially leading to increased expression of GIOT-2, a testament to the intricacy and interconnectedness of cellular regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
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 | $152.00 $479.00 $632.00 $1223.00 $2132.00 | 33 | |
Trichostatin A may upregulate GIOT-2 by altering chromatin architecture, rendering the promoter region of the GIOT-2 gene more accessible for transcriptional machinery. | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $218.00 $322.00 $426.00 | 7 | |
By inhibiting DNA methyltransferase, 5-Aza-2′-Deoxycytidine could lead to the hypomethylation of the GIOT-2 gene promoter, resulting in enhanced transcription. | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $63.00 $182.00 | 8 | |
β-Estradiol could stimulate GIOT-2 expression through estrogen receptor-mediated initiation of transcriptional programs, possibly involving the GIOT-2 gene promoter. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $31.00 $47.00 $84.00 $222.00 | 19 | |
Sodium Butyrate may induce the expression of GIOT-2 by inhibiting deacetylation of histones, thus facilitating a transcriptionally active state of associated gene regions. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $78.00 $153.00 $740.00 $1413.00 $2091.00 | 73 | |
Forskolin could increase GIOT-2 levels by raising intracellular cAMP, subsequently activating a cascade that leads to transcriptional activation of target genes such as GIOT-2. | ||||||
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $172.00 $305.00 | 66 | |
Tunicamycin might stimulate the expression of GIOT-2 due to its ability to initiate the unfolded protein response, a mechanism that compensates for ER stress by upregulating specific genes. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $66.00 $325.00 $587.00 $1018.00 | 28 | |
Retinoic Acid could induce the expression of GIOT-2 by binding to retinoic acid receptors that directly interact with the gene's promoter elements to initiate transcription. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $91.00 $139.00 $374.00 | 36 | |
Dexamethasone may upregulate GIOT-2 expression through glucocorticoid receptor activation which binds to glucocorticoid response elements in the GIOT-2 gene regulatory regions. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium Chloride could stimulate GIOT-2 transcription by inhibiting GSK-3, thereby activating transcription factors that bind to the GIOT-2 gene promoter and initiate its expression. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $136.00 $446.00 | 114 | |
Thapsigargin might increase GIOT-2 transcription as a cellular adaptive response to ER stress through the unfolded protein response, which includes upregulation of certain genes. | ||||||