EFO1, known formally as Establishment of Sister Chromatid Cohesion N-Acetyltransferase 1 (ESCO1), is a pivotal protein in the fundamental process of chromosomal segregation during cell division. This protein is instrumental in establishing sister chromatid cohesion, a critical phase in the cell cycle that ensures accurate chromosome alignment and separation. EFO1 exerts its function by facilitating the acetylation of specific lysine residues on the cohesin complex, a protein structure that holds sister chromatids together until they are ready to be pulled apart during mitosis. The precise regulation of ESCO1 expression is, therefore, essential for maintaining genomic stability and preventing anomalies in chromosome number, which are hallmarks of various forms of genomic instability. EFO1 is not only a keystone in the maintenance of genomic integrity but also plays a role in DNA replication and repair, signifying its broader impact on cellular health and function.
The expression of EFO1 can be influenced by a diverse array of chemical compounds, which may act as activators, inducing its transcription and subsequent protein synthesis. These activators can range from natural polyphenolic compounds, such as resveratrol, found in grapes, which may upregulate EFO1 by modulating sirtuin-dependent pathways, to epigenetic modifiers like Trichostatin A, which can increase EFO1 levels by altering the acetylation state of histones associated with its gene promoter. Other potential activators include dietary constituents like sulforaphane from cruciferous vegetables, which can stimulate EFO1 expression indirectly through its effects on histone modification enzymes. Additionally, compounds like Vitamin D3 and its active metabolites could induce EFO1 expression by interacting with vitamin D receptors that bind to EFO1's promoter region, highlighting the interplay between micronutrients and gene regulation. Understanding the myriad ways in which these chemical compounds can influence EFO1 expression is crucial, as it sheds light on the intricate mechanisms governing cellular replication and the preservation of genetic information. It is through these intricate molecular dialogues that the cell orchestrates the correct expression of genes like EFO1, ensuring the fidelity of cellular division and the perpetuation of genomic integrity.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $80.00 $220.00 $460.00 | 64 | |
Resveratrol may upregulate EFO1 by activating sirtuin pathways that are implicated in the acetylation of histones, a modification that could enhance the transcriptional activation of genes like EFO1 that participate in chromatin structure maintenance. | ||||||
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 | |
By inhibiting histone deacetylase, Trichostatin A could directly increase histone acetylation levels, leading to a more accessible chromatin state and the subsequent upregulation of genes including EFO1 involved in sister chromatid cohesion. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
This compound could stimulate EFO1 expression by reducing DNA methylation, thereby promoting the transcriptional activation of genes that play a role in chromatin architecture and function. | ||||||
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 | |
As a histone deacetylase inhibitor, Sodium Butyrate could increase the expression of EFO1 by promoting an open chromatin structure, thereby facilitating the transcription of genes related to chromatin dynamics. | ||||||
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 may stimulate EFO1 transcription by binding to retinoic acid receptors, which then bind to promoter regions of genes, including those involved in cell cycle control and chromatin organization. | ||||||
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 can elevate intracellular cAMP, which in turn may stimulate the transcription of EFO1 through cAMP response element-binding protein (CREB)-mediated pathways. | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-207495A sc-207495B sc-207495C sc-207495 sc-207495E sc-207495D | 5 mg 10 mg 25 mg 1 g 10 g 250 mg | $153.00 $292.00 $489.00 $1325.00 $8465.00 $933.00 | 22 | |
DL-Sulforaphane may upregulate EFO1 by altering gene expression profiles through its influence on histone acetylation and methylation, thereby changing the expression of genes that govern cell cycle and genomic stability. | ||||||
Cholecalciferol | 67-97-0 | sc-205630 sc-205630A sc-205630B | 1 g 5 g 10 g | $71.00 $163.00 $296.00 | 2 | |
The active metabolite of Cholecalciferol may induce EFO1 expression by interacting with vitamin D receptors, which can bind to specific DNA sequences and upregulate genes involved in DNA repair and replication. | ||||||
(−)-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 | $43.00 $73.00 $126.00 $243.00 $530.00 $1259.00 | 11 | |
Epigallocatechin Gallate could stimulate the transcription of EFO1 through its potential to induce changes in DNA methylation and histone modification patterns, which are key processes in gene expression control. | ||||||
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 | $37.00 $69.00 $109.00 $218.00 $239.00 $879.00 $1968.00 | 47 | |
Curcumin may increase EFO1 expression by stimulating transcription factors and altering the epigenetic landscape, which includes changes in the methylation and acetylation status of histones associated with EFO1's promoter region. | ||||||