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What is the mechanism by which the chemical 5-azacytidine enhances gene expression?

Short Answer

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Explain the mechanism by which 5-azacytidine enhances gene expression. 5-azacytidine enhances gene expression through its ability to inhibit DNA methyltransferase enzymes (DNMTs) and decrease DNA methylation. By incorporating into the DNA during replication and trapping DNMTs, 5-azacytidine leads to reduced DNA methylation. Since DNA methylation typically represses gene expression, the decrease in methylation caused by 5-azacytidine allows for silenced or suppressed genes to be reactivated, ultimately resulting in enhanced gene expression. This mechanism is especially important in cancer treatment, as it can reactivate tumor suppressor genes that have been silenced by hypermethylation.

Step by step solution

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1. Define gene expression and 5-azacytidine

Gene expression is the process through which genetic information encoded in a gene is transformed into a functional product, such as a protein or RNA molecule. 5-azacytidine (AZA) is a chemical compound that acts as an analog of the nucleotide cytidine, which is a component of DNA and RNA.
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2. Explain 5-azacytidine action as a DNA methyltransferase inhibitor

5-azacytidine's main mode of action is by inhibiting DNA methyltransferase enzymes (DNMTs). DNMTs are enzymes responsible for adding a methyl group to the cytosine residues in DNA. 5-azacytidine gets incorporated into the DNA during replication, which occurs when the DNA is copied before cell division. When a DNMT tries to methylate this azacytosine, the enzyme becomes trapped and subsequently degraded. This leads to a reduction in DNA methylation.
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3. Describe the role of DNA methylation in gene expression

DNA methylation is an epigenetic modification that occurs when a methyl group is added to the cytosine residue of a CpG dinucleotide in the DNA. Methylation of a gene's promoter region, a regulatory region located upstream of the gene, typically leads to repression of gene expression. This happens because the methyl groups can block the binding of transcription factors, which are necessary for gene expression, and also facilitate the binding of proteins that compact the DNA, making it less accessible to the transcription machinery.
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4. Relate 5-azacytidine's action to enhanced gene expression

By inhibiting DNMTs and decreasing DNA methylation, 5-azacytidine can lead to enhanced gene expression. As mentioned earlier, DNA methylation is usually associated with reduced gene expression. When 5-azacytidine causes a decrease in DNA methylation, it can lead to the reactivation of silenced or suppressed genes, resulting in enhanced gene expression. This can be particularly relevant in the context of cancer treatment, as 5-azacytidine can reactivate tumor suppressor genes that have been silenced by hypermethylation. In conclusion, 5-azacytidine enhances gene expression by inhibiting DNA methyltransferase enzymes, leading to a decrease in DNA methylation. This ultimately results in the reactivation of silenced or suppressed genes and increased gene expression.

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Most popular questions from this chapter

The addition of a " \(5^{\prime}-\operatorname{cap}^{\prime \prime}\) and a \(^{\prime \prime} 3^{\prime}\) poly-A" tail to many nuclear RNA species occurs prior to export of mature mRNAs to the cytoplasm. Such modifications appear to influence mRNA stability. Many assays for gene regulation involve the use of reporter genes such as luciferase from the North American firefly (Photinus pyralis). When the luciferase gene is transcribed and translated, the protein product can be easily assayed in a test tube. In the presence of luciferin, ATP, and oxygen, the luciferase enzyme produces light that can be easily quantified. Assuming that luciferase mRNA can be obtained and differentially modified (5'-capped, poly-A tailed) in a test tube, suggest an assay system that would allow you to determine the influence of \(5^{\prime}-\) capping and poly-A tail addition on mRNA stability.

In this chapter, we focused on how eukaryotic genes are regulated at different steps in their expression, from chromatin modifications to control of protein stability. At the same time, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, (a) How do we know that promoter and enhancer sequences control the initiation of transcription in eukaryotes? (b) How do we know that eukaryotic transcription factors bind to DNA sequences at or near promoter regions? (c) How do we know that double-stranded RNA molecules can control gene expression?

Present an overview of the manner in which chromatin can be remodeled. Describe the manner in which these remodeling processes influence transcription.

Explain the structural features of the Initiator (Inr) elements, BREs, DPEs, and MTEs of focused promoters.

Distinguish between the \(c\) is-acting regulatory elements referred to as promoters and enhancers.

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