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相关概念视频

Epigenetic Regulation01:37

Epigenetic Regulation

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Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
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Master Transcription Regulators02:23

Master Transcription Regulators

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Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a  complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
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Histone Modification02:32

Histone Modification

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The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
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Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

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Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
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Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

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Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
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Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
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相关实验视频

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Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
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甲基化 Mesa定义了针对目标基因激活的功能调节元素.

Y V Liu1,2, J Suryatenggara1, H Wong1

  • 1Cancer Science Institute of Singapore, 117599, Singapore.

Research square
|November 1, 2024
PubMed
概括

新的表观遗传元素称为甲基化Mesas (MM) 驱动基因激活. 这些自我维持的调节元素使用有针对性的去甲基化来启动长期的基因表达和染色质重新连接.

关键词:
这就是CRISPR-DiRR.基因甲基化 DNA 甲基化脱甲基化脱甲基化基因激活 基因激活基因表达 基因表达甲基化敏感地点

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Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
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科学领域:

  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
  • 基因组学就是基因组学.
  • 分子生物学分子生物学

背景情况:

  • DNA甲基化和mRNA表达之间的相关性缺乏一致的因果证据.
  • 假设:因果调节甲基化元素显示出高度的脱甲基化敏感性.

研究的目的:

  • 识别和描述新的表观遗传调节元素.
  • 研究甲基化在基因调节中的因果作用.
  • 开发精确的工具来进行表观遗传操纵.

主要方法:

  • 在去甲基化前后对20个样本进行全基因组二硫酸盐测序.
  • 识别称为甲基化表 (MM) 的窄宽元素.
  • 开发和应用CRISPR-DiR用于有针对性的脱甲基化.

主要成果:

  • 甲基化表 (MM) 是窄宽 (45-294 bp) 的元素,具有短的高原特征.
  • MM签名在物种中保存,独立于CpG岛屿,并且与活性基因素标记相关联.
  • 针对MM的脱甲基化触发了显著的位点和远端染色体重新连接,启动了mRNA的表达.

结论:

  • 甲基化表 (MM) 是自我维持的表观遗传调节元素.
  • 通过集中去甲基化,MM保持长期的基因激活,从而导致基因素修饰和远端元素相互作用.
  • 克里斯普尔-DiR技术可以精确评估表观遗传因果关系.