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相关概念视频

Epigenetic Regulation01:46

Epigenetic Regulation

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Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
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Nucleosome Remodeling02:54

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Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
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Histone Modification02:32

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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.
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The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
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Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
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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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相关实验视频

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Detection of Modified Forms of Cytosine Using Sensitive Immunohistochemistry
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DNA脱甲基化动态的动态

Nidhi Bhutani1, David M Burns, Helen M Blau

  • 1Baxter Laboratory for Stem Cell Biology, Institute for Stem Cell Biology and Regenerative Medicine, Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305-5175, USA.

Cell
|September 20, 2011
PubMed
概括
此摘要是机器生成的。

最初认为简单的DNA脱甲基化,涉及TET和AID/APOBEC酶的复杂的活性和被动机制. 哺乳动物中的这种动态DNA甲基化过程依赖于DNA修复途径进行调节.

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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.
  • 分子生物学分子生物学
  • 遗传学 是一个遗传学.

背景情况:

  • 细胞因子基甲基化 (5hmC) 最初被提出作为一种简单的DNA脱甲基化途径.
  • 早期的理解表明,通过DNA脱甲基化激活基因的简单机制.

研究的目的:

  • 阐明DNA脱甲基化的复杂机制.
  • 研究TET和AID/APOBEC酶在DNA甲基化动态中的作用.
  • 了解控制哺乳动物细胞中DNA甲基化的调节过程.

主要方法:

  • 研究了被动和活性DNA脱甲基化途径.
  • 专注于十个十一个转位 (TET) 酶家族酶的酶活性.
  • 研究了AID/APOBEC家族酶在DNA修饰中的功能.

主要成果:

  • 基因脱甲基化涉及复杂的活性和被动机制.
  • TET和AID/APOBEC酶在活性DNA脱甲基化中起着至关重要的作用.
  • 在哺乳动物细胞中,DNA修复途径是细胞因子甲基化去除的组成部分.

结论:

  • 基因甲基化是一种动态的,而不是固定的,表观遗传标记.
  • 在特定的细胞环境中,不断调节DNA甲基化是必不可少的.
  • 基因甲基化,脱甲基化和修复之间的相互作用凸显了表观遗传可塑性.