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相关概念视频

Chromatin Modification in iPS Cells01:32

Chromatin Modification in iPS Cells

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Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
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Methods of Nuclear Reprogramming01:24

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Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
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Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

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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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Chromatin Position Affects Gene Expression02:35

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Chromatin is the massive complex of DNA and proteins packaged inside the nucleus. The complexity of chromatin folding and how it is packaged inside the nucleus greatly influences  access to genetic information. Generally, the nucleus' periphery is considered transcriptionally repressive, while the cell's interior is considered a transcriptionally active area. 
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Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

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The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer...
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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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相关实验视频

Updated: Mar 2, 2026

An Integrated Platform for Genome-wide Mapping of Chromatin States Using High-throughput ChIP-sequencing in Tumor Tissues
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染色体状态定义瘤特异性T细胞功能障碍和重编程

Mary Philip1, Lauren Fairchild2,3, Liping Sun4

  • 1Immunology Program, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.

Nature
|May 18, 2017
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概括

透瘤的CD8T细胞存在两种状态:一种是可塑性和可重新编程的,另一种是固定的和耐药的. 识别表面标记可以预测哪些功能失调的T细胞可用于癌症免疫治疗.

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An Integrated Platform for Genome-wide Mapping of Chromatin States Using High-throughput ChIP-sequencing in Tumor Tissues
10:41

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科学领域:

  • 免疫学
  • 癌症生物学
  • 表观遗传学

背景情况:

  • 固体瘤中的瘤特异性CD8T细胞往往变得功能障碍,阻碍抗瘤免疫反应.
  • 控制T细胞功能障碍的表观遗传机制及其对免疫检查点阻断等重编程疗法的易感性仍然不明.

研究的目的:

  • 研究瘤中CD8T细胞功能障碍的表观遗传调节.
  • 识别瘤中的特异性T细胞状态及其治疗重编程潜力.
  • 发现可以预测T细胞适用于癌症免疫治疗的表面标记物.

主要方法:

  • 分析小鼠瘤透的CD8T细胞中的染色质状态.
  • 识别区分T细胞亚群的表面标记物.
  • 鼠标和人类透瘤的CD8T细胞的比较.

主要成果:

  • 小鼠瘤中的CD8T细胞分化为两个离散的染色质状态:可重编程的功能障碍状态和固定的抵抗性功能障碍状态.
  • 确定了特定的表面标记物,区分可重编程与不可重编程的PD1hi功能障碍的CD8T细胞.
  • 这些已识别的表面标记物也存在于人类瘤透的CD8T细胞上.

结论:

  • 在瘤中,表观遗传程序决定了不同的CD8T细胞功能失调状态,影响了它们的治疗潜力.
  • 表面标记可以预测功能失调的CD8T细胞的可重编程性,为癌症免疫治疗提供生物标记.
  • 了解这些表观遗传和表面标记特征对于开发有效的免疫疗法至关重要.