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相关概念视频

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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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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Chromatin Structure Regulates pre-mRNA Processing02:41

Chromatin Structure Regulates pre-mRNA Processing

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In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
The chromatin structure, especially...
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Duplication of Chromatin Structure02:05

Duplication of Chromatin Structure

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The process of chromosome duplication during cell division requires genome-wide disruption and re-assembly of chromatin. The chromatin structure must be accurately inherited, reassembled, and maintained in the daughter cells to ensure lineage propagation.
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...
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Heterochromatin02:38

Heterochromatin

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The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions that take up more dye are called heterochromatin. Heterochromatin is further classified into two forms – constitutive heterochromatin and facultative heterochromatin.
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at...
13.7K
Nucleosome Remodeling02:54

Nucleosome Remodeling

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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
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
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相关实验视频

Updated: Jul 12, 2025

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
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染色化调节了topoisomerase II的过程性.

Jaeyoon Lee1, Meiling Wu1,2, James T Inman1,2

  • 1Physics Department & LASSP, Cornell University, Ithaca, NY, 14853, USA.

Nature communications
|October 27, 2023
PubMed
概括
此摘要是机器生成的。

细胞拓酶II (topo II) 的活性被染色质显著增强,该染色质作为主要的兴奋剂. 这种酶有效地缓解DNA扭曲应激,特别是在复杂的染色质结构中.

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相关实验视频

Last Updated: Jul 12, 2025

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科学领域:

  • 分子生物学分子生物学
  • 生物化学 生物化学
  • 遗传学 遗传学是一种遗传学.

背景情况:

  • 类型IIA拓酶 (topo II) 对于在细胞过程中管理DNA扭曲应激至关重要.
  • 不同的DNA扭曲应力对Topo II功能的影响尚未完全理解.

研究的目的:

  • 为了研究真核细胞的拓酶II活性对裸体DNA和染色质的扭曲依赖性.
  • 阐明DNA结构,特别是染色质如何影响Topo II的过程性和功能.

主要方法:

  • 利用多种单分子方法来分析Topo II活动.
  • 在DNA扭曲和结构的不同条件下检查了酶行为 (裸体DNA与染色质).

主要成果:

  • 比以前报道的,Topo II 在曲DNA上表现出明显更高的过程性.
  • 托波II在积聚体形成之前放松超绕的DNA,并降低了过程性.
  • 染色体通过促进DNA交叉,甚至在低扭力压力下,也大大提高了topo II的过程性.

结论:

  • 染色体是真核生物的托聚酶II功能的关键刺激剂.
  • 染色质的DNA结合特性显著影响TOPO II解决扭曲应力的能力.
  • 了解Topo II与染色质的相互作用对于理解DNA拓调节至关重要.