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相关概念视频

Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

9.9K
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...
9.9K
Histone Modification02:32

Histone Modification

16.9K
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...
16.9K
Histone Modification02:32

Histone Modification

4.8K
4.8K
Nucleosome Remodeling02:54

Nucleosome Remodeling

11.6K
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...
11.6K
Chromatin Modification in iPS Cells01:32

Chromatin Modification in iPS Cells

2.3K
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...
2.3K
Heterochromatin02:38

Heterochromatin

18.9K
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...
18.9K

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相关实验视频

Updated: Mar 17, 2026

Author Spotlight: Developing Acetyl-Click Assay for HAT1 Inhibitor Screening
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Author Spotlight: Developing Acetyl-Click Assay for HAT1 Inhibitor Screening

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关于"基因素乙化开关通过SWR-C重塑酶调节H2A.Z沉积"的评论

Feng Wang1, Anand Ranjan2, Debbie Wei1

  • 1Laboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, Building 37, Room 6114, Bethesda, MD 20892, USA.

Science (New York, N.Y.)
|July 28, 2016
PubMed
概括

研究人员研究了SWR1/SWR-C复合体

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Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
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Complete Workflow for Analysis of Histone Post-translational Modifications Using Bottom-up Mass Spectrometry: From Histone Extraction to Data Analysis
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Complete Workflow for Analysis of Histone Post-translational Modifications Using Bottom-up Mass Spectrometry: From Histone Extraction to Data Analysis

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Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
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Complete Workflow for Analysis of Histone Post-translational Modifications Using Bottom-up Mass Spectrometry: From Histone Extraction to Data Analysis
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科学领域:

  • 分子生物学
  • 染色体生物学
  • 酵母遗传学

背景情况:

  • SWR1/SWR-C复合物有助于基因组变体的交换.
  • 基因组变异H2A.Z在转录和基因组稳定性中起作用.
  • 了解H2A.Z沉积和除去的动态至关重要.

研究的目的:

  • 调查由SWR1/SWR-C复合体替代H2A.Z的报道.
  • 要确定H3K56Q的修饰是否影响H2A.Z核细胞的动态.

主要方法:

  • 在体外生化测试.
  • 分析SWR1/SWR-C复合物的活性.
  • 采用了多种反应条件和测量方法.

主要成果:

  • 没有证据支持H2A.Z替代的逆转.
  • 证实了SWR1/SWR-C复合体在H2A.Z沉积中的作用.
  • 在测试条件下,H3K56Q的修饰似乎没有转变.

结论:

  • 这些发现与之前关于H2AZ替代逆转的报道相矛盾.
  • 需要进一步研究以充分阐明H2A.Z动态的调节机制.
  • 这项研究强调了在染色体重塑研究中严格验证的重要性.