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相关概念视频

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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DNA Topoisomerases02:02

DNA Topoisomerases

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Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
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Transcription Elongation Factors02:35

Transcription Elongation Factors

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Transcription elongation is a dynamic process that alters depending upon the sequence heterogeneity of the DNA being transcribed. Hence, it is not surprising that the elongation complex's composition also varies along the way while transcribing a gene.
The transcription elongation is regulated via pausing of RNA polymerase on several occasions during transcription. In bacteria, these halts are necessary because the transcription of DNA into mRNA is coupled to the translation of that mRNA...
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Bacterial Transcription01:53

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RNA polymerase (RNAP) carries out DNA-dependent RNA synthesis in both bacteria and eukaryotes. Bacteria do not have a membrane-bound nucleus. So, transcription and translation occur simultaneously, on the same DNA template.
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RNA Polymerase II Accessory Proteins02:36

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Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...
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DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
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相关实验视频

Updated: Jul 11, 2025

Chromatin Interaction Analysis with Paired-End Tag Sequencing ChIA-PET for Mapping Chromatin Interactions and Understanding Transcription Regulation
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Chromatin Interaction Analysis with Paired-End Tag Sequencing ChIA-PET for Mapping Chromatin Interactions and Understanding Transcription Regulation

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XPF与TOP2B相互作用,用于R循环处理和DNA循环在活跃转录的基因上.

Georgia Chatzinikolaou1, Kalliopi Stratigi1, Athanasios Siametis1,2

  • 1Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, GR70013, Heraklion, Crete, Greece.

Science advances
|November 8, 2023
PubMed
概括
此摘要是机器生成的。

这项研究揭示了RNA-DNA混合体 (R环) 在转录过程中是如何处理的. 核酸切除修复因子XPF,与TOP2B和CTCF/凝聚素一起,促进R循环分辨率,影响DNA循环和基因激活.

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相关实验视频

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Chromatin Interaction Analysis with Paired-End Tag Sequencing ChIA-PET for Mapping Chromatin Interactions and Understanding Transcription Regulation
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Chromatin Interaction Analysis with Paired-End Tag Sequencing ChIA-PET for Mapping Chromatin Interactions and Understanding Transcription Regulation

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科学领域:

  • 分子生物学分子生物学
  • 遗传学 是一个遗传学.
  • 生物化学 生化学

背景情况:

  • 协同转录的RNA-DNA混合体 (R-循环) 通过导致DNA损伤,对基因组完整性构成风险.
  • 通过R循环调节基因活性的精确机制在很大程度上是未知的.

研究的目的:

  • 阐明转录期间R循环处理的基础分子机制.
  • 研究核酸切除修复因子XPF在R循环分辨率和基因调节中的作用.

主要方法:

  • 同免疫沉测试以确定蛋白质相互作用.
  • 染色体免疫沉 (ChIP) 评估蛋白质对基因促进体的招募.
  • 对DNA损伤反应标记物和DNA循环的分析.

主要成果:

  • XPF与CTCF和凝聚素子单元 (SMC1A,SMC3) 相互作用,在转录激活过程中调解R循环依赖的DNA循环.
  • XPF将TOP2B招募到活跃的基因促进器中,促进双链断裂和DNA损伤反应激活.
  • TOP2B 废除损害了 XPF,CTCF 和凝聚素的招募,阻碍了 DNA 循环和 R 循环处理.

结论:

  • 在转录激活过程中,XPF,TOP2B和CTCF/凝聚素复合体对于处理R循环至关重要.
  • 这一途径对于保持基因组完整性和调节基因表达至关重要.
  • 这些发现对理解与转录相关的DNA损伤相关的DNA修复缺陷综合征有意义.