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相关概念视频

RNA Polymerase II Accessory Proteins02:36

RNA Polymerase II Accessory Proteins

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...
Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form dimers that...
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
Eukaryotic Transcription Inhibitors01:52

Eukaryotic Transcription Inhibitors

Certain biochemical processes, such as embryonic development and cell growth regulation, depend on the repression of specific genes. DNA binding proteins known as eukaryotic transcription inhibitors regulate the repression of gene expression in eukaryotes. The presence of these inhibitors at the required location and time in the cell is triggered by the presence of hormones and additional signals from other cells.
Eukaryotic transcription inhibitors usually contain two distinct domains, a DNA...
Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form dimers that...
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...

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相关实验视频

Updated: Jun 23, 2026

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
10:28

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers

Published on: September 20, 2018

改变抑制剂的DNA结合特异性

P Youderian, A Vershon, S Bouvier

    Cell
    |December 1, 1983
    PubMed
    概括

    研究人员在Mnt抑制蛋白中发现了特定的突变,这些突变改变了其DNA结合特异性. 这种沙门氏菌P22抑制剂现在比原始更强烈地结合了突变的运营者,表明其遗传识别的关键变化.

    科学领域:

    • 分子生物学分子生物学
    • 遗传学 是一个遗传学.
    • 病毒学 病毒学

    背景情况:

    • 来自沙门氏菌P22的Mnt抑制剂通过与特定的操作者DNA序列结合来调节基因表达至关重要.
    • 了解抑制剂-运营者相互作用是破译病毒遗传控制机制的关键.

    研究的目的:

    • 研究Mnt抑制器中的特定突变如何影响其DNA结合特异性.
    • 为了确定负责改变结合亲和力和特异性的氨基酸变化.

    主要方法:

    • 构建一个突变的Mnt结合位点,具有对称的,操作者构成突变.
    • 选择具有改变结合偏好的Mnt抑制器突变.
    • 在体外DNA结合测试中使用纯化的野生类型和突变的Mnt蛋白.

    主要成果:

    • 在Mnt抑制器的CAC编码子 (His6到Pro) 中的突变导致了DNA结合特异性的显著变化.
    • 野生类型的Mnt与野生类型的操作员有很强的结合,但与突变型的操作员的结合关系要小1000倍.
    • 突变的Mnt蛋白质表现出反向的结合亲缘关系,有利于突变的操作者.

    结论:

    • 在Mnt抑制器中,His6到Pro的替代对于其DNA结合特异性至关重要.

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    Lentiviral Vector Platform for the Efficient Delivery of Epigenome-editing Tools into Human Induced Pluripotent Stem Cell-derived Disease Models

    Published on: March 29, 2019

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    In Vitro Selection of Engineered Transcriptional Repressors for Targeted Epigenetic Silencing

    Published on: May 5, 2023

  • 这项研究表明,向突变如何可以重新编程抑制剂-DNA相互作用.
  • 这些发现提供了对菌体抑制器中序列识别的分子基础的见解.