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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...
Initiation of Translation02:33

Initiation of Translation

Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
Master Transcription Regulators02:23

Master Transcription Regulators

Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a  complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
Master Transcription Regulators02:23

Master Transcription Regulators

Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a  complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
Calmodulin-dependent Signaling01:16

Calmodulin-dependent Signaling

Calmodulin (CaM) is a calcium-binding protein in eukaryotes that controls various calcium-regulated cellular processes. It has four calcium-binding sites that bind calcium to form the calcium-calmodulin ( Ca2+-CaM) complex. GPCR stimulation increases the calcium levels in the cells that bind to CaM and induces a conformational change.
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
Transducer Mechanism: Enzyme-Linked Receptors01:27

Transducer Mechanism: Enzyme-Linked Receptors

Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:

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相关实验视频

Updated: Jul 6, 2026

The MultiBac Protein Complex Production Platform at the EMBL
13:51

The MultiBac Protein Complex Production Platform at the EMBL

Published on: July 11, 2013

将转录因子加载到MMTV促进器上:促进器激活的双模机制.

T K Archer1, P Lefebvre, R G Wolford

  • 1Hormone Action and Oncogenesis Section, Laboratory of Molecular Virology, National Cancer Institute, Bethesda, MD 20892.

Science (New York, N.Y.)
|March 20, 1992
PubMed
概括

葡萄糖皮质激素在小鼠乳腺瘤病毒促进体中重塑染色质,使转录因子NF1 / CTF结合. 这种依赖激素的过程通过调节对促进者DNA的访问来控制基因诱导.

科学领域:

  • 分子生物学分子生物学
  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
  • 基因规则 基因规则

背景情况:

  • 小鼠乳腺瘤病毒 (MMTV) 促销者的染色质结构影响转录因子的可访问性.
  • 了解促进器架构是如何动态调节的,对于破译基因表达控制至关重要.

研究的目的:

  • 研究染色体重塑在MMTV促进体的荷尔蒙依赖转录中的作用.
  • 阐明核因子1/CCAAT转录因子 (NF1/CTF) 招募到MMTV发起人的机制.

主要方法:

  • 在动物细胞中分析MMTV促进体核细胞分相.
  • 在葡萄糖皮质体治疗前后评估NF1/CTF结合剂和核分解剂的可访问性.
  • 暂时引入与集成促进者的行为比较.

主要成果:

  • 在集成的环境中,MMTV发起者采用分相核素组合,但不包括NF1/CTF.
  • 葡萄糖皮质体治疗诱导染色体重塑,允许NF1 / CTF结合和核分解性访问.
  • 暂时引入的促进体显示构成性NF1/CTF结合和荷尔蒙独立的核分解性攻击.

结论:

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Inducible T7 RNA Polymerase-mediated Multigene Expression System, pMGX
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Inducible T7 RNA Polymerase-mediated Multigene Expression System, pMGX

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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo

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相关实验视频

Last Updated: Jul 6, 2026

The MultiBac Protein Complex Production Platform at the EMBL
13:51

The MultiBac Protein Complex Production Platform at the EMBL

Published on: July 11, 2013

Inducible T7 RNA Polymerase-mediated Multigene Expression System, pMGX
10:09

Inducible T7 RNA Polymerase-mediated Multigene Expression System, pMGX

Published on: June 27, 2017

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
12:42

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo

Published on: January 7, 2019

  • MMTV促进体诱导是一种双式过程,涉及荷尔蒙依赖的染色体重塑.
  • 受体介导的染色质变化促进NF1/CTF加载和招募其他转录因子.