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相关概念视频

Co-activators and Co-repressors02:04

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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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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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Operons02:09

Operons

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Prokaryotes can control gene expression through operons—DNA sequences consisting of regulatory elements and clustered, functionally related protein-coding genes. Operons use a single promoter sequence to initiate transcription of a gene cluster (i.e., a group of structural genes) into a single mRNA molecule. The terminator sequence ends transcription. An operator sequence, located between the promoter and structural genes, prohibits the operon’s transcriptional activity if bound by...
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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...
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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.
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The organization of prokaryotic genes in their genome is notably different from that of eukaryotes. Prokaryotic genes are organized, such that the genes for proteins involved in the same biochemical process or function are located together in groups. This group of genes, along with their regulatory elements, are collectively known as an operon. The functional genes in an operon are transcribed together to give a single strand of mRNA known as polycistronic mRNA.
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Updated: Jun 18, 2025

Lentiviral Vector Platform for the Efficient Delivery of Epigenome-editing Tools into Human Induced Pluripotent Stem Cell-derived Disease Models
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工程转录激活器样效应二分蛋白赋予DNA循环依赖的基因抑制,与Lac抑制剂相当.

Nicole A Becker1, Justin P Peters2, Elizabeth Lewis1

  • 1Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.

Nucleic acids research
|July 30, 2024
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概括

称为转录激活器样效应二极体 (TALED) 的工程DNA结合蛋白可以使用DNA循环强大抑制细菌基因. 这个系统模仿了天然的基因抑制,并为合成生物学应用提供了潜在的潜力.

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科学领域:

  • 合成生物学 合成生物学
  • 分子生物学分子生物学
  • 微生物学 微生物学

背景情况:

  • Prokaryotic 基因抑制通常利用 DNA 循环来增强抑制蛋白度在目标促进体.
  • 以前设计的转录激活器样效应二分子 (TALED) 系统由于蛋白质二分化动态而显示出有限的基于DNA循环的抑制.

研究的目的:

  • 使用共价TALED设计和表征强大的DNA循环依赖的基因抑制系统.
  • 量化评估DNA循环对大肠杆菌促进体抑制的贡献.
  • 建立基于TALED的基因调节的设计原则.

主要方法:

  • 工程共价TALED蛋白质用于细菌促进体抑制.
  • 使用大肠杆菌作为一个模型系统来测试抑制效率.
  • 应用热力学模型来量化DNA循环对抑制的贡献.

主要成果:

  • 共价TALED显示出强大的DNA循环依赖抑制细菌促进体.
  • 在大肠杆菌中,DNA循环显著提高了促进体抑制效率.
  • 工程设计的TALED系统实现了与天然LacI抑制器相比较的抑制.

结论:

  • 优化的TALED蛋白可以有效地驱动大肠杆菌中的循环依赖性促进体抑制.
  • 用TALEDs实现高效基因抑制的关键因素是DNA循环.
  • 这项研究为合成生物学中TALED介导的基因调节提供了基础设计原则.