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相关概念视频

Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

23.6K
RNA Polymerase (RNAP) is conserved in all animals, with bacterial, archaeal, and eukaryotic RNAPs sharing significant sequence, structural, and functional similarities. Among the three eukaryotic RNAPs, RNA Polymerase II is most similar to bacterial RNAP in terms of both structural organization and folding topologies of the enzyme subunits. However, these similarities are not reflected in their mechanism of action.
All three eukaryotic RNAPs require specific transcription factors, of which the...
23.6K
Transcription Initiation01:47

Transcription Initiation

16.2K
Initiation is the first step of transcription in eukaryotes. Prokaryotic RNA Polymerase (RNAP) can bind to the template DNA and start transcribing. On the other hand, transcription in eukaryotes requires additional proteins, called transcription factors, to first bind to the promoter region in the DNA template. This binding helps recruit the specific RNAP that can assemble on the DNA and start transcription.
The promoters and enhancers and their accessory proteins allow tight regulation of...
16.2K
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

28.8K
Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
28.8K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

9.8K
Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
9.8K
Bacterial Transcription01:53

Bacterial Transcription

28.0K
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.
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
28.0K
RNA Polymerase II Accessory Proteins02:36

RNA Polymerase II Accessory Proteins

9.1K
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...
9.1K

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相关实验视频

Updated: Jun 6, 2025

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

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工程制造的停止和开始T7RNA聚合酶.

Zachary T Baumer1, Matilda S Newton1, Lina Löfstrand1

  • 1Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, Colorado 80305, United States.

ACS synthetic biology
|November 29, 2024
PubMed
概括

科学家们开发了由连接体激活的RNA聚合酶 (LARP),这些聚合酶被indoles精确控制. 这一突破使合成生物学应用的"停止和启动"基因表达成为可能.

关键词:
的RNA聚合酶.亚洛斯特菌是什么意思?动态代谢控制 动态代谢控制细胞间的信号传递.蛋白质工程和设计合成生物学 合成生物学

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Last Updated: Jun 6, 2025

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科学领域:

  • 合成生物学 合成生物学
  • 酶工程是什么? 酶工程是什么?
  • 分子生物学分子生物学

背景情况:

  • 精确的酶激活对于合成生物学至关重要.
  • 不调节的T7RNA聚合酶可以阻止细菌的生长.
  • 自然酶是由内源代谢产物调节的.

研究的目的:

  • 通过生理代谢产物激活的T7RNA聚合酶 (T7RNAP) 的工程.
  • 为了创建一个可控制的基因表达系统使用indules.
  • 为合成生物学开发一个"停止和继续"平台.

主要方法:

  • 理性设计和T7RNAP变体的定向进化.
  • 印醇激活酶动态的表征 (EC50).
  • 在各种环境中展示印介导的基因表达控制.

主要成果:

  • 鉴定了T7RNAP变体,基底活性最小,因多尔诱导29倍 (EC50 = 344μM).
  • 印可以调节T7依赖基因表达的外源性,内源性和细胞间表达.
  • 已经证明了因多尔依赖的细菌的传播和工程结合体激活RNA聚合酶 (LARP).

结论:

  • 联体激活RNA聚合酶 (LARP) 提供了一个新的,可化学诱导的平台.
  • 对于合成生物学来说,LARP提供了精确的"停止和启动"控制.
  • 这种系统可以跨越细菌物种并适用于合成共同培养.