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相关概念视频

Transcription Attenuation in Prokaryotes02:42

Transcription Attenuation in Prokaryotes

15.7K
Transcriptional attenuation occurs when RNA transcription is prematurely terminated due to the formation of a terminator mRNA hairpin structure.  Bacteria use these hairpins to regulate the transcription process and control the synthesis of several amino acids including histidine, lysine, threonine, and phenylalanine. Transcription attenuation takes place in the non-coding regions of mRNA.
There are several different mechanisms used to attenuate transcription. In ribosome mediated...
15.7K
Transcription in Prokaryotes01:28

Transcription in Prokaryotes

163
Transcription is a highly regulated process that converts genetic information into RNA molecules. The transcription cycle is divided into three key stages: initiation, elongation, and termination, each driven by specific molecular mechanisms.Initiation of TranscriptionIn bacteria, transcription begins when the RNA polymerase core enzyme associates with a sigma factor to form a holoenzyme. For example, the E. coli sigma factor called σ70 forms a holoenzyme, which recognizes the -10 (Pribnow...
163
Bacterial Transcription01:53

Bacterial Transcription

28.9K
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:
28.9K
Transcription Initiation01:47

Transcription Initiation

16.6K
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...
16.6K
RNA Polymerase II Accessory Proteins02:36

RNA Polymerase II Accessory Proteins

9.3K
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...
9.3K
Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

24.5K
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...
24.5K

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相关实验视频

Updated: Aug 14, 2025

Analysis of Termination of Transcription Using BrUTP-strand-specific Transcription Run-on TRO Approach
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Analysis of Termination of Transcription Using BrUTP-strand-specific Transcription Run-on TRO Approach

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本质转录终止的结构基础

Linlin You1,2, Expery O Omollo3, Chengzhi Yu1,2

  • 1Key Laboratory of Synthetic Biology, CAS Center for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai, China.

Nature
|January 11, 2023
PubMed
概括

研究人员可视化了细菌的内在终结, 揭示了RNA聚合酶如何暂停, 折叠RNA针, 并回滚DNA释放RNA. 这种结构机制是所有生物体中基因转录终结的关键.

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High-throughput Purification of Affinity-tagged Recombinant Proteins
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High-throughput Purification of Affinity-tagged Recombinant Proteins

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Single-Molecule Imaging of EWS-FLI1 Condensates Assembling on DNA
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Single-Molecule Imaging of EWS-FLI1 Condensates Assembling on DNA

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相关实验视频

Last Updated: Aug 14, 2025

Analysis of Termination of Transcription Using BrUTP-strand-specific Transcription Run-on TRO Approach
12:12

Analysis of Termination of Transcription Using BrUTP-strand-specific Transcription Run-on TRO Approach

Published on: March 12, 2017

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High-throughput Purification of Affinity-tagged Recombinant Proteins
07:44

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科学领域:

  • 分子生物学
  • 结构生物学
  • 生物化学

背景情况:

  • 在所有生物体中,基因转录需要高效准确的终止.
  • 独立于因子的内在终止是细菌和真核生物的保存途径.
  • 这一过程涉及RNA聚合酶识别终端序列并释放新生的RNA.

研究的目的:

  • 阐明细菌内在终结的结构机制.
  • 为了可视化转录终止复合体的中间状态.
  • 了解RNA释放和DNA崩的过程.

主要方法:

  • 单粒子冷电子显微镜 (冷EM).
  • 对大肠杆菌转录终结复合物的结构分析.
  • 关键中间状态的可视化.

主要成果:

  • 获得了大肠杆菌转录内在终结复合物的详细结构.
  • 发现了RNA聚合酶在终结序列中暂停的机制.
  • 在RNA释放过程中可视化了终结RNA针和DNA回卷的折叠.

结论:

  • 已经定义了细菌内在终结的综合结构机制.
  • 该研究提供了与因子独立终止相关的RNA释放和DNA崩的见解.
  • 这些发现适用于所有生命形式的RNA聚合酶.