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相关概念视频

Transcription Attenuation in Prokaryotes02:42

Transcription Attenuation in Prokaryotes

15.2K
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...
15.2K
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
Transcription in Prokaryotes01:28

Transcription in Prokaryotes

4
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...
4
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

29.1K
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...
29.1K
Transcription Initiation01:47

Transcription Initiation

16.3K
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...
16.3K
Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

23.7K
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...
23.7K

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相关实验视频

Updated: Jun 10, 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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细菌如何调整转录终止效率?

Kathryn Julia Dierksheide1, Robert A Battaglia1, Gene-Wei Li1

  • 1Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.

Current opinion in microbiology
|October 18, 2024
PubMed
概括

细菌转录终结器控制基因表达,但它们的强度很难从DNA序列中预测. 新的高通量方法有助于理解序列决定因素,以获得更好的预测模型.

科学领域:

  • 微生物学 微生物学
  • 分子生物学分子生物学
  • 遗传学 遗传学 是一个

背景情况:

  • 细菌的操作子利用转录终端器来调节基因表达,并保持固态测量蛋白质比率.
  • 内在终结体是细菌终结体的主要类别,但它们的序列功能关系尚不清楚.
  • 终结者阅读影响下游的基因表达,影响共同调节的基因中的蛋白质水平.

研究的目的:

  • 审查用于识别内在终端器效率的序列决定因素的高通量方法.
  • 讨论跨作用因子对终结器的序列功能关系的影响.
  • 概述开发终端器效率定量模型的实验挑战.

主要方法:

  • 高通量实验方法的总结.
  • 对终结器效率的序列决定因素的分析.
  • 对跨作用因子效应的讨论.

主要成果:

  • 高通量方法为探测终结器序列决定因素提供了新的方法.
  • 交换作用因素显著影响终端器的强度和功能.
  • 从DNA序列预测终结者力量仍然是一个挑战.

结论:

更多相关视频

Rapid Verification of Terminators Using the pGR-Blue Plasmid and Golden Gate Assembly
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Rapid Verification of Terminators Using the pGR-Blue Plasmid and Golden Gate Assembly

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In Vitro Transcription Assays and Their Application in Drug Discovery
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In Vitro Transcription Assays and Their Application in Drug Discovery

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相关实验视频

Last Updated: Jun 10, 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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Rapid Verification of Terminators Using the pGR-Blue Plasmid and Golden Gate Assembly
09:51

Rapid Verification of Terminators Using the pGR-Blue Plasmid and Golden Gate Assembly

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In Vitro Transcription Assays and Their Application in Drug Discovery
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In Vitro Transcription Assays and Their Application in Drug Discovery

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  • 了解内在终结子序列的决定因素对于预测基因表达至关重要.
  • 开发一个定量模型需要克服重要的实验障碍.
  • 需要进一步的研究,以充分阐明细菌转录终结器的序列功能关系.