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相关概念视频

The Eukaryotic Promoter Region02:40

The Eukaryotic Promoter Region

The eukaryotic promoter region is a segment of DNA located upstream of a gene. It contains an RNA polymerase binding site, a transcription start site, and several cis-regulatory sequences.  The proximal promoter region is located in the vicinity of the gene and has cis-regulatory sequences and the core promoter. The core promoter is the binding site for RNA polymerase and is usually located between -35 and +35 nucleotides from the transcription start site. The distal promoter regions are...
Transcription Attenuation in Prokaryotes02:42

Transcription Attenuation in Prokaryotes

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...
The Eukaryotic Promoter Region02:40

The Eukaryotic Promoter Region

The eukaryotic promoter region is a segment of DNA located upstream of a gene. It contains an RNA polymerase binding site, a transcription start site, and several cis-regulatory sequences.  The proximal promoter region is located in the vicinity of the gene and has cis-regulatory sequences and the core promoter. The core promoter is the binding site for RNA polymerase and is usually located between -35 and +35 nucleotides from the transcription start site. The distal promoter regions are...
Prokaryotic Gene Structure and Organization01:28

Prokaryotic Gene Structure and Organization

Prokaryotic genomes exhibit a streamlined organization of coding and non-coding regions essential for gene expression and protein synthesis. While coding regions contain the genetic instructions for proteins or functional RNAs, non-coding regions regulate the precise transcription and translation of these genes.Coding Regions: Proteins and RNAsThe primary coding regions, known as structural genes, include sequences transcribed into messenger RNA (mRNA) and ultimately translated into...
Transcription in Prokaryotes01:28

Transcription in Prokaryotes

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 box)...
Repressible Operon: trp Operon01:21

Repressible Operon: trp Operon

The trp operon in Escherichia coli exemplifies a repressible operon. It regulates the synthesis of tryptophan through repressor-mediated transcriptional control and attenuation. This dual regulatory mechanism ensures tryptophan biosynthesis occurs only when needed, conserving cellular resources.Structure of the trp OperonThe trp operon consists of five structural genes (trpE, trpD, trpC, trpB, and trpA) that encode enzymes for tryptophan biosynthesis. These genes are transcribed as a single...

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相关实验视频

Updated: Jul 19, 2026

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

Published on: April 25, 2016

在大肠杆菌 tyrT 促销者中的 DNA 结构变异.

H R Drew, A A Travers

    Cell
    |June 1, 1984
    PubMed
    概括

    DNA 结构因基序而异,影响蛋白质的识别. 三个核酶揭示了DNA骨干的几何结构,而不仅仅是序列,它决定了裂变模式,突出了结构多态性.

    科学领域:

    • 分子生物学分子生物学
    • 结构生物学 结构生物学
    • 生物化学 生物化学

    背景情况:

    • DNA结构是一个对基序列敏感的双螺旋.
    • 基序变异会导致DNA骨干中的结构变形.
    • 蛋白质和DNA结合试剂能够识别这些结构变化.

    研究的目的:

    • 研究常见核酶与自然DNA序列的相互作用.
    • 为了确定核酶是否对DNA基序或骨干几何敏感.
    • 为DNA结构多态化提供证据.

    主要方法:

    • 使用三个核酶对DNA裂变模式的分析:DNAase I,DNAase II和铜-.
    • 在单键分辨率下检查160bp tyrT促进体DNA序列.
    • 分裂部位与DNA结构特征的相关性.

    主要成果:

    • 这三种核酶都对DNA骨干几何学表现出敏感性,而不是基序.
    • 依赖序列的分裂模式表明了DNA中的结构多态性.
    • 观察到的变化包括螺旋槽宽度,辐射不对称性和酸盐可访问性.

    结论:

    更多相关视频

    Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach
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    Genetic Modification of Cyanobacteria by Conjugation Using the CyanoGate Modular Cloning Toolkit
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    Genetic Modification of Cyanobacteria by Conjugation Using the CyanoGate Modular Cloning Toolkit

    Published on: October 31, 2019

    相关实验视频

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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

    Published on: April 25, 2016

    Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach
    11:12

    Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach

    Published on: September 11, 2017

    Genetic Modification of Cyanobacteria by Conjugation Using the CyanoGate Modular Cloning Toolkit
    08:25

    Genetic Modification of Cyanobacteria by Conjugation Using the CyanoGate Modular Cloning Toolkit

    Published on: October 31, 2019

    • DNA的结构多态性影响着通过结合试剂对DNA的识别.
    • 基组成和 purin-pyrimidine不对称性通过结构变化影响DNA识别.
    • 了解DNA几何学对于解释特定序列相互作用至关重要.