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関連する概念動画

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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関連する実験動画

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

E. coli tyrT プロモーターのDNA構造の変異

H R Drew, A A Travers

    Cell
    |June 1, 1984
    PubMed
    まとめ

    DNAの構造は塩基配列によって変化し,タンパク質の認識に影響を与えます. 3つの核は,配列だけでなく,DNAの脊髄幾何学を明らかにし,分裂パターンを決定し,構造的多形性を強調します.

    科学分野:

    • 分子生物学は分子生物学である.
    • 構造生物学 構造生物学とは
    • バイオケミストリー バイオケミストリー

    背景:

    • DNAの構造は,塩基配列に敏感な二重ヘリックスである.
    • 塩基配列の変異は,DNAの骨格の構造的変形を引き起こします.
    • タンパク質とDNA結合反応剤は,これらの構造変化を認識します.

    研究 の 目的:

    • 自然なDNA配列と一般的な核酸の相互作用を調査する.
    • 核酸がDNA塩基配列や脊髄幾何学に敏感であるかどうかを判断する.
    • DNAの構造的多形化に関する証拠を提供するため.

    主な方法:

    • DNA分裂パターンの分析は,DNAase I,DNAase II,および銅-フェナントロリンという3つの核酸を用いて行われました.
    • シングルボンド解像度で160 bpの tyrT プロモーターDNA配列の検査.
    • 分裂部位とDNA構造的特徴の相関.

    主要な成果:

    • この3つの核酵素は,塩基配列ではなく,DNAの骨幹幾何学に対する感受性を示した.
    • 配列依存の割れ方パターンは,DNAの構造的多形性を示した.

    さらに関連する動画

    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

    関連する実験動画

    Last 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

    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

  • 観測された変動には,ヘリックス・グリューブの幅,放射性非対称性,およびリン酸のアクセシビリティが含まれています.
  • 結論:

    • DNAの構造的多形性は,結合反応剤によるDNAの認識に影響を与えます.
    • 塩基組成とピューリン-ピリミジン非対称性は,構造的変化を通してDNA認識に影響します.
    • DNAの幾何学を理解することは,配列特異の相互作用を説明するために重要である.