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関連する概念動画

Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

17.3K
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...
17.3K
Eukaryotic Transcription Inhibitors01:52

Eukaryotic Transcription Inhibitors

9.1K
Certain biochemical processes, such as embryonic development and cell growth regulation, depend on the repression of specific genes. DNA binding proteins known as eukaryotic transcription inhibitors regulate the repression of gene expression in eukaryotes. The presence of these inhibitors at the required location and time in the cell is triggered by the presence of hormones and additional signals from other cells.
Eukaryotic transcription inhibitors usually contain two distinct domains, a...
9.1K
Transcription Attenuation in Prokaryotes02:42

Transcription Attenuation in Prokaryotes

14.6K
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...
14.6K
Bacterial Transcription01:53

Bacterial Transcription

25.6K
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:
25.6K
Transcription Initiation01:47

Transcription Initiation

17.0K
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...
17.0K
Transcription in Prokaryotes01:28

Transcription in Prokaryotes

4.4K
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...
4.4K

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関連する実験動画

Updated: May 5, 2026

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

9.3K

酵母における効率的な転写終結のために必要なDNA配列

K S Zaret, F Sherman

    Cell
    |March 1, 1982
    PubMed
    まとめ

    イーストの変異 (cyc1-512) は,転写終了を妨害し,CYC1遺伝子産物レベルとmRNAの変化につながります. これは,ポリアデニレーションが酵母における転写終結と結びついていることを示唆している.

    科学分野:

    • 分子生物学は分子生物学である.
    • 遺伝学 遺伝学とは
    • イースト生物学 イースト生物学

    背景:

    • Saccharomyces cerevisiaeのCYC1遺伝子は,イソ-1-サイトクロームcをコードする.
    • 適切な転写終結は,遺伝子調節とゲノム不安定性の防止に不可欠です.

    研究 の 目的:

    • cyc1-512変異の機能的影響を調査する.
    • CYC1遺伝子発現と転写終結における3'非翻訳領域の役割を決定する.

    主な方法:

    • イーストのcyc1-512デレーションミュータントの特徴.
    • CYC1 mRNAレベル,サイズ,およびポリアデニレーションの分析.
    • CYC1ロカスにおける転写パターンの調査.

    主要な成果:

    • cyc1-512変異は38bpの削除で,iso-1-cytochrome cとCYC1 mRNAレベルを低下させます.
    • CYC1 mRNAの異常な長さの3'端は,転写終了の失敗を示しています.
    • CYC1と隣接する遺伝子の間の収束転写が観察されました.

    結論:

    さらに関連する動画

    DNAzyme-dependent Analysis of rRNA 2’-O-Methylation
    09:12

    DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

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    Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC
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    Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC

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    関連する実験動画

    Last Updated: May 5, 2026

    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

    9.3K
    DNAzyme-dependent Analysis of rRNA 2’-O-Methylation
    09:12

    DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

    Published on: September 16, 2019

    8.2K
    Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC
    09:15

    Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC

    Published on: May 9, 2020

    6.1K
    • cyc1-512の削除は,酵母による転写終了を損なう.
    • ポリアデニレーションは,酵母における転写終結と結合されることがあります.
    • 3'非翻訳領域の保存されたシーケンスが終了に関与している可能性があります.