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相关概念视频

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...
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相关实验视频

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

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在酵母中有效地终止转录所需的DNA序列.

K S Zaret, F Sherman

    Cell
    |March 1, 1982
    PubMed
    概括

    一种酵母突变 (cyc1-512) 破坏了转录终止,导致CYC1基因产品水平和mRNA的改变. 这表明多基化与酵母中的转录终止相结合.

    科学领域:

    • 分子生物学分子生物学
    • 遗传学 是一个遗传学.
    • 酵母生物学的酵母生物学

    背景情况:

    • 在Saccharomyces cerevisiae中的CYC1基因编码了iso-1-cytochrome c.
    • 适当的转录终止对于基因调节和预防基因组不稳定性至关重要.

    研究的目的:

    • 研究cyc1-512突变的功能后果.
    • 确定3'非翻译区域在CYC1基因表达和转录终结中的作用.

    主要方法:

    • 酵母中的cyc1-512删除突变体的特征.
    • 分析CYC1mRNA水平,大小和多基化.
    • 研究CYC1位点中的转录模式.

    主要成果:

    • 循环1-512突变,38bp删除,降低了异位-1-细胞染色体c和CYC1mRNA水平.
    • CYC1mRNA的异常长的3'末端表明转录终止失败.
    • 观察到CYC1与相邻基因之间的转录趋同.

    结论:

    • 删除cyc1-512会损害酵母转录终止.

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  • 聚基化可能与酵母体的转录终止相结合.
  • 在3'非翻译区域的保存序列可能参与终结.