Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart, a...
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

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...
Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

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...
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...
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

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...
Stringent Response in E. coli01:23

Stringent Response in E. coli

Bacterial growth is closely tied to nutrient availability, with cells proliferating exponentially under favorable conditions and entering a stationary phase when resources become scarce. This transition is mediated by a regulatory mechanism known as the stringent response, which allows bacteria to adapt to nutrient deprivation by modulating gene expression and metabolic activity.During nutrient scarcity, intracellular amino acid levels decline. It results in the accumulation of uncharged tRNAs...

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Force-Induced Ankle Opening Reveals Mechanical Stabilization of the Ankle of Human β-Cardiac Myosin.

ACS nano·2026
Same author

A Type III secretion system effector evolved to be mechanically labile and initiate unfolding from the N-terminus.

bioRxiv : the preprint server for biology·2026
Same author

A Rapid Host Response Blood Test for Bacterial/Viral Infection Discrimination Using a Portable Molecular Diagnostic Platform.

Open forum infectious diseases·2025
Same author

Quantifying a light-induced energetic change in bacteriorhodopsin by force spectroscopy.

Proceedings of the National Academy of Sciences of the United States of America·2024
Same author

Force-Activated DNA Substrates for In Situ Generation of ssDNA and Designed ssDNA/dsDNA Structures in an Optical-Trapping Assay.

Methods in molecular biology (Clifton, N.J.)·2022
Same author

Free-energy changes of bacteriorhodopsin point mutants measured by single-molecule force spectroscopy.

Proceedings of the National Academy of Sciences of the United States of America·2021
Same journal

Erratum for the Research Article "Detecting supramolecular organic nanoparticles during heat wave".

Science (New York, N.Y.)·2026
Same journal

Local signals, systemic decline.

Science (New York, N.Y.)·2026
Same journal

The mechanics of liver regeneration.

Science (New York, N.Y.)·2026
Same journal

Computing in a memory with physics.

Science (New York, N.Y.)·2026
Same journal

Retraction.

Science (New York, N.Y.)·2026
Same journal

Making time.

Science (New York, N.Y.)·2026
查看所有相关文章

相关实验视频

Updated: Jun 25, 2026

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA
10:15

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA

Published on: July 6, 2012

单个兰巴外核酶分子的依赖序列的暂停.

Thomas T Perkins1, Ravindra V Dalal, Paul G Mitsis

  • 1Department of Biological Sciences, Stanford University, Stanford, CA 94305, USA. tperkins@jila.colorado.edu

Science (New York, N.Y.)
|August 30, 2003
PubMed
概括
此摘要是机器生成的。

兰巴外核酶以恒定的速度消化DNA链,但在特定的DNA序列中暂停. 这些暂停,特别是在GGCGA动机,可能会影响DNA重组效率.

更多相关视频

Electricity-Free, Sequential Nucleic Acid and Protein Isolation
09:52

Electricity-Free, Sequential Nucleic Acid and Protein Isolation

Published on: May 15, 2012

Dual DNA Rulers to Study the Mechanism of Ribosome Translocation with Single-Nucleotide Resolution
10:27

Dual DNA Rulers to Study the Mechanism of Ribosome Translocation with Single-Nucleotide Resolution

Published on: July 8, 2019

相关实验视频

Last Updated: Jun 25, 2026

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA
10:15

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA

Published on: July 6, 2012

Electricity-Free, Sequential Nucleic Acid and Protein Isolation
09:52

Electricity-Free, Sequential Nucleic Acid and Protein Isolation

Published on: May 15, 2012

Dual DNA Rulers to Study the Mechanism of Ribosome Translocation with Single-Nucleotide Resolution
10:27

Dual DNA Rulers to Study the Mechanism of Ribosome Translocation with Single-Nucleotide Resolution

Published on: July 8, 2019

科学领域:

  • 分子生物学分子生物学
  • 生物化学 生物化学
  • 遗传学 是一个遗传学.

背景情况:

  • 兰巴达外核酶是DNA代谢中的一个关键酶.
  • 在单个分子水平上了解它的酶活性,为DNA处理提供了洞见.
  • 之前的研究已经描述了它的一般过程性和方向性.

研究的目的:

  • 为了研究兰巴外核酶消化的单分子动力学.
  • 在DNA降解过程中识别特定序列的暂停事件.
  • 为了将暂停与DNA序列和潜在的生物学影响相关联.

主要方法:

  • 单分子观察兰巴外核酶活性.
  • 测量DNA消化速度和暂停时间.
  • 凝电泳以确定强大的暂停序列.
  • 序列分析以将暂停与特定动机相关联.

主要成果:

  • 兰巴达外核酶以几乎恒定的速度 (4纳米/秒) 呈现过程性降解.
  • 消化过程中,在特定的部位会有不同长度的暂停.
  • 暂停是线程特定的和依赖于序列的,在GGCGA图案中识别出一个强大的暂停.
  • GGCGA图案位于左边的羊羔结合端.

结论:

  • 单分子分析揭示了兰巴外核酶的细微动力学,包括依赖序列的暂停.
  • 已识别的GGCGA图案作为一个显著的暂停地点.
  • 在这种动机上对外核酶的抑制可能有助于在lambda凝聚端降低重组效率.