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Translesion DNA Polymerases02:10

Translesion DNA Polymerases

10.2K
Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
10.2K
RNA Polymerase II Accessory Proteins02:36

RNA Polymerase II Accessory Proteins

9.6K
Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...
9.6K
Allosteric Proteins-ATCase01:19

Allosteric Proteins-ATCase

5.9K
Binding sites linkages can regulate a protein's function.  For example, enzyme activity is often regulated through a feedback mechanism where the end product of the biochemical process serves as an inhibitor.
Aspartate transcarbamoylase (ATCase) is a cytosolic enzyme that catalyzes the condensation of L-aspartate and carbamoyl phosphate to  N-carbamoyl-L-aspartate. This reaction is the first step in pyrimidine biosynthesis. UTP and CTP, the end products of the pyrimidine synthesis...
5.9K
Eukaryotic Transcription Activators02:42

Eukaryotic Transcription Activators

11.3K
Transcription activators are proteins that promote the transcription of genes from DNA to RNA. In most cases, these proteins contain two separate domains ‒ a domain that binds to DNA and a domain for activating transcription; however, in some cases, a single domain is responsible for both binding and activation of transcription, as seen in the glucocorticoid receptor and MyoD.
The binding domains are capable of recognizing and interacting with regulatory sequences on the DNA. These...
11.3K
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

7.6K
Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
7.6K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.9K
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,...
5.9K

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相关实验视频

Updated: Sep 19, 2025

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
09:26

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

Published on: December 29, 2021

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推进:转化合成驱动的层次调节,使用模板激活器构造用于Cas12a活动.

Lulu Qin1, Wen-Jin Wang2, Xinyi Xia1

  • 1School of Pharmacy, Nanjing Medical University Nanjing Jiangsu 211166 China.

Chemical science
|June 18, 2025
PubMed
概括

我们开发了一种新的CRISPR/Cas12a调节策略,称为THRUST. 这种经济的方法精确地控制了Cas12a活动,用于先进的生物传感和分子诊断.

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相关实验视频

Last Updated: Sep 19, 2025

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

Published on: December 29, 2021

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Gene Digital Circuits Based on CRISPR-Cas Systems and Anti-CRISPR Proteins
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Gene Digital Circuits Based on CRISPR-Cas Systems and Anti-CRISPR Proteins

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Lentiviral Vector Platform for the Efficient Delivery of Epigenome-editing Tools into Human Induced Pluripotent Stem Cell-derived Disease Models
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Lentiviral Vector Platform for the Efficient Delivery of Epigenome-editing Tools into Human Induced Pluripotent Stem Cell-derived Disease Models

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科学领域:

  • 分子生物学分子生物学
  • 生物技术是生物技术.
  • 诊断 诊断 诊断 诊断

背景情况:

  • 由于CRISPR/Cas12a具有特定的识别和跨裂变活性,它是生物传感和分子诊断的强大工具.
  • 目前基于crRNA的Cas12a调节方法复杂,昂贵,需要多个组件.

研究的目的:

  • 开发一种新的,经济的,精确的CRISPR/Cas12a调节策略.
  • 加强CRISPR/Cas12a系统,以改善分子诊断.

主要方法:

  • 开发了转化合成驱动的层次调节,使用Cas12a活动 (THRUST) 的模板激活器构造.
  • 使用了一种双功能模板激活器结构 (TAC),作为T7RNA聚合酶转录模板和Cas12a激活器.
  • 具有脱氧氨 (dU) 病变和阿布里尼克/阿比里米尼克 (AP) 位点的工程 TAC,以控制转录和crRNA长度.
  • 战略位置的转录性调节单元用于Cas12a的层次调节.

主要成果:

  • 推力可以精确控制crRNA长度和Cas12a激活.
  • 证明了THRUST在"淡化"和"亮化"生物传感平台中的有效性.
  • 在分子诊断的聚合诱导排放侧流试验中成功应用了THRUST.

结论:

  • 推力为CRISPR/Cas12a提供了一个强大的,经济的和分层的调节策略.
  • 这种方法简化了CRISPR/Cas12a系统的复杂性,并降低了成本.
  • 推力显著丰富了基于CRISPR/Cas12a的分子诊断的监管工具箱.