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相关概念视频

CRISPR01:59

CRISPR

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Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
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DNA-only Transposons02:57

DNA-only Transposons

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DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
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Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
6.0K
CRISPR and crRNAs02:53

CRISPR and crRNAs

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Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
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Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

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Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
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Homologous Recombination02:31

Homologous Recombination

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The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
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相关实验视频

Updated: Jul 4, 2025

In Vitro Selection of Engineered Transcriptional Repressors for Targeted Epigenetic Silencing
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In Vitro Selection of Engineered Transcriptional Repressors for Targeted Epigenetic Silencing

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克里斯普尔-TE:一种基于网络的工具,用于生成单一指导RNA,针对可转移元素.

Yixin Guo1, Ziwei Xue1,2, Meiting Gong1

  • 1Department of Orthopedic Surgery of the Second Affiliated Hospital, and Centre of Biomedical Systems and Informatics of Zhejiang University-University of Edinburgh Institute (ZJU-UoE Institute), Zhejiang University School of Medicine, Zhejiang University, Zhejiang, Hangzhou, 310003, China.

Mobile DNA
|February 2, 2024
PubMed
概括
此摘要是机器生成的。

克里斯普尔-TE是设计单向导RNA (sgRNA) 的新工具,以有效地准可转移元素 (TE). 这个网络应用程序帮助研究人员操纵TE用于人类和小鼠基因组的功能研究.

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Efficient Production and Identification of CRISPR/Cas9-generated Gene Knockouts in the Model System Danio rerio
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CRISPR Guide RNA Cloning for Mammalian Systems
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Efficient Production and Identification of CRISPR/Cas9-generated Gene Knockouts in the Model System Danio rerio
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科学领域:

  • 基因组学就是基因组学.
  • 分子生物学分子生物学
  • 生物信息学是一种生物信息学.

背景情况:

  • 克里斯普尔/卡斯系统是强大的基因组工程工具.
  • 可转换的元素 (TE) 起着至关重要的作用,需要对其进行功能研究进行操纵.
  • 设计用于重复性TE的特定和高效的sgRNA是具有挑战性的.

研究的目的:

  • 开发一个优化的 sgRNA 设计工具,用于可转换元素 (TE) 操纵.
  • 在单个副本和子家族层面提供一个全面的解决方案,以有效地针对 TE.
  • 用CRISPR/Cas技术促进对TE功能的研究.

主要方法:

  • 开发一个基于Web的应用程序,CRISPR-TE,具有图形用户界面.
  • 为人类和小鼠基因组量身定制该工具.
  • 识别潜在的sgRNAs特定于TE.

主要成果:

  • 克里斯普尔-TE成功识别了用于TE向的sgRNA.
  • 该工具可以在单个副本和子家族层面高效地定位TEs.
  • 针对TEs的sgRNA对具有保存序列的进化年轻TEs更有效.

结论:

  • 克里斯普尔-TE提供了一个多功能框架,用于设计用于TE向的sgRNA.
  • 该应用程序作为在线网络服务公开可访问.
  • 对CRISPR-TE的源代码可供进一步开发和使用.