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相关概念视频

CRISPR/Cas9 Genome Editing01:28

CRISPR/Cas9 Genome Editing

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The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
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Gene Conversion02:08

Gene Conversion

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Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
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Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

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Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
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Base Excision Repair01:54

Base Excision Repair

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One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
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What is Genetic Engineering?00:49

What is Genetic Engineering?

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Overview
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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: Jan 15, 2026

Engineering Oncogenic Heterozygous Gain-of-Function Mutations in Human Hematopoietic Stem and Progenitor Cells
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通过移植进行基因组编辑

Samuel Simoni1, Marco Fambrini1, Claudio Pugliesi1

  • 1Department of Agriculture, Food and Environment, University of Pisa, Via del Borghetto, 80, I-56124 Pisa, Italy.

International journal of molecular sciences
|October 16, 2025
PubMed
概括

通过移植进行基因组编辑,可以通过通过RNA转移CRISPR-Cas9组件来实现无转基因植物修饰. 这种创新技术为改善作物,特别是对具有挑战性的物种提供了一个有希望的,可遗传的解决方案.

科学领域:

  • 植物生物技术 植物生物技术
  • 分子生物学分子生物学
  • 农业科学 农业科学

背景情况:

  • 移植促进了植物组织之间的分子交换 (小RNA,蛋白质).
  • 传统上,植物的基因组编辑需要外来DNA的整合.

研究的目的:

  • 审查通过移植编辑基因组的创新技术.
  • 突出其在传统方法上的优势及其潜在应用.
  • 讨论当前的局限性和未来的前景.

主要方法:

  • 利用RNA分子 (例如tRNA类序列) 来提供CRISPR-Cas9组件.
  • 利用转基因根茎为野生类型的种子提供编辑机械.
  • 在没有将外来DNA整合到后代中的情况下实现基因组修饰.

主要成果:

  • 在植物中可以实现可遗传的,无转基因的基因组编辑.
  • 这种方法解决了监管方面的问题,并改善了作物回收和选择.
  • 它为病毒载体提供了替代方案,可能减少非目标效应.

结论:

  • 通过移植进行基因组编辑对那些不愿接受体外培养的植物和植物繁殖物种具有显著的前景.
关键词:
这就是CRISPR/CasPR.基因组编辑 基因组编辑接种方式 接种方式移动RNARNA是一种移动RNA.与tRNA类似的序列.没有转基因的无基因植物.

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  • 该技术可以保持对植物生产力和质量至关重要的异构性.
  • 需要进一步改进,以解决变量效率,移植不兼容性和更广泛的作物育种应用的可扩展性.