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相关概念视频

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...
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Size and Structure of Viral Genomes01:26

Size and Structure of Viral Genomes

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Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
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Retroviruses02:33

Retroviruses

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Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
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Retrovirus Life Cycles01:10

Retrovirus Life Cycles

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Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
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Methods of Nuclear Reprogramming01:24

Methods of Nuclear Reprogramming

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Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
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Mechanisms of Retrovirus-induced Cancers01:51

Mechanisms of Retrovirus-induced Cancers

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Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...
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相关实验视频

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Designing, Packaging, and Delivery of High Titer CRISPR Retro and Lentiviruses via Stereotaxic Injection
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[利用逆转录病毒工程进行基因组重编程]

Philippe-Emmanuel Mangeot1, Théophile Ohlmann1

  • 1CIRI, Centre international de recherche en infectiologie Université de Lyon, Inserm U1111, Université Claude Bernard Lyon 1, CNRS UMR5308, ENS de Lyon, Lyon, France.

Medecine sciences : M/S
|September 8, 2025
PubMed
概括

逆转录病毒载体学利用隐形病毒载体进行基因传递. 新兴的有缺陷的逆转录病毒粒子提供了像CRISPR Cas9这样的基因组编辑工具的短暂传递,解决了基因工程中的关键挑战.

科学领域:

  • 分子生物学分子生物学
  • 病毒学 病毒学
  • 生物技术是生物技术.

背景情况:

  • 艾滋病毒-1生物学的进步刺激了逆转录病毒载体学的发展.
  • 病毒载体是实验室中广泛用于基因传递应用的工具.

研究的目的:

  • 审查用于基因组操纵的主要逆转录病毒系统.
  • 探索基因组工程技术的演变和应用.

主要方法:

  • 对逆转录病毒组装和整合机制的分析.
  • 关于CRISPR-Cas9及其用于精确基因组修改的衍生物的概述.
  • 讨论缺陷的逆转录病毒颗粒用于短暂的效应器传递.

主要成果:

  • 逆转录病毒载体学已经显著发展,为遗传操纵提供了各种工具.
  • 有缺陷的逆转录病毒颗粒显示出对基因组编辑器的短暂传递有希望.
  • 克里斯普尔-卡斯9系统可以实现高精度的基因组编辑.

结论:

  • 逆转录病毒系统对于推进基因组工程至关重要.
  • 克服效应器传递方面的挑战是有效基因组操纵的关键.

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  • 该领域继续开发用于精确基因改造的创新工具.