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相关概念视频

In-vitro Mutagenesis01:16

In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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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Mouse Models of Cancer Study

Mice have long served as models for studying human biology and pathology because of their phylogenetic and physiological similarity with humans. They are also easy to maintain and breed in the laboratory, and hence, many inbred strains are now available for research. Studies on mice have contributed immeasurably to our understanding of cancer biology.
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...

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相关实验视频

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Mouse Genome Engineering Using Designer Nucleases
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操纵小鼠基因组以设计精确的功能合成替代与人类序列.

Helen A C Wallace1, Fatima Marques-Kranc, Melville Richardson

  • 1Institute for Stem Cell Research, University of Edinburgh, King's Buildings, West Mains Road, Edinburgh EH9 3JQ, United Kingdom.

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概括

重组酶介导的基因组替代 (RMGR) 能够进行大规模的小鼠基因组编辑. 这种方法成功地用人类DNA取代了小鼠DNA,为阿尔法沙拉西米亚等遗传疾病创建了准确的模型.

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科学领域:

  • 遗传学 是一个遗传学.
  • 基因组工程是基因组工程.
  • 转基因技术转基因技术

背景情况:

  • 目前的转基因技术在研究大型基因组区域方面存在局限性.
  • 对小鼠人类遗传疾病的准确建模对于研究至关重要.

研究的目的:

  • 开发一种新的策略,用人类合成区域取代大小鼠基因组段.
  • 为研究人类基因表达和遗传疾病创建先进的小鼠模型.

主要方法:

  • 开发了使用异型位和Cre.recombinase的复合酶介导基因组替代 (RMGR).
  • 修改的小鼠ES细胞和人类BACs用于细分基因组交换.
  • 产生了具有人类α球蛋白调节域的同卵性小鼠.

主要成果:

  • 成功地用人类对应物替换了一个>100 kb小鼠基因组段.
  • 创造出只产生人类α球蛋白链的小鼠.
  • 开发了一个精确的小鼠模型,用于人类的阿尔法血症.

结论:

  • RMGR是一种可行且强大的技术,用于大规模的基因组替代.
  • 这种方法克服了当前转基因方法的局限性.
  • RMGR促进了人类基因表达的研究和遗传疾病的建模.