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Phenotyping analysis of p53 knockout mice produced by gene editing and comparison with conventional p53 knockout mice

机译:基因编辑和常规P53敲除小鼠产生P53敲除小鼠的表型分析

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摘要

BackgroundKnockout (KO) mice developed by homologous recombination (HR) have become useful tools to elucidate gene function. However, HR has low KO efficiency and is time-consuming, labor-intensive, and expensive. Gene editing' has received much attention for efficient genetic manipulation.ObjectiveAs generation of KO mice is simplified, KO mice produced by HR can be feasibly reproduced using gene editing. However, phenotyping analysis and comparison between KO mice produced by these two techniques is necessary.MethodsWe generated p53 KO mice through gene editing and compared their phenotype with the already reported HR-mediated p53 KO mice.ResultsTumors occurred in 36 (73%) of 49 homozygous KO mice and the mean age of occurrence was 23weeks, with lymphoma (64%) and sarcoma (23%) being the most common. Tumors were also developed in 12 heterozygous mice and the mean age of occurrence was 40weeks, with sarcoma (54%) and lymphoma (46%) in high proportion. Homozygotes had a mean life span of 15752days and developmental abnormalities were found in females compared to in males (P<0.05, P<0.001).ConclusionWe analyzed the basic phenotype of p53 KO mice and observed no significant difference from the conventional HR-mediated p53 KO mice.
机译:背景值(KO)由同源重组(HR)开发的小鼠已成为阐明基因功能的有用工具。然而,人力资源效率低,耗时,劳动密集型和昂贵。基因编辑'已获得高效遗传操作的关注。毒品群体产生的KO小鼠被简化,通过基因编辑可以可行再现HR生产的KO小鼠。然而,通过这两种技术产生的KO小鼠之间的表型分析和比较是必要的。通过基因编辑生成P53 KO小鼠,并将其表型与已经报道的HR介导的P53 KO小鼠进行比较。方法发生在36(73%)49中发生纯合KO小鼠和平均发生的年龄是23周,淋巴瘤(64%)和肉瘤(23%)是最常见的。在12只杂合小鼠中也开发了肿瘤,平均发生年龄为40周,肉瘤(54%)和淋巴瘤(46%)高比例。 Homozygotes具有平均寿命为15752天的寿命,与男性相比,女性在女性中发现了发育异常(P <0.05,P <0.001)。CollusionWe分析了P53 Ko小鼠的基本表型,观察到与传统的HR介导的P53没有显着差异Ko小鼠。

著录项

  • 来源
    《Genes and genomics》 |2019年第6期|共12页
  • 作者单位

    Seoul Natl Univ Dept Lab Anim Med BK21 PLUS Program Creat Vet Sci Res Res Inst Vet Sci Seoul 08826 South Korea;

    Konkuk Univ Sch Med Dept Stem Cell Biol Seoul 05029 South Korea;

    Seoul Natl Univ Dept Lab Anim Med BK21 PLUS Program Creat Vet Sci Res Res Inst Vet Sci Seoul 08826 South Korea;

    Seoul Natl Univ Dept Lab Anim Med BK21 PLUS Program Creat Vet Sci Res Res Inst Vet Sci Seoul 08826 South Korea;

    Seoul Natl Univ Dept Lab Anim Med BK21 PLUS Program Creat Vet Sci Res Res Inst Vet Sci Seoul 08826 South Korea;

    Seoul Natl Univ Dept Lab Anim Med BK21 PLUS Program Creat Vet Sci Res Res Inst Vet Sci Seoul 08826 South Korea;

    Seoul Natl Univ Dept Lab Anim Med BK21 PLUS Program Creat Vet Sci Res Res Inst Vet Sci Seoul 08826 South Korea;

    Yonsei Univ Dept Biochem Coll Life Sctalenience &

    Biotechnol Seoul 03722 South Korea;

    Seoul Natl Univ Dept Lab Anim Med BK21 PLUS Program Creat Vet Sci Res Res Inst Vet Sci Seoul 08826 South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物科学;
  • 关键词

    Mouse cancer model; Homologous recombination; Gene editing; TALEN; P53;

    机译:小鼠癌症模型;同源重组;基因编辑;TALEN;P53;

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