...
首页> 外文期刊>Experimental Animals >Simple generation of hairless mice for in vivo imaging
【24h】

Simple generation of hairless mice for in vivo imaging

机译:简单生成用于体内成像的无毛小鼠

获取原文
           

摘要

The in vivo imaging of mice makes it possible to analyze disease progress non-invasively through reporter gene expression. As the removal of hair improves the accuracy of in vivo imaging, gene-modified mice with a reporter gene are often crossed with Hos:HR-1 mutant mice homozygous for the spontaneous Hrhr mutation that exhibit a hair loss phenotype. However, it is time consuming to produce mice carrying both the reporter gene and mutant Hrhr gene by mating. In addition, there is a risk that genetic background of the gene-modified mice would be altered by mating. To resolve these issues, we established a simple method to generate hairless mice maintaining the original genetic background by CRISPR technology. First, we constructed the pX330 vector, which targets exon 3 of Hr . This DNA vector (5 ng/ μ l) was microinjected into the pronuclei of C57BL/6J mice. Induced Hr gene mutations were found in many founders (76.1%) and these mutations were heritable. Next, we performed in vivo imaging using these gene-modified hairless mice. As expected, luminescent objects in their body were detected by in vivo imaging. This study clearly showed that hairless mice could be simply generated by the CRISPR/Cas9 system, and this method may be useful for in vivo imaging studies with various gene-modified mice.
机译:小鼠的体内成像使通过报道基因表达无创地分析疾病进展成为可能。由于脱毛提高了体内成像的准确性,带有报告基因的基因修饰小鼠经常与表现出毛发的自发Hr hr 突变纯合的Hos:HR-1突变小鼠杂交丢失表型。然而,通过交配生产既携带报告基因又携带突变体Hr hr 基因的小鼠是费时的。另外,存在通过交配而改变基因修饰小鼠的遗传背景的风险。为了解决这些问题,我们建立了一种简单的方法,通过CRISPR技术生成维持原始遗传背景的无毛小鼠。首先,我们构建了靶向Xh Hr外显子3的pX330载体。将该DNA载体(5ng /μl)显微注射到C57BL / 6J小鼠的前核中。在许多创始人中(76.1%)发现了诱导型Hr基因突变,这些突变是可遗传的。接下来,我们使用这些基因修饰的无毛小鼠进行了体内成像。如预期的那样,通过体内成像检测了其体内的发光物体。这项研究清楚地表明,可以通过CRISPR / Cas9系统简单地产生无毛小鼠,并且这种方法可能适用于各种基因修饰小鼠的体内成像研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号