Chd7-iCreERT2-tdTomato小鼠的产生和表征。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Zi'ang Han, Ze Wang, Zhuxi Huang, Weijun Feng
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引用次数: 0

摘要

CHD7基因的杂合突变会导致严重的发育障碍,称为CHARGE综合征。为了进一步探索Chd7在体内的表达和功能,我们利用CRISPR/Cas9技术构建了Chd7- p2a - icreert2 - p2a - tdtomato(简称Chd7- ct - tdt)敲入小鼠细胞系。验证了两个敲入基因元件的特异性和效率。Chd7- ct - tdt报告基因既能准确反映内源性Chd7在神经发育过程中的动态表达模式,又能准确反映脑、眼细胞类型特异性表达。Chd7-CT-tdT在出生后小脑中的重组效率非常高。此外,谱系追踪实验表明Chd7在肠干细胞中表达。综上所述,新构建的Chd7- ct - tdt小鼠系为研究Chd7的功能提供了有益的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Generation and characterization of Chd7-iCreERT2-tdTomato mice

Heterozygous mutation of CHD7 gene causes a severe developmental disorder called CHARGE syndrome. In order to further explore the expression and function of Chd7 in vivo, we generated a Chd7-P2A-iCreERT2-P2A-tdTomato (in short, Chd7-CT-tdT) knockin mouse line using the CRISPR/Cas9 technology. The specificity and efficiency of two knockin genetic elements were validated. The Chd7-CT-tdT reporter gene could accurately reflect both the dynamic expression pattern of endogenous Chd7 during neurodevelopment and cell-type specific expression in the brain and eye. The recombination efficiency of Chd7-CT-tdT in postnatal cerebellum is very high. Moreover, lineage tracing experiment showed that Chd7 is expressed in intestinal stem cells. In summary, the newly constructed Chd7-CT-tdT mouse line provide a useful tool to study the function of Chd7.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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