Pax9 encodes a paired-box homeodomain (Pax) transcription factor and is critical for the development of multiple organs. Using CrispR/Cas9-mediated homologous directed repair (HDR), we generated a new Pax9-CreER knock-in mouse line in which the CreER(T2) fusion protein is produced after synthesis of endogenous Pax9 protein. We found that tdTomato reporter expression in Pax9-CreER;tdTomato reporter mice is detectable in a similar pattern to the endogenous Pax9 expression, faithfully recapitulating the Pax9 expression domains throughout the embryo and in the adult mouse. At early embryonic stages, the tdTomato reporter is expressed first in the pharyngeal pouch region and later in the craniofacial mesenchyme, somites, limbs, and lingual papillae in the adult tongue. These results demonstrate that this new Pax9-CreER knock-in mouse line can be used for lineage tracing and genetic targeting of Pax9-expressing cells and their progeny in a temporally and spatially controlled manner during development and organogenesis.
Generation and characterization of tamoxifen-inducible Pax9-CreER knock-in mice using CrispR/Cas9.
利用 CrispR/Cas9 构建和表征他莫昔芬诱导的 Pax9-CreER 敲入小鼠
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作者:Feng Jifan, Jing Junjun, Sanchez-Lara Pedro A, Bootwalla Moiz S, Buckley Jonathan, Wu Nancy, Yan Youzhen, Chai Yang
| 期刊: | Genesis | 影响因子: | 2.500 |
| 时间: | 2016 | 起止号: | 2016 Sep;54(9):490-6 |
| doi: | 10.1002/dvg.22956 | ||
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