Suppr超能文献

用于小鼠内耳毛细胞特异性基因操作的Gfi1-GCE诱导型Cre品系

Gfi1-GCE inducible Cre line for hair cell-specific gene manipulation in mouse inner ear.

作者信息

Tang Qi, Xu Mei, Xu Jiadong, Xie Xiaoling, Yang Hua, Gan Lin

机构信息

Department of Otolaryngology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Department of Ophthalmology and Flaum Eye Institute, University of Rochester, Rochester, New York.

出版信息

Genesis. 2019 Sep;57(9):e23304. doi: 10.1002/dvg.23304. Epub 2019 May 11.

Abstract

Tissue-specific inducible Cre recombinase mouse lines allow precise genetic manipulations in spatiotemporal manners and are pivotal for functional studies of genes during development and in adults. Growth factor independence 1 (GFI1) is an essential transcription factor expressed in the hair cells of mouse inner ear and Gfi1 locus serves as an excellent anchor site to drive the expression of inducible Cre recombinase in mouse inner hair cells. In this study, we have generated Gfi1-P2A-GFP-CreERT2 (Gfi1-GCE) knock-in mouse line by in-frame fusion of a self-cleaving GCE to the C-terminus of GFI1. We have shown that as predicted, the expression of GCE and GFI1 was detected specifically in the cytosol and nuclei of hair cells, respectively, of uninduced Gfi1-GCE mice, suggesting the successful cleavage and simultaneous expression of GFI1 and GCE. In addition, the in-frame fusion of the self-cleaving GCE does not interrupt the function of Gfi1 in the inner ear. Administration of tamoxifen leads to nuclear translocation of GCE and results in an efficient activation of tdTomato reporter gene expression specifically in most hair cells throughout development and in adults. Thus, this inducible Gfi1-GCE mouse line is a highly efficient Cre deleter and is suitable for gene manipulation in developing and adult inner ear hair cells.

摘要

组织特异性诱导型Cre重组酶小鼠品系能够以时空特异性方式进行精确的基因操作,对于研究发育过程中和成年期基因的功能至关重要。生长因子独立性1(GFI1)是一种在小鼠内耳毛细胞中表达的重要转录因子,Gfi1基因座是驱动诱导型Cre重组酶在小鼠内毛细胞中表达的理想锚定位点。在本研究中,我们通过将自我切割的GCE与GFI1的C末端进行读码框融合,构建了Gfi1-P2A-GFP-CreERT2(Gfi1-GCE)敲入小鼠品系。我们发现,正如预期的那样,在未诱导的Gfi1-GCE小鼠中,分别在毛细胞的细胞质和细胞核中特异性检测到了GCE和GFI1的表达,这表明GFI1和GCE成功切割并同时表达。此外,自我切割的GCE的读码框融合并未干扰Gfi1在内耳中的功能。给予他莫昔芬会导致GCE的核转位,并在整个发育过程和成年期的大多数毛细胞中特异性地有效激活tdTomato报告基因的表达。因此,这种诱导型Gfi1-GCE小鼠品系是一种高效的Cre删除工具,适用于发育中和成年内耳毛细胞中的基因操作。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验