Generation of a Wt1 conditional deletion, nuclear red fluorescent protein reporter allele in the mouse

IF 2.2 3区 生物学 Q4 CELL BIOLOGY
Jace A. Aloway , E. Cristy Ruteshouser , Vicki Huff , Richard R. Behringer
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引用次数: 0

Abstract

A Wt1 conditional deletion, nuclear red fluorescent protein (RFP) reporter allele was generated in the mouse by gene targeting in embryonic stem cells. Upon Cre-mediated recombination, a deletion allele is generated that expresses RFP in a Wt1-specific pattern. RFP expression was detected in embryonic and adult tissues known to express Wt1, including the kidney, mesonephros, and testis. In addition, RFP expression and WT1 co-localization was detected in the adult uterine stroma and myometrium, suggesting a role in uterine function. Crosses with Wnt7a-Cre transgenic mice that express Cre in the Müllerian duct epithelium activate Wt1-directed RFP expression in the epithelium of the oviduct but not the stroma and myometrium of the uterus. This new mouse strain should be a useful resource for studies of Wt1 function and marking Wt1-expressing cells.

在小鼠体内产生 Wt1 条件性缺失、核红色荧光蛋白报告等位基因。
通过在胚胎干细胞中进行基因打靶,在小鼠体内产生了 Wt1 条件性缺失、核红色荧光蛋白(RFP)报告等位基因。在 Cre 介导的重组过程中,产生的缺失等位基因以 Wt1 特异性模式表达 RFP。在已知表达 Wt1 的胚胎和成体组织中,包括肾脏、肾间质和睾丸,都检测到了 RFP 的表达。此外,在成体子宫基质和子宫肌层中也检测到了 RFP 表达和 WT1 共定位,表明其在子宫功能中发挥作用。与在输卵管上皮表达 Cre 的 Wnt7a-Cre 转基因小鼠杂交可激活输卵管上皮的 Wt1 定向 RFP 表达,但不能激活子宫基质和子宫肌层的 RFP 表达。这种新的小鼠品系应该是研究Wt1功能和标记Wt1表达细胞的有用资源。
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来源期刊
Differentiation
Differentiation 生物-发育生物学
CiteScore
4.10
自引率
3.40%
发文量
38
审稿时长
51 days
期刊介绍: Differentiation is a multidisciplinary journal dealing with topics relating to cell differentiation, development, cellular structure and function, and cancer. Differentiation of eukaryotes at the molecular level and the use of transgenic and targeted mutagenesis approaches to problems of differentiation are of particular interest to the journal. The journal will publish full-length articles containing original work in any of these areas. We will also publish reviews and commentaries on topics of current interest. The principal subject areas the journal covers are: • embryonic patterning and organogenesis • human development and congenital malformation • mechanisms of cell lineage commitment • tissue homeostasis and oncogenic transformation • establishment of cellular polarity • stem cell differentiation • cell reprogramming mechanisms • stability of the differentiated state • cell and tissue interactions in vivo and in vitro • signal transduction pathways in development and differentiation • carcinogenesis and cancer • mechanisms involved in cell growth and division especially relating to cancer • differentiation in regeneration and ageing • therapeutic applications of differentiation processes.
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