A Cxcl15 Cre Recombinase Mouse Model Useful to Study Gland Development in the Uterus

IF 2.4 4区 生物学 Q2 DEVELOPMENTAL BIOLOGY
genesis Pub Date : 2025-09-01 DOI:10.1002/dvg.70026
Andrew M. Kelleher, Hong Im Kim, Greeshma Sai Bayammagari, Daniel J. Davis, Thomas E. Spencer
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引用次数: 0

Abstract

The mammalian uterus contains glands in the endometrium that develop only or primarily after birth. In the mouse, endometrial glands govern post implantation pregnancy establishment via regulation of blastocyst implantation, stromal cell decidualization, and placental development. Here, we describe a new uterine glandular epithelium (GE) specific Cre recombinase mouse line that is useful to study endometrial gland development and function. Utilizing CRISPR-Cas9 genome editing, improved Cre recombinase (iCre) was inserted into the endogenous C-X-C motif chemokine ligand 15 (Cxcl15) gene. Cxcl15 mRNA, Cxcl15 protein, and Cxcl15-iCre recombinase activity were specific to the developing GE of the uterus. Cxcl15-iCre mice were crossed with floxed Foxa2 mice to conditionally delete Foxa2 specifically in the glands of the neonatal mouse uterus. This conditional deletion of Foxa2 in the developing neonatal uterus resulted in adult mice that lacked Foxa2 in the GE of the uterus, and the adult mice were infertile. The studies described here establish that Cxcl15-iCre mice are a valuable resource to elucidate and explore mechanisms regulating the development and function of glands in the uterus.

一种用于研究子宫腺体发育的cxcl15cre重组酶小鼠模型
哺乳动物的子宫在子宫内膜中含有腺体,这些腺体只在出生后或主要在出生后发育。在小鼠中,子宫内膜腺通过调节囊胚着床、间质细胞脱胞和胎盘发育来控制着床后妊娠的建立。在这里,我们描述了一个新的子宫腺上皮(GE)特异性Cre重组酶小鼠系,这有助于研究子宫内膜腺的发育和功能。利用CRISPR-Cas9基因组编辑技术,将改良的Cre重组酶(iCre)插入内源性C-X-C基序趋化因子配体15 (Cxcl15)基因中。Cxcl15 mRNA、Cxcl15蛋白和Cxcl15- icre重组酶活性与子宫GE的发生有关。将Cxcl15-iCre小鼠与Foxa2小鼠杂交,有条件地特异性删除新生小鼠子宫腺体中的Foxa2。发育中的新生子宫中Foxa2的条件缺失导致成年小鼠在子宫GE中缺乏Foxa2,并且成年小鼠不育。本文所述的研究表明,Cxcl15-iCre小鼠是阐明和探索子宫腺体发育和功能调节机制的宝贵资源。
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来源期刊
genesis
genesis 生物-发育生物学
CiteScore
3.60
自引率
0.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: As of January 2000, Developmental Genetics was renamed and relaunched as genesis: The Journal of Genetics and Development, with a new scope and Editorial Board. The journal focuses on work that addresses the genetics of development and the fundamental mechanisms of embryological processes in animals and plants. With increased awareness of the interplay between genetics and evolutionary change, particularly during developmental processes, we encourage submission of manuscripts from all ecological niches. The expanded numbers of genomes for which sequencing is being completed will facilitate genetic and genomic examination of developmental issues, even if the model system does not fit the “classical genetic” mold. Therefore, we encourage submission of manuscripts from all species. Other areas of particular interest include: 1) the roles of epigenetics, microRNAs and environment on developmental processes; 2) genome-wide studies; 3) novel imaging techniques for the study of gene expression and cellular function; 4) comparative genetics and genomics and 5) animal models of human genetic and developmental disorders. genesis presents reviews, full research articles, short research letters, and state-of-the-art technology reports that promote an understanding of the function of genes and the roles they play in complex developmental processes.
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