Grb7 基因敲除的小鼠发育正常,但基因敲除的雌性小鼠所生的仔鼠却不能茁壮成长。

IF 2 3区 生物学 Q2 ANATOMY & MORPHOLOGY
Kristopher A. Lofgren, Paraic A. Kenny
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引用次数: 0

摘要

背景:生长因子受体结合7(Grb7)是一种适配蛋白,参与多种受体酪氨酸激酶下游的信号转导,包括ERBB、FGFR和PDGFR通路。实验研究表明,Grb7 通过其大量的蛋白-蛋白相互作用调节细胞的增殖、存活、迁移和侵袭:结果:在此,我们描述了 Grb7 基因敲除小鼠的产生和特征。这些小鼠可以存活并繁殖。我们用lacZ基因敲入报告基因来观察成年组织中Grb7启动子的活动模式,结果表明Grb7在腺上皮、中枢神经系统和其他组织中广泛表达。在这些动物中观察到的唯一缺陷是,Grb7基因敲除的雌性动物不能成功地将幼崽养育到断奶年龄,这种表型与父代和幼崽的基因型无关:这些数据表明,Grb7在乳腺泌乳生理中起着调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Grb7 knockout mice develop normally but litters born to knockout females fail to thrive

Grb7 knockout mice develop normally but litters born to knockout females fail to thrive

Background

Growth factor receptor-bound 7 (Grb7) is an adaptor protein involved in signal transduction downstream of multiple receptor tyrosine kinases, including ERBB, FGFR, and PDGFR pathways. Experimental studies have implicated Grb7 in regulating cell proliferation, survival, migration, and invasion through its large repertoire of protein–protein interactions.

Results

Here, we describe the generation and characterization of a Grb7 knockout mouse. These mice are viable and fertile. A lacZ knock-in reporter was used to visualize Grb7 promoter activity patterns in adult tissues, indicating widespread Grb7 expression in glandular epithelium, the central nervous system, and other tissues. The sole defect observed in these animals was a failure of Grb7 knockout females to successfully raise pups to weaning age, a phenotype that was independent of both paternal and pup genotypes.

Conclusions

These data suggest a regulatory role for Grb7 in mammary lactational physiology.

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来源期刊
Developmental Dynamics
Developmental Dynamics 生物-发育生物学
CiteScore
5.10
自引率
8.00%
发文量
116
审稿时长
3-8 weeks
期刊介绍: Developmental Dynamics, is an official publication of the American Association for Anatomy. This peer reviewed journal provides an international forum for publishing novel discoveries, using any model system, that advances our understanding of development, morphology, form and function, evolution, disease, stem cells, repair and regeneration.
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