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使用ROSA26报告基因小鼠进行Nkx2-5/Cre基因的胚胎表达。

Embryonic expression of an Nkx2-5/Cre gene using ROSA26 reporter mice.

作者信息

Moses K A, DeMayo F, Braun R M, Reecy J L, Schwartz R J

机构信息

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Genesis. 2001 Dec;31(4):176-80. doi: 10.1002/gene.10022.

Abstract

Nkx2-5, one of the earliest cardiac-specific markers in vertebrate embryos, was used as a genetic locus to knock in the Cre recombinase gene by homologous recombination. Offspring resulting from heterozygous Nkx2-5/Cre mice mated to ROSA26 (R26R) reporter mice provided a model system for following Nkx2-5 gene activity by beta-galactosidase (beta-gal) activity. beta-gal activity was initially observed in the early cardiac crescent, cardiomyocytes of the looping heart tube, and in the epithelium of the first pharyngeal arch. In later stage embryos (10.5-13.5 days postcoitum, dpc), beta-gal activity was observed in the stomach and spleen, the dorsum of the tongue, and in the condensing primordium of the tooth. The Nkx2-5/Cre mouse model should provide a useful genetic resource to elucidate the role of loxP manipulated genetic targets in cardiogenesis and other developmental processes.

摘要

Nkx2-5是脊椎动物胚胎中最早出现的心脏特异性标志物之一,被用作通过同源重组敲入Cre重组酶基因的遗传位点。将杂合的Nkx2-5/Cre小鼠与ROSA26(R26R)报告基因小鼠交配产生的后代,提供了一个通过β-半乳糖苷酶(β-gal)活性追踪Nkx2-5基因活性的模型系统。最初在早期心脏半月体、环状心管的心肌细胞以及第一咽弓的上皮中观察到β-gal活性。在胚胎后期(妊娠后10.5 - 13.5天,dpc),在胃和脾脏、舌背以及牙齿的凝聚原基中观察到β-gal活性。Nkx2-5/Cre小鼠模型应该为阐明loxP操纵的遗传靶点在心脏发生和其他发育过程中的作用提供一个有用的遗传资源。

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