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通过体细胞核移植生成囊性纤维化雪貂模型的进展。

Progress toward generating a ferret model of cystic fibrosis by somatic cell nuclear transfer.

作者信息

Li Ziyi, Engelhardt John F

机构信息

Department of Anatomy & Cell Biology, College of Medicine, University of Iowa, 1-111 BSB, 51 Newton Road, Iowa City, IA 52242, USA.

出版信息

Reprod Biol Endocrinol. 2003 Nov 7;1:83. doi: 10.1186/1477-7827-1-83.

Abstract

Mammalian cloning by nuclear transfer from somatic cells has created new opportunities to generate animal models of genetic diseases in species other than mice. Although genetic mouse models play a critical role in basic and applied research for numerous diseases, often mouse models do not adequately reproduce the human disease phenotype. Cystic fibrosis (CF) is one such disease. Targeted ablation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in mice does not adequately replicate spontaneous bacterial infections observed in the human CF lung. Hence, several laboratories are pursuing alternative animal models of CF in larger species such as the pig, sheep, rabbits, and ferrets. Our laboratory has focused on developing the ferret as a CF animal model. Over the past few years, we have investigated several experimental parameters required for gene targeting and nuclear transfer (NT) cloning in the ferret using somatic cells. In this review, we will discuss our progress and the hurdles to NT cloning and gene-targeting that accompany efforts to generate animal models of genetic diseases in species such as the ferret.

摘要

通过体细胞核移植进行哺乳动物克隆为在小鼠以外的物种中建立遗传疾病动物模型创造了新机会。尽管基因小鼠模型在众多疾病的基础研究和应用研究中发挥着关键作用,但小鼠模型往往无法充分再现人类疾病表型。囊性纤维化(CF)就是这样一种疾病。在小鼠中靶向敲除囊性纤维化跨膜传导调节因子(CFTR)基因并不能充分复制人类CF肺中观察到的自发性细菌感染。因此,几个实验室正在猪、羊、兔和雪貂等较大物种中寻求CF的替代动物模型。我们实验室专注于将雪貂开发为CF动物模型。在过去几年中,我们研究了利用体细胞在雪貂中进行基因靶向和核移植(NT)克隆所需的几个实验参数。在这篇综述中,我们将讨论我们在NT克隆和基因靶向方面的进展以及在诸如雪貂等物种中建立遗传疾病动物模型过程中所面临的障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dca/280727/92bcdf75571a/1477-7827-1-83-1.jpg

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