Genetic ablation in transgenic mice.

Molecular biology & medicine Pub Date : 1989-12-01
A Bernstein, M Breitman
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Abstract

The study of mammalian development has very quickly moved from a largely descriptive endeavour to one in which very precise mechanistic questions can now be formulated and answered. Undoubtedly, advances in this area have been the result of a strong foundation in experimental embryology, the application of molecular genetic techniques to the isolation and analysis of genes of developmental interest, and the ability to manipulate genetically the embryo through transgenic mouse technology. Perhaps the most dramatic illustration of the power of these new technologies is the potential ability to generate mice either that carry mutations in virtually any gene in the germ line through gene targeting in totipotent embryonic stem (ES) cells or that lack specific cell types through the genetic ablation technology reviewed here. Together, these two approaches have made it possible to knock out either a specific gene or a specific cell type in an intact animal and thus offer almost unlimited possibilities for addressing questions concerning the molecular and cellular biology of development. As well, animal models for various human diseases such as dwarfism, immunodeficiencies and demyelination can now be generated. It is clear that further refinements in both gene targeting and genetic ablation technologies are necessary before the full potential of either approach will be realized. Further development of conditional or inducible ablation strategies, coupled with a more precise definition of the cis-acting sequences, responsible for directing gene expression in fully differentiated and more primitive cells, will greatly broaden the range of questions that can be addressed by this approach.(ABSTRACT TRUNCATED AT 250 WORDS)

转基因小鼠的基因消融。
对哺乳动物发育的研究已经非常迅速地从一个主要是描述性的努力转变为一个现在可以制定和回答非常精确的机械问题的努力。毫无疑问,这一领域的进步是实验胚胎学的坚实基础、分子遗传技术在分离和分析发育相关基因方面的应用以及通过转基因小鼠技术对胚胎进行遗传操作的能力的结果。也许这些新技术的力量最引人注目的例子是,通过在全能胚胎干细胞(ES)中进行基因靶向,可以产生携带生殖系中几乎任何基因突变的小鼠,或者通过本文综述的基因消融技术产生缺乏特定细胞类型的小鼠。总之,这两种方法使得敲除完整动物体内的特定基因或特定细胞类型成为可能,从而为解决有关发育的分子和细胞生物学问题提供了几乎无限的可能性。此外,各种人类疾病的动物模型,如侏儒症、免疫缺陷和脱髓鞘,现在也可以生成。很明显,在实现这两种方法的全部潜力之前,基因靶向和基因消融技术的进一步改进是必要的。条件或诱导消融策略的进一步发展,加上对顺式作用序列的更精确定义,负责在完全分化和更原始的细胞中指导基因表达,将大大拓宽该方法可以解决的问题范围。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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