Bernstein A, Breitman M
Division of Molecular and Developmental Biology Mount Sinai Hospital Research Institute, Toronto, Ontario, Canada.
Mol Biol Med. 1989 Dec;6(6):523-30.
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)
哺乳动物发育的研究很快从主要是描述性的工作转向了现在能够提出并回答非常精确的机制性问题的阶段。毫无疑问,这一领域的进展得益于实验胚胎学的坚实基础、将分子遗传学技术应用于分离和分析发育相关基因,以及通过转基因小鼠技术对胚胎进行基因操作的能力。这些新技术力量最引人注目的例证或许是,通过在全能胚胎干细胞中进行基因打靶,有可能产生在种系中几乎任何基因都携带突变的小鼠,或者通过本文所述的基因消融技术产生缺乏特定细胞类型的小鼠。这两种方法共同使得在完整动物中敲除特定基因或特定细胞类型成为可能,从而为解决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,现在可以生成各种人类疾病的动物模型,如侏儒症、免疫缺陷和脱髓鞘疾病。显然,在实现这两种方法的全部潜力之前,基因打靶和基因消融技术都需要进一步完善。条件性或诱导性消融策略的进一步发展,再加上对负责在完全分化和更原始细胞中指导基因表达的顺式作用序列进行更精确的定义,将极大地拓宽这种方法能够解决的问题范围。(摘要截选至250词)