Dietrich W F, Copeland N G, Gilbert D J, Miller J C, Jenkins N A, Lander E S
Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):10849-53. doi: 10.1073/pnas.92.24.10849.
The mouse is the best model system for the study of mammalian genetics and physiology. Because of the feasibility and importance of studying genetic crosses, the mouse genetic map has received tremendous attention in recent years. It currently contains over 14,000 genetically mapped markers, including 700 mutant loci, 3500 genes, and 6500 simple sequence length polymorphisms (SSLPs). The mutant loci and genes allow insights and correlations concerning physiology and development. The SSLPs provide highly polymorphic anchor points that allow inheritance to be traced in any cross and provide a scaffold for assembling physical maps. Adequate physical mapping resources--notably large-insert yeast artificial chromosome (YAC) libraries--are available to support positional cloning projects based on the genetic map, but a comprehensive physical map is still a few years away. Large-scale sequencing efforts have not yet begun in mouse, but comparative sequence analysis between mouse and human is likely to provide tremendous information about gene structure and regulation.
小鼠是研究哺乳动物遗传学和生理学的最佳模式系统。由于研究遗传杂交的可行性和重要性,小鼠遗传图谱近年来受到了极大关注。目前它包含超过14000个遗传定位标记,包括700个突变位点、3500个基因和6500个简单序列长度多态性(SSLP)。突变位点和基因有助于深入了解生理学和发育过程并建立相关性。SSLP提供了高度多态的锚定位点,可用于追踪任何杂交中的遗传情况,并为组装物理图谱提供支架。有足够的物理图谱绘制资源——尤其是大插入片段酵母人工染色体(YAC)文库——可用于支持基于遗传图谱的定位克隆项目,但全面的物理图谱仍需数年时间才能完成。小鼠的大规模测序工作尚未开始,但小鼠与人类之间的比较序列分析可能会提供有关基因结构和调控的大量信息。