McNeish J D, Scott W J, Potter S S
Division of Basic Science Research, Children's Hospital Research Foundation, Cincinnati, OH.
Science. 1988 Aug 12;241(4867):837-9. doi: 10.1126/science.3406741.
In this report it is shown that the PHT1-1 line of transgenic mice exhibited a pattern of developmental abnormalities when the mice were homozygous for the transgene insertion. Hindlimbs were uniformly truncated at the distal end of the femur, resulting in a "legless" appearance. Forelimbs lacked anterior structures including digits and the radius. The brains had many defects, particularly in the anterior structures of the cerebrum, including the olfactory lobes. Craniofacial malformations in the form of facial clefts also commonly occurred. Furthermore, heterozygotes of this line, with only one copy of the DNA insertion, and other transgenic lines carrying the same DNA construct appeared normal, suggesting that in the PHT1-1 line a gene significant in mammalian development has been disrupted.
本报告显示,当转基因小鼠的PHT1-1系为转基因插入纯合子时,表现出发育异常模式。后肢在股骨远端均匀截断,导致呈现“无腿”外观。前肢缺少包括指骨和桡骨在内的前部结构。大脑有许多缺陷,特别是在大脑前部结构,包括嗅叶。面部裂隙形式的颅面畸形也很常见。此外,该系的杂合子(仅携带一份DNA插入拷贝)以及携带相同DNA构建体的其他转基因系看起来正常,这表明在PHT1-1系中,一个对哺乳动物发育至关重要的基因已被破坏。