Pollock R A, Jay G, Bieberich C J
Jerome H. Holland Laboratory, American Red Cross, Rockville, Maryland 20855.
Cell. 1992 Dec 11;71(6):911-23. doi: 10.1016/0092-8674(92)90388-s.
To investigate the function of region-specific patterns of mouse homeobox gene expression during embryogenesis, we programmed a minimal change in the distribution of Hox3.1 transcripts along the anteroposterior body axis in transgenic mice. Regulatory sequences from Hox1.4, a gene normally expressed more anteriorly than Hox3.1, were chosen to direct expression of a Hox3.1 transgene. Offspring of independent transgenic lines expressed the transgene more anteriorly than the Hox3.1 gene. Rather than predicted posterior transformations, we observed anterior transformations of vertebrae in newborn mice. Transgenic mice also developed profound gastrointestinal tissue malformations, which may provide a molecular explanation for human developmental disorders often involving these same two regions. Paradoxically, vertebral transformations in the transgenic mice were strikingly similar to those reported in mice homozygous for a null mutation of the Hox3.1 gene. This observation suggests that Hox genes may be regulated antipodally, with over- or underexpression resulting in similar phenotypes.
为了研究小鼠同源框基因在胚胎发生过程中区域特异性表达模式的功能,我们对转基因小鼠中Hox3.1转录本沿前后体轴的分布进行了最小程度的改变。选择通常比Hox3.1表达更靠前的Hox1.4基因的调控序列来指导Hox3.1转基因的表达。独立转基因系的后代比Hox3.1基因更靠前地表达转基因。我们没有观察到预测的后部转化,而是在新生小鼠中观察到了椎骨的前部转化。转基因小鼠还出现了严重的胃肠道组织畸形,这可能为经常涉及这两个相同区域的人类发育障碍提供分子解释。矛盾的是,转基因小鼠中的椎骨转化与Hox3.1基因无效突变纯合子小鼠中报道的转化惊人地相似。这一观察结果表明,Hox基因可能受到反向调控,过表达或低表达会导致相似的表型。