Schedl A, Ross A, Lee M, Engelkamp D, Rashbass P, van Heyningen V, Hastie N D
MRC Human Genetics Unit, Western General Hospital, Edinburgh, United Kingdom.
Cell. 1996 Jul 12;86(1):71-82. doi: 10.1016/s0092-8674(00)80078-1.
Aniridia in man and Small eye in mice are semidominant developmental disorders caused by mutations within the paired box gene PAX6. Whereas heterozygotes suffer from iris hypoplasia, homozygous mice lack eyes and nasal cavities and exhibit brain abnormalities. To investigate the role of gene dosage in more detail, we have generated yeast artificial chromosome transgenic mice carrying the human PAX6 locus. When crossed onto the Small eye background, the transgene rescues the mutant phenotype. Strikingly, mice carrying multiple copies on a wild-type background show specific developmental abnormalities of the eye, but not of other tissues expressing the gene. Thus, at least five different eye phenotypes are associated with changes in PAX6 expression. We provide evidence that not only reduced, but also increased levels of transcriptional regulators can cause developmental defects.
人类的无虹膜症和小鼠的小眼症是由配对盒基因PAX6内的突变引起的半显性发育障碍。杂合子患有虹膜发育不全,而纯合子小鼠没有眼睛和鼻腔,并表现出脑部异常。为了更详细地研究基因剂量的作用,我们构建了携带人类PAX6基因座的酵母人工染色体转基因小鼠。当与小眼背景杂交时,转基因挽救了突变表型。令人惊讶的是,在野生型背景上携带多个拷贝的小鼠表现出眼睛的特定发育异常,但在表达该基因的其他组织中则没有。因此,至少五种不同的眼睛表型与PAX6表达的变化有关。我们提供的证据表明,转录调节因子水平的降低和升高都可能导致发育缺陷。