Ashery-Padan R, Marquardt T, Zhou X, Gruss P
Max-Planck Institute of Biophysical Chemistry, Department of Molecular Cell Biology, Goettingen D-37077, Germany.
Genes Dev. 2000 Nov 1;14(21):2701-11. doi: 10.1101/gad.184000.
The Pax6 transcription factor plays a key role in ocular development of vertebrates and invertebrates. Homozygosity of the Pax6 null mutation in human and mice results in arrest of optic vesicle development and failure to initiate lens formation. This phenotype obscures the understanding of autonomous function of Pax6 in these tissue components and during later developmental stages. We employed the Cre/loxP approach to inactivate Pax6 specifically in the eye surface ectoderm concomitantly with lens induction. Although lens induction occurred in the mutant, as indicated by Sox2 up-regulation in the surface ectoderm, further development of the lens was arrested. Hence, Pax6 activity was found to be essential in the specified ectoderm for lens placode formation. Furthermore, this mutant model allowed us for the first time to address in vivo the development of a completely normal retina in the absence of early lens structures. Remarkably, several independent, fully differentiated neuroretinas developed in a single optic vesicle in the absence of a lens, demonstrating that the developing lens is not necessary to instruct the differentiation of the neuroretina but is, rather, required for the correct placement of a single retina in the eye.
Pax6转录因子在脊椎动物和无脊椎动物的眼发育过程中发挥关键作用。人类和小鼠中Pax6无效突变的纯合性会导致视泡发育停滞以及晶状体形成起始失败。这种表型模糊了对Pax6在这些组织成分以及后期发育阶段自主功能的理解。我们采用Cre/loxP方法,在晶状体诱导的同时,特异性地使眼表面外胚层中的Pax6失活。尽管如表面外胚层中Sox2上调所示,突变体中发生了晶状体诱导,但晶状体的进一步发育停滞。因此,发现Pax6活性在特定外胚层中对于晶状体板形成至关重要。此外,这个突变体模型首次让我们能够在体内研究在没有早期晶状体结构的情况下完全正常视网膜的发育。值得注意的是,在没有晶状体的情况下,单个视泡中发育出了几个独立的、完全分化的神经视网膜,这表明发育中的晶状体对于指导神经视网膜的分化并非必要,而是对于单个视网膜在眼中的正确定位是必需的。