Zygar C A, Cook T L, Grainger R M
University of Virginia, Department of Biology, Charlottesville, VA, USA.
Development. 1998 Sep;125(17):3509-19. doi: 10.1242/dev.125.17.3509.
Several stages in the lens determination process have been defined, though it is not known which gene products control these events. At mid-gastrula stages in Xenopus, ectoderm is transiently competent to respond to lens-inducing signals. Between late gastrula and neural tube stages, the presumptive lens ectoderm acquires a lens-forming bias, becomes specified to form lens and begins differentiation. Several genes have been identified, either by expression pattern, mutant phenotype or involvement in crystallin gene regulation, that may play a role in lens bias and specification, and we focus on these roles here. Fate mapping shows that the transcriptional regulators Otx-2, Pax-6 and Sox-3 are expressed in the presumptive lens ectoderm prior to lens differentiation. Otx-2 appears first, followed by Pax-6, during the stages of lens bias (late neural plate stages); expression of Sox-3 follows neural tube closure and lens specification. We also demonstrate the expression of these genes in competent ectoderm transplanted to the lens-forming region. Expression of these genes is maintained or activated preferentially in ectoderm in response to the anterior head environment. Finally, we examined activation of these genes in response to early and late lens-inducing signals. Activation of Otx-2, Pax-6 and Sox-3 in competent ectoderm occurs in response to the early inducing tissue, the anterior neural plate. Since Sox-3 is activated following neural tube closure, we tested its dependence on the later inducing tissue, the optic vesicle, which contacts lens ectoderm at this stage. Sox-3 is not expressed in lens ectoderm, nor does a lens form, when the optic vesicle anlage is removed at late neural plate stages. Expression of these genes demarcates patterning events preceding differentiation and is tightly coupled to particular phases of lens induction.
晶状体决定过程中的几个阶段已被明确,尽管尚不清楚哪些基因产物控制这些事件。在非洲爪蟾原肠胚中期,外胚层短暂具备对晶状体诱导信号作出反应的能力。在原肠胚后期到神经管形成阶段之间,预定晶状体外胚层获得形成晶状体的偏向性,开始被指定形成晶状体并开始分化。通过表达模式、突变体表型或参与晶状体蛋白基因调控等方式,已经鉴定出几个可能在晶状体偏向性和特化过程中发挥作用的基因,我们在此聚焦于这些作用。命运图谱显示,转录调节因子Otx - 2、Pax - 6和Sox - 3在晶状体分化之前就在预定晶状体外胚层中表达。在晶状体偏向性阶段(神经板后期),Otx - 2最先出现,随后是Pax - 6;Sox - 3的表达在神经管闭合和晶状体特化之后。我们还证明了这些基因在移植到晶状体形成区域的感受态外胚层中的表达。这些基因的表达在外胚层中因前脑环境而被优先维持或激活。最后,我们检测了这些基因对早期和晚期晶状体诱导信号的反应激活情况。感受态外胚层中Otx - 2、Pax - 6和Sox - 3的激活是对早期诱导组织即前神经板的反应。由于Sox - 3在神经管闭合后被激活,我们测试了它对后期诱导组织即视泡的依赖性,视泡在这个阶段与晶状体外胚层接触。当在神经板后期移除视泡原基时,Sox - 3不在晶状体外胚层中表达,也不会形成晶状体。这些基因的表达划分了分化之前的模式形成事件,并且与晶状体诱导的特定阶段紧密相关。