Kamachi Y, Uchikawa M, Collignon J, Lovell-Badge R, Kondoh H
Institute for Molecular and Cellular Biology, Osaka University, Suita, Osaka 565-0871, Japan.
Development. 1998 Jul;125(13):2521-32. doi: 10.1242/dev.125.13.2521.
Activation of the first lens-specific gene of the chicken, delta 1-crystallin, is dependent on a group of lens nuclear factors, deltaEF2, interacting with the delta1-crystallin minimal enhancer, DC5. One of the deltaEF2 factors was previously identified as SOX2. We show that two related SOX proteins, SOX1 and SOX3, account for the remaining members of deltaEF2. Activation of the DC5 enhancer is dependent on their C-terminal domains. Expression of Sox1-3 in the eye region during lens induction was studied in comparison with Pax6 and delta1-crystallin. Pax6, known to be required for the inductive response of the ectoderm, is broadly expressed in the lateral head ectoderm from before lens induction. After tight association of the optic vesicle (around stage 10-11, 40 hours after egg incubation), expression of Sox2 and Sox3 is activated in the vesicle-facing ectoderm at stage 12 (44 hours). These cells, expressing together Pax6 and Sox2/3, subsequently give rise to the lens, beginning with formation of the lens placode and expression of delta-crystallin at stage 13 (48 hours). Sox1 then starts to be expessed in the lens-forming cells at stage 14. When the prospective retina area of the neural plate was unilaterally ablated at stage 7, expression of Sox2/3 was lost in the side of lateral head ectoderm lacking the optic cup, implying that an inductive signal from the optic cup activates Sox2/3 expression. In the mouse embryonic lens, this subfamily of Sox genes is expressed in an analogous fashion, although Sox3 transcripts have not been detected and Sox2 expression is down-regulated when Sox1 is activated. In ectodermal tissues of the chicken embryo, delta -crystallin expression occurs in a few ectopic sites. These are always characterized by overlapping expression of Sox2/3 and Pax6. Thus, an essential molecular event in lens induction is the 'turning on' of the transcriptional regulators SOX2/3 in the Pax6-expressing ectoderm and these SOX proteins activate crystallin gene expression. Continued activity, especially of SOX1, is then essential for further development of the lens.
鸡的第一个晶状体特异性基因δ1-晶状体蛋白的激活依赖于一组晶状体核因子δEF2,其与δ1-晶状体蛋白最小增强子DC5相互作用。δEF2因子之一先前被鉴定为SOX2。我们发现另外两个相关的SOX蛋白SOX1和SOX3构成了δEF2的其余成员。DC5增强子的激活依赖于它们的C末端结构域。我们将Sox1-3在晶状体诱导期间眼部区域的表达与Pax6和δ1-晶状体蛋白的表达进行了比较研究。已知外胚层的诱导反应需要Pax6,它在晶状体诱导之前就在侧头外胚层中广泛表达。在视泡紧密关联后(大约在第10-11阶段,即卵孵化后40小时),Sox2和Sox3的表达在第12阶段(44小时)在面向视泡的外胚层中被激活。这些同时表达Pax6和Sox2/3的细胞随后形成晶状体,并从第13阶段(48小时)晶状体板的形成和δ-晶状体蛋白的表达开始。然后Sox1在第14阶段开始在晶状体形成细胞中表达。当在第7阶段单侧切除神经板的预期视网膜区域时,Sox/3在缺乏视杯的侧头外胚层一侧的表达消失,这意味着来自视杯的诱导信号激活了Sox2/3的表达。在小鼠胚胎晶状体中,这个Sox基因亚家族以类似的方式表达,尽管未检测到Sox3转录本,并且当Sox1被激活时Sox2的表达下调。在鸡胚的外胚层组织中,δ-晶状体蛋白在一些异位位点表达。这些位点总是以Sox2/3和Pax6的重叠表达为特征。因此,晶状体诱导中的一个关键分子事件是在表达Pax6的外胚层中转录调节因子SOX2/3的“开启”,并且这些SOX蛋白激活晶状体蛋白基因的表达。持续活性,尤其是SOX1的活性,对于晶状体的进一步发育至关重要。