Matsumata Miho, Uchikawa Masanori, Kamachi Yusuke, Kondoh Hisato
Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, Osaka 565-0871, Japan.
Dev Biol. 2005 Oct 15;286(2):601-17. doi: 10.1016/j.ydbio.2005.08.005. Epub 2005 Sep 16.
Neural plate and sensory placodes share the expression of N-cadherin and Group B1 Sox genes, represented by Sox2. A 219-kb region of the chicken genome centered by the N-cadherin gene was scanned for neural and placodal enhancers. Random subfragments of 4.5 kb average length were prepared and inserted into tkEGFP reporter vector to construct a library with threefold coverage of the region. Each clone was then transfected into N-cadherin-positive (lens, retina and forebrain) or -negative embryonic cells, or electroporated into early chicken embryos to examine enhancer activity. Enhancers 1-4 active in the CNS/placode derivatives and non-specific Enhancer 5 were identified by transfection, while electroporation of early embryos confirmed enhancers 2-4 as having activity in the early CNS and/or sensory placodes but with unique spatiotemporal specificities. Enhancers 2-4 are dependent on SOX-binding sites, and misexpression of Group B1 Sox genes in the head ectoderm caused ectopic development of placodes expressing N-cadherin, indicating the involvement of Group B1 Sox functions in N-cadherin regulation. Enhancers 1, 2 and 4 correspond to sequence blocks conserved between the chicken and mammalian genomes, but enhancers 3 and 5 are unique to the chicken.
神经板和感觉基板共享N-钙黏着蛋白和以Sox2为代表的B1组Sox基因的表达。以N-钙黏着蛋白基因为中心,扫描鸡基因组的一个219 kb区域,寻找神经和基板增强子。制备平均长度为4.5 kb的随机亚片段,并将其插入tkEGFP报告载体,构建该区域三倍覆盖的文库。然后将每个克隆转染到N-钙黏着蛋白阳性(晶状体、视网膜和前脑)或阴性胚胎细胞中,或电穿孔导入早期鸡胚中,以检测增强子活性。通过转染鉴定出在中枢神经系统/基板衍生物中具有活性的增强子1-4和非特异性增强子5,而早期胚胎的电穿孔证实增强子2-4在早期中枢神经系统和/或感觉基板中具有活性,但具有独特的时空特异性。增强子2-4依赖于SOX结合位点,并且头部外胚层中B1组Sox基因的错误表达导致表达N-钙黏着蛋白的基板异位发育,这表明B1组Sox功能参与了N-钙黏着蛋白的调控。增强子1、2和4对应于鸡和哺乳动物基因组之间保守的序列块,但增强子3和5是鸡特有的。