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首页> 外文期刊>The Journal of Comparative Neurology >Vsx-1 and Vsx-2: differential expression of two paired-like homeobox genes during zebrafish and goldfish retinogenesis.
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Vsx-1 and Vsx-2: differential expression of two paired-like homeobox genes during zebrafish and goldfish retinogenesis.

机译:Vsx-1和Vsx-2:斑马鱼和金鱼视网膜发生过程中两个成对的同源盒基因的差异表达。

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Vsx-1 and Vsx-2 are two homeobox genes that were cloned originally from an adult goldfish retinal library. They are members of the paired-like:CVC gene family, which is characterized by the presence of a paired homeodomain and an additional conserved region, termed the CVC domain. To analyze the possible roles for Vsx-1 and Vsx-2 in eye development, we used in situ hybridization to examine their expression patterns in zebrafish and goldfish embryos. Vsx-2 is initially expressed by proliferating neuroepithelial cells of the presumptive neural retina, then it is down-regulated as differentiation begins, and it is finally reexpressed at later stages of differentiation in a subset of cells, presumed to be bipolar cells, in the inner nuclear layer. In contrast, Vsx-1 is expressed only weakly in undifferentiated, presumptive neural retina and is then up-regulated selectively in presumptive bipolar cells at early stages of differentiation (when Vsx-2 is turned off), before decreasing to an intermediate level,which is maintained in the differentiated (adult) retina. The restricted expression patterns of Vsx-2 correspond to the observed phenotypes in mice with the ocular retardation mutation (orJ), further supporting the notion that Vsx-2 and Chx10 are homologues. The sequential complimentary and then corresponding expression patterns of Vsx-1 and Vsx-2 suggest that these similar transcription factors may be recruited for partially overlapping, but distinct, functions during the development of the retina.
机译:Vsx-1和Vsx-2是两个同源盒基因,最初是从成年金鱼视网膜文库中克隆的。它们是成对的:CVC基因家族的成员,其特征是存在配对的同源结构域和一个称为CVC结构域的保守区域。为了分析Vsx-1和Vsx-2在眼睛发育中的可能作用,我们使用原位杂交技术检查了它们在斑马鱼和金鱼胚胎中的表达模式。 Vsx-2最初由假定的神经视网膜的神经上皮细胞增殖表达,然后在分化开始时被下调,最后在分化的后期阶段在假定为双极细胞的一组细胞中重新表达。内核层。相比之下,Vsx-1在未分化的推测性神经视网膜中仅微弱表达,然后在分化的早期阶段(当Vsx-2关闭时)在推测的双极细胞中选择性上调,然后降低至中等水平。保持在分化的(成人)视网膜中。 Vsx-2的限制性表达模式对应于具有眼智障碍突变(orJ)的小鼠中观察到的表型,进一步支持了Vsx-2和Chx10是同源物的观点。 Vsx-1和Vsx-2的顺序互补和随后对应的表达模式表明,可以募集这些相似的转录因子,以在视网膜发育过程中部分重叠但截然不同的功能。

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