首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Characterizing gene expression during lens formation in Xenopus laevis: evaluating the model for embryonic lens induction.
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Characterizing gene expression during lens formation in Xenopus laevis: evaluating the model for embryonic lens induction.

机译:在非洲爪蟾晶状体形成过程中表征基因表达:评估胚胎晶状体诱导模型。

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Few directed searches have been undertaken to identify the genes involved in vertebrate lens formation. In the frog Xenopus, the larval cornea can undergo a process of transdifferentiation to form a new lens once the original lens is removed. Based on preliminary evidence, we have shown that this process shares many elements of a common molecular/genetic pathway to that involved in embryonic lens development. A subtracted cDNA library, enriched for genes expressed during cornea-lens transdifferentiation, was prepared. The similarities/identities of specific clones isolated from the subtracted cDNA library define an expression profile of cells undergoing cornea-lens transdifferentiation ("lens regeneration") and corneal wound healing (the latter representing a consequence of the surgery required to trigger transdifferentiation). Screens were undertaken to search for genes expressed during both transdifferentiation and embryonic lens development. Significantly, new genes were recovered that are also expressed during embryonic lens development. The expression of these genes, as well as others known to be expressed during embryonic development in Xenopus, can be correlated with different periods of embryonic lens induction and development, in an attempt to define these events in a molecular context. This information is considered in light of our current working model of embryonic lens induction, in which specific tissue properties and phases of induction have been previously defined in an experimental context. Expression data reveal the existence of further levels of complexity in this process and suggests that individual phases of lens induction and specific tissue properties are not strictly characterized or defined by expression of individual genes.
机译:很少进行定向搜索来鉴定参与脊椎动物晶状体形成的基因。在青蛙爪蟾中,一旦去除原始晶状体,幼虫角膜会经历转分化过程以形成新晶状体。根据初步证据,我们已经表明,该过程与参与胚胎晶状体发育的分子/遗传途径共有许多共同的分子/遗传途径。制备了一个减去的cDNA文库,该文库富含角膜透镜转分化过程中表达的基因。从减去的cDNA文库中分离的特定克隆的相似性/同一性定义了经历角膜-晶状体分化(“晶状体再生”)和角膜伤口愈合(后者代表触发转分化所需要的手术的结果)的细胞的表达谱。进行筛选以寻找在转分化和胚胎晶状体发育期间表达的基因。重要的是,回收了在胚胎晶状体发育过程中也表达的新基因。这些基因以及其他已知在非洲爪蟾胚胎发育过程中表达的基因的表达,可能与胚胎晶状体诱导和发育的不同时期相关联,以试图在分子环境中定义这些事件。根据我们当前的胚胎晶状体诱导工作模型来考虑此信息,在该模型中,特定的组织特性和诱导阶段已在实验中预先定义。表达数据揭示了该过程中进一步复杂性的存在,并表明晶状体诱导和特定组织特性的各个阶段没有通过单个基因的表达来严格表征或定义。

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