Dong Zimei, Yuwen Yanqing, Wang Qinghua, Chen Guangwen, Liu Dezeng
Life Science College, Henan Normal University, People's Republic of China.
Gene Expr Patterns. 2012 Jan-Feb;12(1-2):1-6. doi: 10.1016/j.gep.2011.08.001. Epub 2011 Aug 6.
Dugesia japonica has become the suitable model system for studying the visual system molecular developmental processes because of their simple structure and high regenerative capacity. To further dissect the molecular events of genetic network controlling the visual system regeneration in D. japonica, we investigated the morphogenesis of regenerating eyes under the stereomicroscope and the transcripts expression levels of eight genes involved in this process by quantitative real-time PCR. The eight genes were Djeya, Djsix-1, Eye53, DjotxA, Djpax6, Djopsin, Djnetrin and 1020HH. The results showed that each gene was of different expression pattern at distinct regeneration stage and these eight genes could be divided into three groups according to the expression levels at different time points and the morphogenesis during eye reconstruction: (1) the early expression group, including Djeya, Djsix-1, Eye53, and DjotxA, which expression levels were significant increase from 1 to 3days after amputation; (2) the medium-term expression group, only including one gene, Djpax6, which expression level reached the peak on day 5; and (3) the late expression genes, including Djopsin, Djnetrin and 1020HH, which gradually increase transcription with the eye regeneration. Our data suggested that eye reconstruction was the results of polygenic services and the genes in the same group might have similar role or function in symphony.
日本三角涡虫因其结构简单和再生能力强,已成为研究视觉系统分子发育过程的合适模型系统。为了进一步剖析控制日本三角涡虫视觉系统再生的遗传网络的分子事件,我们在体视显微镜下研究了再生眼的形态发生,并通过定量实时PCR检测了参与这一过程的八个基因的转录本表达水平。这八个基因分别是Djeya、Djsix-1、Eye53、DjotxA、Djpax6、Djopsin、Djnetrin和1020HH。结果表明,每个基因在不同的再生阶段具有不同的表达模式,根据不同时间点的表达水平和眼重建过程中的形态发生,这八个基因可分为三组:(1)早期表达组,包括Djeya、Djsix-1、Eye53和DjotxA,其表达水平在截肢后1至3天显著增加;(2)中期表达组,仅包括一个基因Djpax6,其表达水平在第5天达到峰值;(3)晚期表达基因,包括Djopsin、Djnetrin和1020HH,它们随着眼再生而逐渐增加转录。我们的数据表明,眼重建是多基因协同作用的结果,同一组中的基因可能在协同作用中具有相似的作用或功能。