首页> 外文期刊>Hydrobiologia >Comparative analysis of genes expressed in regenerating intestine andnon-eviscerated intestine of Apostichopus japonicus Selenka(Aspidochirotida: Stichopodidae) and cloning of ependymin gene
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Comparative analysis of genes expressed in regenerating intestine andnon-eviscerated intestine of Apostichopus japonicus Selenka(Aspidochirotida: Stichopodidae) and cloning of ependymin gene

机译:刺参再生肠和非去肠肠中表达基因的比较分析及鸭e藤素基因的克隆

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The regeneration of the intestine of sea cucumber (Apostichopus japonicus) was studied by describing historically the changes that occurred during intestine regeneration on the fifth day after chemically-induced evisceration. An expressed sequence tag (EST) analysis was undertaken to identify major genes, which might be involved in intestine regeneration of A. japonicus. Two cDNA libraries were constructed with directional cloning method, one for regenerating intestine collected on the third, fourth and fifth day after evisceration (post-evisceration, PE), and the other for the non-eviscerated (NE). A total of 730 ESTs were generated by sequencing cDNA clones from the two libraries (372 from PE and 358 from NE). The results showed that the number of genes that were involved in primary metabolism of PE library was less than that of NE library, while the number of genes involved in cell defense/immunity, cell division, cell signal transduction/communication of PE library was more than that of NE library. The results also revealed that the expression of the genes which might be involved in regeneration was enhanced to some extent after evisceration. Only about 11.54% of the sequenced clones were shared by two libraries, which provided some clues for the existence of differential gene expression between PE and NE intestines. A gene named epenAj was also characterized in this study.
机译:通过历史描述化学诱导内脏后第五天肠道再生过程中发生的变化,研究了海参(Apostichopus japonicus)肠道的再生。进行了表达序列标签(EST)分析,以鉴定可能与日本根瘤菌肠道再生有关的主要基因。使用定向克隆方法构建了两个cDNA文库,一个用于再生在内脏后第三天,第四天和第五天收集的肠道(内脏后,PE),另一个用于非内脏(NE)。通过对来自两个文库的cDNA克隆进行测序,总共产生了730个EST(来自PE的372个和来自NE的358个)。结果表明,PE文库一级代谢所涉及的基因数量少于NE文库,而PE文库的细胞防御/免疫,细胞分裂,细胞信号转导/通讯的基因数量较多。比NE库结果还表明,去内脏后,可能参与再生的基因的表达有所增强。两个文库仅共享约11.54%的测序克隆,这为PE和NE肠之间存在差异基因表达提供了一些线索。在这项研究中还表征了一个名为epenAj的基因。

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