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Discovery of the genes in response to white spot syndrome virus (WSSV) infection in Fenneropenaeus chinensis through cDNA microarray.

机译:通过cDNA微阵列发现中华白粉病对白斑综合症病毒(WSSV)感染的响应基因。

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We used microarray technology to study differentially expressed genes in white spot syndrome virus (WSSV)-infected shrimp. A total of 3136 cDNA targets, including 1578 unique genes from a cephalothorax cDNA library and 1536 cDNA clones from reverse and forward suppression subtractive hybridization (SSH) libraries of Fenneropenaeus chinensis, plus 14 negative and 8 blank control clones, were spotted onto a 18x18 mm area of NH2-modified glass slides. Gene expression patterns in the cephalothorax of shrimp at 6 h after WSSV injection and moribund shrimp naturally infected by WSSV were analyzed. A total of 105 elements on the arrays showed a similar regulation pattern in artificially infected shrimp and naturally infected moribund shrimp; parts of the results were confirmed by semiquantitative reverse transcriptase-polymerase chain reaction (RT-PCR). The up-regulated expression of immune-related genes, including heat shock proteins (HSP70 and HSP90), trehalose-phosphate synthase (TPS), ubiquitin C, and so forth, were observed when shrimp were challenged with WSSV. Genes including myosin LC2, ATP synthase A chain, and arginine kinase were found to be down-regulated after WSSV infection. The expression of housekeeping genes such as actin, elongation factor, and tubulin is not stable, and so these genes are not suitable as internal standards for semiquantitative RT-PCR when shrimp are challenged by WSSV. As a substitute, we found that triosephosphate isomerase (TPI) was an ideal candidate of interstandards in this situation..
机译:我们使用微阵列技术研究了白斑综合症病毒(WSSV)感染的虾中差异表达的基因。将总共​​3136个cDNA靶标点到一个18x18 mm的斑点上,其中包括来自头胸部cDNA文库的1578个独特基因和来自中国猪鞭草的反向和正向抑制消减杂交(SSH)文库的1536个cDNA克隆,以及14个阴性和8个空白对照克隆。 NH2修饰的玻璃片的面积。分析了注射WSSV后6小时虾的胸胸中的基因表达模式和被WSSV自然感染的垂死虾。阵列上总共有105个元素在人工感染的虾和自然感染的垂死虾中显示出相似的调控模式。半定量逆转录聚合酶链反应(RT-PCR)证实了部分结果。当虾受到WSSV攻击时,观察到免疫相关基因的表达上调,包括热休克蛋白(HSP70和HSP90),海藻糖磷酸合酶(TPS),泛素C等。发现包括肌球蛋白LC2,ATP合酶A链和精氨酸激酶在内的基因在WSSV感染后被下调。管家基因如肌动蛋白,延伸因子和微管蛋白的表达不稳定,因此当虾受到WSSV攻击时,这些基因不适合用作半定量RT-PCR的内部标准。作为替代品,我们发现在这种情况下,磷酸三糖异构酶(TPI)是标准品的理想选择。

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