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Use of human cDNA microarrays for identification of differentially expressed genes in Atlantic salmon liver during Aeromonas salmonicida infection

机译:人类cDNA芯片用于鉴定鲑鱼气单胞菌感染期间大西洋鲑鱼肝脏中差异表达的基因的用途

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Commercially available human complementary DNA microarrays were used to compare differential expression in the livers of Atlantic salmon (Salmo salar) infected with Aeromonas salmonicida and of healthy fish. Complementary DNA probes were prepared from total RNA isolated from livers of control salmon and infected salmon by reverse transcription in the presence of P-33-dCTP and independently hybridized to human GENE-FILTERS GF211 microarrays. Of the 4131 known genes on the microarray, 241 spots gave clearly detectable signals using labeled RNA from the control salmon liver. Of these, 4 spots were consistently found to have a greater than 2-fold increase in infected salmon compared with controls when using the same pair of filters to generate hybridization data from triplicates. These up-regulated genes were ADP/ATP translocase (AAT2), Na+/K+ ATPase, acyloxyacyl hydrolase (AOAH), and platelet-derived growth factor (PDFG-A). A BlastN search revealed an AAT2 homolog from Atlantic salmon, and a reverse transcriptase polymerase chain reaction assay using primers based on this sequence confirmed its up-regulation (approx. 1.8-fold) during early infection. This work demonstrates the feasibility of using human microarrays to facilitate the discovery of differentially expressed genes in Atlantic salmon I, for which no homologous microarrays are available.
机译:使用可商购的人互补DNA微阵列来比较感染鲑鱼气单胞菌和健康鱼的大西洋鲑鱼(Salmo salar)肝脏中的差异表达。在存在P-33-dCTP的条件下,通过逆转录从分离自对照鲑鱼和受感染鲑鱼肝脏的总RNA中制备互补DNA探针,并与人GENE-FILTERS GF211微阵列独立杂交。在微阵列上的4131个已知基因中,有241个点使用来自对照鲑鱼肝的标记RNA发出了清晰可检测的信号。其中,使用同一对过滤器从一式三份生成杂交数据时,与对照相比,始终发现4个斑点的受感染鲑鱼增加了2倍以上。这些上调的基因是ADP / ATP转位酶(AAT2),Na + / K + ATPase,酰氧基酰基水解酶(AOAH)和血小板衍生的生长因子(PDFG-A)。 BlastN搜索显示了来自大西洋鲑鱼的AAT2同源物,使用基于该序列的引物进行的逆转录酶聚合酶链反应测定证实了其在早期感染期间的上调(约1.8倍)。这项工作证明了使用人类微阵列来促进大西洋鲑I中差异表达基因的发现的可行性,而大西洋鲑I没有同源微阵列。

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