首页> 外文期刊>农业科学与技术(英文版) >3种微生物诱导的家蚕attacin基因异常表达形式的研究
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3种微生物诱导的家蚕attacin基因异常表达形式的研究

机译:3种微生物诱导的家蚕attacin基因异常表达形式的研究Abnormal Expression of Silkworm Attacin Gene Induced by 3 Kinds of Microorganisms

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[Objective] The aim of this research was to study the expression of silkworm attacin gene induced by some different microorganisms. [Method] Three kinds of microorganism, BmNPV, JM109 and Agrobacterium LBA4404, were ingested to silkworm and the expression profile of attacin gene in hemocyte and fat body was detected by semi-quantitative PCR. And subsequently, the PCR products were cloned and sequenced for further analysis. [Result] A specific band, about 800 bp, appeared in fat body of all induced silkworms. As indicated by the results of cloning and sequencing (GenBank accession number: FJ373019), the band was produced because the 2 introns existing in normal expression form were not spliced. Furthermore, when the extended expression sequence was translated into amino acids, the translation stopped earlier by the stop codon TGA at the 5' end of the first intron of the original sequence, leading the loss of attacin C terminus. [Conclusion] There were two splicesomes of attacin gene, which had reference value to study the role of the attacin gene in silkworm immunity.
机译:[目的]研究一些不同微生物诱导的蚕琼脂蛋白基因的表达。 [方法]采用半定量PCR检测三种微生物,BMNPV,JM109和土壤杆菌LBA4404,血细胞和脂肪体中的宿主基因的表达谱。随后,克隆并测序PCR产物以进一步分析。 [结果]特定带,约800bp,出现在所有诱导的家蚕的脂肪体中。如克隆和测序结果所示(GenBank登录号:FJ373019),产生带的频带是因为在正常表达形式中存在的2个内含子没有拼接。此外,当将延长的表达序列翻译成氨基酸时,通过原始序列的第一个内含子的5'末端的止芯密码子TGA之前更早地停止翻译,导致止损Atacin C末端。 [结论]有两种分析蛋白基因的剪接组,具有参考值,以研究宿主基因在蚕免疫中的作用。

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