首页> 外文期刊>Journal of Agricultural and Food Chemistry >Molecular Cloning and Characterization of Two 12 kDa FK506-Binding Protein Genes in the Chinese Oak Silkworm, Antheraea pernyi
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Molecular Cloning and Characterization of Two 12 kDa FK506-Binding Protein Genes in the Chinese Oak Silkworm, Antheraea pernyi

机译:中国橡蚕An蚕两个12 kDa FK506结合蛋白基因的分子克隆与鉴定

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摘要

Two 12 kDa FK506-binding protein (FKBP12) genes were isolated and characterized from Chinese oak silkworm Antheraea pernyi, an important agricultural and edible insect, designated ApFKBP12 A and B, respectively. Both ApFKBP12 A and B contained 108 amino acids with 82% sequence identity. Phylogenetic analysis showed that FKBP12 B sequences of A. pernyi, Bombyx mori, and Danaus plexippus were clearly separated from FKBP12 A sequences of these three species, suggesting that insect FKBP12 A and B may have been evolving independently. RT-PCR analyses revealed that two ApFKBP12 genes were expressed during the four developmental stages and in all tested tissues, and that the mRNA expression level of the ApFKBP12 A gene was significantly higher than that of the ApFKBP12 B gene. After heat shock treatment, expressions of the two FKBP12 genes were up-regulated, but at different time points. The results suggested that each paralogue of the FKBP12 genes may play a distinct functional role in the development of A. pernyi.
机译:从中国橡树蚕Antheraea pernyi(一种重要的农业和食用昆虫,分别命名为ApFKBP12 A和B)分离并鉴定了两个12 kDa FK506结合蛋白(FKBP12)基因。 ApFKBP12 A和B都包含108个氨基酸,序列同一性为82%。系统发育分析表明,A。pernyi,Bombyx mori和Danaus plexippus的FKBP12 B序列与这三个物种的FKBP12 A序列明显分离,表明昆虫FKBP12 A和B可能已经独立进化。 RT-PCR分析显示,在四个发育阶段和所有受检组织中均表达了两个ApFKBP12基因,并且ApFKBP12A基因的mRNA表达水平明显高于ApFKBP12B基因。热激处理后,两个FKBP12基因的表达上调,但在不同的时间点。结果表明,FKBP12基因的每个旁系同源物可能在peryi。pernyi的发育中发挥独特的功能作用。

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