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首页> 外文期刊>BMC Molecular Biology >Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus)
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Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus)

机译:在日本比目鱼(Paralichthys olivaceus)中对免疫刺激物应答的PoAkirin1和两个相关基因的筛选和分析

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A member of the NF-κB signaling pathway, PoAkirin1, was cloned from a full-length cDNA library of Japanese flounder (Paralichthys olivaceus). The full-length cDNA comprises a 5′UTR of 202?bp, an open reading frame of 564?bp encoding a 187-amino-acid polypeptide and a 521-bp 3′UTR with a poly (A) tail. The putative protein has a predicted molecular mass of 21?kDa and an isoelectric point (pI) of 9.22. Amino acid sequence alignments showed that PoAkirin1 was 99% identical to the Scophthalmus maximus Akirin protein (ADK27484). Yeast two-hybrid assays identified two proteins that interact with PoAkirin1: PoHEPN and PoC1q. The cDNA sequences of PoHEPN and PoC1q are 672?bp and 528?bp, respectively. Real-time quantitative reverse-transcriptase polymerase chain reaction analysis showed that bacteria could induce the expressions of PoAkirin1, PoHEPN and PoC1q. However, the responses of PoHEPN and PoC1q to the bacterial challenge were slower than that of PoAkirin1. To further study the function of PoAkirin1, recombinant PoAkirin1 and PoHEPN were expressed in Escherichia coli and would be used to verify the PoAkirin1-PoHEPN binding activity. These results identified two proteins that potentially interact with PoAkirin1 and that bacteria could induce their expression.
机译:从日本比目鱼(Paralichthys olivaceus)的全长cDNA文库中克隆了NF-κB信号通路的成员PoAkirin1。全长cDNA包括202′bp的5′UTR,564′bp的开放阅读框,其编码187个氨基酸的多肽和521bp的具有聚(A)尾的3′UTR。推定的蛋白质的预测分子量为21 kkDa,等电点(pI)为9.22。氨基酸序列比对显示,PoAkirin1与最大隐球菌Akirin蛋白(ADK27484)99%相同。酵母双杂交测定法鉴定了与PoAkirin1相互作用的两种蛋白质:PoHEPN和PoC1q。 PoHEPN和PoC1q的cDNA序列分别为672bp和528bp。实时定量逆转录酶聚合酶链反应分析表明,细菌可以诱导PoAkirin1,PoHEPN和PoC1q的表达。但是,PoHEPN和PoC1q对细菌攻击的反应要慢于PoAkirin1。为了进一步研究PoAkirin1的功能,重组PoAkirin1和PoHEPN在大肠杆菌中表达,将用于验证PoAkirin1-PoHEPN的结合活性。这些结果确定了可能与PoAkirin1相互作用的两种蛋白质,细菌可以诱导其表达。

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