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Expression and subcellular localization of a novel gene Bm-X of the silkworm, Bombyx mori

机译:家蚕新基因Bm-X的表达和亚细胞定位

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According to the large-scale sequencing of cDNA library from silkworm pupae, the cDNA of a novel gene with blank research background was identified and temporarily named Bm-X. The length of this cDNA is 778 bp. We obtained its ORF for further study by bioinformatics analysis. It is 444 bp and encodes 147 amino acid residues, with a predicted molecular weight (MW) of 16.4 kD and an isoelectric point (pI) of 3.69. In this study, we successfully constructed a recombinant plasmid pET-28a(+)-Bm-X and expressed it in Escherichia coli. We used the fusion protein rBm-X which purified by Niaffinity chromatography to produce polyclonal antibodies against Bm-X for Western blot analysis. The analysis revealed that Bm-X was expressed in the larval midgut, the epidermis and the silk gland. In addition, the subcellular localization analysis of silkworm ovary epithelial cells (BmN cells) showed that Bm-X protein was located both in cytoplasm and nucleus, and the signal was stronger in cytoplasm than in nucleus. Our findings indicate that Bm-X gene is a novel species-specificity gene and its expression product can be detected in tissues of the fifth silkworm instar larvae and BmN cells.
机译:根据蚕pcDNA文库的大规模测序,鉴定了一个具有空白研究背景的新基因的cDNA,并暂时命名为Bm-X。该cDNA的长度是778bp。我们通过生物信息学分析获得了ORF,供进一步研究。它是444 bp,编码147个氨基酸残基,预测分子量(MW)为16.4 kD,等电点(pI)为3.69。在这项研究中,我们成功构建了重组质粒pET-28a(+)-Bm-X,并在大肠杆菌中表达。我们使用通过Niaffinity层析纯化的融合蛋白rBm-X产生针对Bm-X的多克隆抗体,进行蛋白质印迹分析。分析表明,Bm-X在幼虫中肠,表皮和丝腺中表达。此外,家蚕卵巢上皮细胞(BmN细胞)的亚细胞定位分析表明,Bm-X蛋白位于细胞质和细胞核中,并且在细胞质中的信号强于细胞核中的信号。我们的发现表明,Bm-X基因是一种新型的物种特异性基因,其表达产物可以在第五家蚕龄幼虫和BmN细胞的组织中检测到。

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