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Gene Structural Analysis and Expression of Human Renal Dipeptidase

机译:人肾二肽酶的基因结构分析与表达

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AbstractHuman renal dipeptidase cDNA and genomic DNA were isolated from human kidney cDNA and genomic libraries, respectively. The human renal dipeptidase gene has a total length of approximately 6 kb and consists of ten exons and nine introns. The exons and cDNA each encode the 411 amino acid residues of the precursor protein, including 16 amino acid residues of signal sequence and a hydrophobic carboxyl terminal sequence for the attachment of a phosphatidylinositol glycan. Although the cDNA was slightly different from the cDNA reported by Adachi et al. (1990), the differences observed suggest, by comparison with human genomic DNA, that it may not represent an allelic variant but a cloning artifact. The recombinant human renal dipeptidase was produced on the surface of transfected L929 cells and had the same character as native renal dipeptidase. Northern blotting hybridization analysis showed that renal dipeptidase mRNA is only transcribed in kidney.
机译:摘要 分别从人肾cDNA和基因组文库中分离出人肾二肽酶cDNA和基因组DNA。人肾二肽酶基因的总长度约为 6 kb,由 10 个外显子和 9 个内含子组成。外显子和 cDNA 分别编码前体蛋白的 411 个氨基酸残基,包括 16 个信号序列的氨基酸残基和用于连接磷脂酰肌醇聚糖的疏水羧基末端序列。尽管cDNA与Adachi等人(1990)报道的cDNA略有不同,但观察到的差异表明,与人类基因组DNA相比,它可能不代表等位基因变异,而是一种克隆伪影。重组人肾二肽酶在转染的L929细胞表面产生,与天然肾二肽酶具有相同的特性。Northern印迹杂交分析显示,肾二肽酶mRNA仅在肾脏中转录。

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