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首页> 外文期刊>DNA and Cell Biology >Xuhuai Goat H-FABP Gene Clone, Subcellular Localization of Expression Products and the Preparation of Transgenic Mice
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Xuhuai Goat H-FABP Gene Clone, Subcellular Localization of Expression Products and the Preparation of Transgenic Mice

机译:徐淮山羊H-FABP基因克隆,表达产物亚细胞定位及转基因小鼠制备

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摘要

The aim of this study was to clone the heart-type fatty acid binding protein (H-FABP) gene of Xuhuai goat, to explore it bioinformatically, and analyze the subcellular localization using enhanced green fluorescent protein (EGFP). The results showed that the coding sequence (CDS) length of Xuhuai goat H-FABP gene was 402 bp, encoding 133 amino acids (GenBank accession number AY466498.1). The H-FABP cDNA coding sequence was compared with the corresponding region of human, chicken, brown rat, cow, wild boar, donkey, and zebrafish. The similarity were 89%, 76%, 85%, 84%, 93%, 91%, 70%, respectively. For the corresponding amino acid sequences, the similarity were 90%, 79%, 88%, 97%, 95%, 94%, 72%, respectively. This study did not find the signal peptide region in the H-FABP protein; it revealed that H-FABP protein might be a nonsecreted protein. H-FABP expression was detected in vitro by reverse transcription-polymerase chain reaction (RT-PCR), and the EGFP-H-FABP fusion protein was localized to the cytoplasm. The gene could also be transiently and permanently expressed in mice.
机译:这项研究的目的是克隆徐淮山羊的心型脂肪酸结合蛋白(H-FABP)基因,进行生物信息学探索,并使用增强型绿色荧光蛋白(EGFP)分析亚细胞定位。结果表明,徐淮山羊H-FABP基因的编码序列(CDS)长度为402 bp,编码133个氨基酸(GenBank登录号AY466498.1)。将H-FABP cDNA编码序列与人,鸡,褐鼠,牛,野猪,驴和斑马鱼的相应区域进行比较。相似度分别为89%,76%,85%,84%,93%,91%,70%。对于相应的氨基酸序列,相似性分别为90%,79%,88%,97%,95%,94%,72%。该研究未在H-FABP蛋白中发现信号肽区域。它揭示了H-FABP蛋白可能是非分泌蛋白。通过逆转录-聚合酶链反应(RT-PCR)在体外检测到H-FABP表达,并且EGFP-H-FABP融合蛋白定位在细胞质中。该基因还可以在小鼠中瞬时和永久表达。

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