Cloning and characterization of transferrin cDNA and rapid detection of transferrin gene polymorphism in rainbow trout (Oncorhynchus mykiss).

N Tange, L Jong-Young, N Mikawa, I Hirono, T Aoki
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Abstract

A cDNA clone of rainbow trout (Oncorhynchus mykiss) transferrin was obtained from a liver cDNA library. The 2537-bp cDNA sequence contained an open reading frame encoding 691 amino acids and the 5' and 3' noncoding regions. The amino acid sequences at the iron-binding sites and the two N-linked glycosylation sites, and the cysteine residues were consistent with known, conserved vertebrate transferrin cDNA sequences. Single N-linked glycosylation sites existed on the N- and C-lobe. The deduced amino acid sequence of the rainbow trout transferrin cDNA had 92.9% identities with transferrin of coho salmon (Oncorhynchus kisutch); 85%, Atlantic salmon (Salmo salar); 67.3%, medaka (Oryzias latipes); 61.3% Atlantic cod (Gadus morhua); and 59.7%, Japanese flounder (Paralichthys olivaceus). The long and accurate polymerase chain reaction (LA-PCR) was used to amplify approximately 6.5 kb of the transferrin gene from rainbow trout genomic DNA. Restriction fragment length polymorphisms (RFLPs) of the LA-PCR products revealed three digestion patterns in 22 samples.

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虹鳟(Oncorhynchus mykiss)转铁蛋白cDNA的克隆、鉴定及基因多态性快速检测。
从虹鳟肝脏cDNA文库中获得了虹鳟转铁蛋白的cDNA克隆。2537bp的cDNA序列包含一个编码691个氨基酸的开放阅读框以及5'和3'非编码区。铁结合位点和两个n链糖基化位点的氨基酸序列以及半胱氨酸残基与已知的保守的脊椎动物转铁蛋白cDNA序列一致。单个N-链糖基化位点存在于N-叶和c -叶。所得的虹鳟转铁蛋白cDNA序列与银鲑转铁蛋白的同源性为92.9%;85%为大西洋鲑(Salmo salar);67.3%为稻科植物(Oryzias latipes);61.3%大西洋鳕鱼(Gadus morhua);59.7%为牙鲆(parichthys olivaceus)。采用精确的长链聚合酶链反应(LA-PCR)从虹鳟基因组DNA中扩增出约6.5 kb的转铁蛋白基因。LA-PCR产物的限制性内切片段长度多态性(RFLPs)在22个样品中显示出三种消化模式。
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