Suzuki T, Nishikawa T
Department of Biology, Faculty of Science, Kochi University, Japan. suzuki@ cc.kochi.u.ac.jp
J Protein Chem. 1996 May;15(4):389-94. doi: 10.1007/BF01886865.
Hemoglobin beta chains were isolated from the catfish Parasilurus asotus, the scad Decapterus maruadsi, the filefish Thamnaconus modestus, and the scorpaenoid Sebastiscus marmoratus by reverse-phase chromatography, and the N-terminal sequences were determined. To obtain the complete amino acid sequence, a 20-meric redundant consensus primer based on the N-terminal amino acid sequences of the beta chains was designed. Using this primer and oligo-dT adaptor, we amplified successfully the beta-chain cDNAs of about 600 bp from the four fishes. The amplified products from Parasilurus and Decapterus were subcloned in the SmaI site of pUC18 and cDNA-derived amino acid sequences of 147 residues were determined, of which 69 and 76 residues, respectively, were identified by the chemical amino acid sequencing of internal peptides. Thus this PCR methodology using the consensus primer should be widely applicable for amplifying hemoglobin beta chains from teleosts.
通过反相色谱法从鲶鱼(鲇鱼)、蓝圆鲹、绿鳍马面鲀和褐菖鲉中分离出血红蛋白β链,并测定其N端序列。为获得完整的氨基酸序列,基于β链的N端氨基酸序列设计了一个20聚体冗余共有引物。使用该引物和寡聚-dT接头,我们成功地从这四种鱼类中扩增出约600 bp的β链cDNA。将鲶鱼和蓝圆鲹的扩增产物亚克隆到pUC18的SmaI位点,并测定了147个残基的cDNA衍生氨基酸序列,其中分别有69个和76个残基通过内部肽段的化学氨基酸测序得以鉴定。因此,这种使用共有引物的PCR方法应广泛适用于扩增硬骨鱼类的血红蛋白β链。