Cho J J, Sung B K, Lee J H, Chung J K, Choi T J, Kim Y T
Department of Microbiology, Pukyong National University, Pusan, Korea.
Mol Cells. 2001 Apr 30;11(2):226-30.
The cDNA for an immune response gene encoding the low molecular weight polypeptide (LMP7) was cloned and sequenced from a flounder (Paralichthys olivaceus) leukocyte cDNA library. The cDNA clone was 1,160 bp, and composed of an open reading frame of 822 bp that corresponded to a protein of 273 amino acid residues with a calculated mass of 30.5 kDa. The ScanProsite search indicated that the deduced amino acid sequence from the flounder LMP7 contains a proteasome beta-type subunit signature, which is well conserved during evolution. The sequence shares a high degree of identity with other LMP7 sequences varying from a 66% identity with zebra fish (Danio renio) to a 57% identity with the African clawed frog (Xenopus laevis), which was confirmed from a phylogenetic tree. A reverse transcription-polymerase chain reaction (RT-PCR) was used to determine tissue specificity, and the expression of LMP7 was detected from the liver, kidney, leukocyte, and spleen of the flounder.
从牙鲆(Paralichthys olivaceus)白细胞cDNA文库中克隆并测序了编码低分子量多肽(LMP7)的免疫反应基因的cDNA。该cDNA克隆为1160 bp,由一个822 bp的开放阅读框组成,该开放阅读框对应于一个含有273个氨基酸残基的蛋白质,计算分子量为30.5 kDa。ScanProsite搜索表明,牙鲆LMP7推导的氨基酸序列包含一个蛋白酶体β型亚基特征,该特征在进化过程中高度保守。该序列与其他LMP7序列具有高度同源性,与斑马鱼(Danio renio)的同源性为66%,与非洲爪蟾(Xenopus laevis)的同源性为57%,这一点从系统发育树中得到了证实。采用逆转录聚合酶链反应(RT-PCR)来确定组织特异性,在牙鲆的肝脏、肾脏、白细胞和脾脏中检测到了LMP7的表达。