Characterization and expression of AmphiCL encoding cathepsin L proteinase from amphioxus Branchiostoma belcheri tsingtauense

被引:19
作者
Wang, YJ
Zhang, SC
Liu, ZH
Li, HY
Wang, L
机构
[1] Ocean Univ China, Dept Marine Biol, Qingdao 266003, Peoples R China
[2] Nantong Agr Coll, Dept Fishery, Nantong 226007, Peoples R China
关键词
amphioxus; Branchiostoma; cathepsin L; spirulina; lipopolysaccharide; expression;
D O I
10.1007/s10126-004-4084-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
An amphioxus complementary DNA, AmphiCL, encoding cathepsin L proteinase was isolated from the gut cDNA library of Branchiostoma belcheri tsingtauense. It is 1480 bp long, and its longest open reading frame codes for a precursor protein, which consists of 327 amino acid residues including a signal peptide (preregion), a propeptide, and a mature proteinase. Northern blot showed that AmphiCL was expressed in the gill, testis, hepatic cecum, and hind-gut with a molecular size of about 1480 bp. AmphiCL was also expressed at low level in the muscle, notochord, and ovary as revealed by the more sensitive reverse transcriptase polymerase chain reaction techniques. Semiquantitative RT-PCR also showed that although AmphiCL expression in the gut was significantly downregulated by feeding Arthrospira platensis powder, a protein-rich food, its expression in the same tissue was upregulated by exposure to lipopolysaccharide, an integral component of the outer membrane of gram-negative bacteria. This suggests that although the involvement of AmphiCL in food digestion remains to be confirmed, AmphiCL may play a role in inflammatory reaction in amphioxus.
引用
收藏
页码:279 / 286
页数:8
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