Cystatin B homolog from rock bream Oplegnathus fasciatus: Genomic characterization, transcriptional profiling and protease-inhibitory activity of recombinant protein

被引:17
作者
Premachandra, H. K. A. [1 ]
Whang, Ilson [1 ]
Lee, Young-Deuk [1 ]
Lee, Sukkyoung [1 ]
De Zoysa, Mahanama [3 ]
Oh, Myung-Joo [4 ]
Jung, Sung-Ju [4 ]
Lim, Bong-Soo [6 ]
Noh, Jae Koo [5 ]
Park, Hae-Chul [2 ]
Lee, Jehee [1 ,6 ]
机构
[1] Jeju Natl Univ, Sch Marine Biomed Sci, Dept Marine Life Sci, Cheju 690756, Jeju Special Se, South Korea
[2] Korea Univ, Grad Sch Med, Ansan 425707, Gyeonggido, South Korea
[3] Chungnam Natl Univ, Coll Vet Med, Taejon 305764, South Korea
[4] Chonnam Natl Univ, Dept Aqualife Med, Chungnam 550749, South Korea
[5] Natl Fisheries Res & Dev Inst, Genet & Breeding Res Ctr, Geoje 656842, South Korea
[6] Jeju Natl Univ, Marine & Environm Inst, Cheju 690814, Jeju Special Se, South Korea
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY | 2012年 / 163卷 / 01期
关键词
Rock bream; Cystatin B; Papain inhibition; Bacterial challenge; Transcriptional analysis; PROGRESSIVE MYOCLONUS EPILEPSY; CYSTEINE PROTEASES; EGG-WHITE; GENE; PURIFICATION; ROLES; CELLS; SKIN;
D O I
10.1016/j.cbpb.2012.05.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cysteine proteases are present in all living organisms and, in animals, function in a vast array of physiological and pathological processes. Cysteine protease inhibitors act upon the cysteine proteases to regulate their activity. The cystatin superfamily of cysteine protease inhibitors has members represented in all living organisms studied to date. Here, we report the identification of a new member of the family 1 cystatin in Oplegnathus fasciatus rock bream (denoted as RbCyt B) and the characterization at the molecular level. The complete genomic sequence of RbCyt B consists of three exons and a promoter region. The open reading frame (ORF) encodes for a 100 amino acids length polypeptide with a single cystatin-like domain and a cysteine protease inhibitor signature motif. The conserved N-terminal glycine, glutamine-valine-glycine motif, QxVxG, and a variant of the proline-tryptophan. PW, motif were identified. RbCyt B showed closest phylogenetic distance to Dicentrarchus labrax cystatin B, and shared up to 73% amino add identity and 90% amino acid similarity with known cystatin B genes. RbCyt B mRNA expression was detected in nine different tissues and was highly expressed in liver, spleen, gill, brain, intestine, kidney, head kidney, and blood, as compared with muscle. In vivo immune stimulation with Edwardsiella tarda bacteria caused significant up-regulation of RbCyt B mRNA in head kidney and spleen at 24 h post-infection (P<0.05). Recombinant RbCyt B was expressed in Escherichia coli, and the purified protein demonstrated 82% papain inhibitory activity at 500 x 10(-3) mu g mu L-1 in a concentration-dependent manner. These results suggest that RbCyt B is a member of family 1 cystatin with high homology to cystatin B, and is a biologically active protein possessing papain inhibitory activity and potentially involved in immune responses against invading Gram-negative bacteria in rock bream. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:138 / 146
页数:9
相关论文
共 40 条
[1]   Cystatins [J].
Abrahamson, M ;
Alvarez-Fernandez, M ;
Nathanson, CM .
PROTEASES AND THE REGULATION OF BIOLOGICAL PROCESSES, 2003, 70 :179-199
[2]  
Agarwala KL, 1996, J BIOCHEM, V119, P85
[3]   CYSTATIN, A PROTEIN INHIBITOR OF CYSTEINE PROTEINASES - IMPROVED PURIFICATION FROM EGG-WHITE, CHARACTERIZATION, AND DETECTION IN CHICKEN SERUM [J].
ANASTASI, A ;
BROWN, MA ;
KEMBHAVI, AA ;
NICKLIN, MJH ;
SAYERS, CA ;
SUNTER, DC ;
BARRETT, AJ .
BIOCHEMICAL JOURNAL, 1983, 211 (01) :129-138
[4]  
[Anonymous], 2006, ENCYCL RESPIR MED FO, DOI DOI 10.1016/B0-12-370879-6/00329-X
[5]   THE CYSTATINS - A NEW CLASS OF PEPTIDASE INHIBITORS [J].
BARRETT, AJ .
TRENDS IN BIOCHEMICAL SCIENCES, 1987, 12 (05) :193-196
[6]   NOMENCLATURE AND CLASSIFICATION OF THE PROTEINS HOMOLOGOUS WITH THE CYSTEINE-PROTEINASE INHIBITOR CHICKEN CYSTATIN [J].
BARRETT, AJ ;
FRITZ, H ;
GRUBB, A ;
ISEMURA, S ;
JARVINEN, M ;
KATUNUMA, N ;
MACHLEIDT, W ;
MULLERESTERL, W ;
SASAKI, M ;
TURK, V .
BIOCHEMICAL JOURNAL, 1986, 236 (01) :312-312
[7]   THE 2.0 A X-RAY CRYSTAL-STRUCTURE OF CHICKEN EGG-WHITE CYSTATIN AND ITS POSSIBLE MODE OF INTERACTION WITH CYSTEINE PROTEINASES [J].
BODE, W ;
ENGH, R ;
MUSIL, D ;
THIELE, U ;
HUBER, R ;
KARSHIKOV, A ;
BRZIN, J ;
KOS, J ;
TURK, V .
EMBO JOURNAL, 1988, 7 (08) :2593-2599
[8]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[9]  
CALKINS CC, 1995, BIOL CHEM H-S, V376, P71
[10]   Emerging roles for cysteine proteases in human biology [J].
Chapman, HA ;
Riese, RJ ;
Shi, GP .
ANNUAL REVIEW OF PHYSIOLOGY, 1997, 59 :63-88