Identification and characterization of matrix metalloproteinase-13 sequence structure and expression during embryogenesis and infection in channel catfish (Ictalurus punctatus)

被引:13
作者
Jiang, Yanliang [1 ,3 ]
Abernathy, Jason W. [1 ]
Peatman, Eric [1 ]
Liu, Hong [1 ,2 ]
Wang, Shaolin [1 ]
Xu, De-Hai [4 ]
Kucuktas, Huseyin [1 ]
Klesius, Phillip [4 ]
Liu, Zhanjiang [1 ]
机构
[1] Auburn Univ, Dept Fisheries & Allied Aquacultures, Program Cell & Mol Biosci, Fish Mol Genet & Biotechnol Lab,Aquat Genom Unit, Auburn, AL 36849 USA
[2] Huazhong Agr Univ, Coll Fisheries, Wuhan 430070, Peoples R China
[3] Hunan Normal Univ, Coll Life Sci, State Educ Minist China, Key Lab Prot Chem & Dev Biol, Changsha 410081, Hunan, Peoples R China
[4] ARS, Aquat Anim Hlth Res Lab, USDA, Auburn, AL 36832 USA
关键词
Extracellular matrix; Metalloproteinase; Catfish; Matrix metalloproteinase-13; MMP-13; Collagenase-3; Embryogenesis; Edwardsiella ictaluri; COLLAGENASE-3; MMP-13; GENE-EXPRESSION; ANGIOGENESIS; CLONING; ACTIVATION; MATRILYSIN; MODULATORS; APOPTOSIS; IMMUNITY; PEPTIDE;
D O I
10.1016/j.dci.2010.01.001
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Matrix metalloproteinase-13 (MMP-13), referred to as collagenase-3, is a proteolytic enzyme that plays a key role in degradation and remodelling of host extracellular matrix proteins. The objective of this study was to characterize the MMP-13 gene in channel catfish, and to determine its pattern of expression in various healthy tissues and during embryogenesis. Since MMP-13 has been shown to have importance in tissue remodelling and some pathological processes, we further studied its involvement in the defense responses of catfish after bacterial infection. The channel catfish MMP-13 cDNA contains an open reading frame of 1416 bp encoding 471 amino acids. Using RT-PCR analysis, MMP-13 was widely expressed in various health tissues. Using quantitative real-time PCR analysis, expression of MMP-13 gene was up-regulated by bacterial infection. During normal embryological development, MMP-13 expression was slightly increased in the first day post-fertilization and sharply up-regulated from 1-day post-fertilization through hatching. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:590 / 597
页数:8
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