Lysozyme is one of the important effectors involved in a variety of immune responses in innate immune system of organisms. A conservative i-type lysozyme cDNA sequence was cloned from Crassostrea hongkongensis and its expression in different tissues was studied. The effects of different temperatures on the gene expression in the experiment were also studied. The cloned conservative i-type lysozyme cDNA sequence contained 634 bp with a 420 bp open reading frame and the cDNA encoded 139 amino acids. A new conservative amino acid sequence, HNGGPRGC, and the typical features were found in the protein sequence of the i-type lysozyme from C. hongkongensis, including specific amino acid residue sequence, CL(E/L/R/H)C(I/M)C, a partial highly conservative sequence, SCG(P/Y)FQI, and the enzyme active site (Glu34, Asp45, Ser48, Trp61). Real-time quantitative PCR was used to assess the expression pattern of the i-type lysozyme gene in the digestive gland, muscle, gill, mantle, and labial palps of C. hongkongensis. The highest expression level of the i-type lysozyme gene was found in the digestive gland, the second in the gill, and the lowest in the muscle. A temperature stress experiment was conducted to study the expression control of the i-type lysozyme gene. The expression level was stable when the water temperature was at 20?25℃. A tendency to decrease expression was found at 6 or 13℃. The expression was maintained at a relatively high level throughout of 96 h at 27℃. The expression level was found the highest at 12 h and sharply declined after 48 h at 34℃. It is concluded that the expression of the i-type lysozyme gene was affected by temperature, which could be used to control the immune function of C. hongkongensis in response to external environment
XU You-qing, WU Wei-jun, DING Zhao-kun, PAN Zhi-zhong, HE Wei, WU Tie-jun, CHEN Xiu-li, LI Yong-mei, JIANG Wei-ming
. Analysis of i-type lysozyme gene from Crassostrea hongkongensis and the effect of temperature on the gene expression[J]. Journal of Tropical Oceanography, 2012
, 31(6)
: 69
-75
.
DOI: 10.11978/j.issn.1009-5470.2012.06.011
[1] BACHALI S, JAGER M, HASSANIN A, et al. Phylogenetic analysis of invertebrate lysozymes and the evolution of lysozyme function [J]. J Mol Evol , 2002 , 54(5) : 652-664.
[2] ZHAO J, QIU L, NING X X, et al. Cloning and characterization of an invertebrate type lysozyme from Venerupis philippinarum [J]. Comp Biochem Physiol B, 2010, 156(1) : 56-60.
[3] KYOMUHENDO P, MYRNES B, NILSEN I W. A cold-active salmon goose-type lysozyme with high heat tolerance [J]. Cell Mol Life Sci, 2007, 64(21) : 2841-2847.
[4] KIM M, AHN I Y, CHEON J, et al. Molecular cloning and thermal stress-induced expression of a pi-class glutathione S-transferase (GST) in the Antarctic bivalve Laternula elliptica [J]. Comp Biochem Physiol A, 2009, 152(2): 207-213.
[5] MONARI M, MATOZZO V, FOSCHI J, et al. Effects of high temperatures on functional responses of haemocytes in the clam Chamelea gallina [J]. Fish Shellfish Immun, 2007, 22(1-2) : 98-114.
[6] YU J H, SONG J H, CHOI M C, et al. Effects of water temperature change on immune function in surf clams, Mactra veneriformis (Bivalvia: Mactridae) [J]. J Invertebr Pathol, 2009, 102(1) : 30-35.
[7] DE ZOYSA M, WHANG I, LEE Y, et al. Transcriptional analysis of antioxidant and immune defense genes in disk abalone (Haliotis discus discus) during thermal, low-salinity and hypoxic stress [J]. Comp Biochem Phys B, 2009, 154(4) : 387-395.
[8] 许友卿, 吴卫君, 蒋伟明, 等. 温度对贝类免疫系统的影响及其机理研究进展[J]. 水产科学, 2012, 31(3): 176?180.
[9] 林群, 梁旭方, 王琳, 等. 近江牡蛎等7种养殖鱼虾贝类参照基因β-肌动蛋白cDNA序列的克隆与比较分析[J]. 生态毒理学报, 2008, 3(3) : 256-261.
[10] LIVAK K J, SCHMITTGEN T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2?ΔΔCT method [J]. Methods, 2001, 25(4) : 402-408.
[11] ITOH N, TAKAHASHI K G. A novel peptidoglycan recognition protein containing a goose-type lysozyme domain from the Pacific oyster, Crassostrea gigas [J]. Mol Immunol, 2009, 46(8?9) : 1768-1774.
[12] JOSKOV? R, ?ILEROV? M, PROCH?ZKOV? P, et al.
Identification and cloning of an invertebrate-type lysozyme from Eisenia andrei [J]. Develop Com Immunol, 2009, 33(8) : 932-938.
[13] ITOH N, OKADA Y, TAKAHASHI K G, et al. Presence and characterization of multiple mantle lysozymes in the Pacific oyster, Crassostrea gigas [J]. Fish Shellfish Immun, 2010, 29(1) : 126-135.
[14] SAITOU N, NEI M. The neighbor-joining method: A new method for reconstructing phylogenetic trees [J]. Mol Biol Evol, 1987, 4(4) : 406-425.
[15] CONG L, YANG X, WANG X, et al. Characterization of an i-type lysozyme gene from the sea cucumber Stichopus japonicus, and enzymatic and nonenzymatic antimicrobial activities of its recombinant protein [J]. J Biosci Bioeng, 2009, 107(6) : 583-588.
[16] KAWAMURA S, OHNO K, OHKUMA M, et al. Experimental verification of the crucial roles of Glu73 in the catalytic activity and structural stability of goose type lysozyme [J]. J Biochem, 2006, 140(1) : 75-85.
[17] PIPE R K. Hydrolytic enzymes associates with the granular hemocytes of the marine mussel Mytilud edulis [J]. Histochem J, 1992, 22(11) : 529-603.
[18] XUE Q G, ITOH N, SCHEY K L, et al. A new lysozyme from the eastern oyster (Crassostrea virginica) indicates adaptive evolution of i-type lysozymes [J]. Cell Mol Life Sci, 2007, 64(1) : 82-95.
[19] FEARMAN J, MOLTSCHANIWSKYJ N A. Warmer temperatures reduce rates of gametogenesis in temperate mussels, Mytilus galloprovincialis[J]. Aquaculture, 2010, 305(1?4) : 20?25.
[20] VERLECAR X N, JENA K B, CHAINY G B. Biochemical markers of oxidative stress in Perna viridis exposed to mercury and temperature [J]. Chem Biol Interact, 2007, 167(3) : 219-226.
[21] PARK H, AHN I Y, KIM H, et al. Analysis of ESTs and expression of two peroxiredoxins in the thermally stressed Antarctic bivalve Laternula elliptica [J]. Fish Shellfish Immun, 2008, 25(5) : 550-559.
[22] WANG F Y, YANG H S, GAO F, et al. Effects of acute temperature or salinity stress on the immune response in sea cucumber, Apostichopus japonicus [J]. Comp Biochem Physiol A, 2008, 151(4) : 491-498.