低盐协迫对大黄鱼gh、igf-1、hsp90和pparβ基因表达变化的影响
PDF下载 (509)李明云,苗 亮,张 浩,王 涛,胡 谋,刘连亮,陈 炯.低盐协迫对大黄鱼gh、igf-1、hsp90和pparβ基因表达变化的影响[J].宁波大学学报(理工版),2015,28(04):1-6.DOI:
LI Ming-yun,MIAO Liang,ZHANG Hao,WANG Tao,HU Mou,LIU Lian-liang,CHEN Jiong.Effects of Low Salt Stress on Expression of gh, igf-1, hsp90 and pparβ Gene in Pseudosciaena crocea[J].Journal of Ningbo University(Natural Science & Engineering Edition),2015,28(04):1-6.DOI:
| Title: | Effects of Low Salt Stress on Expression of gh, igf-1, hsp90 and pparβ Gene in Pseudosciaena crocea |
| 作者: | 李明云, 苗 亮, 张 浩, 王 涛, 胡 谋, 刘连亮, 陈 炯 |
| Author(s): | LI Ming-yun, MIAO Liang, ZHANG Hao, WANG Tao, HU Mou, LIU Lian-liang, CHEN Jiong |
| 关键词: | 大黄鱼; 低盐协迫; 基因表达 |
| Keywords: | Pseudosciaena crocea; low salt stress; gene expression |
| 分类号: | Q785; S965 |
| 文献标识码: | A |
| 摘要: | 为了解大黄鱼在低盐胁迫下相关基因的表达变化, 采用实时荧光定量PCR技术检测了正常盐度25和降低盐度后3个节点(盐度8、盐度3和盐度1.5)鳃、肾、肝、心、脾、肌肉、脑和肠8组织中gh、igf-1、hsp90和pparβ基因mRNA的表达量变化. 研究表明: 低盐胁迫可显著影响大黄鱼中这4个基因的表达量. gh基因在盐度1.5节点除心脏外各组织中表达量均显著高于正常盐度(P<0.05), 其中脾的升幅最大; 盐度8和盐度3节点, 均是肝中gh表达量升高幅度最大, 分别为正常盐度的5.21和3.11倍. igf-1基因在盐度1.5节点除肌肉和脑外表达量均显著上调(P<0.05), 鳃中表达量最高, 为正常盐度的5.28倍, 其次为肾(3.05倍)和肝(2.20倍). hsp90基因在盐度8节点时心和肝中的表达量显著升高(P<0.05); 盐度1.5节点心中表达量显著降低(P<0.05), 而在其他组织中的表达量均显著升高(P<0.05). 在盐度8节点pparβ基因在心、肌肉、肝和脾中的表达量均显著高于其他3个盐度点(P<0.05); 盐度1.5节点鳃、脑、肾和肠中的表达量均显著升高(P<0.05), 分别为正常盐度时的9.04、7.36、3.39和3.19倍. 上述结果可为深入研究大黄鱼应对低渗环境的分子调控机制提供基础资料. |
| Abstract: | In order to investigate the gene expression changes responding to low salt stress, we detected the expression level of gh, igf-1, hsp90 and pparβ gene in different tissues of large yellow crocea (Pseudosciaena crocea) by real-time quantitative PCR. The samples were collected at normal salinity (25) and three low salt nodes (8, 3 and 1.5). The result shows that the expression of these four genes is significantly altered under low salt stress. At salinity 1.5 node, the expression level of gh rises significantly (P<0.05) in all tissues except heart, and the most significant increase of amplitude is observed in spleen. Among all the sampled tissues, liver shows the most notable increase of amplitude of gh expression both at salinity 8 and 3 nodes, and the expression level is 5.21 and 3.11 times the normal salinity, respectively. The expression of igf-1 mRNA goes up significantly (P<0.05) in all tissues at salinity 1.5 node, except muscle and brain. At salinity 1.5 node, the expression level of igf-1 is found in gill, which turns out to be 5.28 fold to normal salinity, and followed by kidney (3.05 fold) and liver (2.20 fold). The expression level of hsp90 rises significantly (P<0.05) in heart and liver at salinity 8 node. At salinity 1.5 node, the expression of hsp90 is declined significantly (P<0.05) in heart, while all the other tissues climbs significantly (P<0.05). At salinity 8 node, the expression level of pparβ in heart, muscle, liver and spleen are all significantly higher than the other three salinities (P<0.05). At salinity 1.5 node, the expression of pparβ in gill, brain, kidney and gut all raised significantly (P<0.05), and are 9.04, 7.36, 3.39 and 3.19 fold to normal salinity. These results are expected to provide fundamental data for further research on the molecular mechanism of response to low salt stress in Pseudosciaena crocea. |
| 参考文献 /References: | [1] 李兵, 王帅, 张伟. 室内低盐度饲养大黄鱼的初步研究[J]. 上海海洋大学学报, 2012, 21(4):524-529. [2] 汤瑜瑛, 张志良. 大黄鱼低盐度养殖[J]. 科学养鱼, 2003(8):25. [3] 邓利, 张为民, 林浩然. 盐度变化对黑鲷生长激素及其受体的影响[J]. 热带海洋学报, 2003, 22(6):9-14. [4] Kelly S P, Chow N K, Woo N Y S. Effects of prolactin and growth hormone on strategies of hypoosmotic adapration in a marine teleost, Sparus sarha[J]. Gen Comp Endocrinol, 1999, 113(1):9-22. [5] 张殿昌. 鱼类胰岛素样生长因子研究进展[J]. 上海水产大学学报, 2005, 14(1):66-71. [6] 刘红云, 童富淡. 鱼类IGF-I生理功能及其表达调控的研究进展[J]. 水产科学, 2004, 23(5):37-40. [7] 董云伟, 董双林, 纪婷婷. 水生动物热休克蛋白研究进展[J]. 中国海洋大学学报, 2008, 38(1):39-44. [8] Fu D, Chen J, Zhang Y, et al. Cloning and expression of a heat shock protein (HSP) 90 gene in the haemocytes of Crassostrea hongkongensis under osmotic stress and bacterial challenge[J]. Fish & Shellfish Immunology, 2011(31):118-125. [9] Pan F, Zarate J M, Tremblay G C, et al. Cloning and characterization of salmon HSP90 cDNA up regulation by thermal and hyperosmotic stress[J]. Journal of Experimental Zoology, 2000, 287(3):199-212. [10] Yang W K, Hseu J R, Tang C H, et al. Na+/K+-ATPase expression in gills of the euryhaline sailfin molly, Poecilia latipinna, is altered in response to salinity challenge[J]. Journal of Experimental Marine Biology and Ecology, 2009, 375(1/2):41-50. [11] Hummasti S, Tontono Z P. The peroxisome proliferator- activated receptor N-terminal domain controls isotype- selective gene expression and adipogenesis[J]. Molecular Endocrinology, 2006, 20(6):1261-1275. [12] Bhatia V, Viswanatan P. Insulin resistance and PPAR insulin sensitizers[J]. Current Opinion in Investigational Drugs, 2006, 7(10):891-897. [13] 方文良, 鞠志花, 黄金明, 等. 过氧化物酶体增殖剂激活受体的研究进展[J]. 家畜生态学报, 2011, 32(3):1-5. [14] Richter H, Albrektsen T, Billestrup B. The role of signal transducer and activator of transcription 5 in inhibitory effects of GH on adipocyte differentiation[J]. Journal of Molecular Endocrinology, 2003, 30:139-150. [15] Jung H S, Lee Y J, Kim Y H, et al. Peroxisome proliferator-activated receptor gamma/signal transducers and activators of transcription 5A pathway plays a key factor in adipogenesis of human bone marrow-derived stromal cells and 3T3-L1 preadipocytes[J]. Stem Cells and Development, 2011, 21:465-475. [16] Livak K J, Schmittgen T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method[J]. Methods, 2001, 25(4): 402-408. [17] 张殿昌, 江世贵. 黄鳍鲷生长激素cDNA的分子克隆和序列分析[J]. 湛江海洋大学学报, 2002, 22(4):62-65. [18] Madsen S S, Bern H A. Antagonism of prolactin and growth hormone: Impact on seawater adaptation in two salmonids, Salmon trutta and Oncorhynchus mykiss[J]. Zool Sci, 1992, 4:775-784. [19] 王涛, 苗亮, 李明云, 等. 突降盐度胁迫对大黄鱼(Pseudosciaena crocea)血清生理生化及鳃丝Na+/K+- ATP酶活性的影响[J]. 海洋与湖沼, 2013, 44(2):421- 426. [20] McCormick S D, Sakamoto T, Hasegawa S, et al. Osmoregulatory action of insulin-like growth factor-I in rainbow trout (Oncorhynchus mykiss)[J]. Endocrinol, 1991, 130:87-92. [21] Madsen S S, Bern H A. In-vitro effects of insulin-like growth factor-I on gill Na+, K+-ATPase in coho salmon, Oncorhynchus kisutch[J]. Journal of Endocrinology, 1993, 138:23-30. [22] Sakamato T, Hirano T. Expression of insulin-like growth factor I gene I osmoregulatory argans during seawater adaptation of the Salmonid fish: Possible mode of osmoregulatory action of growth hormone[J]. Proc Natul Acad Sci USA, 1993, 90:1912-1916. [23] Dubeau S F, Pan F, Tremblay G C, et al. Thermal shock of salmon in vivo induces the heat shock protein (Hsp70) and confers protection against osmotic shock[J]. Aquaculture, 1998, 168:311-323. [24] 覃烨, 许强华. 盐度胁迫下三疣梭子蟹热休克蛋白HSP90a的原核表达[J]. 水产学报, 2012, 36(5):681-685. [25] 于姗姗, 王青林, 孟宪亮, 等. 盐度骤变对仿刺参HSP70及HSP90基因表达的影响[J]. 中国海洋大学学报, 2012, 42(9):22-27. [26] Tomanek L, Somero G N. Time course and magitude of synthesis of heat shock proteins in congeneric marine snails (genus Tegula) from different tidal heights[J]. Physiol Biochem Zool, 2000, 73:249-256. [27] Jugeaubry C E, Cottlicher M, Schmidt A, et al. Peroxisome proliferator activated receptor-mediates crosstalk with thyroid receptor by competition for retinoid X receptor[J]. The Journal of Biological Chemistry, 1995, 270(30):18117-18120. [28] 王艳, 胡先成, 罗颖. 盐度对鲈鱼稚鱼的生长及脂肪酸组成的影响[J]. 重庆师范大学学报: 自然科学版, 2007, 24(2):1-5. |
| 备注/Memo: | 收稿日期: 2015-03-17. 宁波大学学报(理工版)网址: http://journallg.nbu.edu.cn/ 基金项目: 国家高技术研究发展计划(2012AA10A403-4); 浙江省重大科技专项优先主题(2009C12077, 2012C12907-8); 宁波市重大项目(2008C3005). 第一作者: 李明云(1942-), 男, 浙江舟山人, 教授, 主要研究方向: 鱼类遗传育种与种质保护. E-mail: limingyun@nbu.edu.cn 宁波大学学报(理工版)网址:http://journallg.nbu.edu.cn/ |