何鹏, 江世贵, 李运东, 杨其彬, 姜松, 杨丽诗, 黄建华, 周发林. 斑节对虾GLUT1基因cDNA的克隆与表达分析[J]. 南方水产科学, 2019, 15(2): 72-82. DOI: 10.12131/20180264
引用本文: 何鹏, 江世贵, 李运东, 杨其彬, 姜松, 杨丽诗, 黄建华, 周发林. 斑节对虾GLUT1基因cDNA的克隆与表达分析[J]. 南方水产科学, 2019, 15(2): 72-82. DOI: 10.12131/20180264
HE Peng, JIANG Shigui, LI Yundong, YANG Qibin, JIANG Song, YANG Lishi, HUANG Jianhua, ZHOU Falin. Molecular cloning and expression pattern analysis of GLUT1 in black tiger shrimp (Penaeus monodon)[J]. South China Fisheries Science, 2019, 15(2): 72-82. DOI: 10.12131/20180264
Citation: HE Peng, JIANG Shigui, LI Yundong, YANG Qibin, JIANG Song, YANG Lishi, HUANG Jianhua, ZHOU Falin. Molecular cloning and expression pattern analysis of GLUT1 in black tiger shrimp (Penaeus monodon)[J]. South China Fisheries Science, 2019, 15(2): 72-82. DOI: 10.12131/20180264

斑节对虾GLUT1基因cDNA的克隆与表达分析

Molecular cloning and expression pattern analysis of GLUT1 in black tiger shrimp (Penaeus monodon)

  • 摘要: 该研究利用RACE技术克隆获得了斑节对虾(Penaeus monodon) GLUT1 (glucose transporter type 1)的cDNA全长序列;采用实时荧光定量的方法研究了PmGLUT1在斑节对虾幼体发育过程中、各个组织中及低盐胁迫下的差异表达情况。该基因cDNA开放阅读框(ORF)全长1 476 bp,可编码491个氨基酸。检测PmGLUT1基因从受精卵至仔虾期发育过程的表达情况,结果显示,PmGLUT1在幼体发育各期的表达量有所波动,但总体呈现上升趋势。组织表达分析发现,PmGLUT1在鳃组织中的表达量最高,肝胰腺次之,在卵巢中的表达量最低。急性低盐胁迫后,PmGLUT1在肝胰腺中的表达水平显著高于对照组(P<0.05),但在鳃中的表达水平显著低于对照组(P<0.05)。研究结果表明,PmGLUT1可能在斑节对虾幼体发育及机体应对低盐胁迫过程中具有重要作用,这为进一步研究葡萄糖转运蛋白基因在斑节对虾幼体发育调控和耐低盐胁迫应答中的分子机制提供了理论依据。

     

    Abstract: We obtained the full-length cDNA sequence of GLUT1 from Penaeus monodon by rapid amplification of cDNA ends (RACE), and investigated the expression of GLUT1 at different larval developmental stages, in different tissues, and under low salinity stress by quantitative real-time PCR. The total cDNA sequence of PmGLUT1 open reading frame (ORF) was 1 476 bp, encoding 491 amino acids. From zygote to postlarva stages, the expression of PmGLUT1 fluctuated but showed an increasing trend. The PmGLUT1 was expressed in all tested tissues with the highest expression in gill tissue, followed by hepatopancreas, and the lowest expression was in ovary. After acute low salinity stress, the expression level of PmGLUT1 mRNA in hepatopancreas was significantly higher than that in the control group, while the expression level in gill was significantly lower than that in the control group (P<0.05). The results show that PmGLUT1 might play an important role at different larval developmental stages and under low salinity stress, which provides a theoretical basis for studying the molecular mechanism of PmGLUT1 in larval development and salinity adaptation of P. monodon.

     

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