浙江农业学报 ›› 2016, Vol. 28 ›› Issue (11): 1862-1866.DOI: 10.3969/j.issn.1004-1524.2016.11.09

• 动物科学 • 上一篇    下一篇

南极鱼Ⅲ型抗冻基因真核表达质粒的构建及其细胞表达

杨敏, 黄巧, 陈良标*   

  1. 上海海洋大学 水产与生命学院 水产种质资源发掘与利用省部共建教育部重点实验室,上海201306
  • 收稿日期:2016-02-29 出版日期:2016-11-15 发布日期:2016-11-16
  • 通讯作者: 陈良标,E-mail:lbchen@shou.edu.cn
  • 作者简介:杨敏(1989—),女,山东临沂人,硕士研究生,主要从事南极鱼抗冻蛋白机制研究。E-mail:ymcassie@foxmail.com
  • 基金资助:
    国家自然科学基金 (31572611)

Construction of type Ⅲ antifreeze protein eukaryotic expression plasmid and expression in zebrafish cell line

YANG Min, HUANG Qiao, CHEN Liang-biao*   

  1. College of Fisheries and Life Sciences,Key Laboratory of Aquaculture Resources and Utilization,Ministry of Education,Shanghai Ocean University,Shanghai 201306,China
  • Received:2016-02-29 Online:2016-11-15 Published:2016-11-16

摘要: 为了探讨多聚AFPⅢ的作用机制,从南极鱼Lycodichthys dearborni的多聚三型抗冻蛋白基因LD12 cDNA中克隆得到AFPⅢ的四聚体,命名为LD4,并构建真核表达质粒Tol2-actin-LD4-2A-EGFP。将表达质粒转染到斑马鱼细胞系ZF4中,发现LD4可以在ZF4中大量表达并且能够减少斑马鱼细胞在低温胁迫下的死亡率。通过对不同处理温度(28、18、10 ℃)下的WT、EGFP和LD4细胞进行转录组测序分析,找出26个表达差异转录因子,其中I3MB13、ZNF687b等表达上调,JUNCremb等表达下调,并且通过荧光定量PCR的验证。通过KEGG pathway分析发现,这些差异性基因主要参与细胞凋亡、细胞周期、增殖等调节通路。采用 Annexin V-PE/7-AAD双染色法对3种不同温度下的WT、EGFP和LD4细胞进行细胞凋亡检测,结果显示,LD4在低温下与对照组相比凋亡率没有显著差异,说明LD4可能是通过其他通路而不是通过抑制细胞凋亡来抵御低温胁迫,这为LD4作用机制的进一步研究提供了理论基础。

关键词: 多聚Ⅲ, 型抗冻蛋白, 斑马鱼细胞系, 转录组测序, 细胞凋亡

Abstract: To elucidate the AFPⅢ multimerization molecular mechanisms on cold tolerance, we cloned tetramer (LD4) of the type Ⅲ AFP from a multimer type Ⅲ antifreeze protein gene LD12 cDNA which was characterized from the Antarctic eelpout (Lycodichthys dearborni). The eukaryotic expression plasmid Tol2-actin-LD4-2A-EGFP was constructed and transfected into zebrafish cells (ZF4). It was found that LD4 was abundantly expressed in ZF4 cell line and reduced mortality of zebrafish cells under low temperature stress. Transcriptome sequencing and gene expression analysis were carried out at WT, EGFP and LD4 cells under different processing temperatures (28 ℃, 18 ℃ for 2 days, 18 ℃ for 2 days and 10 ℃ for 2 days), the results indicated 26 differentially expressed transcription factors, in which I3MB13 and ZNF687b were up-regulated and JUN and Cremb were down-regulated. The expression patterns of 26 selected genes were verified by qRT-PCR (quantitative real-time PCR). Based on the KEGG pathway analysis, the transcription factors were suggested to be involved in apoptosis, cell cycle and proliferation regulation. So, AnnexinV-PE/7-AAD double staining was used to detect the effect of LD4 on apoptosis. Unfortunately, apoptosis rate was not significantly decreased in LD4 cells compared with the control group (EGFP and WT). That is, LD4 might be involved in another channel rather than inhibiting apoptosis to resist low temperature, which provides a certain theoretical basis for further research on the mechanism of LD4.

Key words: multimer type Ⅲ, antifreeze protein, zebrafish cell line, transcriptome sequencing, cell apoptosis

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