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三角帆蚌热休克蛋白70基因克隆及其表达分析

吴圣楠 隗黎丽 李海军 付建平 刘毅

水生生物学报2017,Vol.41Issue(1):50-55,6.
水生生物学报2017,Vol.41Issue(1):50-55,6.DOI:10.7541/2017.7

三角帆蚌热休克蛋白70基因克隆及其表达分析

CLONING AND EXPRESSION ANALYSIS OF HEAT SHOCK PROTEIN 70 GENE FROM HYRIOPSISCUMINGII

吴圣楠 1隗黎丽 2李海军 1付建平 1刘毅1

作者信息

  • 1. 江西师范大学生命科学学院,南昌330022
  • 2. 江西农业大学动物科学学院,南昌330045
  • 折叠

摘要

Abstract

In the present study, the cDNA sequence of Hyriopsis cumingii HSP70 (HcHSP70) was cloned by 3′rapid amplification of cDNA ends methods (3′-RACE) based on a long chain sequence of HcHSP70 and it was determined by high flux sequencing for transcriptome of H. cumingii blood cells, and its expression in the different tissues was detec-ted with quantitative real time polymerase chain reaction (qRT-PCR). Results showed that the full-length of HcHSP70 cDNA was 2298 bp long including a 1974 bp open reading frame (ORF) encoding a polypeptide of 657 amino acids that estimated molecular mass of 71.6 Ku and an isoelectric point of 5.67. Sequence comparison indicated that HcHSP70 shares the highest identity (91%) with HSP70 of Tegillarca granosa and Crassostrea gigas. HcHSP70 mRNA expressed in all 5 detected tissues (hepatopancreas, gonad, gill, mantle, muscle) with the highest expression in hepatopancreas. Both mRNA and protein level of HcHSP70 in gill significantly up-regulated at 37℃and rapidly re-duced to normal level under 40℃.

关键词

三角帆蚌/热休克蛋白70/序列分析/基因表达/水温刺激

Key words

Hyriopsis cumingii/Heat shock protein 70/Cloning/Gene expression/Thermal stress

分类

生物科学

引用本文复制引用

吴圣楠,隗黎丽,李海军,付建平,刘毅..三角帆蚌热休克蛋白70基因克隆及其表达分析[J].水生生物学报,2017,41(1):50-55,6.

基金项目

国家自然科学基金项目(31060359) (31060359)

江西省自然科学基金(20122BAB204017)资助[Supported by the National Natural Science Foundation of China (31060359) (20122BAB204017)

the Natural Science Foundation of Jiangxi Province (20122BAB204017) (20122BAB204017)

水生生物学报

OA北大核心CSCDCSTPCD

1000-3207

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