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沙葱萤叶甲丝氨酸蛋白酶基因GdSP的克隆及对温度胁迫的响应

单艳敏 张玉 霍志家 庞保平 孙学涛

昆虫学报2018,Vol.61Issue(7):761-770,10.
昆虫学报2018,Vol.61Issue(7):761-770,10.DOI:10.16380/j.kcxb.2018.07.002

沙葱萤叶甲丝氨酸蛋白酶基因GdSP的克隆及对温度胁迫的响应

Molecular cloning of a serine protease gene DdSP and its response to temperature stress in Galeruca daurica (Coleoptera: Chrysomelidae)

单艳敏 1张玉 2霍志家 1庞保平 1孙学涛1

作者信息

  • 1. 内蒙古农业大学草原昆虫研究中心,呼和浩特 010010
  • 2. 内蒙古自治区草原工作站,呼和浩特 010020
  • 折叠

摘要

Abstract

[Aim]Serine protease (SP) is an important proteolytic enzyme, with serine as its active center. This study aims to clone a serine protease gene from Galeruca daurica and to analyze its expression levels in response to temperature stress so as to lay a foundation for further investigation on the regulation mechanisms of temperature tolerance and other physiological functions in G. daurica.[Methods]Based on the transcriptome data of the 2 nd instar larvae of G. daurica, the full-length cDNA of the serine protease gene was cloned from G. daurica by RACE, and its sequence was subjected to bioinformatics analysis. Its expression profiles in the 2 nd instar larvae of G. daurica exposed to differenttemperatures (-10,-5, 0, 5, 25, and 35℃) for 1 h and recovered at 25℃ for 30 min were detected by qPCR. [Results]A serine protease gene was cloned from G. daurica, and named GdSP (GenBank accession no.: MG797556). GdSP is 1 110 bp in length with an open reading frame (ORF) of 969 bp, encoding a protein of 322 amino acids with the predicted molecular weight of 35. 41 kD and p I of 5. 61.The encoded protein shares the typical structural features of serine proteases, with a transmembrane domain but no signal peptide. Homologous sequence alignment and phylogenetic analysis showed that GdSP has the highest amino acid sequence identity (30. 53%) with Anoplophora glabripennis SP. qPCR results showed that the expression levels of GdSP had no significant difference in the 2 nd instar larvae of G. daurica exposed to different temperatures whereas increased significantly after recovery from the low (except-10℃) and high temperature stresses. [Conclusion]Rapid cold-hardening has no significant effects on the expression of GdSP while recovery from cold shock elicits its up-regulated expression.

关键词

沙葱萤叶甲/丝氨酸蛋白酶/基因克隆/温度胁迫/表达分析

Key words

Galeruca daurica/serine protease/gene cloning/temperature stress/expression profiling

分类

生物科学

引用本文复制引用

单艳敏,张玉,霍志家,庞保平,孙学涛..沙葱萤叶甲丝氨酸蛋白酶基因GdSP的克隆及对温度胁迫的响应[J].昆虫学报,2018,61(7):761-770,10.

基金项目

国家自然科学基金项目(31360441) (31360441)

昆虫学报

OA北大核心CSCDCSTPCD

0454-6296

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