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青杄 PwRbcS 基因克隆及对逆境响应分析

鞠丹 胡安妮 张杰 张凌云

生物技术通报2016,Vol.32Issue(10):154-162,9.
生物技术通报2016,Vol.32Issue(10):154-162,9.DOI:10.13560/j.cnki.biotech.bull.1985.2016.10.019

青杄 PwRbcS 基因克隆及对逆境响应分析

Cloning and Stress Response Analysis of PwRbcS in Picea wilsonii

鞠丹 1胡安妮 1张杰 1张凌云1

作者信息

  • 1. 北京林业大学 省部共建森林培育与保护教育部重点实验室,北京 100083
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摘要

Abstract

RbcS gene encodes a subunit of nuclear plant photosynthesis 1,5 two ribulose bisphosphate carboxylase / oxygenase. In this study,PwRbcS cDNA was obtained using RACE -PCR method. Bioinformatics analysis and real-time PCR technique were used to determine the relative expression of PwRbcS. The results showed that the full-length of PwRbcS cDNA was 936 bp,including the ORF of 552 bp encoding 186 amino acids. The theoretical molecular weight of PwRbcS is 20.712 6 kD and the pI value was 9.07. RT-qPCR showed that PwRbcS is mainly expressed in the needles,especially in mature needles. The expression of PwRbcS changed obviously under the treatment of NaCl,ABA and low temperature,respectively. After NaCl treatment,the expression level of PwRbcS changed significantly,reaching to 14 times than the control at 6 h. The expression level of PwRbcS reached to 24 times than the control after 8 h-ABA-treatment. And under low temperature stress, the expression increased gradually to 12 times than the control and followed by a drop,while under high temperature and PEG stress expression level did not change significantly. Therefore,PwRbcS may play an important role during abiotic stresses in planta.

关键词

Picea wilsonii/RbcS/生物信息学分析/组织表达/胁迫响应

Key words

Picea wilsonii/RbcS/bioinformatics/tissue expression/stress response

引用本文复制引用

鞠丹,胡安妮,张杰,张凌云..青杄 PwRbcS 基因克隆及对逆境响应分析[J].生物技术通报,2016,32(10):154-162,9.

基金项目

国家自然科学基金项目(31270663),国家转基因生物新品种培育科技重大专项 ()

生物技术通报

OA北大核心CSCDCSTPCD

1002-5464

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