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首页> 外文期刊>International Sugar Journal >Effects of chilling stress on protein and related gene expression in chloroplasts of sugarcane
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Effects of chilling stress on protein and related gene expression in chloroplasts of sugarcane

机译:低温胁迫对甘蔗叶绿体蛋白质及相关基因表达的影响

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摘要

The effects of chilling stress on chloroplasts at protein and mRNA levels to provide a reference for further investigation on the molecular mechanism of chilling stress in sugarcane was investigated. Sugarcane varieties GT28 (strong cold resistant) and ROC22 (weak cold resistant) were used as plant materials, and treated under 9 d, 15 d and 24 d of chilling stress, respectively. The chloroplast protein was extracted and used for electrophoresis analysis, and expressions of the genes were analysed using real-time PCR. Electrophoresis analysis showed that, for both sugarcane varieties, the relative content of chloroplast protein decreased with increase in chilling time. The protein bands of 39.92, 32.95 and 22.87 kDa were down-regulated. Mass spectrometry revealed that they were ATP synthase subunit gamma, oxygen-evolving enhancer protein 1 and chloroplast 23 kDa polypeptide of photosystem II, and they were encoded by atpC, PsbO and PsbP genes, respectively. Their fragment lengths were 937, 996 and 721 bp respectively. The obtained fragment of PsbO gene, in its complete open reading frame, has been registered in the GenBank database with the accession number JQ898540. Real-time PCR analysis showed that chilling stress suppressed the expression of atpC gene, but induced the expressions of PsbO and PsbP genes, which reached a maximum at 15 d. Generally, chilling stress promoted protein degradation, and the protein declined more in ROC22 than that in GT28. Chilling stress suppressed the expression of atpC gene, but induced the expressions of PsbO and PsbP genes in chloroplasts of sugarcane.
机译:低温胁迫对叶绿体蛋白质和mRNA水平的影响,为进一步研究甘蔗低温胁迫的分子机制提供参考。将甘蔗品种GT28(耐强寒性)和ROC22(耐弱寒性)用作植物材料,分别在9 d,15 d和24 d的低温胁迫下进行了处理。提取叶绿体蛋白并用于电泳分析,并使用实时PCR分析基因的表达。电泳分析表明,对于两种甘蔗品种,叶绿体蛋白的相对含量均随着冷却时间的增加而降低。 39.92、32.95和22.87 kDa的蛋白条带被下调。质谱显示它们是光合系统II的ATP合酶亚基γ,放氧增强蛋白1和叶绿体23 kDa多肽,分别由atpC,PsbO和PsbP基因编码。它们的片段长度分别为937、996和721bp。所获得的PsbO基因的片段,在其完整的开放阅读框中,已在GenBank数据库中注册,登录号为JQ898540。实时PCR分析表明,低温胁迫抑制了atpC基因的表达,但诱导了PsbO和PsbP基因的表达,在15 d时达到最大值。通常,低温胁迫促进蛋白质降解,ROC22中的蛋白质下降比GT28中的下降更多。低温胁迫抑制了甘蔗叶绿体中atpC基因的表达,但诱导了PsbO和PsbP基因的表达。

著录项

  • 来源
    《International Sugar Journal》 |2015年第1404期|884-889|共6页
  • 作者单位

    Chinese Acad Agr Sci, Guangxi Crop Genet Improvement & Biotechnol Lab, Key Lab Sugarcane Biotechnol & Genet Improvement, Guangxi Key Lab Sugarcane Genet Improvement,Sugar, Nanning 530007, Peoples R China|Guangxi Univ, Coll Agr, State Key Lab Conservat & Utilizat Subtrop Agrobi, Nanning 530005, Peoples R China;

    Chinese Acad Agr Sci, Guangxi Crop Genet Improvement & Biotechnol Lab, Key Lab Sugarcane Biotechnol & Genet Improvement, Guangxi Key Lab Sugarcane Genet Improvement,Sugar, Nanning 530007, Peoples R China;

    Chinese Acad Agr Sci, Guangxi Crop Genet Improvement & Biotechnol Lab, Key Lab Sugarcane Biotechnol & Genet Improvement, Guangxi Key Lab Sugarcane Genet Improvement,Sugar, Nanning 530007, Peoples R China;

    Chinese Acad Agr Sci, Guangxi Crop Genet Improvement & Biotechnol Lab, Key Lab Sugarcane Biotechnol & Genet Improvement, Guangxi Key Lab Sugarcane Genet Improvement,Sugar, Nanning 530007, Peoples R China;

    Chinese Acad Agr Sci, Guangxi Crop Genet Improvement & Biotechnol Lab, Key Lab Sugarcane Biotechnol & Genet Improvement, Guangxi Key Lab Sugarcane Genet Improvement,Sugar, Nanning 530007, Peoples R China;

    Chinese Acad Agr Sci, Guangxi Crop Genet Improvement & Biotechnol Lab, Key Lab Sugarcane Biotechnol & Genet Improvement, Guangxi Key Lab Sugarcane Genet Improvement,Sugar, Nanning 530007, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    chilling stress; sugarcane; chloroplast; proteome; differential expression;

    机译:低温胁迫;蔗糖烷;叶绿体;蛋白质组;差异表达;

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