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小麦Na+/H+反转运蛋白基因的克隆和特性

机译:小麦Na+/H+反转运蛋白基因的克隆和特性

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摘要

以水稻(Oryza sativa L.) Na+/H+反转运蛋白cDNA片段为探针,从小麦盐胁迫cDNA文库中筛选和克隆了2个小麦Na+/H+反转运蛋白基因,分别命名为TaNHX1 和 TaNHX2.序列分析表明TaNHX1为2 029 bp,包含一个完整的1 638 bp的ORF,编码546个氨基酸,其中含有DIFFIYLLPPI跨膜区.TaNHX2为1 693 bp,包含部分ORF及808 bp的3′-UTR.这2个基因与已知的水稻、拟南芥(Arabidopsis thialiana)和滨藜(Atriplex gmelini)中的同类基因NHX的相似性约为70%.RT-PCR分析表明小麦苗经400 mmol/L NaCl处理1 h后,TaNHX1的转录水平有所提高.%The Na+/H+ antiport genes named TaNHX1 and TaNHX2 were cloned by screening a salt-stressed wheat cDNA library using rice Na+/H+ antiport cDNA fragment as the probe. Sequencing analysis showed that TaNHX1 was 2 029 bp in length and contained a complete ORF of 1 638 bp. The TaNHX1 encodes a polypeptide of 546 amino acids with a transmembrane domain DIFFIYLLPPI. TaNHX2 was 1 693 bp in length consisting of a partial ORF followed by a 3′-UTR of 808 bp. The amino acid sequence of these two genes were about 70% identical to the known NHX genes from rice, Arabidopsis and Atriplex. A RT-PCR assay showed that the level of TaNHX1 transcripts was increased and reached a steady higher level in the seedlings after 3 h treatment with 400 mmol/L NaCl.
机译:以水稻(Oryza sativa L.) Na+/H+反转运蛋白cDNA片段为探针,从小麦盐胁迫cDNA文库中筛选和克隆了2个小麦Na+/H+反转运蛋白基因,分别命名为TaNHX1 和 TaNHX2.序列分析表明TaNHX1为2 029 bp,包含一个完整的1 638 bp的ORF,编码546个氨基酸,其中含有DIFFIYLLPPI跨膜区.TaNHX2为1 693 bp,包含部分ORF及808 bp的3′-UTR.这2个基因与已知的水稻、拟南芥(Arabidopsis thialiana)和滨藜(Atriplex gmelini)中的同类基因NHX的相似性约为70%.RT-PCR分析表明小麦苗经400 mmol/L NaCl处理1 h后,TaNHX1的转录水平有所提高.%The Na+/H+ antiport genes named TaNHX1 and TaNHX2 were cloned by screening a salt-stressed wheat cDNA library using rice Na+/H+ antiport cDNA fragment as the probe. Sequencing analysis showed that TaNHX1 was 2 029 bp in length and contained a complete ORF of 1 638 bp. The TaNHX1 encodes a polypeptide of 546 amino acids with a transmembrane domain DIFFIYLLPPI. TaNHX2 was 1 693 bp in length consisting of a partial ORF followed by a 3′-UTR of 808 bp. The amino acid sequence of these two genes were about 70% identical to the known NHX genes from rice, Arabidopsis and Atriplex. A RT-PCR assay showed that the level of TaNHX1 transcripts was increased and reached a steady higher level in the seedlings after 3 h treatment with 400 mmol/L NaCl.

著录项

  • 来源
    《植物学报(英文版)》 |2002年第10期|1203-1208|共6页
  • 作者单位

    中国科学院遗传研究所植物生物技术重点实验室,北京,100101;

    河北农林科学院粮油作物研究所作物育种室,石家庄,050031;

    中国科学院遗传研究所植物生物技术重点实验室,北京,100101;

    河北农林科学院粮油作物研究所作物育种室,石家庄,050031;

    中国科学院遗传研究所植物生物技术重点实验室,北京,100101;

    中国科学院遗传研究所植物生物技术重点实验室,北京,100101;

    中国科学院遗传研究所植物生物技术重点实验室,北京,100101;

  • 收录信息 中国科学引文数据库(CSCD);
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 植物基因工程;
  • 关键词

    小麦; Na+/H+反转运蛋白基因; 盐诱导;

  • 入库时间 2022-08-19 04:02:32

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