首页> 外文期刊>Planta >Identification of a novel low-temperature-response element in the promoter of the barley (Hordeum vulgare L) gene blt101.1
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Identification of a novel low-temperature-response element in the promoter of the barley (Hordeum vulgare L) gene blt101.1

机译:大麦(Hordeum vulgare L)基因blt101.1启动子中的新型低温响应元件的鉴定

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摘要

Two winter barley (Hordeum vulgare L. cv. Igri) genomic clones, λgblt101.1 and λgblt101.2, encoding the blt101 gene family, were isolated from a genomic library. Deletion analysis of the blt101.1 promoter, using transient β-glucuronidase (GUS) reporter expression assays, indicated that it contains at least three regulatory regions. A 107-bp region between nucleotides –168 and –275 with respect to the translation initiation codon, confers high -level GUS reporter expression at low temperature and contains a sequence (designated CR1) that is highly conserved in equivalent positions within the promoters of both members of the blt101 gene family. A 10-bp motif contained within CR1 binds proteins present in nuclear extracts from both control and low-temperature-treated barley tissue. Loss-of-function experiments, using transient-expression analysis, confirmed that this motif acts as a previously unreported low-temperature-responsive element. Nuclease sensitivity analysis of intact chromatin indicated that the blt101.1 promoter becomes more susceptible to DNase and micrococcal nuclease at low temperature, consistent with chromatin reorganisation upon transcriptional induction. It is proposed that both the 10-bp motif and chromatin reorganisation are involved in the regulation of blt101.1 at low temperature. This is the first detailed analysis of a low-temperature-specific plant promoter and identifies a novel low-temperature-response element.
机译:从一个基因组文库中分离出两个冬小麦(Hordeum vulgare L. cv。Igri)基因组克隆,分别编码blt101基因家族的λgblt101.1和λgblt101.2。使用瞬时β-葡糖醛酸糖苷酶(GUS)报告基因表达分析法对blt101.1启动子进行缺失分析,表明其至少包含三个调控区。相对于翻译起始密码子,核苷酸–168和–275之间有107 bp的区域,可在低温下提供高水平的GUS报告基因表达,并包含一个在两个启动子内等价位置均高度保守的序列(称为CR1) blt101基因家族的成员。 CR1中包含的10 bp基序与来自对照和低温处理的大麦组织的核提取物中存在的蛋白质结合。使用瞬时表达分析的功能丧失实验证实,该基序充当了以前未报道的低温反应元件。完整染色质的核酸酶敏感性分析表明,blt101.1启动子在低温下对DNase和微球菌核酸酶更敏感,这与转录诱导后的染色质重组一致。有人提出10bp的基序和染色质重组都参与低温blt101.1的调节。这是对低温特异性植物启动子的首次详细分析,并确定了一种新型的低温响应元件。

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  • 来源
    《Planta》 |2001年第5期|770-780|共11页
  • 作者单位

    School of Biochemistry and Genetics The Medical School University of Newcastle upon Tyne Framlington Place Newcastle upon Tyne NE2 4HH UK;

    School of Biochemistry and Genetics The Medical School University of Newcastle upon Tyne Framlington Place Newcastle upon Tyne NE2 4HH UK;

    School of Biochemistry and Genetics The Medical School University of Newcastle upon Tyne Framlington Place Newcastle upon Tyne NE2 4HH UK;

    School of Biochemistry and Genetics The Medical School University of Newcastle upon Tyne Framlington Place Newcastle upon Tyne NE2 4HH UK;

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  • 原文格式 PDF
  • 正文语种 eng
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  • 关键词

    Chromatin Hordeum (LTRE) Low temperature Nuclear protein-DNA binding Promoter Transient expression;

    机译:染色质大麦(LTRE)低温核蛋白-DNA结合启动子瞬时表达;

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