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首页> 外文期刊>Plant Molecular Biology >Identification of a dehydration and ABA-responsive promoter regulon and isolation of corresponding DNA binding proteins for the group 4 LEA gene CpC2 from C. plantagineum
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Identification of a dehydration and ABA-responsive promoter regulon and isolation of corresponding DNA binding proteins for the group 4 LEA gene CpC2 from C. plantagineum

机译:鉴定脱水和ABA反应性启动子调节子,并从植物假丝酵母中分离出第4组LEA基因CpC2的相应DNA结合蛋白

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摘要

The resurrection plant Craterostigma plantagineum (Scrophulariaceae) is used as a model system to investigate the molecular and biochemical basis of desiccation tolerance. Genes which contribute to desiccation tolerance are expressed during dehydration of this plant. One of the dehydration-induced genes is CpC2, a group 4 LEA gene. The CpC2 promoter was analysed and a core promoter region (CPR) was identified which is critical for the responsiveness of the gene to dehydration and the plant hormone ABA. The CPR motif contains two ABA-response elements (ABRE) and a binding site for HDZIP transcription factors. A yeast one-hybrid screen was performed to isolate CPR binding proteins. This resulted in the isolation of a bZIP transcription factor (CpbZIP1) and three highly conserved CpHistone H3 proteins. Two of these CpHistone H3 proteins are constitutively expressed histone H3 variants which are suggested to be involved in gene regulation via histone modification. The CpbZIP1 belongs to the group S of bZIP genes which possess long 5'-UTRs with a putative regulatory function. A second very similar bZIP clone, CpbZIP2, was isolated which contains a conserved small upstream open reading frame (uORF) within the 5'-leader sequence. A possible regulatory role of the uORF is discussed.
机译:使用复活植物Craterostigma plantagineum(Scrophulariaceae)作为模型系统,研究干燥耐性的分子和生化基础。在该植物的脱水过程中表达有助于脱水耐受的基因。脱水诱导的基因之一是CpC2,第4组LEA基因。分析了CpC2启动子并鉴定了核心启动子区域(CPR),该区域对于基因对脱水和植物激素ABA的响应性至关重要。 CPR基序包含两个ABA反应元件(ABRE)和一个HDZIP转录因子的结合位点。进行酵母一杂交筛选以分离CPR结合蛋白。这导致了bZIP转录因子(CpbZIP1)和三个高度保守的CpHistone H3蛋白的分离。这些CpHistone H3蛋白中有两个是组成性表达的组蛋白H3变体,提示它们通过组蛋白修饰参与基因调控。 CpbZIP1属于bZIP基因的S组,该基因具有较长的5'-UTR,具有可能的调控功能。分离出第二个非常相似的bZIP克隆CpbZIP2,其在5'-leader序列内包含一个保守的上游小开放阅读框(uORF)。讨论了uORF的可能调控作用。

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