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Regulated AtHKT1 Gene Expression by a Distal Enhancer Element and DNA Methylation in the Promoter Plays an Important Rolen in Salt Tolerance

机译:调控AtHKT1基因表达的远端增强子和启动子中的DNA甲基化在耐盐性中起重要作用

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摘要

Through sos3 (salt overly sensitive 3) suppressor screening, two allelic suppressor mutants that are weak alleles of the strong sos3 suppressor sos3hkt1-1 were recovered. Molecular characterization identified T-DNA insertions in the distal promoter region of the Arabidopsis thaliana HKT1 (AtHKT1, At4g10310) in these two weak sos3 suppressors, which results in physical separation of a tandem repeat from the proximal region of the AtHKT1 promoter. The tandem repeat is approximately 3.9 kb upstream of the ATG start codon and functions as an enhancer element to promote reporter gene expression. A putative small RNA target region about 2.6 kb upstream of the ATG start codon is heavily methylated. CHG and CHH methylation but not CG methylation is significantly reduced in the small RNA biogenesis mutant rdr2, indicating that non-CG methylation in this region is mediated by small RNAs. Analysis of AtHKT1 expression in rdr2 suggests that non-CG methylation in the putative small RNA target region represses AtHKT1 expression in shoots. The DNA methylation-deficient mutant met1-3 has nearly complete loss of total cytosine methylation in the putative small RNA target region and is hypersensitive to salt stress. The putative small RNA target region and the tandem repeat are essential for maintaining AtHKT1 expression patterns crucial for salt tolerance.
机译:通过sos3(盐敏感性3)抑制剂筛选,回收了两个等位基因抑制剂突变体,它们是强sos3抑制剂sos3hkt1-1的弱等位基因。分子表征鉴定了在这两个弱的sos3抑制子中拟南芥HKT1(AtHKT1,At4g10310)的远端启动子区域中的T-DNA插入,​​这导致串联重复序列与AtHKT1启动子的近端区域物理分离。串联重复序列在ATG起始密码子上游约3.9kb处,并用作促进报告基因表达的增强子。假定的ATG起始密码子上游约2.6 kb的小RNA靶区域被高度甲基化。在小RNA生物发生突变体rdr2中,CHG和CHH甲基化程度显着降低,但CG甲基化程度却未显着降低,表明该区域的非CG甲基化是由小RNA介导的。对rdr2中AtHKT1表达的分析表明,假定的小RNA靶区域中的非CG甲基化抑制了芽中AtHKT1的表达。 DNA甲基化不足的突变体met1-3在假定的小RNA靶区域中几乎完全丧失了总胞嘧啶甲基化,并且对盐胁迫高度敏感。假定的小RNA靶区域和串联重复序列对于维持AtHKT1表达模式对于耐盐性至关重要。

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