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DNA Methylation is a Determinative Element of Photosynthesis Gene Expression in Amyloplasts from Liquid-Cultured Cells of Sycamore (Acer pseudoplatanus L.)

机译:DNA甲基化是美国梧桐(Acer pseudoplatanus L.)液体培养细胞的淀粉体中光合作用基因表达的决定性因素

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References(44) Cited-By(7) Transcriptional regulation has been shownto operate as a selective control mechanismof expression of photosynthetic genes in the nonphotosynthetic plastids, amyloplasts, of a white-wild cell line of sycamore (Acer pseudoplatanus L.). To elaborate the mechanisms governing the transcriptional regulation at the molecular level, we have examined the template activity of the amyloplast DNA compared to the chloroplast DNA by using the in vitro run-off transcription assay system with extracts of the two plastid types. The results of these assays clearly indicate that most of the amyloplast DNA regions do not serve as a template for the in vitro transcription regardless of the plastid extracts; this is in contrast to the chloroplast DNA which serves as an active template. It is highly likely that the template activity of amyloplast DNA per se is the modulating element of transcriptional regulation. Parallel experiments determining the DNA base content by HPLC analysis have shown that a variety of methylated bases, especially 5-methylcytosine, are localized in the DNAregions containing suppressed genes of the amyloplast genome. In sharp contrast, methylated bases were undetectable in the expressed gene regions of amyloplast and whole chloroplast genomes. The overall findings strongly support the notion that DNAmethylation is involved in the selective suppression of photosynthetic genes in the nonphotosynthetic plastids of cultured sycamore cells.
机译:参考文献(44)Cited-By(7)转录调控已显示为美国梧桐白野生细胞系(Acer pseudoplatanus L.)的非光合质体,淀粉质体中光合基因表达的选择性控制机制。为了详细阐述在分子水平上调控转录调控的机制,我们使用了两种质体类型的提取物,通过体外径流转录检测系统,检查了与叶绿体DNA相比,淀粉体DNA的模板活性。这些测定的结果清楚地表明,无论质体提取物是什么,大多数淀粉质体DNA区都不能作为体外转录的模板。这与用作活性模板的叶绿体DNA相反。淀粉酶DNA本身的模板活性很可能是转录调控的调节元件。通过HPLC分析确定DNA碱基含量的平行实验表明,各种甲基化碱基,特别是5-甲基胞嘧啶,位于含有淀粉体基因组基因被抑制基因的DNA区域中。与之形成鲜明对比的是,在淀粉状塑料和整个叶绿体基因组的表达基因区域中,甲基化的碱基是不可检测的。总的发现强烈支持DNA甲基化参与选择性抑制培养的梧桐细胞的非光合质体中的光合基因的观点。

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