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首页> 外文期刊>Frontiers in Plant Science >P1 Epigenetic Regulation in Leaves of High Altitude Maize Landraces: Effect of UV-B Radiation
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P1 Epigenetic Regulation in Leaves of High Altitude Maize Landraces: Effect of UV-B Radiation

机译:<斜视> P1 高空玉米实地叶片中的表观遗传调节:UV-B辐射的影响

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P1 is a R2R3-MYB transcription factor that regulates the accumulation of a specific group of flavonoids in maize floral tissues, such as flavones and phlobaphenes. P1 is also highly expressed in leaves of maize landraces adapted to high altitudes and higher levels of UV-B radiation. In this work, we analyzed the epigenetic regulation of the P1 gene by UV-B in leaves of different maize landraces. Our results demonstrate that DNA methylation in the P1 proximal promoter, intron1 and intron2 is decreased by UV-B in all lines analyzed; however, the basal DNA methylation levels are lower in the landraces than in B73, a low altitude inbred line. DNA demethylation by UV-B is accompanied by a decrease in H3 methylation at Lys 9 and 27, and by an increase in H3 acetylation. smRNAs complementary to specific regions of the proximal promoter and of intron 2 3′ end are also decreased by UV-B; interestingly, P1 smRNA levels are lower in the landraces than in B73 both under control conditions and after UV-B exposure, suggesting that smRNAs regulate P1 expression by UV-B in maize leaves. Finally, we investigated if different P1 targets in flower tissues are also regulated by this transcription factor in response to UV-B. Some targets analyzed show an induction in maize landraces in response to UV-B, with higher basal expression levels in the landraces than in B73; however, not all the transcripts analyzed were found to be regulated by UV-B in leaves.
机译:P1是R2R3-MYB转录因子,其调节玉米花组织中特定类黄酮组的积累,例如黄酮和磷酰比。 P1也高于玉米地体的叶子表达,适用于高海拔高度和更高水平的UV-B辐射。在这项工作中,我们在不同玉米体力素的叶片中分析了UV-B中P1基因的表观遗传调节。我们的结果表明,P1近端启动子,Intron1和Intron2中的DNA甲基化在分析的所有线中通过UV-B降低;然而,基础DNA甲基化水平比在B73中低于B73,低海拔近红线。通过UV-B的DNA去甲基化伴随着Lys 9和27处的H3甲基化的降低,并通过增加H3乙酰化。 UV-B也降低了近端启动子和Intron 2 3'末端的特定区域的SMRNA;有趣的是,在对照条件下,P1 SMRNA水平低于B73在控制条件下和UV-B暴露后的B73,表明SMRNA通过玉米叶中的UV-B调节P1表达。最后,我们研究了花组织中的不同P1靶的响应于UV-B的转录因子。分析的一些靶标显示玉米背包响应于UV-B的诱导,体重率高于B73中的较高基础表达水平;然而,并非分析的所有转录物被发现由叶片中的UV-B调节。

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