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首页> 外文期刊>Plant physiology >The Exosome and Trans-Acting Small Interfering RNAs Regulate Cuticular Wax Biosynthesis during Arabidopsis Inflorescence Stem Development
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The Exosome and Trans-Acting Small Interfering RNAs Regulate Cuticular Wax Biosynthesis during Arabidopsis Inflorescence Stem Development

机译:外来体和反式作用的小干扰RNA调节拟南芥花序茎发育过程中的表皮蜡生物合成。

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The primary aerial surfaces of land plants are covered with a cuticle, a protective layer composed of the cutin polyester matrix and cuticular waxes. Previously, we discovered a unique mechanism of regulating cuticular wax biosynthesis during Arabidopsis (Arabidopsis thaliana) stem elongation that involves ECERIFERUM7 (CER7), a core subunit of the exosome. Because loss-of-function mutations in CER7 result in reduced expression of the wax biosynthetic gene CER3, we proposed that CER7 is involved in degrading a messenger RNA encoding a CER3 repressor. To identify this putative repressor, we performed a cer7 suppressor screen that resulted in the isolation of the posttranscriptional gene-silencing components RNA-DEPENDENT RNA POLYMERASE1 and SUPPRESSOR OF GENE SILENCING3, indicating that small RNAs regulate CER3 expression. To establish the identity of the effector RNA species and determine whether these RNAs control CER3 transcript levels directly, we cloned additional genes identified in our suppressor screen and performed next-generation sequencing of small RNA populations that differentially accumulate in the cer7 mutant in comparison with the wild type. Our results demonstrate that the trans-acting small interfering RNA class of small RNAs are the effector molecules involved in direct silencing of CER3 and that the expression of five additional genes (EARLY RESPONSE TO DEHYDRATION14, AUXIN RESISTANT1, a translation initiation factor SUI1 family protein, and two genes of unknown function) is controlled by both CER7 and trans-acting small interfering RNAs.
机译:陆地植物的主要空中表面覆盖有角质层,由角质聚酯基质和角质层蜡组成的保护层。以前,我们发现了在拟南芥(Arabidopsis thaliana)茎伸长过程中调节表皮蜡生物合成的独特机制,该机制涉及外泌体的核心亚基ECERIFERUM7(CER7)。由于CER7中的功能丧失突变导致蜡生物合成基因CER3的表达降低,因此我们建议CER7参与降解编码CER3阻遏物的信使RNA。为了鉴定该推定的阻遏物,我们进行了cer7抑制子筛选,该转录物导致转录后基因沉默组件RNA依赖性RNA POLYMERASE1和基因SILENCING3的抑制子的分离,表明小RNA调节CER3的表达。为了确定效应RNA种类的身份并确定这些RNA是否直接控制CER3转录水平,我们克隆了在抑制子筛选中鉴定的其他基因,并对与cer7突变体相比有差异积聚的小RNA群体进行了下一代测序。野生型。我们的研究结果表明,小分子RNA的反式作用小分子RNA是影响CER3直接沉默的效应子分子,并且另外五个基因的表达(对脱水的早期反应14,AUXIN RESISTANT1,翻译起始因子SUI1家族蛋白,和两个功能未知的基因)都受CER7和反式作用的小干扰RNA的控制。

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