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首页> 外文期刊>Plant and cell physiology >Arabidopsis Zinc-Finger-Like Protein ASYMMETRIC LEAVES2 (AS2) and Two Nucleolar Proteins Maintain Gene Body DNA Methylation in the Leaf Polarity Gene ETTIN (ARF3)
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Arabidopsis Zinc-Finger-Like Protein ASYMMETRIC LEAVES2 (AS2) and Two Nucleolar Proteins Maintain Gene Body DNA Methylation in the Leaf Polarity Gene ETTIN (ARF3)

机译:拟南芥锌 - 指状物的蛋白质不对称叶片2(AS2)和两个核菌蛋白在叶子极性基因ETTIN中维持基因体DNA甲基化(ARF3)

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Arabidopsis ASYMMETRIC LEAVES2 (AS2) plays a critical role in leaf adaxial–abaxial partitioning by repressing expression of the abaxial-determining gene ETTIN/AUXIN RESPONSE FACTOR3 (ETT/ARF3). We previously reported that six CpG dinucleotides in its exon 6 are thoroughly methylated by METHYLTRASFERASE1, that CpG methylation levels are inversely correlated with ETT/ARF3 transcript levels and that methylation levels at three out of the six CpG dinucleotides are decreased in as2-1. All these imply that AS2 is involved in epigenetic repression of ETT/ARF3 by gene body DNA methylation. The mechanism of the epigenetic repression by AS2, however, is unknown. Here, we tested mutations of NUCLEOLIN1 (NUC1) and RNA HELICASE10 (RH10) encoding nucleolus-localized proteins for the methylation in exon 6 as these mutations enhance the level of ETT/ARF3 transcripts in as2-1. Methylation levels at three specific CpGs were decreased in rh10-1, and two of those three overlapped with those in as2-1. Methylation levels at two specific CpGs were decreased in nuc1-1, and one of those three overlapped with that in as2-1. No site was affected by both rh10-1 and nuc1-1. One specific CpG was unaffected by these mutations. These results imply that the way in which RH10, NUC1 and AS2 are involved in maintaining methylation at five CpGs in exon 6 might be through at least several independent pathways, which might interact with each other. Furthermore, we found that AS2 binds specifically the sequence containing CpGs in exon 1 of ETT/ARF3, and that the binding requires the zinc-finger-like motif in AS2 that is structurally similar to the zinc finger-CxxC domain in vertebrate DNA methyltransferase1.
机译:Arabidopsis不对称的叶片2(AS2)通过抑制释放的确定基因ETTIN / AUXIN响应因子3(ETT / ARF3)的表达,在叶形和释录分区中起着关键作用。我们之前报道,其外显子6中的六个CpG二核苷酸通过甲基转移酶1彻底甲基化,CpG甲基化水平与ETT / ARF3转录物水平同时相关,并且在六个CPG二核苷酸中的三个中的甲基化水平在AS2-1中降低。所有这些都意味着AS2通过基因体DNA甲基化参与ETT / ARF3的表观遗传抑制。然而,由AS2的表观遗传抑制的机制是未知的。这里,我们测试了在外显子6中甲基化的核仁局部化蛋白的核仁1(NUC1)和RNA Helicase10(RH10)的突变,因为这些突变增强了AS2-1中的ETT / ARF3转录物的水平。三种特异性CPG的甲基化水平在RH10-1中降低,并且其中两种中的两种与AS2-1中的两种相比重叠。在NUC1-1中,两种特异性CPG的甲基化水平降低,并且在AS2-1中重叠的那些中的三个中的一个。 RH10-1和NUC1-1的任何网站都不受到影响。一个特定的CPG不受这些突变的影响。这些结果意味着RH10,NUC1和AS2参与在外显子6中的五个CPG中涉及维持甲基化的方式可能是通过至少几个独立的途径,这可能相互作用。此外,我们发现AS2特别结合含有ETT / ARF3的外显子1中的含有CPG的序列,并且结合需要在AS2中的锌指状基序,其在结构上类似于脊椎动物DNA甲基转移酶1的锌指-CXXC结构域。

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