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首页> 外文期刊>The Plant Cell >The WD40-repeat proteins NFC101 and NFC102 regulate different aspects of maize development through chromatin modification.
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The WD40-repeat proteins NFC101 and NFC102 regulate different aspects of maize development through chromatin modification.

机译:WD40重复蛋白NFC101和NFC102通过染色质修饰来调节玉米发育的不同方面。

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The maize (Zea mays) nucleosome remodeling factor complex component101 (nfc101) and nfc102 are putative paralogs encoding WD-repeat proteins with homology to plant and mammalian components of various chromatin modifying complexes. In this study, we generated transgenic lines with simultaneous nfc101 and nfc102 downregulation and analyzed phenotypic alterations, along with effects on RNA levels, the binding of NFC101/NFC102, and Rpd3-type histone deacetylases (HDACs), and histone modifications at selected targets. Direct NFC101/NFC102 binding and negative correlation with mRNA levels were observed for indeterminate1 (id1) and the florigen Zea mays CENTRORADIALIS8 (ZCN8), key activators of the floral transition. In addition, the abolition of NFC101/NFC102 association with repetitive sequences of different transposable elements (TEs) resulted in tissue-specific upregulation of nonpolyadenylated RNAs produced by these regions. All direct nfc101fc102 targets showed histone modification patterns linked to active chromatin in nfc101fc102 downregulation lines. However, different mechanisms may be involved because NFC101/NFC102 proteins mediate HDAC recruitment at id1 and TE repeats but not at ZCN8. These results, along with the pleiotropic effects observed in nfc101fc102 downregulation lines, suggest that NFC101 and NFC102 are components of distinct chromatin modifying complexes, which operate in different pathways and influence diverse aspects of maize development.
机译:玉米(Zea mays)核小体重塑因子复合物组分101(nfc101)和nfc102是编码WD重复蛋白的推定旁系同源物,其与各种染色质修饰复合物的植物和哺乳动物组分具有同源性。在这项研究中,我们产生了同时具有nfc101和nfc102下调的转基因品系,并分析了表型变化,以及对RNA水平,NFC101 / NFC102和Rpd3型组蛋白脱乙酰基酶(HDAC)的结合以及选定靶标上的组蛋白修饰的影响。观察到直接不确定的1(id1)和花的过渡的主要激活物玉米黄玉米CENTRORADIALIS8(ZCN8)与NFC101 / NFC102的直接结合和与mRNA水平的负相关。此外,取消了NFC101 / NFC102与不同转座因子(TEs)的重复序列的结合,导致这些区域产生的非聚腺苷酸RNA的组织特异性上调。所有直接的nfc101 / nfc102靶标均显示了与nfc101 / nfc102下调谱系中的活性染色质相关的组蛋白修饰模式。但是,可能涉及不同的机制,因为NFC101 / NFC102蛋白在id1和TE重复处介导HDAC募集,但不在ZCN8处介导HDAC募集。这些结果,以及在nfc101 / nfc102下调系中观察到的多效性效应表明,NFC101和NFC102是不同的染色质修饰复合物的组成部分,它们以不同的途径起作用并影响玉米发育的各个方面。

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