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Metal A and Metal B Sites of Nuclear RNA Polymerases Pol IV and Pol V Are Required for siRNA-Dependent DNA Methylation and Gene Silencing

机译:siRNA依赖的DNA甲基化和基因沉默需要核RNA聚合酶Pol IV和Pol V的金属A和金属B位点

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摘要

Plants are unique among eukaryotes in having five multi-subunit nuclear RNA polymerases: the ubiquitous RNA polymerases I, II and III plus two plant-specific activities, nuclear RNA polymerases IV and V (previously known as Polymerases IVa and IVb). Pol IV and Pol V are not required for viability but play non-redundant roles in small interfering RNA (siRNA)-mediated pathways, including a pathway that silences retrotransposons and endogenous repeats via siRNA-directed DNA methylation. RNA polymerase activity has not been demonstrated for Polymerases IV or V in vitro, making it unclear whether they are catalytically active enzymes. Their largest and second-largest subunit sequences have diverged considerably from Pol I, II and III in the vicinity of the catalytic center, yet retain the invariant Metal A and Metal B amino acid motifs that bind magnesium ions essential for RNA polymerization. By using site-directed mutagenesis in conjunction with in vivo functional assays, we show that the Metal A and Metal B motifs of Polymerases IV and V are essential for siRNA production, siRNA-directed DNA methylation, retrotransposon silencing, and the punctate nuclear localization patterns typical of both polymerases. Collectively, these data show that the minimal core sequences of polymerase active sites, the Metal A and B sites, are essential for Pol IV and Pol V biological functions, implying that both are catalytically active.
机译:在真核生物中,植物具有五个多亚基核RNA聚合酶,它们是独特的:普遍存在的RNA聚合酶I,II和III加上两个植物特有的活性,即核RNA聚合酶IV和V(以前称为聚合酶IVa和IVb)。 Pol IV和Pol V不是生存力所必需的,但在小干扰RNA(siRNA)介导的途径中发挥非冗余作用,包括通过siRNA定向的DNA甲基化使逆转座子和内源重复序列沉默的途径。 RNA聚合酶的活性尚未在体外证明为聚合酶IV或V,尚不清楚它们是否为催化活性酶。它们的最大和第二大亚基序列已在催化中心附近与Pol I,II和III发生了很大的差异,但保留了结合RNA聚合所必需的镁离子的不变的Metal A和Metal B氨基酸基序。通过使用定点诱变结合体内功能测定,我们显示了聚合酶IV和V的金属A和金属B基序对于siRNA生产,siRNA定向DNA甲基化,反转录转座子沉默和点状核定位模式必不可少这两种聚合酶都是典型的。总体而言,这些数据表明,聚合酶活性位点(金属A和B位点)的最小核心序列对于Pol IV和Pol V的生物学功能至关重要,这意味着两者均具有催化活性。

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