Preuss Sasha B, Costa-Nunes Pedro, Tucker Sarah, Pontes Olga, Lawrence Richard J, Mosher Rebecca, Kasschau Kristin D, Carrington James C, Baulcombe David C, Viegas Wanda, Pikaard Craig S
Biology Department, Washington University, St. Louis, MO 63130, USA.
Mol Cell. 2008 Dec 5;32(5):673-84. doi: 10.1016/j.molcel.2008.11.009.
In genetic hybrids, the silencing of nucleolar rRNA genes inherited from one progenitor is the epigenetic phenomenon known as nucleolar dominance. An RNAi knockdown screen identified the Arabidopsis de novo cytosine methyltransferase, DRM2, and the methylcytosine binding domain proteins, MBD6 and MBD10, as activities required for nucleolar dominance. MBD10 localizes throughout the nucleus, but MBD6 preferentially associates with silenced rRNA genes and does so in a DRM2-dependent manner. DRM2 methylation is thought to be guided by siRNAs whose biogenesis requires RNA-DEPENDENT RNA POLYMERASE 2 (RDR2) and DICER-LIKE 3 (DCL3). Consistent with this hypothesis, knockdown of DCL3 or RDR2 disrupts nucleolar dominance. Collectively, these results indicate that in addition to directing the silencing of retrotransposons and noncoding repeats, siRNAs specify de novo cytosine methylation patterns that are recognized by MBD6 and MBD10 in the large-scale silencing of rRNA gene loci.
在遗传杂种中,从一个亲本遗传而来的核仁rRNA基因的沉默是一种被称为核仁显性的表观遗传现象。一项RNA干扰敲低筛选确定了拟南芥从头胞嘧啶甲基转移酶DRM2以及甲基胞嘧啶结合结构域蛋白MBD6和MBD10是核仁显性所需的活性因子。MBD10定位于整个细胞核,但MBD6优先与沉默的rRNA基因结合,且以依赖DRM2的方式进行。DRM2甲基化被认为是由小干扰RNA(siRNA)引导的,其生物合成需要RNA依赖的RNA聚合酶2(RDR2)和类Dicer 3(DCL3)。与该假设一致,敲低DCL3或RDR2会破坏核仁显性。总体而言,这些结果表明,除了指导逆转座子和非编码重复序列的沉默外,siRNA还指定了从头胞嘧啶甲基化模式,这些模式在rRNA基因座的大规模沉默中被MBD6和MBD10识别。