LGDP-UMR5096, CNRS, Perpignan, France.
LGDP-UMR5096, Université de Perpignan Via Domitia, France.
FEBS Open Bio. 2019 May;9(5):973-985. doi: 10.1002/2211-5463.12627. Epub 2019 Apr 5.
Repeated sequence expression and transposable element mobilization are tightly controlled by multilayer processes, which include DNA 5'-cytosine methylation. The RNA-directed DNA methylation (RdDM) pathway, which uses siRNAs to guide sequence-specific directed DNA methylation, emerged specifically in plants. RdDM ensures DNA methylation maintenance on asymmetric CHH sites and specifically initiates de novo methylation in all cytosine sequence contexts through the action of DRM DNA methyltransferases, of which DRM2 is the most prominent. The RdDM pathway has been well described, but how DRM2 is recruited onto DNA targets and associates with other RdDM factors remains unknown. To address these questions, we developed biochemical approaches to allow the identification of factors that may escape genetic screens, such as proteins encoded by multigenic families. Through both conventional and affinity purification of DRM2, we identified DEAD box RNA helicases U2AF56 Associated Protein 56 (UAP56a/b), which are widespread among eukaryotes, as new DRM2 partners. We have shown that, similar to DRM2 and other RdDM actors, UAP56 has chromatin-associated protein properties. We confirmed this association both in vitro and in vivo in reproductive tissues. In addition, our experiments also suggest that UAP56 may exhibit differential distribution in cells depending on plant organ. While originally identified for its role in splicing, our study suggests that UAP56 may also have other roles, and our findings allow us to initiate discussion about its potential role in the RdDM pathway.
重复序列的表达和转座元件的激活受到多层过程的严格控制,包括 DNA 5'-胞嘧啶甲基化。RNA 指导的 DNA 甲基化(RdDM)途径利用 siRNA 指导序列特异性的定向 DNA 甲基化,它是植物特有的。RdDM 确保了不对称 CHH 位点上的 DNA 甲基化维持,并通过 DRM DNA 甲基转移酶的作用特异性地在所有胞嘧啶序列背景下起始从头甲基化,其中 DRM2 最为突出。RdDM 途径已经得到了很好的描述,但 DRM2 如何被招募到 DNA 靶标上并与其他 RdDM 因子相关联仍然未知。为了解决这些问题,我们开发了生化方法来识别可能逃避遗传筛选的因素,例如多基因家族编码的蛋白质。通过 DRM2 的常规和亲和纯化,我们鉴定了 DEAD 盒 RNA 解旋酶 U2AF56 相关蛋白 56(UAP56a/b),它在真核生物中广泛存在,是新的 DRM2 伴侣。我们已经表明,与 DRM2 和其他 RdDM 因子相似,UAP56 具有染色质相关蛋白的特性。我们在生殖组织中既在体外又在体内证实了这种关联。此外,我们的实验还表明,UAP56 可能根据植物器官的不同而在细胞中表现出不同的分布。虽然最初是因其在剪接中的作用而被鉴定出来的,但我们的研究表明 UAP56 可能还有其他作用,我们的发现使我们能够开始讨论它在 RdDM 途径中的潜在作用。