Abstract

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.

Highlights

  • HAL is a multi-disciplinary open access archive for the deposit and dissemination of scientific research documents, whether they are published or not

  • An attractive hypothesis is that UAP56 plays a new role through its partnership with DRM2 potentially linked to the RNA-directed DNA methylation (RdDM) pathway in reproductive organs

  • Knowing the functional links between UAP56 and polymerase II (Pol II), the most obvious hypothesis would be that UAP56/DRM2 association may contribute to the non-canonical RdDM pathways initiated by Pol II transcription

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Summary

Introduction

HAL is a multi-disciplinary open access archive for the deposit and dissemination of scientific research documents, whether they are published or not. 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. 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. The first one is MET1, which is a conserved DNA methyltransferase homologous to mammalian DNMT1, which targets cytosines in a CG context [2] Unlike their animal counterparts, plants target methylation in a non-CG context. The chromomethylases proteins, mainly CMT2 and CMT3, Abbreviations GST, glutathione-S-transferase; HRP, horseradish peroxidase; IP, immunoprecipitation; lncRNA, long non-coding RNA; MNase, micrococcal nuclease; RdDM, RNA-directed DNA methylation; UAP56a/b, U2AF56 Associated Protein 56

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