2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      An siRNA-guided ARGONAUTE protein directs RNA polymerase V to initiate DNA methylation

      research-article

      Read this article at

          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In mammals and plants, cytosine DNA methylation is essential for the epigenetic repression of transposable elements and foreign DNA. In plants, DNA methylation is guided by small interfering RNAs (siRNAs) in a self-reinforcing cycle termed RNA-directed DNA methylation (RdDM). RdDM requires the specialized RNA polymerase V (Pol V), and the key unanswered question is how Pol V is first recruited to new target sites without pre-existing DNA methylation. We find that Pol V follows and is dependent on the recruitment of an AGO4-clade ARGONAUTE protein, and any siRNA can guide the ARGONAUTE protein to the new target locus independent of pre-existing DNA methylation. These findings reject long-standing models of RdDM initiation and instead demonstrate that siRNA-guided ARGONAUTE targeting is necessary, sufficient and first to target Pol V recruitment and trigger the cycle of RdDM at a transcribed target locus, thereby establishing epigenetic silencing.

          Abstract

          This study finds that siRNA-guided ARGONAUTE first recruits polymerase V to new target sites without pre-existing DNA methylation and triggers the cycle of RdDM at the target sites, thereby establishing epigenetic silencing.

          Related collections

          Most cited references57

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          BEDTools: a flexible suite of utilities for comparing genomic features

          Motivation: Testing for correlations between different sets of genomic features is a fundamental task in genomics research. However, searching for overlaps between features with existing web-based methods is complicated by the massive datasets that are routinely produced with current sequencing technologies. Fast and flexible tools are therefore required to ask complex questions of these data in an efficient manner. Results: This article introduces a new software suite for the comparison, manipulation and annotation of genomic features in Browser Extensible Data (BED) and General Feature Format (GFF) format. BEDTools also supports the comparison of sequence alignments in BAM format to both BED and GFF features. The tools are extremely efficient and allow the user to compare large datasets (e.g. next-generation sequencing data) with both public and custom genome annotation tracks. BEDTools can be combined with one another as well as with standard UNIX commands, thus facilitating routine genomics tasks as well as pipelines that can quickly answer intricate questions of large genomic datasets. Availability and implementation: BEDTools was written in C++. Source code and a comprehensive user manual are freely available at http://code.google.com/p/bedtools Contact: aaronquinlan@gmail.com; imh4y@virginia.edu Supplementary information: Supplementary data are available at Bioinformatics online.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Dynamics and function of DNA methylation in plants

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              DNA interrogation by the CRISPR RNA-guided endonuclease Cas9

              The CRISPR-associated enzyme Cas9 is an RNA-guided endonuclease that uses RNA:DNA base-pairing to target foreign DNA in bacteria. Cas9:guide RNA complexes are also effective genome engineering agents in animals and plants. Here we use single-molecule and bulk biochemical experiments to determine how Cas9:RNA interrogates DNA to find specific cleavage sites. We show that both binding and cleavage of DNA by Cas9:RNA require recognition of a short trinucleotide protospacer adjacent motif (PAM). Non-target DNA binding affinity scales with PAM density, and sequences fully complementary to the guide RNA but lacking a nearby PAM are ignored by Cas9:RNA. DNA strand separation and RNA:DNA heteroduplex formation initiate at the PAM and proceed directionally towards the distal end of the target sequence. Furthermore, PAM interactions trigger Cas9 catalytic activity. These results reveal how Cas9 employs PAM recognition to quickly identify potential target sites while scanning large DNA molecules, and to regulate dsDNA scission.
                Bookmark

                Author and article information

                Contributors
                kslotkin@danforthcenter.org
                Journal
                Nat Plants
                Nat Plants
                Nature Plants
                Nature Publishing Group UK (London )
                2055-0278
                8 November 2021
                8 November 2021
                2021
                : 7
                : 11
                : 1461-1474
                Affiliations
                [1 ]GRID grid.261331.4, ISNI 0000 0001 2285 7943, Department of Molecular Genetics, , The Ohio State University, ; Columbus, OH USA
                [2 ]GRID grid.34424.35, ISNI 0000 0004 0466 6352, Donald Danforth Plant Science Center, ; St. Louis, MO USA
                [3 ]GRID grid.262962.b, ISNI 0000 0004 1936 9342, Bioinformatics and Computational Biology Program, , Saint Louis University, ; St. Louis, MO USA
                [4 ]GRID grid.134936.a, ISNI 0000 0001 2162 3504, Division of Biological Sciences, , University of Missouri, ; Columbia, MO USA
                [5 ]GRID grid.28803.31, ISNI 0000 0001 0701 8607, Present Address: Medical Scientist Training Program, , University of Wisconsin, ; Madison, WI USA
                [6 ]GRID grid.134563.6, ISNI 0000 0001 2168 186X, Present Address: Graduate Program in the School of Plant Sciences, , University of Arizona, ; Tucson, AZ USA
                Author information
                http://orcid.org/0000-0001-5847-0206
                http://orcid.org/0000-0002-8217-472X
                http://orcid.org/0000-0001-9925-8009
                http://orcid.org/0000-0001-9582-3533
                Article
                1008
                10.1038/s41477-021-01008-7
                8592841
                34750500
                a47d471b-63d4-4fa3-9013-6e71779ca71a
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 12 March 2021
                : 9 September 2021
                Funding
                Funded by: FundRef https://doi.org/10.13039/100000001, National Science Foundation (NSF);
                Award ID: MCB-1908521
                Award ID: MCB-1908521
                Award ID: MCB-1908521
                Award ID: MCB-1908521
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s), under exclusive licence to Springer Nature Limited 2021

                transgenic plants,dna methylation,rnai
                transgenic plants, dna methylation, rnai

                Comments

                Comment on this article