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FVE directly enriches to RdDM target loci.

ABSTRACT: FVE directly enriches to RdDM target loci.

PROVIDER: PRJNA720941 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR14199890_1.fastq.gz	Fastqsanger.gz
	SRR14199890_2.fastq.gz	Fastqsanger.gz
	SRR14199891_1.fastq.gz	Fastqsanger.gz
	SRR14199891_2.fastq.gz	Fastqsanger.gz
	SRR14199892_1.fastq.gz	Fastqsanger.gz

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FVE directly enriches to RdDM target loci.

Project description:Using ChIP-seq to study the deposition of FVE on the chromatin

2021-04-10 | GSE171808 | GEO

FVE regulates DNA methylation levels at a subset of RdDM loci.

Project description:Using BS-Seq to provide single-base resolution of DNA methylation status in Col-0 WT, nrpd1-3, nrpe1-11 and fve-4.

2021-04-10 | GSE171805 | GEO

FVE regulates DNA methylation levels at a subset of RdDM loci.

Project description:FVE regulates DNA methylation levels at a subset of RdDM loci.

| PRJNA720939 | ENA

FVE promotes RNA-directed DNA methylation by facilitating the association of RNA polymerase V with chromatin [ChIP-seq]

Project description:DNA methylation can be established by RNA-directed DNA methylation (RdDM) in plants. The association of RNA polymerase V (Pol V) with chromatin is a critical step for RdDM. While the SRA-domain-containing proteins SUVH2 and SUVH9 and the DDR complex are known to be required for the association of Pol V with chromatin, it is unknown whether the association of Pol V with chromatin requires other unidentified regulators. Here we found that SUVH9 is able to interact with a conserved histone-interaction protein, FVE, and a previously uncharacterized RRM domain-containing protein, which we named RRM1. We demonstrated that FVE facilitates the association of Pol V with chromatin and thus contributes to DNA methylation at a substantial subset of RdDM target loci, while RRM1 is only slightly involved in RdDM. FVE-dependent RdDM target loci are more abundant in gene-rich chromosome arms than FVE-independent RdDM target loci. FVE was previously shown to be a shared subunit of the RPD3-type histone deacetylase complex and the polycomb-type histone H3K27 trimethyltransferase complex, both of which are involved in transcriptional repression. This study reveals a previously uncharacterized role of FVE in RdDM and suggests that FVE may coordinate RdDM, histone deacetylation, and H3K27 trimethylation, thus ensuring transcriptional silencing of TEs in gene-rich chromosome arms to protect genes from harmful effects of potentially transcribed TEs.

2021-06-12 | GSE169179 | GEO

FVE promotes RNA-directed DNA methylation by facilitating the association of RNA polymerase V with chromatin [Bisulfite-seq]

2021-06-12 | GSE169178 | GEO

FVE promotes RNA-directed DNA methylation by facilitating the association of RNA polymerase V with chromatin [RNA-seq]

2021-06-12 | GSE169174 | GEO

FVE promotes RNA-directed DNA methylation by facilitating the association of RNA polymerase V with chromatin [H3K27me3 ChIP-Seq].

2021-06-01 | GSE173630 | GEO

FVE affects 24-nt siRNA accumulation downstream of RdDM pathway

Project description:FVE affects 24-nt siRNA accumulation downstream of RdDM pathway

| PRJNA720952 | ENA

FVE affects 24-nt siRNA accumulation downstream of RdDM pathway

Project description:Using siRNA-Seq to provide siRNA accumulation status in fve mutant.

2021-04-10 | GSE171813 | GEO

The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation.

Project description:MOM1 is an Arabidopsis factor previously shown to mediate transcriptional silencing independent of major DNA methylation changes. Here we found that MOM1 localizes with sites of RNA-directed DNA methylation (RdDM). Tethering MOM1 with artificial zinc finger to unmethylated FWA promoter led to establishment of DNA methylation and FWA silencing. This process was blocked by mutations in components of the Pol V arm of the RdDM machinery, as well as by mutation of MORC6. We found that at some endogenous RdDM sites, MOM1 is required to maintain DNA methylation and a closed chromatin state. In addition, efficient silencing of newly introduced FWA transgenes was impaired by mutation of MOM1 or mutation of genes encoding the MOM1 interacting PIAL1/2 proteins. In addition to RdDM sites, we identified a group of MOM1 peaks at active chromatin near genes that colocalized with MORC6. These findings demonstrate a multifaceted role of MOM1 in genome regulation.

2023-06-10 | PXD039991 | Pride

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