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SRX1609652: GSM2078422: BSseq wt rep 2; Arabidopsis thaliana; Bisulfite-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 116M spots, 5.9G bases, 4.5Gb downloads

Submitted by: NCBI (GEO)
Study: Arabidopsis AtMORC4 and AtMORC7 form Nuclear Bodies and Repress a Large Number of Protein-Coding Genes
show Abstracthide Abstract
The MORC family of GHKL ATPases are an enigmatic class of proteins with diverse chromatin related functions. In Arabidopsis, AtMORC1, AtMORC2, and AtMORC6 act together in heterodimeric complexes to mediate transcriptional silencing of methylated DNA elements. Here, we studied Arabidopsis AtMORC4 and AtMORC7. We found that, in contrast to AtMORC1,2,6, they act to suppress a wide set of non-methylated protein-coding genes that are enriched for those involved in pathogen response. Furthermore, atmorc4 atmorc7 double mutants show a pathogen response phenotype. We found that AtMORC4 and AtMORC7 form homomeric complexes in vivo and are concentrated in discrete nuclear bodies adjacent to chromocenters. Analysis of an atmorc1,2,4,5,6,7 hextuple mutant demonstrates that transcriptional de-repression is largely uncoupled from changes in DNA methylation in plants devoid of MORC function. However, we also uncover a requirement for MORC in both DNA methylation and silencing at a small but distinct subset of RNA-directed DNA methylation target loci. These regions are characterized by poised transcriptional potential and a low density of sites for symmetric cytosine methylation. These results provide insights into the biological function of MORC proteins in higher eukaryotes. Overall design: This dataset includes: 6 BS-seq and 26 RNA-seq datasets
Sample: BSseq wt rep 2
SAMN04528874 • SRS1319105 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: Bisulfite-Seq
Source: GENOMIC
Selection: RANDOM
Layout: SINGLE
Construction protocol: Qiagen DNeasy Plant Mini kit (#69106) For each library, 500ng of genomic DNA from a Qiagen DNeasy Plant Mini kit (#69106) extraction from 2-3 leaves of an individual plant was fragmented with a Covaris S2 instrument, end repaired using KAPA hyper prep kit (#KK8502), bisulphite converted using EZ DNA methylation lightning kit (#D5030)Kit, and amplified during 13 PCR cycles using MyTaq DNA polymerase (Bioline) and Illumina TruSeq PCR primers. The 6 BSseq libraries were multiplexed and sequenced on three lanes.
Experiment attributes:
GEO Accession: GSM2078422
Links:
Runs: 1 run, 116M spots, 5.9G bases, 4.5Gb
Run# of Spots# of BasesSizePublished
SRR3199815115,971,2835.9G4.5Gb2016-05-11

ID:
2301910

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