U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX1609647: GSM2078417: RNAseq round 2 atmorc4/6/7 rep 3; Arabidopsis thaliana; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 7.4M spots, 379.3M bases, 211.8Mb 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: RNAseq round 2 atmorc4/6/7 rep 3
SAMN04528867 • SRS1319100 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: TRIzol (#15596018) For each library, 2ug of total RNA from a TRIzol extraction of 2-3 leaves from an individual plant was DNase treated (Ambion TURBO DNase AM2238) then depleted for ribosomal RNA using Epicentre RiboZero (MRZPL1224), and strand specific libraries were generated using Epicentre ScriptSeqv2 (SSV21124) according to manufacturers instructions. Round 1 (R1) and Round 2 (R2) were each multiplexed and sequenced on a single lane.
Experiment attributes:
GEO Accession: GSM2078417
Links:
Runs: 1 run, 7.4M spots, 379.3M bases, 211.8Mb
Run# of Spots# of BasesSizePublished
SRR31998107,437,764379.3M211.8Mb2016-05-11

ID:
2301905

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...