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SRX3312758: GSM2828148: Wild type 18 DAP embryo BS-seq,rep2; Zea mays; Bisulfite-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 113.6M spots, 28.4G bases, 9.4Gb downloads

Submitted by: NCBI (GEO)
Study: Decrease in DNA methylation 1(DDM1) is required for the establishement of CHH islands in maize
show Abstracthide Abstract
DNA methylation plays a crucial role in suppressing mobilization of transposable elements and regulation of gene expression. A number of studies have indicated that DNA methylation pathways and patterns exhibit distinct properties in different species, including Arabidopsis, rice, and maize. Here, we characterized the function of DDM1 in regulating genome-wide DNA methylation in maize. Two homologs of ZmDDM1 are abundantly expressed in the embryo and their simultaneous disruption caused embryo lethality with abnormalities in cell proliferation from the early stage of kernel development. We establish that ZmDDM1 is critical for DNA methylation, at CHG sites, and to a lesser extent at CG sites, in heterochromatic regions, and unexpectedly, it is required for the formation of m CHH islands. In addition, ZmDDM1 is indispensable for the presence of 24-nt siRNA, suggesting its involvement in the RdDM pathway. Our results provide novel insight into the role of ZmDDM1 in regulating the formation of m CHH islands, via the RdDM pathway maize, suggesting that, in comparison to Arabidopsis, maize may have adopted distinct mechanisms for regulating m CHH. Overall design: Characterize the function of chromatin remodeling factor DDM1 on DNA methylation in zea mays
Sample: Wild type 18 DAP embryo BS-seq,rep2
SAMN07822310 • SRS2618714 • All experiments • All runs
Organism: Zea mays
Library:
Instrument: Illumina HiSeq 2500
Strategy: Bisulfite-Seq
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Genomic DNA was extracted using CTAB method. 10 ug of genomic DNA was sheared to fragments between 300 and 500 bp. The fragments were subject to end repair, dA tailing, and ligating to methylated adapters, followed by bisulfate conversion.The bisulfate converted library were then PCR amplified (13 cycle) and purified, and sequenced on Illumina Hiseq 2500 platform.
Experiment attributes:
GEO Accession: GSM2828148
Links:
Runs: 1 run, 113.6M spots, 28.4G bases, 9.4Gb
Run# of Spots# of BasesSizePublished
SRR6202836113,572,61028.4G9.4Gb2017-10-30

ID:
4640667

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