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Series GSE169070 Query DataSets for GSE169070
Status Public on Mar 01, 2023
Title GwEEP - A comprehensive approach for the profiling of DNA modifying enzymes
Organism Mus musculus
Experiment type Methylation profiling by high throughput sequencing
Summary A precise understanding of DNA methylation dynamics on a genome wide scale is of great importance for the comprehensive investigation of a variety of biological processes such as reprogramming of somatic cells to iPSCs, cell differentiation and also cancer development. To date, a complex integration of multiple and distinct genome wide data sets is required to derive the global activity of DNA modifying enzymes.
We present GwEEP - Genome-wide Epigenetic Efficiency Profiling as a versatile approach to infer dynamic efficiency changes of DNA modifying enzymes at base pair resolution on a genome wide scale. GwEEP relies on genome wide oxidative Hairpin Bisulfite sequencing (HPoxBS) data sets, which are translated by a sophisticated hidden Markov model into quantitative enzyme efficiencies with reported confidence around the estimates. GwEEP in its present form predicts de novo and maintenance methylation efficiencies of Dnmts, as well as the hydroxylation efficiency of Tets but its purposefully flexible design allows to capture further oxidation processes such as formylation and carboxylation given available data in the future.
Applied to a well characterized ES cell model, GwEEP precisely predicts the complex epigenetic changes following a Serum-to-2i shift i.e., (i) instant reduction in maintenance efficiency (ii) gradually decreasing de novo methylation efficiency and (iii) increasing Tet efficiencies. In addition, a complementary analysis of Tet triple knock-out ES cells confirms the previous hypothesized mutual interference of Dnmts and Tets. GwEEP is applicable to a wide range of biological samples including cell lines, but also tissues and primary cell types.

 
Overall design In total we generated eight hairpin libraries (BS and oxBS, respectively) for WT ES cells at three distinct time points - Serum/Lif(d0), 2i 72h (d3) and 2i 144h (d6); four libraries for TetTKO cells (BS only) - Serum/LIF, 2i 48h (d2), 2i 96h (d4) and 168h (d7), as well as two low-input libraries for WT ES cells 72h 2i (BS and oxBS).
 
Contributor(s) Kyriakopoulos C, Nordström K, Kramer P, Gottfreund J, Salhab A, Arand J, Müller F, von Meyenn F, Ficz G, Reik W, Wolf V, Walter J, Giehr P
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Submission date Mar 17, 2021
Last update date Mar 04, 2023
Contact name Jörn Walter
E-mail(s) j.walter@mx.uni-saarland.de
Phone +496813022425
Organization name Saarland University
Department Genetics and Epigenetics
Street address Campus A2.4
City Saarbrücken
State/province Saarland
ZIP/Postal code 66123
Country Germany
 
Platforms (2)
GPL16417 Illumina MiSeq (Mus musculus)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
Samples (12)
GSM5176043 WT-Serum-BS
GSM5176044 WT-Serum-oxBS
GSM5176045 WT-72h-2i-BS
Relations
BioProject PRJNA715106
SRA SRP311034

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE169070_RAW.tar 347.6 Mb (http)(custom) TAR (of TXT)
GSE169070_Tet_TKO_Enzyme_Efficiencies.igv.gz 380.5 Mb (ftp)(http) IGV
GSE169070_WT_Enzyme_Efficiencies.igv.gz 504.5 Mb (ftp)(http) IGV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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