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Status |
Public on Apr 21, 2020 |
Title |
Genomewide nucleotide-resolution mapping of single-strand breaks and lesions by GLOE-Seq [Human_Ligase_inactivation] |
Organism |
Homo sapiens |
Experiment type |
Other
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Summary |
Numerous methods are available for the mapping of DNA lesions ranging from double-strand breaks (DSBs) to incorporated ribonucleotides. We now present a technology based on the Genomewide Ligation of 3’-OH Ends (GLOE-Seq) and an associated computational pipeline designed for single-stranded breaks (SSBs), but versatile enough to be applied to any lesion that is convertible into a free 3’-OH terminus. We demonstrate its applicability to the mapping of Okazaki fragments without prior size selection and detect biases and asymmetries in the distribution of spontaneous SSBs in budding yeast and human DNA.
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Overall design |
V. Analysis of Okazaki fragments and global DNA single-strand breaks in human cells DNA ligase-competent and -compromised HCT116 cells were subjected to GLOE-Seq analysis in two replicates each. Ligase-competent cells were used to map the genomewide distribution of DNA single-strand breaks. Cells with inactivated DNA Ligase 1 and 3 were used to map the distribution of Okazaki fragments.
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Contributor(s) |
Sriramachandran AM, Petrosino G, Méndez-Lago M, Schäfer A, Batista-Nascimento LS, Zilio N, Ulrich HD |
Citation(s) |
32320643 |
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Submission date |
Jul 12, 2019 |
Last update date |
Jun 16, 2020 |
Contact name |
Helle Ulrich |
E-mail(s) |
h.ulrich@imb-mainz.de
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Organization name |
Institute of Molecular Biology
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Street address |
Ackermannweg 4
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City |
Mainz |
State/province |
Germany |
ZIP/Postal code |
55128 |
Country |
Germany |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE134225 |
Genome-wide nucleotide-resolution mapping of DNA replication patterns, single-strand breaks and lesions by GLOE-Seq |
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Relations |
BioProject |
PRJNA554350 |
SRA |
SRP214484 |