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Status |
Public on Jul 01, 2016 |
Title |
Replication timing of control and suv4-20h (KO and inducible mutant) cells |
Platform organism |
Homo sapiens |
Sample organism |
Mus musculus |
Experiment type |
Genome variation profiling by genome tiling array
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Summary |
Although histone modifications have been implicated in many DNA-dependent processes, their precise role in DNA replication remains poorly understood. Here, we show that the regulation of histone H4-K20 methylation states, in particular for the trimethylation, is a critical determinant of licensing and time activation of replication origins in mammalian cells.
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Overall design |
WT cells versus suv4-20h KO cells, and non-induced cells versus induced cells
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Contributor(s) |
Brustel J, Dulev S, Kirstein N, Izard F, Grimaud C, Cayrou C, Schotta G, Mechali M, Baldacci G, Sardet C, Batada NN, Cadoret J, Schepers A, Julien E |
Citation(s) |
28778956 |
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Submission date |
May 20, 2015 |
Last update date |
Jun 05, 2019 |
Contact name |
Jean-Charles Cadoret |
E-mail(s) |
jean-charles.cadoret@ijm.fr
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Organization name |
CNRS/ Université de Paris
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Street address |
15 rue hélène Brion
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City |
Paris |
ZIP/Postal code |
75013 |
Country |
France |
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Platforms (1) |
GPL10123 |
Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Feature Number version) |
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Samples (4)
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GSM1692640 |
induced suv4-20h mutant replication timing |
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This SubSeries is part of SuperSeries: |
GSE69085 |
Degree of H4-K20me defines distinct subsets of replication origins in active and silent chromatin domains of mammalian cells |
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Relations |
BioProject |
PRJNA284498 |