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dc.contributor.authorPabba, Maruthi Kumar
dc.contributor.authorRitter, Christian
dc.contributor.authorChagin, Vadim
dc.contributor.authorStear, Jeffrey
dc.contributor.authorLoerke, Dinah
dc.contributor.authorProrok, Paulina
dc.contributor.authorSchmid, Alice Kristin
dc.contributor.authorLeonhardt, Heinrich
dc.contributor.authorRohr, Karl
dc.contributor.authorCardoso, Cristina
dc.contributor.authorKolobynina, Ksenia
dc.contributor.authorCelikay, Kerem
dc.contributor.authorKolobynina, Ksenia
dc.date.accessioned2023-07-07T11:56:08Z
dc.date.available2022-05-11T07:21:00Z
dc.date.available2023-07-07T11:56:08Z
dc.date.issued2022
dc.identifier.urihttps://tudatalib.ulb.tu-darmstadt.de/handle/tudatalib/3462.2
dc.descriptionChromatin has been shown to undergo diffusional motion, and during active gene transcription the RNA polymerase activity negatively affects chromatin motion. However, the relationship between chromatin motion and other genomic processes remains unclear. Hence, we set out to label the DNA directly in a sequence unbiased manner and recorded labeled chromatin dynamics in interphase human cells expressing GFP-tagged PCNA, a cell cycle marker and core component of the replication machinery. We detected decreased chromatin mobility during S-phase compared to G1 and G2 phases using automated particle tracking. To gain insight into the organization and dynamics of the genome during DNA replication, we analyzed labeled chromatin domain size and motion in replicating cells. By correlating chromatin mobility with proximity to sites of active DNA synthesis, we show that chromatin motion is locally constrained at the sites of DNA replication. Furthermore, inhibiting DNA synthesis activity leads to increase loading of DNA polymerases and further restricts local chromatin motion. The polymerases under stress no longer reel DNA through, as they normally do during DNA synthesis, which may explain the further restriction of chromatin motion and the fact that loading the helicase/polymerase already restricts it during active DNA synthesis. We, therefore, propose that increased polymerase loading but not their catalytic activity reduces genome dynamics and its accessibility and interaction with other genomic regions.de_DE
dc.language.isoende_DE
dc.rightsCreative Commons Attribution-NonCommercial 4.0
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subjectAphidicolinde_DE
dc.subjectcell cyclede_DE
dc.subjectchromatin trackingde_DE
dc.subjectdiffusionde_DE
dc.subjectDNA labelingde_DE
dc.subjectDNA replicationde_DE
dc.subjectgenome architecturede_DE
dc.subjecthydroxyureade_DE
dc.subjectmean square displacementde_DE
dc.subjectS-phasede_DE
dc.subject.classification201-03 Zellbiologiede_DE
dc.subject.ddc570
dc.titleReplisome loading reduces chromatin motion independent of DNA synthesisde_DE
dc.typeSoftwarede_DE
dc.typeImagede_DE
dc.description.versionPrepublication with Access for Reviewerde_DE
tud.projectDFG | SFB1361,TP06 | TP_06_Cardoso_Mainzde_DE
tud.projectDFG | CA198/9-2 | Hochauflösende Analyde_DE
tud.projectDFG | CA198/15-1 | Regulation der Säugede_DE
tud.unitTUDa


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Creative Commons Attribution-NonCommercial 4.0
Solange nicht anders angezeigt, wird die Lizenz wie folgt beschrieben: Creative Commons Attribution-NonCommercial 4.0
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