TU Darmstadt / ULB / TUbiblio

Developmental Changes in Genome Replication Progression in Pluripotent versus Differentiated Human Cells

Pradhan, Sunil Kumar ; Lozoya, Teresa ; Prorok, Paulina ; Yuan, Yue ; Lehmkuhl, Anne ; Zhang, Peng ; Cardoso, M. Cristina (2024)
Developmental Changes in Genome Replication Progression in Pluripotent versus Differentiated Human Cells.
In: Genes, 2024, 15 (3)
doi: 10.26083/tuprints-00027162
Artikel, Zweitveröffentlichung, Verlagsversion

WarnungEs ist eine neuere Version dieses Eintrags verfügbar.

Kurzbeschreibung (Abstract)

DNA replication is a fundamental process ensuring the maintenance of the genome each time cells divide. This is particularly relevant early in development when cells divide profusely, later giving rise to entire organs. Here, we analyze and compare the genome replication progression in human embryonic stem cells, induced pluripotent stem cells, and differentiated cells. Using single-cell microscopic approaches, we map the spatio-temporal genome replication as a function of chromatin marks/compaction level. Furthermore, we mapped the replication timing of subchromosomal tandem repeat regions and interspersed repeat sequence elements. Albeit the majority of these genomic repeats did not change their replication timing from pluripotent to differentiated cells, we found developmental changes in the replication timing of rDNA repeats. Comparing single-cell super-resolution microscopic data with data from genome-wide sequencing approaches showed comparable numbers of replicons and large overlap in origins numbers and genomic location among developmental states with a generally higher origin variability in pluripotent cells. Using ratiometric analysis of incorporated nucleotides normalized per replisome in single cells, we uncovered differences in fork speed throughout the S phase in pluripotent cells but not in somatic cells. Altogether, our data define similarities and differences on the replication program and characteristics in human cells at different developmental states.

Typ des Eintrags: Artikel
Erschienen: 2024
Autor(en): Pradhan, Sunil Kumar ; Lozoya, Teresa ; Prorok, Paulina ; Yuan, Yue ; Lehmkuhl, Anne ; Zhang, Peng ; Cardoso, M. Cristina
Art des Eintrags: Zweitveröffentlichung
Titel: Developmental Changes in Genome Replication Progression in Pluripotent versus Differentiated Human Cells
Sprache: Englisch
Publikationsjahr: 14 Mai 2024
Ort: Darmstadt
Publikationsdatum der Erstveröffentlichung: 27 Februar 2024
Ort der Erstveröffentlichung: Basel
Verlag: MDPI
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Genes
Jahrgang/Volume einer Zeitschrift: 15
(Heft-)Nummer: 3
Kollation: 26 Seiten
DOI: 10.26083/tuprints-00027162
URL / URN: https://tuprints.ulb.tu-darmstadt.de/27162
Zugehörige Links:
Herkunft: Zweitveröffentlichung DeepGreen
Kurzbeschreibung (Abstract):

DNA replication is a fundamental process ensuring the maintenance of the genome each time cells divide. This is particularly relevant early in development when cells divide profusely, later giving rise to entire organs. Here, we analyze and compare the genome replication progression in human embryonic stem cells, induced pluripotent stem cells, and differentiated cells. Using single-cell microscopic approaches, we map the spatio-temporal genome replication as a function of chromatin marks/compaction level. Furthermore, we mapped the replication timing of subchromosomal tandem repeat regions and interspersed repeat sequence elements. Albeit the majority of these genomic repeats did not change their replication timing from pluripotent to differentiated cells, we found developmental changes in the replication timing of rDNA repeats. Comparing single-cell super-resolution microscopic data with data from genome-wide sequencing approaches showed comparable numbers of replicons and large overlap in origins numbers and genomic location among developmental states with a generally higher origin variability in pluripotent cells. Using ratiometric analysis of incorporated nucleotides normalized per replisome in single cells, we uncovered differences in fork speed throughout the S phase in pluripotent cells but not in somatic cells. Altogether, our data define similarities and differences on the replication program and characteristics in human cells at different developmental states.

Freie Schlagworte: human cells, induced pluripotent stem cells, pluripotent embryonic stem cells, genome replication progression, repli-FISH, rDNA, centromere, chromatin compaction
ID-Nummer: Artikel-ID: 305
Status: Verlagsversion
URN: urn:nbn:de:tuda-tuprints-271629
Zusätzliche Informationen:

This article belongs to the Special Issue Mechanisms and Regulation of Human DNA Replication

Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
Fachbereich(e)/-gebiet(e): 10 Fachbereich Biologie
10 Fachbereich Biologie > Cell Biology and Epigenetics
Hinterlegungsdatum: 14 Mai 2024 13:35
Letzte Änderung: 15 Mai 2024 05:20
PPN:
Export:
Suche nach Titel in: TUfind oder in Google

Verfügbare Versionen dieses Eintrags

Frage zum Eintrag Frage zum Eintrag

Optionen (nur für Redakteure)
Redaktionelle Details anzeigen Redaktionelle Details anzeigen