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Series GSE271478 Query DataSets for GSE271478
Status Public on Jul 08, 2024
Title Developmental signals control chromosome segregation fidelity during early lineage specification and neurogenesis by modulating replicative stress
Organism Homo sapiens
Experiment type Other
Summary Human development and homeostasis rely on the correct replication, maintenance and segregation of our genetic blueprints. How these intracellular processes are monitored across different human cellular lineages, and why the spatio-temporal distribution of mosaicism varies during development remain unknown. Using human and mouse pluripotent stem cells, we identify that several lineage specification signals –including WNT, BMP and FGF– converge into the modulation of DNA replication stress and damage during S-phase, which in turn controls spindle dynamics and chromosome segregation fidelity in mitosis. We show that patterning signals associated with anteriorisation during mammalian gastrulation increase chromosome missegregation, while the posteriorising signals WNT and BMP protect pluripotent stem cells from excessive origin firing, DNA damage and chromosome missegregation derived from stalled forks. Through epistasis experiments, we find that WNT, BMP and FGF have distinct roles during DNA replication, and demonstrate that WNT/GSK3 signalling sits at the helm of this regulatory cascade. Cell signalling control of chromosome segregation declines after pluripotency exit and specification into the three human germ layers, but re-emerges in differentiating neural progenitors. Through ex vivo and in vivo analyses, we also show that FGF and WNT signalling display opposite roles in chromosome segregation fidelity in mouse neural progenitors during the onset of neurogenesis (E14.5), but not during their expansion (E12.5). In particular, we find that the neurogenic factor FGF2 induces DNA replication stress-mediated chromosome missegregation, which could provide a rationale for the elevated chromosomal mosaicism of the developing brain. Our results highlight a role for patterning signals and cellular identity in genome maintenance that contributes to somatic mosaicism during mouse and human early lineage specification and neurogenesis.
 
Overall design hiPSC were treated with DMSO, Aphidicolin (200nM) or DKK1 (250ng/ml) for 3hrs prior to double pulse EdU labeling, single cells were sorted and subjected to scEdU-seq (van den Berg, et al., Nature Methods,2024
 
Contributor(s) van den Berg J, De Jaime-Soguero A, Acebrón S
Citation(s) 39191776
Submission date Jul 04, 2024
Last update date Sep 30, 2024
Contact name Jeroen van den Berg
E-mail(s) jervdberg@gmail.com
Phone +31610597913
Organization name Hubrecht Institute
Lab van Oudenaarden lab
Street address Uppsalalaan 8
City Utrecht
State/province Utrecht
ZIP/Postal code 3584 CT
Country Netherlands
 
Platforms (1)
GPL30173 NextSeq 2000 (Homo sapiens)
Samples (12)
GSM8377755 DMSO treated hIPSC labeled with double pulse of EdU plate 1
GSM8377756 DMSO treated hIPSC labeled with double pulse of EdU plate 2
GSM8377757 DMSO treated hIPSC labeled with double pulse of EdU plate 3
Relations
BioProject PRJNA1131787

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Supplementary file Size Download File type/resource
GSE271478_RAW.tar 291.3 Mb (http)(custom) TAR (of TSV)
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Raw data are available in SRA

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