Increased levels of lagging strand polymerase α in an adult stem cell lineage affect replication-coupled histone incorporation

Stem cells display asymmetric histone inheritance, while nonstem progenitor cells exhibit symmetric patterns in the <i>Drosophila</i> male germ line. Here, we report that components involved in lagging strand synthesis, DNA polymerases α and δ, have substantially reduced levels in stem cells compared to progenitor cells, and this promotes local asymmetry of parental histone incorporation at the replication fork. Compromising Polα genetically induces the local replication-coupled histone incorporation pattern in progenitor cells to resemble that in stem cells, seen by both nuclear localization patterns and chromatin fibers. This is recapitulated using a Polα inhibitor in a concentration-dependent manner. The local old versus new histone asymmetry is comparable between stem cells and progenitor cells at both S phase and M phase. Together, these results indicate that developmentally programmed expression of key DNA replication components is important to shape stem cell chromatin. Furthermore, manipulating one crucial DNA replication component can induce replication-coupled histone dynamics in nonstem cells to resemble those in stem cells.

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Journal
Science Advances
Published
2025-02-28
DOI
https://doi.org/10.1126/sciadv.adu6799
Citations
1
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.81
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article

Increased levels of lagging strand polymerase α in an adult stem cell lineage affect replication-coupled histone incorporation

Brendon E. M. Davis, Joshua Blundon, Xin Chen, Simon Barton et al.
1 citations
Science Advances
Genomics and Chromatin Dynamics
0.81
article

Increased levels of lagging strand polymerase α in an adult stem cell lineage affect replication-coupled histone incorporation

Brendon E. M. Davis, Joshua Blundon, Xin Chen, Simon Barton, Matthew Wooten, Jonathan C. Snedeker, Rajesh Ranjan
article en
1 citations

Abstract

Stem cells display asymmetric histone inheritance, while nonstem progenitor cells exhibit symmetric patterns in the <i>Drosophila</i> male germ line. Here, we report that components involved in lagging strand synthesis, DNA polymerases α and δ, have substantially reduced levels in stem cells compared to progenitor cells, and this promotes local asymmetry of parental histone incorporation at the replication fork. Compromising Polα genetically induces the local replication-coupled histone incorporation pattern in progenitor cells to resemble that in stem cells, seen by both nuclear localization patterns and chromatin fibers. This is recapitulated using a Polα inhibitor in a concentration-dependent manner. The local old versus new histone asymmetry is comparable between stem cells and progenitor cells at both S phase and M phase. Together, these results indicate that developmentally programmed expression of key DNA replication components is important to shape stem cell chromatin. Furthermore, manipulating one crucial DNA replication component can induce replication-coupled histone dynamics in nonstem cells to resemble those in stem cells.

Science AdvancesVol. 11(9)
Howard Hughes Medical Institute (US), Johns Hopkins University (US)
Openalex Percentile: Top 31%
Genomics and Chromatin Dynamics
0.81
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Increased levels of lagging strand polymerase α in an adult stem cell lineage affect replication-coupled histone incorporation — Brendon E. M. Davis, Joshua Blundon, et al. · Science Advances (2025) | TGRS Research Map | TGRS