Repair at Single Targeted DNA Double-Strand Breaks in Pluripotent and Differentiated Human Cells
2011

Repair of DNA Breaks in Human Stem Cells

Sample size: 194 publication 10 minutes Evidence: high

Author Information

Author(s): Fung Hua Weinstock, David M. Weinstock, Marinus Martin G.

Primary Institution: Dana-Farber Cancer Institute, Harvard Medical School

Hypothesis

Differences in ex vivo cell culture conditions can drastically affect stem cell physiology and the precision of DNA repair.

Conclusion

The study shows that the efficiency and precision of DNA repair at a single double-strand break differ significantly between human embryonic stem cells and somatic cells, with differentiation into astrocytes reducing both.

Supporting Evidence

  • The frequency of homologous recombination at a single DNA double-strand break differs up to 20-fold between isogenic human embryonic stem cells based on the site of the break.
  • Repair at a targeted double-strand break is highly precise in human embryonic stem cells compared to somatic cells.
  • Differentiation of human embryonic stem cells into astrocytes reduces both the efficiency and precision of DNA repair.

Takeaway

This study found that how well stem cells fix broken DNA can change a lot depending on how they are grown and what type of cells they become.

Methodology

The study used a targeted DNA repair reporter system to analyze the effects of various conditions on the repair of a single DNA double-strand break in human embryonic stem cells and differentiated cells.

Limitations

The study primarily focused on specific cell lines and conditions, which may not represent all human stem cells or their responses to DNA damage.

Participant Demographics

Human embryonic stem cells and somatic human cell lines were used in the study.

Statistical Information

P-Value

p<0.01

Statistical Significance

p<0.01

Digital Object Identifier (DOI)

10.1371/journal.pone.0020514

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