DNA damage triggers reprogramming of differentiated cells into stem cells in Physcomitrella
DNA damage can result from intrinsic cellular processes and from exposure to stressful environments. Such DNA damage generally threatens genome integrity and cell viability 1 . However, here we report that the transient induction of DNA strand breaks (single-strand breaks, double-strand breaks or bo...
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Veröffentlicht in: | Nature plants 2020-09, Vol.6 (9), p.1098-1105 |
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Zusammenfassung: | DNA damage can result from intrinsic cellular processes and from exposure to stressful environments. Such DNA damage generally threatens genome integrity and cell viability
1
. However, here we report that the transient induction of DNA strand breaks (single-strand breaks, double-strand breaks or both) in the moss
Physcomitrella patens
can trigger the reprogramming of differentiated leaf cells into stem cells without cell death. After intact leafy shoots (gametophores) were exposed to zeocin, an inducer of DNA strand breaks, the
STEM
CELL-
IN
DUCING FACTOR 1
(
STEMIN1
)
2
promoter was activated in some leaf cells. These cells subsequently initiated tip growth and underwent asymmetric cell divisions to form chloronema apical stem cells, which are in an earlier phase of the life cycle than leaf cells and have the ability to form new gametophores. This DNA-strand-break-induced reprogramming required the DNA damage sensor ATR kinase, but not ATM kinase, together with STEMIN1 and closely related proteins. ATR was also indispensable for the induction of
STEMIN1
by DNA strand breaks. Our findings indicate that DNA strand breaks, which are usually considered to pose a severe threat to cells, trigger cellular reprogramming towards stem cells via the activity of ATR and STEMINs.
This study reports that DNA strand breaks trigger the reprogramming of differentiated leaf cells into stem cells without cell death in
Physcomitrella
, which requires the DNA damage sensor ATR kinase and the STEM-CELL INDUCING FACTORs (STEMINs). |
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ISSN: | 2055-026X 2055-0278 2055-0278 |
DOI: | 10.1038/s41477-020-0745-9 |