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Lgr5+ intestinal stem cells reside in an unlicensed G1 phase.


ABSTRACT: During late mitosis and the early G1 phase, the origins of replication are licensed by binding to double hexamers of MCM2-7. In this study, we investigated how licensing and proliferative commitment are coupled in the epithelium of the small intestine. We developed a method for identifying cells in intact tissue containing DNA-bound MCM2-7. Interphase cells above the transit-amplifying compartment had no DNA-bound MCM2-7, but still expressed the MCM2-7 protein, suggesting that licensing is inhibited immediately upon differentiation. Strikingly, we found most proliferative Lgr5+ stem cells are in an unlicensed state. This suggests that the elongated cell-cycle of intestinal stem cells is caused by an increased G1 length, characterized by dormant periods with unlicensed origins. Significantly, the unlicensed state is lost in Apc-mutant epithelium, which lacks a functional restriction point, causing licensing immediately upon G1 entry. We propose that the unlicensed G1 phase of intestinal stem cells creates a temporal window when proliferative fate decisions can be made.

SUBMITTER: Carroll TD 

PROVIDER: S-EPMC5940300 | biostudies-other | 2018 May

REPOSITORIES: biostudies-other

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Lgr5<sup>+</sup> intestinal stem cells reside in an unlicensed G<sub>1</sub> phase.

Carroll Thomas D TD   Newton Ian P IP   Chen Yu Y   Blow J Julian JJ   Näthke Inke I  

The Journal of cell biology 20180329 5


During late mitosis and the early G<sub>1</sub> phase, the origins of replication are licensed by binding to double hexamers of MCM2-7. In this study, we investigated how licensing and proliferative commitment are coupled in the epithelium of the small intestine. We developed a method for identifying cells in intact tissue containing DNA-bound MCM2-7. Interphase cells above the transit-amplifying compartment had no DNA-bound MCM2-7, but still expressed the MCM2-7 protein, suggesting that licensi  ...[more]

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