Background: Stem cells are thought to play a critical role in minimizing the accumulation of mutations, but it is not
\nclear which strategies they follow to fulfill that performance objective. Slow cycling of stem cells provides a simple
\nstrategy that can minimize cell pedigree depth and thereby minimize the accumulation of replication-dependent
\nmutations. Although the power of this strategy was recognized early on, a quantitative assessment of whether and
\nhow it is employed by biological systems is missing.<\/p>\n
Results: Here we address this problem using a simple self-renewing organ \u2013 the C. elegans gonad \u2013 whose overall
\norganization is shared with many self-renewing organs. Computational simulations of mutation accumulation
\ncharacterize a tradeoff between fast development and low mutation accumulation, and show that slow-cycling stem
\ncells allow for an advantageous compromise to be reached. This compromise is such that worm germ-line stem cells
\nshould cycle more slowly than their differentiating counterparts, but only by a modest amount. Experimental
\nmeasurements of cell cycle lengths derived using a new, quantitative technique are consistent with these predictions.<\/p>\n
Conclusions: Our findings shed light both on design principles that underlie the role of stem cells in delaying aging
\nand on evolutionary forces that shape stem-cell gene regulatory networks.<\/p>\n","protected":false},"excerpt":{"rendered":"
Background: Stem cells are thought to play a critical role in minimizing the accumulation of mutations, but it is not clear which strategies they follow to fulfill that performance objective. Slow cycling of stem cells provides a simple strategy that can minimize cell pedigree depth and thereby minimize the accumulation of replication-dependent mutations. 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