TY - JOUR
T1 - Toward stem cell systems biology: From molecules to networks and landscapes
AU - MacArthur, B. D.
AU - Ma'ayan, A.
AU - Lemischka, I. R.
N1 - P50 GM071558-01A20007, NIGMS NIH HHS, United StatesP50 GM071558-020007, NIGMS NIH HHS, United StatesP50 GM071558-030007, NIGMS NIH HHS, United StatesR01 GM078465-02, NIGMS NIH HHS, United States
PY - 2008
Y1 - 2008
N2 - The last few years have seen significant advances in our understanding of the molecular mechanisms of stem-cell-fate specification. Newand emerging high-throughput techniques, aswell as increasingly accurate loss-of-function perturbation techniques, are allowing us to dissect the interplay among genetic, epigenetic, proteomic, and signaling mechanisms in stem-cell-fate determination with ever-increasing fidelity (Boyer et al. 2005, 2006; Ivanova et al. 2006; Loh et al. 2006; Cole et al. 2008; Jiang et al. 2008; Johnson et al. 2008; Kim et al. 2008; Liu et al. 2008; Marson et al. 2008; Mathur et al. 2008). Taken together, recent reports using these new techniques demonstrate that stem-cell-fate specification is an extremely complex process, regulated by multiple mutually interacting molecular mechanisms involving multiple regulatory feedback loops. Given this complexity and the sensitive dependence of stem cell differentiation on signaling cues from the extracellular environment, how are we best to develop a coherent quantitative understanding of stem cell fate at the systems level? One approach that we and other researchers have begun to investigate is the application of techniques derived in the computational disciplines (mathematics, physics, computer science, etc.) to problems in stemcell biology. Here, we briefly sketch a few pertinent results fromthe literature in this area and discuss future potential applications of computational techniques to stem cell systems biology. ©2008 Cold Spring Harbor Laboratory Press.
AB - The last few years have seen significant advances in our understanding of the molecular mechanisms of stem-cell-fate specification. Newand emerging high-throughput techniques, aswell as increasingly accurate loss-of-function perturbation techniques, are allowing us to dissect the interplay among genetic, epigenetic, proteomic, and signaling mechanisms in stem-cell-fate determination with ever-increasing fidelity (Boyer et al. 2005, 2006; Ivanova et al. 2006; Loh et al. 2006; Cole et al. 2008; Jiang et al. 2008; Johnson et al. 2008; Kim et al. 2008; Liu et al. 2008; Marson et al. 2008; Mathur et al. 2008). Taken together, recent reports using these new techniques demonstrate that stem-cell-fate specification is an extremely complex process, regulated by multiple mutually interacting molecular mechanisms involving multiple regulatory feedback loops. Given this complexity and the sensitive dependence of stem cell differentiation on signaling cues from the extracellular environment, how are we best to develop a coherent quantitative understanding of stem cell fate at the systems level? One approach that we and other researchers have begun to investigate is the application of techniques derived in the computational disciplines (mathematics, physics, computer science, etc.) to problems in stemcell biology. Here, we briefly sketch a few pertinent results fromthe literature in this area and discuss future potential applications of computational techniques to stem cell systems biology. ©2008 Cold Spring Harbor Laboratory Press.
U2 - 10.1101/sqb.2008.73.061
DO - 10.1101/sqb.2008.73.061
M3 - Article
C2 - 19329576
VL - 73
SP - 211
EP - 215
JO - Cold Spring Harbor Symposia on Quantitative Biology
JF - Cold Spring Harbor Symposia on Quantitative Biology
ER -