Transcription Factor Competition Allows Embryonic Stem Cells to Distinguish Authentic Signals from Noise
Abstract
Stem cells occupy variable environments where they must distinguish stochastic fluctuations from developmental cues. Here, we use optogenetics to investigate how the pluripotency network in embryonic stem cells (ESCs) achieves a robust response to differentiation cues but not to gene expression fluctuations. We engineered mouse ESCs to allow quantitative control over the endogenous mechanism of neural differentiation through a light-inducible Brn2 transgene and monitored differentiation status through a genome-integrated Nanog-GFP reporter. By exposing cells to pulses of Brn2, we find that the pluripotency network rejects Brn2 inputs that are below specific magnitude or duration thresholds, but allows rapid differentiation when both thresholds are satisfied. The filtering properties of the network arise through its positive feedback architecture and the intrinsic half-life of Nanog, which determines the duration threshold in the network. Together our results suggest that the dynamic properties of positive feedback networks might determine how inputs are classified as signal or noise by stem cells.
Additional Information
© 2015 Elsevier Inc. Received: January 7, 2015. Revised: May 18, 2015. Accepted: August 3, 2015. Published: August 26, 2015. The authors thank Eric Siggia, Leor Weinberger, Saul Villeda, Long Cai, Carl Pabo, Angela Andersen, David Schaffer, Belinda Waltman, and Benoit Bruneau for scientific discussions and careful reading of the manuscript; Wendell Lim, Ron Vale, and Leo Morsut for scientific discussions. We thank Kurt Thorn, Eric Chow, Mekhala Maiti, DNA 2.0, and Pickersgill and Andersen for advice and technical assistance. This work was supported by the UCSF Center for Systems and Synthetic Biology NIGMS P50 GM081879 (L.S.Q., D.A.S., M.T.). M.T. acknowledges support from the NIH Office of the Director (OD), the National Cancer Institute, and the National Institute of Dental & Craniofacial Research (NIDCR) NIH DP5 OD012194. L.S.Q. acknowledges support from the UCSF Center for Systems and Synthetic Biology, NIH Office of the Director (OD), and National Institute of Dental and Craniofacial Research (NIDCR) NIH DP5 OD017887 (Y.L. and L.S.Q.).Attached Files
Accepted Version - nihms714076.pdf
Supplemental Material - mmc1.pdf
Supplemental Material - mmc2.mp4
Supplemental Material - mmc3.mp4
Supplemental Material - mmc4.mp4
Supplemental Material - mmc5.mp4
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Additional details
- PMCID
- PMC4576702
- Eprint ID
- 74082
- Resolver ID
- CaltechAUTHORS:20170206-125245319
- NIH
- P50 GM081879
- NIH
- DP5 OD012194
- University of California, San Francisco (UCSF)
- NIH
- DP5 OD017887
- National Institute of Dental and Craniofacial Research (NIDCR)
- Created
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2017-02-06Created from EPrint's datestamp field
- Updated
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2021-11-11Created from EPrint's last_modified field