Abstract
Embryonic zebrafish have long been used for lineage-tracing studies. In zebrafish embryos, the cell fate identities can be determined by whole-mount in situ hybridization, or by visualization of live embryos if using fluorescent reporter lines. We use embryonic zebrafish to study the effects of a leukemic oncogene AML1-ETO on modulating hematopoietic cell fate. Induced expression of AML1-ETO is able to efficiently reprogram hematopoietic progenitor cells from erythroid to myeloid cell fate. Using the zebrafish model of AML1-ETO, we performed a chemical screen to identify small molecules that suppress the cell fate switch in the presence of AML1-ETO. The methods discussed herein may be broadly applicable for identifying small molecules that modulate other cell fate decisions.
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Acknowledgments
The authors would like to thank Dr. Randall T. Peterson for his advice and support during the development of this project. J.-R. J. Yeh is supported by a Career Development Award (AG031300) from the National Institute of Aging. This work was supported by RO1 CA118498 and the Claflin Distinguished Scholar Award.
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Yeh, JR.J., Munson, K.M. (2010). Zebrafish Small Molecule Screen in Reprogramming/Cell Fate Modulation. In: Ding, S. (eds) Cellular Programming and Reprogramming. Methods in Molecular Biology, vol 636. Humana Press. https://doi.org/10.1007/978-1-60761-691-7_20
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DOI: https://doi.org/10.1007/978-1-60761-691-7_20
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Publisher Name: Humana Press
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Online ISBN: 978-1-60761-691-7
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