Please use this identifier to cite or link to this item: https://doi.org/10.3390/genes9020101
Title: Modeling the role of wnt signaling in human and Drosophila stem cells
Authors: Kaur, P 
Jin, H.J
Lusk, J.B
Tolwinski, N.S 
Keywords: beta catenin
bone morphogenetic protein
G protein coupled receptor
kruppel like factor 4
LGR5 protein
mitogen activated protein kinase
Myc protein
octamer transcription factor 4
RING finger protein
RNF43 protein
transcription factor 4
transcription factor Sox2
unclassified drug
Wnt protein
Wnt3a protein
ZNRF3 protein
Article
clustered regularly interspaced short palindromic repeat
CRISPR-CAS9 system
embryonic stem cell
fruit fly model
gene editing
hedgehog signaling
human
induced pluripotent stem cell
nonhuman
protein expression
protein function
Wnt signaling
Issue Date: 2018
Citation: Kaur, P, Jin, H.J, Lusk, J.B, Tolwinski, N.S (2018). Modeling the role of wnt signaling in human and Drosophila stem cells. Genes 9 (2) : 101. ScholarBank@NUS Repository. https://doi.org/10.3390/genes9020101
Abstract: The discovery of induced pluripotent stem (iPS) cells, barely more than a decade ago, dramatically transformed the study of stem cells and introduced a completely new way to approach many human health concerns. Although advances have pushed the field forward, human application remains some years away, in part due to the need for an in-depth mechanistic understanding. The role of Wnts in stem cells predates the discovery of iPS cells with Wnts established as major pluripotency promoting factors. Most work to date has been done using mouse and tissue culture models and few attempts have been made in other model organisms, but the recent combination of clustered regularly interspaced short palindromic repeats (CRISPR) gene editing with iPS cell technology provides a perfect avenue for exploring iPS cells in model organisms. Drosophila is an ideal organism for such studies, but fly iPS cells have not yet been made. In this opinion article, we draw parallels between Wnt signaling in human and Drosophila stem cell systems, propose ways to obtain Drosophila iPS cells, and suggest ways to exploit the versatility of the Drosophila system for future stem cell studies. © 2018 by the authors. Licensee MDPI, Basel, Switzerland.
Source Title: Genes
URI: https://scholarbank.nus.edu.sg/handle/10635/175070
ISSN: 20734425
DOI: 10.3390/genes9020101
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