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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 |
Appears in Collections: | Elements Staff Publications |
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