| Literature DB >> 29207259 |
Xi Chen1, Ruizhe Wang1, Xu Liu2, Yongming Wu1, Tao Zhou1, Yujia Yang1, Andrew Perez1, Ying-Chu Chen2, Liang Hu1, Jean Paul Chadarevian1, Amir Assadieskandar2, Chao Zhang3, Qi-Long Ying4.
Abstract
Glycogen synthase kinase 3 (GSK3) plays a central role in diverse cellular processes. GSK3 has two mammalian isozymes, GSK3α and GSK3β, whose functions remain ill-defined because of a lack of inhibitors that can distinguish between the two highly homologous isozymes. Here, we show that GSK3α and GSK3β can be selectively inhibited in mouse embryonic stem cells (ESCs) using a chemical-genetic approach. Selective inhibition of GSK3β is sufficient to maintain mouse ESC self-renewal, whereas GSK3α inhibition promotes mouse ESC differentiation toward neural lineages. Genome-wide transcriptional analysis reveals that GSK3α and GSK3β have distinct sets of downstream targets. Furthermore, selective inhibition of individual GSK3 isozymes yields distinct phenotypes from gene deletion, highlighting the power of the chemical-genetic approach in dissecting kinase catalytic functions from the protein's scaffolding functions. Our study opens new avenues for defining GSK3 isozyme-specific functions in various cellular processes.Entities:
Keywords: GSK3; Wnt/β-catenin pathway; chemical genetics; embryonic stem cell; neural differentiation; self-renewal
Mesh:
Substances:
Year: 2017 PMID: 29207259 PMCID: PMC5851779 DOI: 10.1016/j.devcel.2017.11.007
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270