| Literature DB >> 25320084 |
Lianxin Hu1, Hongling Huang1, Jinhui Li1, Meng-Xin Yin1, Yi Lu1, Wenqing Wu1, Rong Zeng2, Jin Jiang3, Yun Zhao1, Lei Zhang4.
Abstract
Drosophila Hippo signaling regulates Wts activity to phosphorylate and inhibit Yki in order to control tissue growth. CK2 is widely expressed and involved in a variety of signaling pathways. In this study we report that Drosophila CK2 promotes Wts activity to phosphorylate and inhibit Yki activity, which is independent of Hpo-induced Wts promotion. In vivo, CK2 overexpression suppresses hpo mutant-induced expanded (Ex) up-regulation and overgrowth phenotype, whereas it cannot affect wts mutant. Consistent with this, knockdown of CK2 up-regulates Hpo pathway target expression. We also found that Drosophila CK2 is essential for tissue growth as a cell death inhibitor as knockdown of CK2 in the developing disc induces severe growth defects as well as caspase3 signals. Taken together, our results uncover a dual role of CK2; although its major role is promoting cell survive, it may potentially be a growth inhibitor as well.Entities:
Keywords: Cell Signaling; Drosophila; Hippo Pathway; Phosphorylation; Tumor Promoter; Tumor Suppressor Gene
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Year: 2014 PMID: 25320084 PMCID: PMC4246111 DOI: 10.1074/jbc.M114.580456
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157