| Literature DB >> 26887950 |
Shimin Wang1, Yi Lu1, Meng-Xin Yin1, Chao Wang1, Wei Wu1, Jinhui Li1, Wenqing Wu1, Ling Ge1, Lianxin Hu1, Yun Zhao2, Lei Zhang3.
Abstract
The Hippo signaling pathway controls organ size by orchestrating cell proliferation and apoptosis. When the Hippo pathway was inactivated, the transcriptional co-activator Yorkie translocates into the nucleus and forms a complex with transcription factor Scalloped to promote the expression of Hippo pathway target genes. Therefore, the nuclear translocation of Yorkie is a critical step in Hippo signaling. Here, we provide evidence that the N-terminal 1-55 amino acids of Yorkie, especially Arg-15, were essential for its nuclear localization. By mass spectrometry and biochemical analyses, we found that Importin α1 can directly interact with the Yorkie N terminus and drive Yorkie into the nucleus. Further experiments show that the upstream component Hippo can inhibit Importin α1-mediated Yorkie nuclear import. Taken together, we identified a potential nuclear localization signal at the N-terminal end of Yorkie as well as a critical role for Importin α1 in Yorkie nuclear import.Entities:
Keywords: Hippo pathway; Importin; NLS; nuclear translocation; nuclear transport; oncogene; yes-associated protein (YAP); yorkie
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Year: 2016 PMID: 26887950 PMCID: PMC4825000 DOI: 10.1074/jbc.M115.700823
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157