| Literature DB >> 25038227 |
Kelly L Weaver1, Marie-Clotilde Alves-Guerra2, Ke Jin1, Zhiqiang Wang1, Xiaoqing Han1, Prathibha Ranganathan1, Xiaoxia Zhu1, Thiago DaSilva1, Wei Liu3, Francesca Ratti4, Renee M Demarest5, Cristos Tzimas6, Meghan Rice1, Rodrigo Vasquez-Del Carpio7, Nadia Dahmane8, David J Robbins1, Anthony J Capobianco9.
Abstract
The Notch signaling pathway governs many distinct cellular processes by regulating transcriptional programs. The transcriptional response initiated by Notch is highly cell context dependent, indicating that multiple factors influence Notch target gene selection and activity. However, the mechanism by which Notch drives target gene transcription is not well understood. Herein, we identify and characterize a novel Notch-interacting protein, Notch activation complex kinase (NACK), which acts as a Notch transcriptional coactivator. We show that NACK associates with the Notch transcriptional activation complex on DNA, mediates Notch transcriptional activity, and is required for Notch-mediated tumorigenesis. We demonstrate that Notch1 and NACK are coexpressed during mouse development and that homozygous loss of NACK is embryonic lethal. Finally, we show that NACK is also a Notch target gene, establishing a feed-forward loop. Thus, our data indicate that NACK is a key component of the Notch transcriptional complex and is an essential regulator of Notch-mediated tumorigenesis and development. ©2014 American Association for Cancer Research.Entities:
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Year: 2014 PMID: 25038227 PMCID: PMC4154994 DOI: 10.1158/0008-5472.CAN-14-1547
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701