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  4. CCAR1 is required for Ngn3-mediated endocrine differentiation
 
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CCAR1 is required for Ngn3-mediated endocrine differentiation

Journal
Biochemical and Biophysical Research Communications
Date Issued
2012-02-10
Author(s)
YI-CHYI LAI  
DOI
10.1016/j.bbrc.2012.01.016
URI
https://www.scopus.com/pages/publications/84862817272
https://scholars.csmu.edu.tw/handle/123456789/32548
Abstract
Neurogenin3 (Ngn3) is a basic helix-loop-helix transcription factor that specifies pancreatic endocrine cell fates during pancreas development. It can also initiate a transdifferentiation program when expressed in pancreatic exocrine and ductal cells. However, how Ngn3 initiates a transcriptional cascade to achieve endocrine differentiation is still poorly understood. Here, we show that cell cycle and apoptosis regulator 1 (CCAR1), which is a transcriptional coactivator for nuclear receptors, also interacts with Ngn3. The association between Ngn3 and CCAR1 was verified by pull-down assays and co-immunoprecipitation analyses. Using gene reporter assays, we found that CCAR1 is essential for Ngn3 to activate the expression of the reporter genes containing the NeuroD promoter. Moreover, down-regulation of endogenous CCAR1 in the PANC-1 pancreatic ductal cell line inhibits the transdifferentiation program initiated by Ngn3. CCAR1 is, therefore, a novel partner of Ngn3 in mediating endocrine differentiation.
Type
journal article
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