Identification of the GTPase-activating protein DEP domain containing 1B (DEPDC1B) as a transcriptional target of Pitx2

Item Type:	Article
Title:	Identification of the GTPase-activating protein DEP domain containing 1B (DEPDC1B) as a transcriptional target of Pitx2
Creators Name:	Wu, D. and Zhu, X. and Jimenez-Cowell, K. and Mold, A.J. and Sollecito, C.C. and Lombana, N. and Jiao, M. and Wei, Q.
Abstract:	Pitx2 is a bicoid-related homeobox transcription factor implicated in regulating left-right patterning and organogenesis. However, only a limited number of Pitx2 downstream target genes have been identified and characterized. Here we demonstrate that Pitx2 is a transcriptional repressor of DEP domain containing 1B (DEPDC1B). The first intron of the human and mouse DEP domain containing 1B genes contains multiple consensus DNA-binding sites for Pitx2. Chromatin immunoprecipitation assays revealed that Pitx2, along with histone deacetylase 1, was recruited to the first intron of Depdc1b. In contrast, RNAi-mediated depletion of Pitx2 not only enhanced the acetylation of histone H4 in the first intron of Depdc1b, but also increased the protein level of Depdc1b. Luciferase reporter assays also showed that Pitx2 could repress the transcriptional activity mediated by the first intron of human DEPDC1B. The GAP domain of DEPDC1B interacted with nucleotide-bound forms of RAC1 in vitro. In addition, exogenous expression of DEPDC1B suppressed RAC1 activation and interfered with actin polymerization induced by the guanine nucleotide exchange factor TRIO. Moreover, DEPDC1B interacted with various signaling molecules such as U2af2, Erh, and Salm. We propose that Pitx2-mediated repression of Depdc1b expression contributes to the regulation of multiple molecular pathways, such as Rho GTPase signaling.
Keywords:	GTPase Signaling, Transcriptional Regulation, Pitx2, DEPDC1B, Animals, Mice
Source:	Experimental Cell Research
ISSN:	0014-4827
Publisher:	Elsevier
Volume:	333
Number:	1
Page Range:	80-92
Date:	10 April 2015
Additional Information:	Copyright © 2015 Elsevier Inc. All rights reserved.
Official Publication:	https://doi.org/10.1016/j.yexcr.2015.02.008
External Fulltext:	View full text on PubMed Central
PubMed:	View item in PubMed

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