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Molecular and Cellular Biology, October 2005, p. 8401-8414, Vol. 25, No. 19
0270-7306/05/$08.00+0     doi:10.1128/MCB.25.19.8401-8414.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Stimulation of GCMa Transcriptional Activity by Cyclic AMP/Protein Kinase A Signaling Is Attributed to CBP-Mediated Acetylation of GCMa

Ching-Wen Chang,¹ Hsiao-Ching Chuang,² Chenchou Yu,¹ Tso-Pang Yao,³ and Hungwen Chen^1,2*

Institute of Biological Chemistry, Academia Sinica, Nankang, Taipei 115, Taiwan,¹ Graduate Institute of Biochemical Sciences, National Taiwan University, Taipei 106, Taiwan,² Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710³

Received 15 February 2005/ Returned for modification 15 March 2005/ Accepted 29 June 2005

Human GCMa is a zinc-containing transcription factor primarily expressed in placenta. GCMa regulates expression of syncytin gene, which encodes for a placenta-specific membrane protein that mediates trophoblastic fusion and the formation of syncytiotrophoblast layer required for efficient fetal-maternal exchange of nutrients and oxygen. The adenylate cyclase activator, forskolin, stimulates syncytin gene expression and cell fusion in cultured placental cells. Here we present evidence that cyclic AMP (cAMP) signaling pathway activates the syncytin gene expression by regulating GCMa activity. We found that forskolin and protein kinase A (PKA) enhances GCMa-mediated transcriptional activation. Furthermore, PKA treatment stimulates the association of GCMa with CBP and increases GCMa acetylation. CBP primarily acetylates GCMa at lysine³⁶⁷, lysine⁴⁰⁶, and lysine⁴⁰⁹ in the transactivation domain (TAD). We found that acetylation of these residues is required to protect GCMa from ubiquitination and increases the TAD stability with a concomitant increase in transcriptional activity, supporting the importance of acetylation in PKA-dependent GCMa activation. Our results reveal a novel regulation of GCMa activity by cAMP-dependent protein acetylation and provide a molecular mechanism by which cAMP signaling regulates trophoblastic fusion.

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* Corresponding author. Mailing address: Institute of Biological Chemistry, Academia Sinica, Nankang, Taipei 115, Taiwan. Phone: 886-2-27855696, ext. 6090. Fax: 886-2-27889759. E-mail: hwchen{at}gate.sinica.edu.tw.

Supplemental material for this article may be found at http://mcb.asm.org/.

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Molecular and Cellular Biology, October 2005, p. 8401-8414, Vol. 25, No. 19
0022-538X/05/$08.00+0     doi:10.1128/MCB.25.19.8401-8414.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

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