| Literature DB >> 24316029 |
Yi Ling Chia1, Chew Har Ng1, Philip Lashmit2, Kai Ling Chu1, Qiao Jing Lew1, Jia Pei Ho1, Hsueh Lee Lim3, Peter Morin Nissom3, Mark F Stinski2, Sheng-Hao Chao4.
Abstract
Expression of the human cytomegalovirus (HCMV) major immediate-early (MIE) genes is regulated by a strong enhancer-containing promoter with multiple binding sites for various transcription factors, including cyclic AMP response element binding protein 1 (CREB1). Here we show that overexpression of CREB1 potently blocked MIE transcription and HCMV replication. Surprisingly, CREB1 still exhibited strong inhibition of the MIE promoter when all five CREB binding sites within the enhancer were mutated, suggesting that CREB1 regulated the MIE gene expression indirectly. Promoter deletion analysis and site-directed mutagenesis identified the region between -130 and -50 upstream of the transcription start site of the MIE gene as the "CREB1 responsive region". Mutations of SP1/3 and NF-κB binding sites within this region interrupted the inhibitory effect induced by CREB1 overexpression. Our findings suggest that overexpression of CREB1 can cause repression of HCMV replication and may contribute to the development of new anti-HCMV strategies.Entities:
Keywords: CREB1; Human cytomegalovirus; Major immediate-early genes; NF-κB; SP1; SP3
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Year: 2013 PMID: 24316029 DOI: 10.1016/j.antiviral.2013.11.012
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970