Abstract
Adar-1 gene plays an important role in the negative regulation of RNA interference. We previously showed that increased adar-1 mRNA level was associated with the rebound of gene expression after RNAi suppression. In this study, we identified a PU.1 binding site upstream from transcription start point of adar-1 gene and is essential for the promoter activity. Knockdown and over-expression of the PU.1 gene resulted in decreased and increased activity of adar-1 promoter, respectively. Our results suggest that transcription factor PU.1, could bind to the adar-1 promoter and play a key role in activating transcription of gene induced by high-dose esiRNAs.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenosine Deaminase / genetics*
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Animals
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CHO Cells
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Cricetinae
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Cricetulus
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Endoribonucleases / genetics*
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Gene Expression Regulation
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Gene Knockdown Techniques
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Genes, Reporter / genetics
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Mice
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Promoter Regions, Genetic / genetics
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Proto-Oncogene Proteins / metabolism*
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RNA, Small Interfering / genetics*
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RNA, Small Interfering / metabolism
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RNA-Binding Proteins
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Trans-Activators / metabolism*
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Transcription, Genetic*
Substances
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Proto-Oncogene Proteins
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RNA, Small Interfering
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RNA-Binding Proteins
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Trans-Activators
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proto-oncogene protein Spi-1
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Endoribonucleases
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ADARB1 protein, human
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Adenosine Deaminase