Abstract
Although much is known about microRNAs' regulation in gene expression and their contributions in cell fate, to date, globally lineage-(cell-) specific identification of the binding events between a transcription factor and its targeting microRNA genes is still waiting for elucidation. In this paper, we performed a ChIP-Seq experiment to find the targeting microRNA genes of a transcription factor, Egr1, in human erythroleukemia cell line K562. We found Egr1 binding sites near the promoters of 124 distinct microRNA genes, accounting for about 42 of the miRNAs which have high-confidence predicted promoters (294). We also found EGR1 bind to another 63 pre-miRNAs. We chose 12 of the 187 microRNAs with Egr1 binding sites to perform ChIP-PCR assays and the positive binding signal from ChIP-PCR confirmed the ChIP-Seq results. Our experiments provide the first global binding profile between Egr1 and its targeting microRNA genes in PMA-treated K562 cells, which may facilitate the understanding of pathways controlling microRNA biology in this specific cell line. © 2010 Wei Wang et al.
Cite
CITATION STYLE
Lu, Z., Wang, W., Zhou, D., Shi, X., Tang, C., Xie, X., … Ge, Q. (2010). Global Egr1-miRNAs binding analysis in PMA-induced K562 cells using ChIP-Seq. Journal of Biomedicine and Biotechnology, 2010. https://doi.org/10.1155/2010/867517
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.