Dissecting the action of an evolutionary conserved non-coding region on renin promoter activity

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Abstract

Elucidating the mechanisms of the human transcriptional regulatory network is a major challenge of the post-genomic era. One important aspect is the identification and functional analysis of regulatory elements in non-coding DNA. Genomic sequence comparisons between related species can guide the discovery of cis-regulatory sequences. Using this technique, we identify a conserved region CNSmd of ∼775 bp in size, ∼14 kb upstream of the renin gene. Renin plays a pivotal role for mammalian blood pressure regulation and electrolyte balance. To analyse the cis-regulatory role of this region in detail, we perform 132 combinatorial reporter gene assays in an in vitro Calu-6 cell line model. To dissect the role of individual subregions, we fit several mathematical models to the experimental data. We show that a multiplicative switch model fits best the experimental data and that one subregion has a dominant effect on promoter activity. Mapping of the sub-sequences on phylogenetic conservation data reveals that the dominant regulatory region is the one with the highest multi-species conservation score. © 2007 The Author(s).

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Mrowka, R., Steege, A., Kaps, C., Herzel, H., Thiele, B. J., Persson, P. B., & Blüthgen, N. (2007). Dissecting the action of an evolutionary conserved non-coding region on renin promoter activity. Nucleic Acids Research, 35(15), 5120–5129. https://doi.org/10.1093/nar/gkm535

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