Functional characterization of enhancer activity during a long terminal repeat's evolution

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 2.
Figure 2.

Schematic of MPRA. (A) Sequence alignment of motif-focused regions to test primate and ancestral reconstructed LTR18A elements. MAFK and DBP motif regions are boxed. (B) Tiling of ancestral and hg19 genomic LTR18A elements in a reconstructed phylogenetic tree. All elements were tiled with 160-bp tiles at 10-bp intervals. (C) Plasmid construct and enrichment score calculation. Each LTR18A fragment was integrated upstream of a minimal promoter (minP) and tagged with 10 unique barcodes (BCs) during library synthesis. The MPRA library was transfected into HepG2 and K562 cells. Enrichment scores are log2 ratios of RNA/DNA normalized to basal.

This Article

  1. Genome Res. 32: 1840-1851

Preprint Server