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. 1998 Dec;18(12):7510–7520. doi: 10.1128/mcb.18.12.7510

FIG. 8.

FIG. 8

Inhibition of U6 snRNA interactions with m7GpppG-capped Ad1WW pre-mRNA by the m7GpppG cap analogue but not the ApppG cap analogue. HeLa nuclear extract was preincubated with the m7GpppG or the ApppG cap analogue for 15 min prior to the addition of the pre-mRNA. The final concentrations of m7GpppG and ApppG were 0, 5, 10, 20, 50, and 100 μM, as marked above the gel. The cross-linked RNA was resolved on a 5% polyacrylamide gel. The bar charts aligned below the image show the relative intensities of specific products and the pre-mRNA (expressed as percentages) for each lane. The products measured are U1 cross-linked to the upstream 5′ splice site (the major site of splicing), U6 cross-linked, and the upstream (u/s) mRNA, as indicated by the y axis labels.