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. Author manuscript; available in PMC: 2017 Aug 25.
Published in final edited form as: Cell. 2016 Aug 25;166(5):1257–1268.e12. doi: 10.1016/j.cell.2016.07.044

Figure 1. CLIP-seq experiments showing HIV-1 IN binding to viral RNA in virions.

Figure 1

(A) A representative autoradiogram of IN-RNA crosslinked adducts from HIV-1NL4-3 and HIV-1NL4-3 ΔIN virions (upper panel). Corresponding western blot analysis of IN in immunoprecipitated fractions (lower panel). (B) Percentage of reads that map to cellular and viral RNA obtained from 2 independent CLIP-Seq analysis of IN-RNA adducts from WT virions. Error bars indicate standard errors. (C) CLIP-seq results showing read densities (frequency distribution of nucleotide occurrence) mapped to the viral genome obtained from HIV-1NL4-3 (red) and HIV-1NL4-3 ΔIN (blue) progeny virions. The read densities have been normalized with respect to total reads for WT HIV-1NL4-3. A collinear schematic diagram of the HIV-1 genome is shown above.