“…The direct effect of PAP on RNAs, namely capped BMV RNAs and capped and uncapped luciferase transcripts, was determined by incubating the PAP-treated RNA with acidic aniline, which causes chain cleavage at the depurination site (Irvin & Uckun, 1992)+ This assay has been widely used for detection of RIPmediated depurination of the large rRNA )+ Depurination results in increased susceptibility of the sugar-phosphate backbone to hydrolysis at the depurination site+ Hence, treatment of depurinated rRNA with aniline breaks the sugar-phosphate bond of the RNA+ Therefore, degradation of the RNA following aniline treatment will occur only if that RNA has been depurinated+ BMV RNAs and luciferase transcripts were incubated with wild-type PAP and one half of the treated RNAs was incubated with aniline, and the other half was incubated with buffer+ After precipitation, RNAs were visualized by urea-polyacrylamide gel analysis and staining with ethidium bromide+ As shown in Figure 9, 10 pg (3+33 pM) of PAP did not affect the integrity of the capped or uncapped luciferase transcripts or the BMV RNAs+ However 5 ng (1+65 nM) of PAP were capable of directly depurinating the capped luciferase transcripts and the BMV RNAs, as shown by degradation of the RNA after treatment with aniline ( Fig+ 9A,B)+ In contrast, 5 ng of PAP did not depurinate the uncapped luciferase transcripts (Fig+ 9C)+ At greater concentration (100 ng, 33+3 nM), PAP was capable of degrading the capped luciferase transcripts or the BMV RNAs even in the absence of aniline treatment ( Fig+ 9A,B), whereas 100 ng of PAP had no effect on the uncapped luciferase RNA (Fig+ 9C)+ These results demonstrate that PAP specifically depurinates the capped RNAs and does not affect the uncapped RNA+…”