Comparison of TRIBE and STAMP for identifying targets of RNA binding proteins in human and Drosophila cells

(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.

TDP-43 TRIBE and TDP-43 STAMP identify editing sites with different characteristics on TDP-43 target transcripts. (A,B) Pie charts showing the relationship between editing sites in two biological replicates. Editing sites identified in both experiments at: identical locations (dark blue), two different locations that are in close proximity in the biological replicates (green and gray; 50–100 bp), within 200 bp (yellow), or >200 bp (dark red). (C) Mean percentage editing for all editing sites identified in TDP-43-ADAR (∼15%) and TDP-43-APOBEC (∼10%). Mean values indicated by X and median values by lines (P-value <0.0001; Wilcoxon rank-sum test). (D) Mean editing sites per transcript generated by TDP-43-APOBEC (∼7) and TDP-43-ADAR (∼5) (mean indicated by X and median indicated by a line; P-value <0.0001; Wilcoxon rank-sum test). (E,F) The near neighbors of all edited nucleotides were identified and quantified (percentage of all editing sites). TDP-43-ADAR (E) preferentially edited adenosines followed by guanosine. TDP-43-APOBEC (F) preferentially edited cytosines that were flanked by A or T.

This Article

  1. RNA 29: 1230-1242