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. 2018 Mar 28;9:1248. doi: 10.1038/s41467-018-03387-6

Fig. 7.

Fig. 7

AID R-mutants are uncoupled from transcription elongation. a, ce ChIP qPCR results using anti-AID antibody on extracts from reconstituted Aicda−/− mouse B cells activated with LPS and IL-4. Means + s.e.m. from two independent experiments are plotted. A scheme of each genomic region analysed is shown at the top of each panel with the qPCR amplicons indicated. b ChIP qPCR for endogenous AID and Spt6 from wt mouse B cells treated and analysed as in a, including amplicons in the non-transcribed Sα region. Means + s.d. from three independent experiments are plotted. f (Bottom) ChIP qPCR for AID from reconstituted DT40 Aicda−/− ΔΨVλ B cells. Means + s.d. from three independent experiments are plotted. An additional amplicon within Gapdh was used as a negative control. g WB of cell extract from reconstituted Aicda−/− mouse B cells, probed with antibodies recognizing GFP and AID. For gel source data, see supplementary Fig. 7