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. 2018 Oct 23;9:4408. doi: 10.1038/s41467-018-06557-8

Fig. 7.

Fig. 7

eRIC identifies m6A-responsive RBPs in vivo. a m6A dot blot of Jurkat cells treated with 0.5 mM DMOG or vehicle for 6 h, using two independent antibodies (Antibody 1: Abcam, Antibody 2: SySy). Serial dilutions of poly(A) RNA were blotted as indicated on the right. A quantification of the signal intensity based on image analysis is shown below each dot. Intensity is expressed relative to the lowest signal in the control. A representative blot of three biologically independent experiments is shown. b Overlap between DMOG-responsive RBPs identified by eRIC/RIC and m6A-regulated RBPs previously reported by Edupuganti et al.21 or Arguello et al.20. Between brackets are the number of proteins with directions of DMOG-induced changes that coincide with previous reports. c Normalized signal sum in eRIC and RIC samples of representative examples of reported m6A readers (left), m6A-repelled RBPs (middle), and RBPs insensitive to m6A (right). −UV non-irradiated controls, +UV irradiated samples. eRIC and RIC values are expressed relative to the respective untreated control (−UV, DMSO). Data are shown as mean from two biologically independent experiments. Asterisk (*) indicates FDR < 0.05 (moderated t test)