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. 2021 May 28;118(22):e2019681118. doi: 10.1073/pnas.2019681118

Fig. 6.

Fig. 6.

TMEM43 interacts with Cx26 and Cx30 gap junction channels. (A) Immunohistochemistry data showing TMEM43 expression with Cx26 and Cx30 in GLSs (P20). Merged images are shown in Bottom. TMEM43, green; Cx26, red; Cx30, magenta; DAPI, blue. (B) Confocal micrographs of Cx26 expression in the organ of Corti (Top) and Stria Vascularis (Bottom) of Tmem43+/+, Tmem43+/KI, and Tmem43KI/KI (5 mo). (C) Confocal micrographs of Cx30 expression in the organ of Corti (Top) and Stria Vascularis (Bottom) of Tmem43+/+, Tmem43+/KI, and Tmem43KI/KI (7 mo). There was no difference among the genotypes. (D) Western blot result from cochlea tissue lysates of Tmem43+/+ and Tmem43KI/KI mice (p6), blotted with anti-Cx26 and anti-Cx30. (E) Co-IP data showing that both TMEM43 WT and TMEM43-p.(Arg372Ter) are immuno-pulled down with Cx26 and Cx30 in in vitro. (F) Duolink PLA with anti-TMEM43 and anti-Cx26 (Top). Duolink PLA signal was amplified as a red fluorescent, indicative of close proximity of TMEM43 and Cx-26. Red signal was pseudo colored as green for better data display. Lower is a negative control data without Cx26 antibody. (G) Co-IP data using cochlea tissue (p6). Protein lysate was pulled down with Cx30 antibody and blotted with anti-TMEM43.