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. 2022 Jun 23;50(12):7097–7114. doi: 10.1093/nar/gkac512

Figure 1.

Figure 1.

An IAV replication defect in TRIM25 KO HEK293 cells can be rescued with RNA binding or ubiquitination deficient TRIM25 mutants. (A) TRIM25 WT, TRIM25ΔRBD or TRIM25ΔRING were re-integrated into HEK293 TRIM25 KO cells using the Flp-In recombinase system. LHS: domain architecture of wild-type TRIM25 and deletion mutants. Relative position of host RNA-binding domain (RBD) is shown in red. RHS: levels of proteins were compared to WT cells by western blot. (B) Cell lines were infected with IAV PR8 WT or PR8 NS1 R38K41A (MOI = 0.0001) and virus titers were assessed by the endpoint dilution assay. Whiskers represent the standard deviation (SD) from three biological replicates. Dpi—days post-inoculation. The asterisk (*) indicates P < 0.05 in mixed-effect model followed by Sidak's multiple comparison test.