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. 2007 Jan 26;3(1):e10. doi: 10.1371/journal.ppat.0030010

Figure 6. Effects of TRIM5 and APOBEC3 Proteins on HERV-KCON Infectivity.

Figure 6

(A) Unmanipulated CHO cells or variants stably expressing human TRIM5α, rhesus monkey TRIM5α, or owl monkey TRIM-Cyp were infected with VSV-G pseudotyped retroviral vectors that are sensitive to one or more of the TRIM5 proteins (N-MLV or HIV-1) or TRIM5-resistant controls (B-MLV or HIV-1 carrying SIVmac CA HIV(SCA)), as indicated. Two days postinfection, the percentage of GFP+ cells was determined using FACS.

(B) The same panel of CHO-derived TRIM5-expressing CHO cell lines were inoculated with HERV-KCON(VSV-G). Two days postinfection, GFP+ foci were quantified.

(C) APOBEC3F and APOBEC3G expression plasmids were cotransfected into 293T cells during generation of CHKCG-containing HERV-KCON(VSV-G) particles. Fresh 293T cells were infected with the resulting viral supernatant, and GFP+ foci were quantified 2 d later.

(D) Western blot analysis, using the anti–HERV-K Gag antibody, of cell and HERV-KCON virion lysates generated upon coexpression of APOBEC3F or APOBEC3G, as indicated.

All data are representative of at least three experiments.