Figure 3.
Figure 3. 729HTLVRex- stable cell line contains the Rex mutation and does not produce detectable Rex. (A) HTLV-1 genome fragment containing the Rex start codon was amplified by PCR from genomic DNA of 729wtHTLV-1 and 729HTLVRex- cells. PCR-amplified product was incubated in the presence (+) or absence (-) of SphI, separated on 2% agarose gel, and visualized by ethidium bromide staining. (B) Rex-1 immunoprecipitation. 729, 729wtHTLV-1, and 729HTLVRex- cells were metabolically labeled with [35S] methionine-cysteine. Cell lysates were immunoprecipitated with polyclonal antibody against the HTLV-1 Rex in the presence of protein A-sepharose. The sizes (in daltons, indicated on the left) were determined by comparison to protein markers.

729HTLVRex- stable cell line contains the Rex mutation and does not produce detectable Rex. (A) HTLV-1 genome fragment containing the Rex start codon was amplified by PCR from genomic DNA of 729wtHTLV-1 and 729HTLVRex- cells. PCR-amplified product was incubated in the presence (+) or absence (-) of SphI, separated on 2% agarose gel, and visualized by ethidium bromide staining. (B) Rex-1 immunoprecipitation. 729, 729wtHTLV-1, and 729HTLVRex- cells were metabolically labeled with [35S] methionine-cysteine. Cell lysates were immunoprecipitated with polyclonal antibody against the HTLV-1 Rex in the presence of protein A-sepharose. The sizes (in daltons, indicated on the left) were determined by comparison to protein markers.

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