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. 1999 Sep;73(9):7175–7184. doi: 10.1128/jvi.73.9.7175-7184.1999

FIG. 3.

FIG. 3

Southern blot analysis of ΔMo+SRS M-MuLV-induced tumors. High-molecular-weight DNAs from ΔMo+SRS M-MuLV-induced tumors were digested with PstI, which cleaves asymmetrically within the SRS enhancer fragment. (A) Hybridization with a labeled SRS enhancer-specific probe would yield a diagnostic 839-bp hybridizing fragment for ΔMo+SRS+ M-MuLV and a 757-bp fragment for ΔMo+SRS M-MuLV. (B) Southern blots of the tumors all show fragments of the expected size when hybridized with an SRS 19-6 MuLV enhancer probe. Larger hybridizing fragments presumably represent endogenous MuLV sequences (also present in control spleen DNA) or host-virus junction fragments from the downstream LTR.