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. 2011 Mar 2;6(3):e17151. doi: 10.1371/journal.pone.0017151

Figure 1. Transient transfection to induce Vpr expression destabilizes both endogenous and GFP-CENP-A.

Figure 1

A. Manual quantitation of GFP-CENP-A cells after transfection with control Vpr mutant W54R or wild-type Vpr. B–CInline graphic. Example images of cells transfected with control Vpr-W54R-HA (B-BInline graphic) or wild-type Vpr-HA (C-CInline graphic) detected with anti-HA in red, DNA in blue, and GFP-CENP-A in green. GFP-CENP-A channel is also shown alone (BInline graphic and CInline graphic). D–E. Example fields of live GFP-CENP-A cells transfected with Vpr-W54R (D) or wild-type Vpr (E). F–GInline graphic. Example fields of fixed HeLa cells after transfection with Vpr-W54R (F-FInline graphic) or wild-type Vpr (G-GInline graphic). Vpr is detected with anti-HA in green. Endogenous CENP-A is detected with anti-centromere autoantisera (ACA) in red.