Skip to main content
. 2018 Jan 24;46(6):2834–2849. doi: 10.1093/nar/gky034

Figure 2.

Figure 2.

PCNA Interacting (PIP) motif of PR-Set7 is not necessary for PR-Set7 degradation and is dispensable for Drosophila development. (A) Immunoblot analysis of whole cell extracts prepared from S2 cells expressing ubiquitously (actin promoter) a wild type (FLAG-PR-Set7, upper panel) or a PIP mutant version of PR-Set7 (FLAG-PR-Set7PIPmutant, lower panel) treated with cycloheximide (CHX) alone or in combination with the proteasome inhibitor MG132 as indicated. Antibodies and relative amounts of each FLAG tagged PR-Set7 protein normalized to Tubulin are indicated on the left and above each panel, respectively. (B) Optic lobes of third instar larvae of different genotypes, as indicated on the left, were stained with DAPI (left panel) and the mitotic marker anti-H3S10p (right panel) and analyzed by immunofluorescence. W1118 corresponds to a wild type control line. Act>GAL4 indicates the expression of GAL4 protein by the actin promoter. pr-set720 corresponds to a loss of function allele of pr-set7. UAS-GFP-PR-Set7 and UAS-GFP-PR-Set7PIPmutant corresponds to transgenic constructs under the control of an UAS sequence. Scale bar represents 50μm.