7 Interactions found (0.03 seconds)

In dre-1 partial loss-of-function mutants (e.g., dre- 1(dh99)) seam cells undergo precocious terminal differentiation in L3, a full stage ahead of schedule. Using the adherens junction marker ajm-1:gfp to mark seam cell boundaries, we observed that blmp-1 knockdown by RNAi reduced dre-1(dh99) precocious seam cell fusion from 90% to 15% of the animals. Similarly only 7.5% of dre-1;blmp-1(tm548) double mutant animals showed seam cell fusion in L3.

che-14 : let-413

"Similarly, a GFP reporter construct of the multi-TM protein CHE-14 (Michaux et al., 2000) was used to mark the apical surface of a subset of epidermal cells (Fig. 3G). We observed that these proteins all remained at the apical surface in dlg-1(RNAi) embryos (Fig. 3B,B',E,E',H), although PAR-3 appeared to move to a position coincident with, or just apical to, the CeAJ (marked by HMP-1) in the intestine (Fig. 3B'), and small areas of subapical localisation were also detected for CHE-14::GFP in the epidermis (arrows in Fig. 3H). In contrast, PAR-3 and PAR-6 became progressively mislocalized basally along the lateral membrane of intestinal cells in let-413(RNAi) embryos (Fig. 3C,F,C',F'). Similarly, CHE-14::GFP was progressively mislocalizedto the lateral cell membrane in LET- 413-deficient embryos (Fig. 3I)."

"Similarly, a GFP reporter construct of the multi-TM protein CHE-14 (Michaux et al., 2000) was used to mark the apical surface of a subset of epidermal cells (Fig. 3G). We observed that these proteins all remained at the apical surface in dlg-1(RNAi) embryos (Fig. 3B,B',E,E',H), although PAR-3 appeared to move to a position coincident with, or just apical to, the CeAJ (marked by HMP-1) in the intestine (Fig. 3B'), and small areas of subapical localisation were also detected for CHE-14::GFP in the epidermis (arrows in Fig. 3H). In contrast, PAR-3 and PAR-6 became progressively mislocalized basally along the lateral membrane of intestinal cells in let-413(RNAi) embryos (Fig. 3C,F,C',F'). Similarly, CHE-14::GFP was progressively mislocalizedto the lateral cell membrane in LET- 413-deficient embryos (Fig. 3I)."

"Similarly, a GFP reporter construct of the multi-TM protein CHE-14 (Michaux et al., 2000) was used to mark the apical surface of a subset of epidermal cells (Fig. 3G). We observed that these proteins all remained at the apical surface in dlg-1(RNAi) embryos (Fig. 3B,B',E,E',H), although PAR-3 appeared to move to a position coincident with, or just apical to, the CeAJ (marked by HMP-1) in the intestine (Fig. 3B'), and small areas of subapical localisation were also detected for CHE-14::GFP in the epidermis (arrows in Fig. 3H). In contrast, PAR-3 and PAR-6 became progressively mislocalized basally along the lateral membrane of intestinal cells in let-413(RNAi) embryos (Fig. 3C,F,C',F'). Similarly, CHE-14::GFP was progressively mislocalizedto the lateral cell membrane in LET- 413-deficient embryos (Fig. 3I)."

let-413 : par-6

"Similarly, a GFP reporter construct of the multi-TM protein CHE-14 (Michaux et al., 2000) was used to mark the apical surface of a subset of epidermal cells (Fig. 3G). We observed that these proteins all remained at the apical surface in dlg-1(RNAi) embryos (Fig. 3B,B',E,E',H), although PAR-3 appeared to move to a position coincident with, or just apical to, the CeAJ (marked by HMP-1) in the intestine (Fig. 3B'), and small areas of subapical localisation were also detected for CHE-14::GFP in the epidermis (arrows in Fig. 3H). In contrast, PAR-3 and PAR-6 became progressively mislocalized basally along the lateral membrane of intestinal cells in let-413(RNAi) embryos (Fig. 3C,F,C',F'). Similarly, CHE-14::GFP was progressively mislocalizedto the lateral cell membrane in LET- 413-deficient embryos (Fig. 3I)."

"Similarly, a GFP reporter construct of the multi-TM protein CHE-14 (Michaux et al., 2000) was used to mark the apical surface of a subset of epidermal cells (Fig. 3G). We observed that these proteins all remained at the apical surface in dlg-1(RNAi) embryos (Fig. 3B,B',E,E',H), although PAR-3 appeared to move to a position coincident with, or just apical to, the CeAJ (marked by HMP-1) in the intestine (Fig. 3B'), and small areas of subapical localisation were also detected for CHE-14::GFP in the epidermis (arrows in Fig. 3H). In contrast, PAR-3 and PAR-6 became progressively mislocalized basally along the lateral membrane of intestinal cells in let-413(RNAi) embryos (Fig. 3C,F,C',F'). Similarly, CHE-14::GFP was progressively mislocalizedto the lateral cell membrane in LET- 413-deficient embryos (Fig. 3I)."

let-413 : par-3

"Similarly, a GFP reporter construct of the multi-TM protein CHE-14 (Michaux et al., 2000) was used to mark the apical surface of a subset of epidermal cells (Fig. 3G). We observed that these proteins all remained at the apical surface in dlg-1(RNAi) embryos (Fig. 3B,B',E,E',H), although PAR-3 appeared to move to a position coincident with, or just apical to, the CeAJ (marked by HMP-1) in the intestine (Fig. 3B'), and small areas of subapical localisation were also detected for CHE-14::GFP in the epidermis (arrows in Fig. 3H). In contrast, PAR-3 and PAR-6 became progressively mislocalized basally along the lateral membrane of intestinal cells in let-413(RNAi) embryos (Fig. 3C,F,C',F'). Similarly, CHE-14::GFP was progressively mislocalizedto the lateral cell membrane in LET- 413-deficient embryos (Fig. 3I)."