Voir la source de We analyzed if the Wg sample was altered in these circumstances as it has been noticed in the existence of ``undead cells''

(D) BrdU staining (white) of the discs demonstrated in (A). (B, E) In RBF expressing discs, as in the handle disc proven in (A,D), BrdU staining is homogeneous in the entire disc, apart from in the ZNC (Zone of Non-proliferating Cells) (white arrow). (C) In RBFD253A expressing discs, cells surrounding the powerful RBF staining show an enhanced BrdU staining, indicating that these cells have an enhanced proliferation price. (G) From still left to appropriate, genotypes of the larvae are: ptcGal4/+, ptc-Gal4/UAS-RBF, and UAS-RBFD253A X ptc-Gal4/+. (G) S period staining by BrdU (inexperienced), and RBF staining (crimson). (J) BrdU staining (white) of the discs revealed in (G) with enlarged check out of boxed area. (G, J) BrdU staining is homogeneous in the total disc, except in the ZNC (white arrow). (IL) In ptc.RBFD253A discs, cells within the ZNC that are adjacent to RBFD253A expressing cells are labeled with BrdU, indicating an abnormal proliferation of these cells. All discs are proven with posterior to the best. 
RBFD253A-induced apoptosis is dependent on the activity of the JNK pathway. In conclusion, we demonstrated that RBF and RBFD253A activate the JNK pathway, that this pathway mediates the two RBF and RBFD253A -induced apoptosis, and is accountable for RBFD253A-induced overgrowth. As beforehand indicated, the JNK pathway is essential to equally RBFD253A-induced overgrowth, and in excess of-proliferation induced by ``undead cells''. Its more than-activation in ``undead cells'' qualified prospects to ectopic synthesis and secretion of the mitogenic proteins Wg and Dpp in a lengthy long lasting [http://www.medchemexpress.com/Peficitinib.html 944118-01-8 citations] fashion, foremost to an in excess of-proliferation of neighboring cells and overgrowth phenotypes [forty three]. Given that RBFD253A-induced overgrowth is dependent on JNK pathway activation, we questioned if this process was provoked by a equivalent mechanism. We as a result co-expressed RBF and p35 in wing discs to make undead cells relying on RBF-induced apoptosis, and examine the wg expression pattern in these discs to wg expression in RBFD253A expressing discs. In vg.RBF, p35 flies lifted at 25uC, only 1 wing observed exhibited overgrowth out of 123 flies counted. As a result, even in the presence of p35, RBF does not seem to be to induce an overgrowth phenotype that would consequence from the presence of undead cells. However, at 29uC, far more wings co-expressing RBF and p35 introduced overgrowth phenotype (ten wings out of 35), but in this kind of excessive circumstances only handful of flies hatched.