Mahjong acts as a downstream target of Lgl in cell competition and basal cell extrusion. TamoriYoichiro Uli BialuchaCarl TianAi-Guo KajitaMihoko HuangYi-Chun NormanMark HarrisonNicholas PoultonJohn IvanovitchKenzo DischLena LiuTao DengWu-Min FujitaYasuyuki 2010 <p>The mosaic analysis with a repressible cell marker (MARCM) system was used to overexpress UAS constructs in either <i>mahj</i><sup>−/−</sup> clones (A) or <i>lgl</i><sup>−/−</sup> clones (B, D, and E). Homozygous mutant clones are marked by the expression of GFP. (A) <i>mahj</i><sup>−/−</sup> MARCM clones overexpressing Lgl at 96 h after clone induction. (B, D, and E) <i>lgl</i><sup>−/−</sup> MARCM clones overexpressing Mahj at 144 h (B and D) or 96 h (E) after clone induction. (C) Quantification of apoptotic cells in the <i>lgl</i><sup>−/−</sup> mosaic wing discs with or without overexpression of Mahj. The percentage of apoptosis occurring in <i>lgl</i><sup>−/−</sup> cells on the boundary with wild-type cells was examined. The results represent means±SD (<i>n</i> = 13 discs, *<i>p</i><0.001). (D) A transverse section. Anti-cleaved Caspase-3 (A and B), anti-DE-Cadherin (D), and anti-phospho JNK (E) antibodies were used for immunostaining. (A, B, D, and E) Nuclei were stained with DAPI (blue).</p>