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. Author manuscript; available in PMC: 2011 May 18.
Published in final edited form as: Neuron. 2010 Nov 18;68(4):695–709. doi: 10.1016/j.neuron.2010.09.027

Figure 2. MADM Analysis of Lis1, Ndel1, and 14-3-3ε in Somatosensory Cortex.

Figure 2

(A) Genomic location of MADM-11 and Lis1, Ndel1 and 14-3-3ε genes on Chr. 11. Physical and genetic distances to the centromere are indicated.

(B–E) MADM-labeled cells in P21 somatosensory barrel cortex in control-MADM (B; MADM-11GT/TG;Emx1Cre/+), Lis1-MADM (C; MADM-11GT/TG,Lis1;Emx1Cre/+), Ndel1-MADM (D; MADM-11GT/TG,Ndel1;Emx1Cre/+) and 14-3-3ε-MADM (E; MADM-11GT/TG, 14-3-3ε;Emx1Cre/+). In control-MADM (B), GFP+ (green), tdT+ (red), and GFP+/tdT+ (yellow) cells are all WT. In Lis1-, Ndel1-, and 14-3-3ε MADM (C–E), homozygous mutants are GFP+ (green), heterozygous cells are GFP+/tdT+ (yellow) or unlabeled (vast majority), and homozygous WT cells are tdT+ (red). Nuclei were stained using DAPI (blue). White star in (B) marks tdT+ cortical astrocytes. Arrows in (C) indicate sparse green Lis1−/− mutant neurons. Arrows in (D) point to Ndel1−/− astrocytes. Cortical layers are numbered in roman digits. WM: white matter. Scale bar, 150 μm.

(F) Quantification of green/red ratio of neurons (upper panel) and cortical astrocytes (lower panel) corresponding to respective genotypes in (B–E). No Lis1−/− mutant astrocytes were observed in any sample analyzed.

(G–J) Quantification of the relative distribution (%) of mutant green, heterozygote yellow and WT red neurons (upper panels) and astrocytes (lower panels) for genotypes corresponding to (B)–(E). Values represent mean ± SEM ns: nonsignificant, *p < 0.05, **p < 0.01, and ***p < 0.001.

See also Figures S2–S4.