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. Author manuscript; available in PMC: 2013 May 11.
Published in final edited form as: Cell. 2012 May 11;149(4):832–846. doi: 10.1016/j.cell.2012.03.032

Figure 1. Subnuclear localization of DFz2C and LamC at larval muscle nuclei and defective NMJs in lamC mutants (also see SF1).

Figure 1

A- LamC and DFz2C labeling (deconvolved) of muscle nucleus containing a DFz2C/LamC focus (box; enlarged in right panels) localized to the nuclear periphery (arrowhead in XZ plane). Arrows=DFz2C granule within the LamC framework-like structure.

B- Number of DFz2C and LamC foci/nucleus. N (same order as in graph)=450, 413, 302, 530, 328, 617, 593.

C- Localization of LamC-GFP and wild type LamC in muscle nucleus from lamCGFP-trap/+ in relationship to DFz2C (box; enlarged in right panels). Inset is the same nucleus but overexposed.

Calibration=5µm A (left), 2µm A and C (right), 7µm C (left). Images are single confocal slices.

D–I- Larval NMJsdouble labeled with antibodies to HRP and DLG in
  • D,E- a wild type NMJ at (A) low and (B) high magnification,
  • F, G- a lamC null mutant NMJ at (C) low and (D) high magnification, and
  • H, I- an NMJ from a larva expressing LamC-RNAi in muscles (LamC-RNAi-muscle).

Arrowheads=ghost boutons. Calibration=30µm D, F, H; 12µm E, G, I.

J, K- Morphometric analysis of NMJs showing
  • J- ghost boutons, and
  • K- bouton number.

N (same order as in graph)= 10, 19, 16, 16.

L- Morphology of synaptic boutons in (top) wild type and (bottom) lamC mutant.

Calibration=12µm.

M–O- Electrophysiological analysis of larval NMJs showing
  • M- mEJP frequency,
  • N- mEJPs amplitude, and
  • O- evoked EJP amplitude.

N (same order as in graph)=8, 8, 5, 5, 7.

P,Q- Larval NMJs labeled with HRP and DGluRIIA antibodies in
  • (P) wild type and
  • (Q) a larva expressing LamC-RNAi in muscles.

Calibration= 5 µm.

R,S- Morphometric analysis of GluRIIA clusters showing
  • (R) GluRIIA label volume and
  • (S) total intensity.
  • ***= p< 0.0001; **= p<0.01; *= p<0.05. Bars in graphs indicate mean±SEM.