FIGURE SUMMARY
Title

Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways

Authors
Blokhuis, A.M., Koppers, M., Groen, E.J., van den Heuvel, D.M., Dini Modigliani, S., Anink, J.J., Fumoto, K., van Diggelen, F., Snelting, A., Sodaar, P., Verheijen, B.M., Demmers, J.A., Veldink, J.H., Aronica, E., Bozzoni, I., den Hertog, J., van den Berg, L.H., Pasterkamp, R.J.
Source
Full text @ Acta Neuropathol.

Exogenous FMRP rescues NMJ and locomotion defects caused by mutant FUS. a Western blot analysis of 72 hpf zebrafish embryo lysates using antibodies against human FUS or FMRP following injection of FUS WT, FUS R521C and/or FMR1 RNAs. Tubulin is used as a loading control. NIC non-injected control. b Representative images of neuromuscular junctions (NMJ) in 72 hpf NIC zebrafish embryos or following injection of FUS WT, FUS R521C, and FUS R521C and FMR1 RNAs. Anti-synaptic vesicles 2 (SV2) and anti-bungarotoxin (BTX) were used to label the pre- and postsynaptic compartments. Arrowheads indicate absence of colocalization between SV2 and BTX staining. c Quantification of the Pearson’s correlation coefficient for overlap between immunolabeling for pre- and post-synaptic markers, as shown in b. n = 20 per condition. IB immunoblot. d Quantification of touch-evoked escape responses (TEER) in zebrafish embryos at 72 hpf following injection of the indicated RNAs. Data is obtained over five experiments with n = 267 for NIC, n = 182 for FUS WT, n = 163 for FUS R521C and n = 111 for FUS R521C + FMR1. *p < 0.05, **p < 0.01, Fisher’s exact test. Scale bar 20 µm

Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Acta Neuropathol.