Rethinking ALS: The FUS about TDP-43

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Rethinking ALS: The FUS about TDP-43 Clotilde Lagier-Tourenne, Don W. Cleveland  Cell  Volume 136, Issue 6, Pages 1001-1004 (March 2009) DOI: 10.1016/j.cell.2009.03.006 Copyright © 2009 Elsevier Inc. Terms and Conditions

Figure 1 TDP-43 and FUS/TLS Mutations in ALS (A) Thirty dominant mutations in TDP-43 have been identified in sporadic (red) and familial (black) ALS patients, with most lying in the C-terminal glycine-rich region of TDP-43. All are missense mutations, except for the truncating mutation TDP-43Y374X. (B) Fourteen mutations in FUS/TLS have been identified in familial ALS cases, with most lying in the final 13 amino acids of this protein (R514S and G515S are found in cis). (Data compiled from Kwiatkowski et al., 2009; Vance et al., 2009; domains from http://www.uniprot.org and http://www.cbs.dtu.dk/services/NetNES.) Cell 2009 136, 1001-1004DOI: (10.1016/j.cell.2009.03.006) Copyright © 2009 Elsevier Inc. Terms and Conditions