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Human Molecular Genetics Advance Access published online on April 18, 2008

Human Molecular Genetics, doi:10.1093/hmg/ddn131
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© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach

Han-Xiang Deng1,*, Hujun Jiang1,2, Ronggen Fu1, Hong Zhai1, Yong Shi1, Erdong Liu1, Makito Hirano1, Mauro C. Dal Canto3 and Teepu Siddique1,4,5

1 Davee Department of Neurology and Clinical Neurosciences, Central South University, Changsha, Hunan, China 2 National Laboratory of Medical Genetics, Central South University, Changsha, Hunan, China 3 Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA 4 Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA 5 Institute for Neuroscience, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA

* Address for correspondence: Dr. Han-Xiang Deng, Davee Department of Neurology and Clinical Neurosciences, Northwestern University Feinberg School of Medicine, Tarry Building 13-715, 303 E. Chicago Ave, Chicago, IL 60611, USA. E-mail: h-deng{at}northwestern.edu Tel: (312) 503-4737 Fax: (312) 908-0865

Received January 24, 2008; Revised April 15, 2008; Accepted April 15, 2008

Mutations in Cu,Zn superoxide dismutase (SOD1) are associated with amyotrophic lateral sclerosis (ALS). Among more than 100 ALS-associated SOD1 mutations, premature termination codon (PTC) mutations exclusively occur in exon 5, the last exon of SOD1. The molecular basis of ALS-associated toxicity of the mutant SOD1 is not fully understood. Here, we show that nonsense-mediated mRNA decay (NMD) underlies clearance of mutant mRNA with a PTC in the non-terminal exons. To further define the crucial ALS-associated SOD1 fragments, we designed and tested an exon-fusion approach using an artificial transgene SOD1T116X that harbors a PTC in exon 4. We found that the SOD1T116X transgene with a fused exon could escape NMD in cellular models. We generated a transgenic mouse model that overexpresses SOD1T116X. This mouse model developed ALS-like phenotype and pathology. Thus, our data have demonstrated that a "mini-SOD1" of only 115 amino acids is sufficient to cause ALS. This is the smallest ALS-causing SOD1 molecule currently defined. This proof of principle result suggests that the exon-fusion approach may have potential not only to further define a shorter ALS-associated SOD1 fragment, thus providing a molecular target for designing rational therapy, but also to dissect toxicities of other proteins encoded by genes of multiple exons through a "gain of function" mechanism.


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