Section 50
Chapter 49,279

Identification of the mutation of SOD1 gene in a familial amyotrophic lateral sclerosis

Shi, S.-g.; Li, L.-s.; Chen, K.-n.; Liu, X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 21(2): 149-152


ISSN/ISBN: 1003-9406
PMID: 15079798
Accession: 049278931

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To identify the mutation of Cu/Zn superoxide dismutase(SOD1) gene in an amyotrophic lateral sclerosis (ALS) family with unique phenotype. Five exons of SOD1 gene were amplified by PCR. The differences of these products were analyzed by PCR-single strand conformation polymorphism and visualized by silver staining. Abnormal bands were found in exons 2 and 5 of SOD1 gene in several familial members. DNA sequence analysis verified that a base pair insertion occurred in the codon area of exon 2 and in the intron area of exon 5. And the insertion mutation of exon 2 led to a frameshift mutation and premature stop. It is a new type of SOD1 mutation which may be associated with familial amyotrophic lateral sclerosis. Insertion mutation of exon 2 may be responsible for the disease of an ALS family in Chongqing.

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