Novel FUS mutation Y526F causing rapidly progressive familial amyotrophic lateral sclerosis

Abstract

FUS gene is one of the most common mutated genes in amyotrophic lateral sclerosis (ALS). We sequenced for FUS mutations in a cohort of 15 familial ALS and 275 sporadic ALS of Chinese origin. All 15 exons of the FUS gene were sequenced by targeted next-generation sequencing in a cohort of 15 familial ALS indexes and 275 sporadic ALS patients of Chinese origin. One novel p.Y526F mutation in FUS was detected in one familial ALS proband. Another novel FUS p.Q140R variant and two known FUS mutations (p.R495Efs*33 and p.R521C) were identified in four sporadic ALS cases. The frequency of FUS mutation in our cohort is 6.7% in familial ALS and 1.5% in sporadic ALS. The familial ALS proband carrying the FUS p.Y526F mutation presented with juvenile-onset lower limbs weakness and demonstrated an aggressive course, with respiratory muscles involvement 6 months after onset. The other patients in the family all had limbs weakness and died 1–2 years after disease onset. Our results strengthen that FUS mutations are the most frequent genetic causes of young-onset aggressive ALS. Genetic testing of the FUS gene should be performed in early-onset ALS patients especially those with a rapid progression.

Keywords:

• Amyotrophic lateral sclerosis
• ALS
• FUS mutation

Acknowledgments

The authors thank the patients and their families for their cooperation in this study.

Disclosure statement

The authors declare no conflicts of interest.

Additional information

Funding

This study was supported by grants from the National Natural Science Foundation of China [grant number 81671271, 81974199], Joint Funds for the innovation of science and Technology, Fujian province [grant number 2017Y91010015] and Program for New Century Excellent Talents in Fujian Province University [grant number 2017B014].