生物
肌萎缩侧索硬化
遗传学
突变
外显子
基因
分子生物学
人口
错义突变
病理
医学
疾病
环境卫生
作者
John E. Landers,A. L. LeClerc,Linchun Shi,A. Virkud,T. Cho,M. M. Maxwell,A. Henry,Michel Polak,J. David Glass,Thomas J. Kwiatkowski,Ammar Al‐Chalabi,Christopher E. Shaw,P. Nigel Leigh,I. Rodriguez-Leyza,D. McKenna-Yasek,Peter C. Sapp,Robert H. Brown
出处
期刊:Neurology
[Ovid Technologies (Wolters Kluwer)]
日期:2008-03-06
卷期号:70 (14): 1179-1185
被引量:58
标识
DOI:10.1212/01.wnl.0000289760.85237.4e
摘要
Amyotrophic lateral sclerosis (ALS) is a progressive, neurodegenerative disorder involving upper and lower motor neurons. The vesicle-associated membrane protein B (VAPB) gene has been genetically linked to ALS in several large Brazilian families in which the disorder is caused by a proline to serine mutation at codon 56 (P56S). No additional mutations have been identified.To establish the prevalence of VAPB mutations, we screened 80 familial ALS samples by DNA sequencing.Our study failed to identify any novel VAPB gene mutations but identified a single Brazilian family harboring the P56S mutation. In a second familial ALS case, we identified a three-base pair deletion within exon 5 of the VAPB gene that deleted the serine residue at position 160 (Delta S160). This variant is detected in a normal population at low frequency (0.45%). Analyses of homology alignment and secondary structure predict that this deletion significantly alters the structure of VAPB, although a GFP-Delta S160 VAPB fusion protein demonstrates a wild-type subcellular localization. This contrasts the aberrant localization observed in a GFP-P56S VAPB fusion protein. The allele frequency of Delta S160 in patients with sporadic ALS does not differ significantly from that in the normal population.Mutations in the VAPB gene are rare and the Delta S160 variant does not contribute to the development of amyotrophic lateral sclerosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI