Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

被引:458
作者
Pennacchio, LA
Lehesjoki, AE
Stone, NE
Willour, VL
Virtaneva, K
Miao, JM
DAmato, E
Ramirez, L
Faham, M
Koskiniemi, M
Warrington, JA
Norio, R
delaChapelle, A
Cox, DR
Myers, RM
机构
[1] STANFORD UNIV,SCH MED,DEPT GENET,STANFORD,CA 94305
[2] STANFORD UNIV,DEPT BIOL,STANFORD,CA 94305
[3] UNIV HELSINKI,DEPT MED GENET,SF-00290 HELSINKI,FINLAND
[4] UNIV HELSINKI,DEPT VIROL,SF-00290 HELSINKI,FINLAND
[5] FINNISH POPULAT & FAMILY WELF FEDERAT,DEPT MED GENET,SF-00100 HELSINKI,FINLAND
关键词
D O I
10.1126/science.271.5256.1731
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is an autosomal recessive inherited form of epilepsy, previously linked to human chromosome 21q22.3. The gene encoding cystatin B was shown to be localized to this region, and levels of messenger RNA encoded by this gene were found to be decreased in cells from affected individuals. Two mutations, a 3' splice site mutation and a stop codon mutation, were identified in the gene encoding cystatin B in EPM1 patients but were not present in unaffected individuals. These results provide evidence that mutations in the gene encoding cystatin B are responsible for the primary defect in patients with EPM1.
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页码:1731 / 1734
页数:4
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