CLONING OF A GENE BEARING MISSENSE MUTATIONS IN EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE

被引:3368
作者
SHERRINGTON, R
ROGAEV, EI
LIANG, Y
ROGAEVA, EA
LEVESQUE, G
IKEDA, M
CHI, H
LIN, C
LI, G
HOLMAN, K
TSUDA, T
MAR, L
FONCIN, JF
BRUNI, AC
MONTESI, MP
SORBI, S
RAINERO, I
PINESSI, L
NEE, L
CHUMAKOV, I
POLLEN, D
BROOKES, A
SANSEAU, P
POLINSKY, RJ
WASCO, W
DASILVA, HAR
HAINES, JL
PERICAKVANCE, MA
TANZI, RE
ROSES, AD
FRASER, PE
ROMMENS, JM
STGEORGEHYSLOP, PH
机构
[1] UNIV TORONTO,DEPT MED NEUROL,CTR RES NEURODEGENERAT DIS,TORONTO,ON,CANADA
[2] UNIV TORONTO,DEPT MED BIOPHYS,TORONTO,ON,CANADA
[3] UNIV TORONTO,DEPT MED,DIV NEUROL,TORONTO,ON M5S 1A8,CANADA
[4] UNIV TORONTO,HOSP SICK CHILDREN,RES INST,TORONTO,ON M5S 1A8,CANADA
[5] UNIV TORONTO,DEPT MED & MOLEC GENET,TORONTO,ON M5S 1A8,CANADA
[6] ECOLE PRAT HAUTES ETUD,NEUROHIST LAB,F-75651 PARIS 13,FRANCE
[7] INSERM LA SALPETRIERE,U106,F-75651 PARIS 13,FRANCE
[8] USL 6,I-88046 LAMEZIA TERME,ITALY
[9] CNR,UO,I-88046 LAMEZIA TERME,ITALY
[10] UNIV FLORENCE,DEPT NEUROL & PSYCHIAT,FLORENCE,ITALY
[11] UNIV TURIN,DEPT NEUROL,I-10126 TURIN,ITALY
[12] NINCDS,CLIN NEUROPHARMACOL SECT,BETHESDA,MD 20892
[13] CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
[14] UNIV MASSACHUSETTS,MED CTR,DEPT NEUROL,WORCESTER,MA 01655
[15] HARVARD UNIV,MASSACHUSETTS GEN HOSP,SCH MED,MOLEC NEUROGENET LAB,BOSTON,MA 02114
[16] HARVARD UNIV,MASSACHUSETTS GEN HOSP,SCH MED,DEPT NEUROL,GENET & AGING LAB,BOSTON,MA 02114
[17] HARVARD UNIV,SCH MED,DEPT GENET,BOSTON,MA 02114
[18] DUKE UNIV,MED CTR,BRYAN ALZHEIMERS DIS RES CTR,DURHAM,NC 27710
[19] GLAXO GRP RES LTD,RES & DEV,MOLEC PATHOL,GREENFORD UB6 0HE,MIDDX,ENGLAND
[20] SANDOZ PHARMACEUT CORP,SANDOZ RES INST,E HANOVER,NJ 07936
[21] WESTERN GEN HOSP,MRC,HUMAN GENET UNIT,EDINBURGH,MIDLOTHIAN,SCOTLAND
关键词
D O I
10.1038/375754a0
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
Some cases of Alzheimer's disease are inherited as an autosomal dominant trait. Genetic linkage studies have mapped a locus (AD3) associated with susceptibility to a very aggressive form of Alzheimer's disease to chromosome 14q24.3. We have defined a minimal cosegregating region containing the AD3 gene, and isolated at least 19 different transcripts encoded within this region. One of these transcripts (S182) corresponds to a novel gene whose product is predicted to contain multiple transmembrane domains and resembles an integral membrane protein. Five different missense mutations have been found that cosegregate with early-onset familial Alzheimer's disease. Because these changes occurred In conserved domains of this gene, and are not present in normal controls, they are likely to be causative of AD3.
引用
收藏
页码:754 / 760
页数:7
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