MITOCHONDRIAL-DNA VARIANTS OBSERVED IN ALZHEIMER-DISEASE AND PARKINSON DISEASE PATIENTS

被引:401
作者
SHOFFNER, JM
BROWN, MD
TORRONI, A
LOTT, MT
CABELL, MF
MIRRA, SS
BEAL, MF
YANG, CC
GEARING, M
SALVO, R
WATTS, RL
JUNCOS, JL
HANSEN, LA
CRAIN, BJ
FAYAD, M
RECKORD, CL
WALLACE, DC
机构
[1] EMORY UNIV, SCH MED,DEPT GENET & MOLEC MED,1462 CLIFTON RD, ROOM 403, ATLANTA, GA 30322 USA
[2] EMORY UNIV, SCH MED, DEPT NEUROL, ATLANTA, GA 30322 USA
[3] EMORY UNIV, SCH MED, DEPT PATHOL, ATLANTA, GA 30322 USA
[4] EMORY UNIV, SCH MED, DEPT LAB MED, ATLANTA, GA 30322 USA
[5] VET AFFAIRS MED CTR, DECATUR, GA 30033 USA
[6] UNIV CALIF SAN DIEGO, DEPT NEUROSCI, LA JOLLA, CA 92093 USA
[7] UNIV CALIF SAN DIEGO, DEPT PATHOL, LA JOLLA, CA 92093 USA
[8] MASSACHUSETTS GEN HOSP, DEPT NEUROL, BOSTON, MA 02114 USA
[9] HARVARD UNIV, SCH MED, BOSTON, MA 02114 USA
[10] DUKE UNIV, MED CTR, DEPT PATHOL, DURHAM, NC 27706 USA
关键词
D O I
10.1006/geno.1993.1299
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Mitochondrial DNA (mtDNA) variants associated with Alzheimer disease (AD) and Parkinson disease (PD) were sought by restriction endonuclease analysis in a cohort of 71 late-onset Caucasian patients. A tRNAGln gene variant at nucleotide pair (np) 4336 that altered a moderately conserved nucleotide was present in 9/173 (5.2%) of the patients surveyed but in only 0.7% of the general Caucasian controls. One of these patients harbored an additional novel 12S rRNA 5-nucleotide insertion at np 956-965, while a second had a missense variant at np 3397 that converted a highly conserved methionine to a valine. This latter mutation was also found in an independent AD + PD patient, as was a heteroplasmic 16S rRNA variant at np 3196. Additional studies will be required to determine the significance, if any, of these mutations. © 1993 Academic Press. All rights reserved.
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页码:171 / 184
页数:14
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