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A presenilin 1 mutation in the first case of Alzheimer's disease: Revisited
Author(s) -
Rupp Carsten,
Beyreuther Konrad,
Maurer Konrad,
Kins Stefan
Publication year - 2014
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2014.06.005
Subject(s) - exon , presenilin , mutation , psen1 , genetics , dna sequencing , nonsynonymous substitution , point mutation , gene , biology , polymerase chain reaction , alzheimer's disease , disease , microbiology and biotechnology , medicine , pathology , genome
Background Recently, a single point mutation in the presenilin 1 ( PSEN1 ) gene of the first described Alzheimer's disease (AD) patient Auguste D was reported by Müller and co‐workers. However, the sequencing results of the DNA from a 100‐year‐old tissue contained some uncertainties. Methods We heat extracted DNA from an original histological slice of Auguste D's brain and used nested polymerase chain reaction for the amplification of different exons of genes known to be affected in familial forms of AD. Results Our sequencing analysis did not validate the reported mutation. Furthermore, an extended sequencing analysis of Auguste D's DNA revealed no indication of a nonsynonymous hetero‐ or homozygous mutation in the exons of APP , PSEN1 , and PSEN2 genes comprising the already known familial AD mutations. Conclusion Despite the wealth of data from Müller and co‐workers, our results emphasize the requirement of more detailed analysis of Auguste D's DNA in future.