Absence of Mutation in the Beta-amyloid Cdnas Cloned From the Brains of 3 Patients With Sporadic Alzheimers-disease
(1988) Molecular Brain Research — Vol. 4, n° 2, p. 121-131 (1988)
Files
pdfdocument.pdf
Restricted Access - Adobe PDF
- 842.34 KB
Details
- Authors
- Abstract
- Using an oligonucleotide probe, we isolated cDNA clones corresponding to the precursor of the β-amyloid peptide (BAP) from brain libraries of 3 patients with sporadic Alzheimer's disease (AD). DNA sequencing showed that the largest cDNA clone encompasses 83% of the open reading frame proposed by Kang et al. to encode the BAP precursor (APP). cDNA clones from each of the 3 AD brain libraries were identical to the sequence of the APP-cDNAs cloned from normal adult human and fetal brain. An antisense-radiolabeled RNA copy of one of the AD clones detected a pattern of 3 gene transcripts measuring 3.5, 3.2 and 1.6 kilobases (kb) in both normal and AD brain RNAs. These data suggest that there are no mutations in or about the 42 amino acid (aa) sequence of BAP and that the accumulation of amyloid consistently found in AD may result from altered post-translational processing of APP.
- Affiliations
Citations
Vitek, MP., Rasool, CG., Desauvage, F., Vitek, SM., Bartus, RT., Beer, B., Ashton, RA., Macq, AF., Maloteaux, J.-M., Blume, AJ., & Octave, J.-N. (1988). Absence of Mutation in the Beta-amyloid Cdnas Cloned From the Brains of 3 Patients With Sporadic Alzheimers-disease. Molecular Brain Research, 4(2), 121-131. https://doi.org/10.1016/0169-328X(88)90004-6 (Original work published 1988)