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Scientific ReportsNeurosciencePeer-reviewed journal article

Genetic dissection of Down syndrome-associated alterations in APP/amyloid-β biology using mouse models

Justin ToshiD, Elena R. RhymesiD, Paige MumfordiD, Heather T. WhittakeriD, Laura J. Pulford, Suzanna NoyiD, Karen CleverleyiD, André StrydomiD, Elizabeth FisheriD, Frances K. WisemaniD, Dean NižetićiD, John HardyiD, Victor L. J. TybulewicziD, Annette Karmiloff‐Smith, Matthew C. WalkeriD, Robert C. WykesiD

PDFDOIPreprint

Abstract

Individuals who have Down syndrome (caused by trisomy of chromosome 21), have a greatly elevated risk of early-onset Alzheimers disease, in which amyloid-{beta} accumulates in the brain. Amyloid-{beta} is a product of the chromosome 21 gene APP (amyloid precursor protein) and the extra copy or dose of APP is thought to be the cause of this early-onset Alzheimers disease. However, other chromosome 21 genes likely modulate disease when in three-copies in people with Down syndrome. Here we show that an extra copy of chromosome 21 genes, other than APP, influences APP/A{beta} biology. We crossed Down syndrome mouse models with partial trisomies, to an APP transgenic model and found that extra copies of subgroups of chromosome 21 gene(s) modulate amyloid-{beta} aggregation and APP transgene-associated mortality, independently of changing amyloid precursor protein abundance. Thus, genes on chromosome 21, other than APP, likely modulate Alzheimers disease in people who have Down syndrome.

Citations
26
FWCI
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top 11%

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