Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.

Nicastrin is an obligatory component of the γ-secretase; the enzyme complex that leads to the production of Aβ fragments critically central to the pathogenesis of Alzheimer's disease (AD). Analyses of the effects of common variation in this gene on risk for late onset AD have been inconclusive....

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Autores principales: Michelle K Lupton, Petroula Proitsi, Makrina Danillidou, Magda Tsolaki, Gillian Hamilton, Richard Wroe, Megan Pritchard, Kathryn Lord, Belinda M Martin, Iwona Kloszewska, Hilkka Soininen, Patrizia Mecocci, Bruno Vellas, Denise Harold, Paul Hollingworth, Simon Lovestone, John F Powell
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Publicado: Public Library of Science (PLoS) 2011
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Acceso en línea:https://doaj.org/article/23a00884875846cc8154fa1c9d1e808c
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spelling oai:doaj.org-article:23a00884875846cc8154fa1c9d1e808c2021-11-18T06:58:13ZDeep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.1932-620310.1371/journal.pone.0017298https://doaj.org/article/23a00884875846cc8154fa1c9d1e808c2011-02-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21364883/?tool=EBIhttps://doaj.org/toc/1932-6203Nicastrin is an obligatory component of the γ-secretase; the enzyme complex that leads to the production of Aβ fragments critically central to the pathogenesis of Alzheimer's disease (AD). Analyses of the effects of common variation in this gene on risk for late onset AD have been inconclusive. We investigated the effect of rare variation in the coding regions of the Nicastrin gene in a cohort of AD patients and matched controls using an innovative pooling approach and next generation sequencing. Five SNPs were identified and validated by individual genotyping from 311 cases and 360 controls. Association analysis identified a non-synonymous rare SNP (N417Y) with a statistically higher frequency in cases compared to controls in the Greek population (OR 3.994, CI 1.105-14.439, p = 0.035). This finding warrants further investigation in a larger cohort and adds weight to the hypothesis that rare variation explains some of genetic heritability still to be identified in Alzheimer's disease.Michelle K LuptonPetroula ProitsiMakrina DanillidouMagda TsolakiGillian HamiltonRichard WroeMegan PritchardKathryn LordBelinda M MartinIwona KloszewskaHilkka SoininenPatrizia MecocciBruno VellasDenise HaroldPaul HollingworthSimon LovestoneJohn F PowellPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 2, p e17298 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Michelle K Lupton
Petroula Proitsi
Makrina Danillidou
Magda Tsolaki
Gillian Hamilton
Richard Wroe
Megan Pritchard
Kathryn Lord
Belinda M Martin
Iwona Kloszewska
Hilkka Soininen
Patrizia Mecocci
Bruno Vellas
Denise Harold
Paul Hollingworth
Simon Lovestone
John F Powell
Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.
description Nicastrin is an obligatory component of the γ-secretase; the enzyme complex that leads to the production of Aβ fragments critically central to the pathogenesis of Alzheimer's disease (AD). Analyses of the effects of common variation in this gene on risk for late onset AD have been inconclusive. We investigated the effect of rare variation in the coding regions of the Nicastrin gene in a cohort of AD patients and matched controls using an innovative pooling approach and next generation sequencing. Five SNPs were identified and validated by individual genotyping from 311 cases and 360 controls. Association analysis identified a non-synonymous rare SNP (N417Y) with a statistically higher frequency in cases compared to controls in the Greek population (OR 3.994, CI 1.105-14.439, p = 0.035). This finding warrants further investigation in a larger cohort and adds weight to the hypothesis that rare variation explains some of genetic heritability still to be identified in Alzheimer's disease.
format article
author Michelle K Lupton
Petroula Proitsi
Makrina Danillidou
Magda Tsolaki
Gillian Hamilton
Richard Wroe
Megan Pritchard
Kathryn Lord
Belinda M Martin
Iwona Kloszewska
Hilkka Soininen
Patrizia Mecocci
Bruno Vellas
Denise Harold
Paul Hollingworth
Simon Lovestone
John F Powell
author_facet Michelle K Lupton
Petroula Proitsi
Makrina Danillidou
Magda Tsolaki
Gillian Hamilton
Richard Wroe
Megan Pritchard
Kathryn Lord
Belinda M Martin
Iwona Kloszewska
Hilkka Soininen
Patrizia Mecocci
Bruno Vellas
Denise Harold
Paul Hollingworth
Simon Lovestone
John F Powell
author_sort Michelle K Lupton
title Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.
title_short Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.
title_full Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.
title_fullStr Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.
title_full_unstemmed Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.
title_sort deep sequencing of the nicastrin gene in pooled dna, the identification of genetic variants that affect risk of alzheimer's disease.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/23a00884875846cc8154fa1c9d1e808c
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