Cited by 164Parkinson's Disease Mechanisms and TreatmentsAlzheimer's disease research and treatmentsGenetic Associations and Epidemiology

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

Rademakers, Rosa, Melquist, Stacey, Cruts, Marc, Theuns, Jessie, Del-Favero, Jurgen, Poorkaj, Parvoneh, Baker, Matt, Sleegers, Kristel +19 more·2005·Human Molecular Genetics

Abstract

Two extended haplotypes exist across the tau gene-H1 and H2-with H1 consistently associated with increased risk of progressive supranuclear palsy (PSP). Using 15 haplotype tagging SNPs (htSNPs), capturing >95% of MAPT haplotype diversity, we performed association analysis in a US sample of 274 predominantly pathologically confirmed PSP patients and 424 matched control individuals. We found that PSP risk is associated with one of two major ancestral H1 haplotypes, H1B, increasing from 14% in control individuals to 22% in PSP patients (P<0.001). In young PSP patients, the H1B risk could be localized to a 22 kb regulatory region in intron 0 (P<0.001) and could be fully explained by one SNP, htSNP167, creating a LBP-1c/LSF/CP2 site, shown to regulate the expression of genes in other neurodegenerative disorders. Luciferase reporter data indicated that the 182 bp conserved regulatory region, in which htSNP167 is located, is transcriptionally active with both alleles differentially influencing expression. Further, we replicated the htSNP167 association in a second, independently ascertained US PSP patient-control sample. However, the htSNP association showed that H1 risk alone could not explain the overall differences in H1 and H2 frequencies in PSP patients and control individuals. Thus, risk variants on different H1 htSNP haplotypes and protective variants on H2 contribute to population risk for PSP.

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Crossref · 10.1093/hmg/ddi361

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Authors
Rademakers, R., Melquist, S., Cruts, M., Theuns, J., Del-Favero, J., Poorkaj, P., Baker, M., Sleegers, K., Crook, R., De Pooter, T., Kacem, S. B., Adamson, J., Van den Bossche, D., Van den Broeck, M., Gass, J., Corsmit, E., De Rijk, P., Thomas, N., Engelborghs, S., Heckman, M., Litvan, I., Crook, J., De Deyn, P. P., Dickson, D., Schellenberg, G. D., Van Broeckhoven, C., & Hutton, M. L.
Affiliations
  • University of Antwerp (BE)
  • Mayo Clinic in Florida (US)
  • Vlaams Instituut voor Biotechnologie (BE)
  • University of Washington (US)
  • University of Louisville (US)
Corresponding author
Rademakers, Rosa
Venue
Human Molecular Genetics
Published
2005-09-29
Volume
14
Issue
21
Pages
3281-3292
ISSN
  • 0964-6906 (ISSN-L)
  • 1460-2083
OpenAlex
W2150655508
Cited by
164
References
2
Citations by year
2026: 1 · 2025: 5 · 2024: 3 · 2023: 2 · 2022: 3 · 2021: 4 · 2020: 4 · 2019: 2 · 2018: 3 · 2017: 7 · 2016: 10 · 2015: 12 · 2014: 8 · 2013: 9 · 2012: 8
FWCI
11.01
Type
journal article
Language
en
Open access
closed
Locations
  • Human Molecular Genetics (publishedVersion)
  • PubMed (publishedVersion)
  • VUBIR (Vrije Universiteit Brussel) (submittedVersion)
Funders
  • Mayo Clinic
  • National Institute on Aging (P01-AG-17216, F32AG024030, AG 24030, P01AG017216)
Topics
  • Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
Keywords
progressive supranuclear palsy, MAPT, tau gene, haplotype-tagging SNPs, genetic risk, transcriptional regulation, haplotype association, neurodegenerative disease genetics
MeSH terms
Age Factors, Aged, Aged, 80 and over, Chromosome Mapping, Gene Expression Regulation, Genotype, Haplotypes, Humans, Luciferases, Middle Aged, Supranuclear Palsy, Progressive, United States, tau Proteins, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Gene Components, White People

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