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Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.

  • Author(s): McClymont, Sarah A
  • Hook, Paul W
  • Soto, Alexandra I
  • Reed, Xylena
  • Law, William D
  • Kerans, Samuel J
  • Waite, Eric L
  • Briceno, Nicole J
  • Thole, Joey F
  • Heckman, Michael G
  • Diehl, Nancy N
  • Wszolek, Zbigniew K
  • Moore, Cedric D
  • Zhu, Heng
  • Akiyama, Jennifer A
  • Dickel, Diane E
  • Visel, Axel
  • Pennacchio, Len A
  • Ross, Owen A
  • Beer, Michael A
  • McCallion, Andrew S
  • et al.

Published Web Location

https://www.cell.com/ajhg/fulltext/S0002-9297(18)30370-7
No data is associated with this publication.
Abstract

The progressive loss of midbrain (MB) dopaminergic (DA) neurons defines the motor features of Parkinson disease (PD), and modulation of risk by common variants in PD has been well established through genome-wide association studies (GWASs). We acquired open chromatin signatures of purified embryonic mouse MB DA neurons because we anticipated that a fraction of PD-associated genetic variation might mediate the variants' effects within this neuronal population. Correlation with >2,300 putative enhancers assayed in mice revealed enrichment for MB cis-regulatory elements (CREs), and these data were reinforced by transgenic analyses of six additional sequences in zebrafish and mice. One CRE, within intron 4 of the familial PD gene SNCA, directed reporter expression in catecholaminergic neurons from transgenic mice and zebrafish. Sequencing of this CRE in 986 individuals with PD and 992 controls revealed two common variants associated with elevated PD risk. To assess potential mechanisms of action, we screened >16,000 proteins for DNA binding capacity and identified a subset whose binding is impacted by these enhancer variants. Additional genotyping across the SNCA locus identified a single PD-associated haplotype, containing the minor alleles of both of the aforementioned PD-risk variants. Our work posits a model for how common variation at SNCA might modulate PD risk and highlights the value of cell-context-dependent guided searches for functional non-coding variation.

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