Integrative analysis identifies bHLH transcription factors as contributors to Parkinson's disease risk mechanisms

Genome-wide association studies (GWAS) have identified multiple genetic risk signals for Parkinson's disease (PD), however translation into underlying biological mechanisms remains scarce. Genomic functional annotations of neurons provide new resources that may be integrated into analyses of GWAS findings. Altered transcription factor binding plays an important role in human diseases. Insight into transcriptional networks involved in PD risk mechanisms may thus improve our understanding of pathogenesis. We analysed overlap between genome-wide association signals in PD and open chromatin in neurons across multiple brain regions, finding a significant enrichment in the superior temporal cortex. The involvement of transcriptional networks was explored in neurons of the superior temporal cortex based on the location of candidate transcription factor motifs identified by two de novo motif discovery methods. Analyses were performed in parallel, both finding that PD risk variants significantly overlap with open chromatin regions harboring motifs of basic Helix-Loop-Helix (bHLH) transcription factors. Our findings show that cortical neurons are likely mediators of genetic risk for PD. The concentration of PD risk variants at sites of open chromatin targeted by members of the bHLH transcription factor family points to an involvement of these transcriptional networks in PD risk mechanisms.

Automated summary

Genome-wide association studies have identified genetic risk signals for Parkinson's disease, with potential biological mechanisms yet to be fully understood. Utilizing genomic functional annotations, researchers found an overlap between PD risk variants and open chromatin regions in neurons, particularly in the superior temporal cortex. This suggests that cortical neurons may play a key role in mediating genetic risk for PD, implicating transcriptional networks involving basic Helix-Loop-Helix transcription factors.