| Literature DB >> 29852216 |
Gincy George1, Sachidanand Singh2, Sowmya Bekshe Lokappa3, Jobin Varkey4.
Abstract
Parkinson's disease (PD) is a neurodegenerative disorder involving progressive deterioration of dopaminergic neurons. Although few genetic markers for familial PD are known, the etiology of sporadic PD remains poorly understood. Microarray data was analysed for induced pluripotent stem cells (iPSCs) derived from PD patients and mature neuronal cells (mDA) differentiated from these iPSCs. Combining expression and semantic similarity, a highly-correlated PD interactome was constructed that included interactions of established Parkinson's disease marker genes. A novel three-way comparative approach was employed, delineating topologically and functionally important genes. These genes showed involvement in pathways like Parkin-ubiquitin proteosomal system (UPS), immune associated biological processes and apoptosis. Of interest are three genes, eEF1A1, CASK, and PSMD6 that are linked to PARK2 activity in the cell and thereby form attractive candidate genes for understanding PD. Network biology approach delineated in this study can be applied to other neurodegenerative disorders for identification of important genetic regulators.Entities:
Keywords: Differential co-expression analysis; Gene expression profile; Gene ontology; Network analysis; Parkinson's disease; α-Synuclein
Mesh:
Year: 2018 PMID: 29852216 DOI: 10.1016/j.ygeno.2018.05.005
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736