Abstract
Abstract
Background: Two of the most prevalent central neuron system disorders are Alzheimer (AD) and Parkinson’s disease (PD). Interestingly, despite their differences in both pathological and molecular basis of the diseases, they exhibit some degrees of similarities. Here, we have conducted a comparative systems-level analysis study for these diseases. Cohort cortex samples from healthy control cases and AD/PD patients were obtained, then we have applied weighted gene co-expression network analysis (WGCNA).
Results: Network analysis identified key modules of genes related to each of these diseases. Gene ontology enrichment of the modules showed the involvement of both disease-specific and shared biological processes, including chemical synaptic transmission, nervous system development, and immune responses that are involved in both AD and PD. Surprisingly, the expression patterns for the gene members of the shared modules were strikingly identical. Additionally, we have introduced a handful of novel genes, including INPP4A, CREG2, ABI3, MYO1F, NAPB, NXN, DOCK6, CPSF6, and IKZF1, with potential functionality in both diseases; AD and PD.
Conclusions: In conclusion, besides unveiling the presence of high molecular level similarities between AD and PD, for the first time, several novel genes have been proposed that can open a new opportunity for diagnostic or treatment applications.
Publisher
Research Square Platform LLC
Reference65 articles.
1. A preliminary study of the whole-genome expression profile of sporadic and monogenic early-onset Alzheimer's disease;Antonell A;Neurobiology of aging,2013
2. Wnt signaling in midbrain dopaminergic neuron development and regenerative medicine for Parkinson's disease;Arenas E;Journal of molecular cell biology,2014
3. Bastian M, Heymann S, Jacomy M (2009) Gephi: an open source software for exploring and manipulating networks. Icwsm 8 (2009):361–362
4. Vulnerability of cortical neurons to Alzheimer's and Parkinson's diseases;Braak H;Journal of Alzheimer's disease,2006
5. Büttner N, Johnsen SA, Kügler S, Vogel T (2010) Af9/Mllt3 interferes with Tbr1 expression through epigenetic modification of histone H3K79 during development of the cerebral cortex. Proceedings of the National Academy of Sciences:200912041