Potential gene identification and pathway crosstalk analysis of age-related macular degeneration

• Published in: Frontiers in genetics Vol. 13; p. 992328
• Main Authors: Ren, Chengda, Yu, Jing
• Format: Journal Article
• Language: English
• Published: Frontiers Media S.A 06.09.2022
• Subjects: AMD; gene identification; Genetics; GO analyses; lipid metabolism; pathway crosstalk
• ISSN: 1664-8021; 1664-8021
• DOI: 10.3389/fgene.2022.992328

Age-related macular degeneration (AMD), the most prevalent visual disorder among the elderly, is confirmed as a multifactorial disease. Studies demonstrated that genetic factors play an essential role in its pathogenesis. Our study aimed to make a relatively comprehensive study about biological functions of AMD related genes and crosstalk of their enriched pathways. 1691 AMD genetic studies were reviewed, GO enrichment and pathway crosstalk analyses were conducted to elucidate the biological features of these genes and to demonstrate the pathways that these genes participate. Moreover, we identified novel AMD-specific genes using shortest path algorithm in the context of human interactome. We retrieved 176 significantly AMD-related genes. GO results showed that the most significant term in each of these three GO categories was: signaling receptor binding (P BH = 4.835 × 10 −7 ), response to oxygen-containing compound (P BH = 2.764 × 10 −21 ), and extracellular space (P BH = 2.081 × 10 −19 ). The pathway enrichment analysis showed that complement pathway is the most enriched. The pathway crosstalk study showed that the pathways could be divided into two main modules. These two modules were connected by cytokine-cytokine receptor interaction pathway. 42 unique genes potentially participating AMD development were obtained. The aberrant expression of the mRNA of FASN and LRP1 were validated in AMD cell and mouse models. Collectively, our study carried out a comprehensive analysis based on genetic association study of AMD and put forward several evidence-based genes for future study of AMD.