8 research outputs found
Computational Modelling Folate Metabolism and DNA Methylation: Implications for Understanding Health and Ageing
This is a pre-copyedited, author-produced PDF of an article accepted for publication in 'Briefings in Bioinformatics' following peer review. The version of record Mc Auley, M. T., Mooney, K. M., & Salcedo-Sora, J. E. (2016). Computational Modelling Folate Metabolism and DNA Methylation: Implications for Understanding Health and Ageing. Briefings in Bioinformatics. DOI: 10.1093/bib/bbw116 is available online at: https://academic.oup.com/bib/article-abstract/doi/10.1093/bib/bbw116/2606065/Computational-modelling-folate-metabolism-and-DNADietary folates have a key role to play in health as deficiencies in the intake of these B vitamins have been implicated in a wide variety of clinical conditions. The reason for this is folates function as single carbon donors in the synthesis of methionine and nucleotides. Moreover, folates have a vital role to play in the epigenetics of mammalian cells by supplying methyl groups for DNA methylation reactions. Intriguingly, a growing body of experimental evidence suggests DNA methylation status could be a central modulator of the ageing process. This has important health implications because the methylation status of the human genome could be used to infer age-related disease risk. Thus, it is imperative we further our understanding of the processes which underpin DNA methylation and how these intersect with folate metabolism and ageing. The biochemical and molecular mechanisms which underpin these processes are complex. However, computational modelling offers an ideal framework for handling this complexity. A number of computational models have been assembled over the years, but to date no model has represented the full scope of the interaction between the folate cycle and the reactions which govern the DNA methylation cycle. In this review we will discuss several of the models which have been developed to represent these systems. In addition we will present a rationale for developing a combined model of folate metabolism and the DNA methylation cycle