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Unravelling epigenetic mechanisms in Cerastoderma edule genome: a comparison of healthy and neoplastic cockles. | LitMetric

AI Article Synopsis

  • Cancer is a complex genetic disease that can spread between different species, including mammals and certain bivalves, with specific attention to hemic neoplasia in bivalves.
  • The study focuses on the epigenetic factors in the bivalve species Cerastoderma edule, using advanced sequencing to compare DNA methylation and hydroxymethylation between healthy specimens and those with cancerous growths.
  • Results showed that neoplastic specimens had lower global methylation and higher hydroxymethylation, indicating that these epigenetic changes play crucial roles in gene expression and tumor development, contributing to our understanding of cancer epigenetics overall.

Article Abstract

Cancer is a multifaceted genetic disease characterized by the acquisition of several essential hallmarks. Notably, certain cancers exhibit horizontal transmissibility, observed across mammalian species and diverse bivalves, the latter referred to as hemic neoplasia. Within this complex landscape, epigenetic mechanisms such as histone modifications and cytosine methylation emerge as fundamental contributors to the pathogenesis of these transmissible cancers. Our study delves into the epigenetic landscape of Cerastoderma edule, focusing on whole-genome methylation and hydroxymethylation profiles in heathy specimens and transmissible neoplasias by means of Nanopore long-read sequencing. Our results unveiled a global hypomethylation in the neoplastic specimens compared to their healthy counterparts, emphasizing the role of DNA methylation in these tumorigenic processes. Furthermore, we verified that intragenic CpG methylation positively correlated with gene expression, emphasizing its role in modulating transcription in healthy and neoplastic cockles, as also highlighted by some up-methylated oncogenic genes. Hydroxymethylation levels were significantly more elevated in the neoplastic samples, particularly within satellites and complex repeats, likely related to structural functions. Additionally, our analysis also revealed distinct methylation and activity patterns in retrotransposons, providing additional insights into bivalve neoplastic processes. Altogether, these findings contribute to understanding the epigenetic dynamics of bivalve neoplasias and shed light on the roles of DNA methylation and hydroxymethylation in tumorigenesis. Understanding these epigenetic alterations holds promise for advancing our broader understanding of cancer epigenetics.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11126487PMC
http://dx.doi.org/10.1007/s00438-024-02148-zDOI Listing

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