Methylation in the CHH Context Allows to Predict Recombination in Rice

Oct 19, 2022·
Mauricio Peñuela
,
Jenny Johana Gallo-Franco
,
Jorge Finke
,
Camilo Rocha
Anestis Gkanogiannis
Anestis Gkanogiannis
,
Thaura Ghneim-Herrera
,
Mathias Lorieux
· 0 min read
Abstract
DNA methylation is the most studied epigenetic trait. It is considered a key factor in regulating plant development and physiology, and has been associated with the regulation of several genomic features, including transposon silencing, regulation of gene expression, and recombination rates. Nonetheless, understanding the relation between DNA methylation and recombination rates remains a challenge. This work explores the association between recombination rates and DNA methylation for two commercial rice varieties. The results show negative correlations between recombination rates and methylated cytosine counts for all contexts tested at the same time, and for CG and CHG contexts independently. In contrast, a positive correlation between recombination rates and methylated cytosine count is reported in CHH contexts. Similar behavior is observed when considering only methylated cytosines within genes, transposons, and retrotransposons. Moreover, it is shown that the centromere region strongly affects the relationship between recombination rates and methylation. Finally, machine learning regression models are applied to predict recombination using the count of methylated cytosines in the CHH context as the entrance feature. These findings shed light on the understanding of the recombination landscape of rice and represent a reference framework for future studies in rice breeding, genetics, and epigenetics.
Type
Publication
Int. J. Mol. Sci. 2022, 23(20), 12505;, 23(20)
publication
Anestis Gkanogiannis
Authors
Senior AI/ML and genomics practitioner

Senior AI/ML and genomics practitioner with ~15 years building open-source, production-grade tools for large-scale biological data. Maintainer of multiple Bioconductor packages (fastreeR, metabinR, jvecfor), and author of agentic, LLM-driven tooling that runs reproducible bioinformatics workflows from natural-language requests.

Broad multi-omics background spanning genome assembly and annotation, population genomics, large-scale NGS and functional-genomics analysis, and metagenomics, backed by reproducible HPC software and end-to-end program leadership. Currently focused on bringing modern AI — embeddings, deep learning, and LLM-based agents — to making complex omics datasets faster and easier to interrogate.