- Kulis, Marta;
- Merkel, Angelika;
- Heath, Simon;
- Queirós, Ana C;
- Schuyler, Ronald P;
- Castellano, Giancarlo;
- Beekman, Renée;
- Raineri, Emanuele;
- Esteve, Anna;
- Clot, Guillem;
- Verdaguer-Dot, Néria;
- Duran-Ferrer, Martí;
- Russiñol, Nuria;
- Vilarrasa-Blasi, Roser;
- Ecker, Simone;
- Pancaldi, Vera;
- Rico, Daniel;
- Agueda, Lidia;
- Blanc, Julie;
- Richardson, David;
- Clarke, Laura;
- Datta, Avik;
- Pascual, Marien;
- Agirre, Xabier;
- Prosper, Felipe;
- Alignani, Diego;
- Paiva, Bruno;
- Caron, Gersende;
- Fest, Thierry;
- Muench, Marcus O;
- Fomin, Marina E;
- Lee, Seung-Tae;
- Wiemels, Joseph L;
- Valencia, Alfonso;
- Gut, Marta;
- Flicek, Paul;
- Stunnenberg, Hendrik G;
- Siebert, Reiner;
- Küppers, Ralf;
- Gut, Ivo G;
- Campo, Elías;
- Martín-Subero, José I
We analyzed the DNA methylome of ten subpopulations spanning the entire B cell differentiation program by whole-genome bisulfite sequencing and high-density microarrays. We observed that non-CpG methylation disappeared upon B cell commitment, whereas CpG methylation changed extensively during B cell maturation, showing an accumulative pattern and affecting around 30% of all measured CpG sites. Early differentiation stages mainly displayed enhancer demethylation, which was associated with upregulation of key B cell transcription factors and affected multiple genes involved in B cell biology. Late differentiation stages, in contrast, showed extensive demethylation of heterochromatin and methylation gain at Polycomb-repressed areas, and genes with apparent functional impact in B cells were not affected. This signature, which has previously been linked to aging and cancer, was particularly widespread in mature cells with an extended lifespan. Comparing B cell neoplasms with their normal counterparts, we determined that they frequently acquire methylation changes in regions already undergoing dynamic methylation during normal B cell differentiation.