作者: Muhammad Assad Aslam , Mir Farshid Alemdehy , Eliza Mari Kwesi-Maliepaard , Marieta Caganova , Iris N. Pardieck
DOI: 10.1101/826370
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摘要: Development of naive peripheral B cells into terminally differentiated plasma is a highly controlled process guided by epigenetic mechanisms. Here we identified central role for the histone H3K79 methyltransferase DOT1L in controlling cell development. Upon deletion Dot1L early B-cell lineage, and activated prematurely acquired features failed to establish germinal centers (GC) normal humoral immune responses vivo. Transcriptome analyses revealed that promotes expression oncogenic, pro-proliferative pro-GC transcription factors. Simultaneously, indirectly repression anti-proliferative targets Polycomb Repressor Complex 2. Our findings show fine tunes transcriptional landscape cells. In doing so it establishes critical barrier warranting naivety prohibiting premature differentiation towards