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Multi-omics integration across RNA-seq, miRNA, scRNA-seq, and scATAC-seq datasets allowed the construction of YY1-dependent regulatory networks that reveal how YY1 influences B-cell lineage plasticity.
It is suggested that YY1 preserves B cell identity through coordinated regulation of transcriptional and post-transcriptional programs, with YY1-dependent miRNA networks contributing to the maintenance of B cell-associated gene expression and restriction of alternative lineage programs.
It is revealed that constitutive Notch2 experience affords lipopolysaccharide (LPS) hyperresponsiveness in Notch2-independent follicular B cells, which resulted in earlier Myc induction and accelerated cell cycle entry, ultimately augmenting division kinetics.
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