Retinoblastoma protein partners
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2019, Cell ReportsCitation Excerpt :The in vivo data here suggest that cells differentiate not by exiting the cell cycle with accumulation of E2F4 after mitosis but more likely in late G1, with accumulation of activating E2Fs, allowing the choice between entering (initiating DNA replication) or exiting (differentiating) the cell cycle. At least in the small intestine of mice, the accumulation of E2F3A in the last G1 coincides with the physical association of hypo-phosphorylated RB (Burkhart and Sage, 2008; Lees et al., 1993; Morris and Dyson, 2001). The subsequent disappearance of E2F3A protein at the crypt-villus junctional zone is tightly coordinated with the nuclear appearance and maintenance of the canonical E2F4 repressor along the entire villus, permanent repression of cell-cycle-regulated genes, and terminal differentiation of enterocytes.
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