“…Subsequently, E2F/DP-dependent transcription of cell cycle genes promotes S phase entry and cell cycle progression. Because of its central role in controlling the transcription of cell cycle genes, RB serves as a convergence point for regulating the cell cycle in response to internal and external mitogenic signals (Nakagami et al, 2002;Stevaux et al, 2002;Cobrinik, 2005;Dimova and Dyson, 2005;Wikenheiser-Brokamp, 2006;Jullien et al, 2008;van den Heuvel and Dyson, 2008;Borghi et al, 2010;Henriques et al, 2010;Johnston et al, 2010;Chen et al, 2011;Gutzat et al, 2011Gutzat et al, , 2012Weimer et al, 2012). Recent studies also provide evidence that RB depletion causes metabolic reprogramming and suggest that the RB pathway in animals exerts part of its effect on cell proliferation through the control of Gln metabolism (Nicolay et al, 2013;Reynolds et al, 2014).…”