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All rights reserved. http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel http://purl.org/dc/elements/1.1/title BEL Framework Large Corpus Document http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel http://purl.org/pav/authoredBy http://www.tkuhn.ch/bel2nanopub/RASxBWPqOWj9XIQgKxGsoxC6W_zCPGcKP7MupG0nB87rA#_6 http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel http://purl.org/pav/version 1.4 http://www.tkuhn.ch/bel2nanopub/RASxBWPqOWj9XIQgKxGsoxC6W_zCPGcKP7MupG0nB87rA#_5 http://www.w3.org/ns/prov#value Previous studies have demonstrated a role for cyclin D1 in the repression of several distinct transcription factors (Fig. 4). In addition to binding CDK4, CDK6, and pRB, cyclin D1 forms physical associations with P/CAF (p300/CB P associated factor), Myb, MyoD, and the cyclin D1 myb-like binding protein (DMP1) [8-11]. Cyclin D1 and D2 are capable of inhibiting MyoD [12]. v-Myb is preferentially repressed by cyclin D1 [9], although cyclin D2 and D3 are also capable of repressing v-Myb; the helix-loop-helix-like protein DMP1 is repressed by each of the D-type cyclins [8]. 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