Figures & data
Figure 1. Kinase-dependent and -independent roles of Cdc28. (A) In late G1, Cdc28 phosphorylates the SBF-bound repressor Whi5. This triggers the release of Whi5 from the SBF, thus stimulating the transcription of the genes belonging to the G1 transcriptional program. (B) Cdc28/Cks1 and the 19S-regulatory particle of the proteasome are recruited to genes such as GAL1 for efficient transcriptional activation by promoting a decrease in nucleosomal density.
![Figure 1. Kinase-dependent and -independent roles of Cdc28. (A) In late G1, Cdc28 phosphorylates the SBF-bound repressor Whi5. This triggers the release of Whi5 from the SBF, thus stimulating the transcription of the genes belonging to the G1 transcriptional program. (B) Cdc28/Cks1 and the 19S-regulatory particle of the proteasome are recruited to genes such as GAL1 for efficient transcriptional activation by promoting a decrease in nucleosomal density.](/cms/asset/536156ec-e9d1-4172-8152-ee986fb8a7dd/ktrn_a_10922456_f0001.gif)
Figure 2. Model for Cdc28-mediated phosphorylation of the CTD. (A) In late G1 Kin28 (or potentially a still uncharacterized kinase) primes the CTD. (B) Phosphorylated TP sites (threonine followed by a proline) and/or multiple phospho-S5 serve as a docking site for Cks1/Cdc28. As Cdc28 becomes active in late G1, Cdc28 further phosphorylates S5 to ensure high rates of transcription and mRNA capping.
![Figure 2. Model for Cdc28-mediated phosphorylation of the CTD. (A) In late G1 Kin28 (or potentially a still uncharacterized kinase) primes the CTD. (B) Phosphorylated TP sites (threonine followed by a proline) and/or multiple phospho-S5 serve as a docking site for Cks1/Cdc28. As Cdc28 becomes active in late G1, Cdc28 further phosphorylates S5 to ensure high rates of transcription and mRNA capping.](/cms/asset/2544ae70-e0b6-497e-a283-4e81be53282b/ktrn_a_10922456_f0002.gif)