BioProject

As part of a study on the mechanism of Sir-based silencing at HML in S.cerevisiae, and the contribution of Rap1 to transcription of the locus, we performed ChIP-seq of multiple components of RNA Pol II machinery in different genetic backgrounds including: sir4∆, SIR+, and with or without a mutation that abbrogated Rap1 binding at the alpha promoter. More...

As part of a study on the mechanism of Sir-based silencing at HML in S.cerevisiae, and the contribution of Rap1 to transcription of the locus, we performed ChIP-seq of multiple components of RNA Pol II machinery in different genetic backgrounds including: sir4∆, SIR+, and with or without a mutation that abbrogated Rap1 binding at the alpha promoter. Overall design: Taf1-3xFLAG ChIPseq; Sua7-3xFLAG ChIPseq; Elf1-3xFLAG ChIPseq; Rpb3-3xFLAG ChIPseq in silenced (SIR) or unsilenced (sir4∆) cells, with or without a mutation in the alpha2 promoter. Less...