The CHR site: definition and genome-wide identification of a cell cycle transcriptional element. Issue 16 (8th August 2014)

• Record Type: Journal Article
• Authors: Müller, Gerd A.; Wintsche, Axel; Stangner, Konstanze; Prohaska, Sonja J.; Stadler, Peter F.; Engeland, Kurt
• Is Part Of: Nucleic acids research. Volume 42:Issue 16(2014)
• Page Start: 10331
• Page End: 10350
• Publication Date: 2014-08-08
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gku696
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: The cell cycle genes homology region (CHR) has been identified as a DNA element with an important role in transcriptional regulation of late cell cycle genes. It has been shown that such genes are controlled by DREAM, MMB and FOXM1-MuvB and that these protein complexes can contact DNA via CHR sites. However, it has not been elucidated which sequence variations of the canonical CHR are functional and how frequent CHR-based regulation is utilized in mammalian genomes. Here, we define the spectrum of functional CHR elements. As the basis for a computational meta-analysis, we identify new CHR sequences and compile phylogenetic motif conservation as well as genome-wide protein-DNA binding and gene expression data. We identify CHR elements in most late cell cycle genes binding DREAM, MMB, or FOXM1-MuvB. In contrast, Myb- and forkhead-binding sites are underrepresented in both early and late cell cycle genes. Our findings support a general mechanism: sequential binding of DREAM, MMB and FOXM1-MuvB complexes to late cell cycle genes requires CHR elements. Taken together, we define the group of CHR-regulated genes in mammalian genomes and provide evidence that the CHR is the central promoter element in transcriptional regulation of late cell cycle genes by DREAM, MMB and FOXM1-MuvB.