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Bugis, J.

Publications and source records attributed to Bugis, J..

2 recordsLinked to original sources

Activator-binding domains are required but insufficient for Med15 recruitment to UAS, revealing a critical role for its disordered C-terminus in directing genome targeting

The Mediator complex is a conserved transcriptional coactivator that bridges transcription factors (TFs) with the core transcriptional machinery. In budding yeast, TFs recruit the Mediator to upstream activation sequences (UASs) by interacting with three activator-binding domains (ABDs) within the Med15 tail subunit. However, these ABD-TF interactions exhibit relatively low affinity, raising the question of whether they fully account for Med15 recruitment in vivo. Here, we address this question by combining genome-wide profiling with systematic mutational analysis. We demonstrate that while the three ABDs are collectively required for Med15 recruitment, they are not individually required and are not sufficient to specify the genomic binding pattern of Med15. Instead, removal of an intrinsically disordered C-terminal redistributes Med15 occupancy across UASs. Notably, C-terminal truncation alters Med15 binding even at TF-depleted regions, and these effects are recapitulated by deleting Med2 or Med3, which further stabilize TF-dependent recruitment. Together, these findings support a dual mechanism of Med15 UAS recruitment, whereby TF-ABD recruitment is directed and stabilized by C-terminal mediated interactions.

genomics↗

Beyond motif recognition: Specificity of human transcription factors in yeast

Transcription factors (TFs) bind DNA through sequence-specific DNA-binding domains (DBDs), yet genome-wide analyses show that TFs occupy only a small fraction of their motif occurrences. This raises the question of how TFs distinguish specific targets from the many potential sites in the genome. To investigate determinants of binding specificity beyond the cognate motif and cofactor influences, we measured the binding of 60 human TFs across the budding yeast genome. Although human TFs robustly recognized their motifs, they displayed strong selectivity in site occupancy. Nucleosome abundance explained this selectivity only in part: among the 5-20% of motif sites that were bound, a substantial fraction remained nucleosome covered. Furthermore, TFs recognizing similar motif sequences independently localized to distinct subsets of sites within different promoters. Despite the absence of human-specific cofactors in yeast, both binding stability and genomic preferences depended on largely disordered non-DBD regions. These findings suggest intrinsically disordered regions (IDRs) may therefore direct genome binding TF target recognition across evolutionarily distant genomes. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=124 SRC="FIGDIR/small/721015v1_ufig1.gif" ALT="Figure 1"> View larger version (31K): org.highwire.dtl.DTLVardef@7db4cborg.highwire.dtl.DTLVardef@e88903org.highwire.dtl.DTLVardef@7b3e11org.highwire.dtl.DTLVardef@127ef29_HPS_FORMAT_FIGEXP M_FIG C_FIG

genetics↗