Project name: The SPARC complex defines RNAPII promoters in Trypanosoma brucei [ChIP-seq]

Description: Kinetoplastids are a highly divergent lineage of eukaryotes with unusual mechanisms for regulating gene expression. We previously surveyed 65 putative chromatin factors in the kinetoplastid Trypanosoma brucei. Our analyses revealed that the predicted histone methyltransferase SET27 and the Chromodomain protein CRD1 are tightly concentrated at RNAPII transcription start regions (TSRs). Here we report that SET27 and CRD1 together with four biologically novel constituents form the SET27 promoter-associated regulatory complex (SPARC), which is specifically enriched at TSRs. SET27 loss leads to aberrant RNAPII recruitment to promoter sites, accumulation of polyadenylated transcripts upstream of normal transcription start sites, and conversion of some normally unidirectional promoters to bidirectional promoters. Transcriptome analysis in the absence of SET27 revealed upregulated  mRNA expression in the vicinity of SPARC peaks on chromosome cores in addition to derepression of genes encoding variant surface glycoproteins (VSGs) located in subtelomeric regions. These analyses uncover a novel chromatin-associated complex required to establish accurate promoter position and directionality.Overall design: This ChIP-seq dataset shows the genomic association of YFP-tagged SPARC complex subunits in bloodstream form (BF) and procyclic form (PF) T. brucei, and the genomic association of YFP-RPB1 in WT, set27D/+ (SKO) and set27D/D (DKO) BF cells. There are three replicates for JBP2 (BF) and SET27 (PF), and two replicates for the remaining YFP-tagged proteins (BF and PF) and for the untagged control (PF).

Data type: Epigenomics

Sample scope: Multiisolate

Relevance: Medical

Last updated: 2022-07-12