Abstract
Eukaryotic cells respond to genomic and environmental stresses, such as DNA damage and heat shock (HS), with the synthesis of poly-[ADP-ribose] (PAR) at specific chromatin regions, such as DNA breaks or HS genes, by PAR polymerases (PARP). Little is known about the role of this modification during cellular stress responses. We show here that the nucleosome remodeler dMi-2 is recruited to active HS genes in a PARP–dependent manner. dMi-2 binds PAR suggesting that this physical interaction is important for recruitment. Indeed, a dMi-2 mutant unable to bind PAR does not localise to active HS loci in vivo. We have identified several dMi-2 regions which bind PAR independently in vitro, including the chromodomains and regions near the N-terminus containing motifs rich in K and R residues. Moreover, upon HS gene activation, dMi-2 associates with nascent HS gene transcripts, and its catalytic activity is required for efficient transcription and co-transcriptional RNA processing. RNA and PAR compete for dMi-2 binding in vitro, suggesting a two step process for dMi-2 association with active HS genes: initial recruitment to the locus via PAR interaction, followed by binding to nascent RNA transcripts. We suggest that stress-induced chromatin PARylation serves to rapidly attract factors that are required for an efficient and timely transcriptional response.
Highlights
The activity of eukaryotic genomes is regulated by dynamic changes in chromatin structure
We have investigated a paradigm of environmental stress, the activation of heat shock (HS) loci in Drosophila and have analyzed the mechanism through which the nucleosome remodeler dMi-2 is recruited to HS genes
Heat shock gene activation involves the synthesis of poly[ADP-ribose] (PAR) at heat shock loci, the opening of chromatin structure, and the coordinated recruitment of transcription factors and chromatin regulators RNA polymerase II and components of the RNA processing machinery
Summary
The activity of eukaryotic genomes is regulated by dynamic changes in chromatin structure. The HS loci of polytene chromosomes form transcriptionally active ‘‘puffs’’. This rapid chromatin decondensation correlates with a strong decrease in nucleosome density [1]. In addition to histone displacement and transcription compartment formation at HS genes, recent evidence suggests that PARylation could act as a signaling scaffold for the recruitment of PARsensing factors during DNA damage. We sought to address whether and how nucleosome remodelers may be recruited to PARP activation sites upon environmental stresses other than DNA damage. We have investigated a paradigm of environmental stress, the activation of HS loci in Drosophila and have analyzed the mechanism through which the nucleosome remodeler dMi-2 is recruited to HS genes
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