End-targeting proteomics of isolated chromatin segments of a mammalian ribosomal RNA gene promoter

Biological Macromolecules Laboratory • Maeshima Group

End-targeting proteomics of isolated chromatin segments of a mammalian ribosomal RNA gene promoter

Ide, S. and Dejardin, J.
Nature Communications, 6, Article number: 6674, DOI: 10.1038/ncomms7674

he unbiased identification of proteins associated with specific loci is crucial for understanding chromatin-based processes. The proteomics of isolated chromatin fragment (PICh) method has previously been developed to purify telomeres and identify associated proteins. This approach is based on the affinity capture of endogenous chromatin segments by hybridization with oligonucleotide containing locked nucleic acids. However, PICh is only efficient with highly abundant genomic targets, limiting its applicability. Here we develop an approach for identifying factors bound to the promoter region of the ribosomal RNA genes that we call end-targeting PICh (ePICh). Using ePICh, we could specifically enrich the RNA polymerase I pre-initiation complex, including the selectivity factor 1. The high purity of the ePICh material allowed the identification of ZFP106, a novel factor regulating transcription initiation by targeting RNA polymerase I to the promoter. Our results demonstrate that ePICh can uncover novel proteins controlling endogenous regulatory elements in mammals.

Figure1

Rules for designing capture probes for the formation of stable oligo-DNA hybrids.


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