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Updated: Apr 26, 2026

Transcriptome-Wide Profiling of Protein-RNA Interactions by Cross-Linking and Immunoprecipitation Mediated by FLAG-Biotin Tandem Purification
Published on: May 18, 2020
Identification of proteins associated with RNA polymerase III using a modified tandem chromatin affinity purification
Ngoc-Thuy-Trinh Nguyen1, Cyril Saguez1, Christine Conesa1
1CEA, iBiTecS, SBIGeM, FRE 3377, Gif-sur-Yvette F-91191, France; CNRS, FRE 3377, Gif-sur-Yvette F-91191, France; Univ Paris-Sud, FRE 3377, Gif-sur-Yvette F-91191, France.
Abstract:
To identify the proteins associated with the RNA polymerase III (Pol III) machinery in exponentially growing yeast cells, we developed our own tandem chromatin affinity purification procedure (TChAP) after in vivo cross-link, allowing a reproducible and good recovery of the protein bait and its associated partners. In contrast to TFIIIA that could only be purified as a free protein, this protocol allows us to capture free Pol III together with Pol III bound on its target genes. Transcription factors, elongation factors, RNA-associated proteins and proteins involved in Pol III biogenesis were identified by mass spectrometry. Interestingly, the presence of all the TFIIIB subunits found associated with Pol III together with the absence of TFIIIC and chromatin factors including histones suggest that DNA-bound Pol III purified using TChAP is mainly engaged in transcription reinitiation.
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