FRET Image Correlation Spectroscopy Reveals RNAPII-Independent P-TEFb Recruitment on Chromatin

• Published in: Biophysical journal Vol. 114; no. 3; pp. 522 - 533
• Main Authors: Bidaux, Gabriel, Le Nézet, Corentin, Pisfil, Mariano Gonzalez, Henry, Mélanie, Furlan, Alessandro, Bensaude, Oliver, Vandenbunder, Bernard, Héliot, Laurent
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 06.02.2018; Biophysical Society; The Biophysical Society
• Subjects: Biological Physics; Cells; Cells (biology); Chromatin; Clusters; Correlation analysis; DNA-directed RNA polymerase; Elongation; Energy transfer; Fluorescence; Fluorescence resonance energy transfer; Genetic engineering; Histidine; Histone H2A; Image acquisition; Image analysis; Image processing; Microscopy; Molecular interactions; Nuclei; Nucleic Acids and Genome Biophysics; Phosphorylation; Physics; Protein interaction; Proteins; Recruitment; Ribonucleic acid; RNA; RNA polymerase II; Spatial distribution; Spectroscopy; Spectrum analysis; Statistical analysis; Transcription elongation factor b
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/j.bpj.2017.11.3783

Biochemical studies have revealed that the RNA Polymerase II (RNAPII) pause release is triggered by phosphorylation of the transcription machinery by the positive transcription elongation factor b (P-TEFb). However, there are no direct report that P-TEFb and RNA polymerase II interact in single living cells and the biophysical mechanisms mediating this association are still unclear. Förster resonance energy transfer (FRET) detects molecular interactions at the subcellular level. Time domain fluorescence lifetime imaging provides an accurate quantification of FRET efficiency, EFRET, because it is fluorochrome concentration-independent and insensitive to fluorescence bleed-through. However, the way FRET signal is usually analyzed does not provide information about the areas where protein-protein interactions take place. In this work, we developed a method, dubbed FRET image correlation spectroscopy (FICS), which relied on FRET fluorescence lifetime imaging image acquisition and image correlation spectroscopy of EFRET clusters to quantify the spatial distribution of interaction clusters in the nucleus. The combination of high content FRET microscopy with batch image analysis allowed a robust statistical analysis. By applying FICS, we characterized the area and density of interaction clusters between P-TEFb and RNAPII or histone H2A in single living cells. The FICS method applied to cells expressing genetically engineered mutated proteins confirmed that the histidine-rich domain of P-TEFb is required for its interaction with RNAPII. Furthermore, it demonstrated that P-TEFb was also located in close vicinity to histone H2A, independently of its interactions with RNAPII. These results support the hypothesis that P-TEFb dynamics on chromatin regulate its recruitment on RNAPII.