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. 2012 Sep 5;103(5):851–859. doi: 10.1016/j.bpj.2012.06.036

Figure 4.

Figure 4

Fluorescent UTPs get incorporated into transcript like RNA aggregates. (A) Raw intensity plots of Alexa546-UTP obtained by FCS measurement in nucleoplasm (red) and in 5 μM solution of Alexa546-UTP (green). (B) Normalized intensity histogram from FCS intensity profiles (pooled from ∼25 independent FCS readings) in Alexa546-UTP in solution, nucleus, and cytoplasm of untreated cells. (C) Fluorescence correlation curves plotted as normalized amplitude and their respective fits with a three-dimensional one-particle anomalous model for Alexa546-UTP in solution and nucleoplasm. (D) Quantification of the mean size of UTP aggregates, estimated from mean correlation time for solution and nucleoplasm (in control and transcription inhibited states) where N ∼ 600 in control and DRB treatment, and N ∼ 500 FCS readings in α-amanitin treatment. P <0.05.