Fig. 6

Measurement of the transcription elongation rate in the PSM of an intact embryo using b21 transgenic fish. (A) The modified transgenic her1/7 locus in b21 fish (compare with Fig. 2A). A ~21 kb artificial intron (brown triangle) was inserted in the second intron of her7. Probes AI1 (red) and AI2 (green) recognise regions of this intron that are ~10 kb apart. The her1 coding sequence is replaced by d1EGFP. (B,C) b21 transgenic embryos fixed at the 10-somite stage (14 hpf) and stained by two-colour FISH with two different probes and with DAPI as nuclear counterstain. Confocal optical sections of the PSM of flat-mounted embryos are shown. The middle image is a merge, with red and green channels shown separately on either side. (B) Co-staining with probes H1 (green; detecting transcripts from endogenous her1) and AI1 (red). (C) Co-staining with probes AI1 (red) and AI2 (green). (D) Processed image of the PSM of an embryo co-stained with AI1 and AI2 as used for intensity plot analysis. The image is warped in Adobe Photoshop to make the stripes of gene expression appear at right angles to the body axis, and the notochord and adaxial cells are blanked out leaving only PSM tissue to contribute to the analysis. (E) Intensity of the red and green fluorescence signals as a function of distance along the body axis. For each point along the axis, we took the total signal summed over the transverse column of pixels, and used Gaussian smoothing to obtain a smooth graph. The offset between the red and green signals was measured as the distance between the points of inflection on the rising parts of the curves, and the corresponding timing difference was calculated as described (Giudicelli et al., 2007).