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. Author manuscript; available in PMC: 2019 Oct 18.
Published in final edited form as: Cell. 2018 Oct 18;175(3):835–847.e25. doi: 10.1016/j.cell.2018.09.056

Figure 1: Absolute quantification of gap gene transcriptional activity.

Figure 1:

(A) Activity of individual nuclei (blue) for the gene hunchback (hb) measured by single molecule mRNA-FISH (green) in nuclear cycle 13 (nc13) of the blastoderm embryo of length L. Red arrowheads: nuclei with two sites of transcription; magenta arrowheads: single site of transcription.

(B) Activity profile of hb as a function of AP position in % egg length for 18 embryos. Activity of individual nuclei from the summed intensity of all transcription sites per nucleus, normalized by the average intensity of a single cytoplasmic mRNA (cytoplasmic unit, C.U.). Blue dots: total mean intensity per nucleus. Vertical dashed lines define AP bins; circles: mean activity in each bin.

(C) Mean activity in C.U. as a function of AP position during nc13 for: hunchback in wild-type (labeled hb wt in blue, N=18 embryos); hunchback deficiency with half the hb dosage (hb def, light blue, N=7); Krüppel (Kr, magenta, N=11); knirps during early (kni early, green, N=14) and late nc13 (kni late, light green, N=16); giant in females with two alleles (gt female, red, N=20) and in males with one (gt male, light red, N=16).

(D) Total variance of transcriptional activity as a function of AP position (colorcode as in C).

All error bars are 68% confidence intervals. See also Figure S1.