Extraction of functional binding sites from unique regulatory regions: the Drosophila early developmental enhancers - PubMed (original) (raw)

Comparative Study

Extraction of functional binding sites from unique regulatory regions: the Drosophila early developmental enhancers

Dmitri A Papatsenko et al. Genome Res. 2002 Mar.

Abstract

The early developmental enhancers of Drosophila melanogaster comprise one of the most sophisticated regulatory systems in higher eukaryotes. An elaborate code in their DNA sequence translates both maternal and early embryonic regulatory signals into spatial distribution of transcription factors. One of the most striking features of this code is the redundancy of binding sites for these transcription factors (BSTF). Using this redundancy, we explored the possibility of predicting functional binding sites in a single enhancer region without any prior consensus/matrix description or evolutionary sequence comparisons. We developed a conceptually simple algorithm, Scanseq, that employs an original statistical evaluation for identifying the most redundant motifs and locates the position of potential BSTF in a given regulatory region. To estimate the biological relevance of our predictions, we built thorough literature-based annotations for the best-known Drosophila developmental enhancers and we generated detailed distribution maps for the most robust binding sites. The high statistical correlation between the location of BSTF in these experiment-based maps and the location predicted in silico by Scanseq confirmed the relevance of our approach. We also discuss the definition of true binding sites and the possible biological principles that govern patterning of regulatory regions and the distribution of transcriptional signals.

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Figures

Figure 1

Figure 1

Strategies for BSTF map construction. Two strategies for constructing maps of binding sites rely on a matrix search for experimentally defined binding sites for transcription factors (BSTF). The first strategy (refined map path) is used to verify the exact location and size of the experimental sites. A second strategy (consistent map path) takes into account both the presence of the experimentally verified sites and the matrix score of found matches. The initial map is the raw footprint data from a literature source.

Figure 2

Figure 2

Scanseq

algorithm. Initial search is performed with words of length m with 0-k mismatches. For each word found in the sequence, the corresponding motif (word set), is refined by positional weight matrix (PWM), and is statistically evaluated through Z score. In the final stage, Z scores for motifs within a range of m and k are compared and a predicted map is generated. Note that the PWM in the

Scanseq

algorithm is not the same as in the strategy of BSTF map construction, and it does not include any a priori information about binding motifs.

Figure 3

Figure 3

Sensitivity of

Scanseq

to the parameters of the initial search. Z-score profile plot (_X_-axis is the position in the sequence) is shown for the even-skipped stripe 2 enhancer using a range of length (m) and divergence (k). Each horizontal line corresponds to a combination of m (7 bp–10 bp) and k (1–3 mismatches) that are shown on the left side. Z-score values are represented by the color scale (bottom left). The bottom bar shows the distribution of binding sites for transcription factors (BSTF; consistent map) in the even-skipped stripe 2 enhancer. The best statistical correlation with the consistent map for eve stripe 2 was observed at the following parameters: {m = 7; k = 1}, {m = 8; k = 1}, and {m = 9; k = 2}.

Figure 4

Figure 4

(see figure on preceding page)

Scanseq

predictions. Z-score profile plots and maps of predictions are shown for even-skipped stripe 2 (panels A, B), hairy stripe 7 (panels C, D), even-skipped stripe 4+6 (panels E, F), and runt stripe 5 (panels G, H). The plots show the maximum observed Z scores (_Y_-axis) for each position in the sequence (_X_-axis) using a selected parameter range (mmin, mmax, kmax, and c). Panels A, C, E, and G (see parameters and statistics in Table 3) show the results after training on the group-of-10 enhancers. The results of individual trainings (see Table 4) are shown in panels B, D, F, and H. The predicted map is shown below each Z-score profile plot. The blue bars represent the most redundant segments (predicted by

Scanseq

); the red bars represent the established distribution for binding sites for transcription factors (BSTF): Consistent maps for even-skipped stripe 2 (Giant sites were not used in the training), hairy stripe 6, and the virtual maps for even-skipped stripe 4+6 and runt stripe 5 are shown.

Figure 5

Figure 5

Detailed map of predictions for even-skipped stripe 2. The comparison between the

Scanseq

predictions (in red) and the consistent map (in green) shows the efficiency of individual training (panel B) versus training on a group of 10 (panel A). In both cases, periodic sequences (ATCCC)n generated very high statistical scores.

Figure 6

Figure 6

Structure and conservation of tandem repeats. Periodic structures of ∼100-bp region from even-skipped stripe 2 (A, D), even-skipped stripe 4+6 (B), and fushi-tarazu proximal enhancer (C) are revealed by matrix search for Bicoid, Knirps, and Tramtrack, respectively (see also Table 5). The red arrows indicate sites that produce a positional weight matrix score in the 4–6 range (shadow sites). Evolutionary conservation in four species of Drosophila is shown for eve stripe 2 (ATCCC)n (D).

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