(A) Qualitatively different classes of two-dimensional patterns based on the annotation of 211 expression patterns from the literature and our own experiments. The numbers indicate the number of times a given pattern is observed in the database.
(B) Counts for the number of genes in a given pattern annotation in the published data (LIT) and our experiments (SCREEN).
(C) Distribution of published (LIT) and new (SCREEN) patterns by the number of primitives required to describe them. ∼80% are described with one or two primitives.

(A) Schematic representation (i) and in situ hybridization image (ii) of ana expression at S10A, lateral view. Changes in the ana pattern in flies with reduced level of EGFR signaling (iii) and DPP signaling (iv). The pattern is greatly reduced in flies with the weak allele of Ras (iii) and is completely obliterated in flies overexpressing Dad, an inhibitor of DPP signaling (iv).
(B) Schematic representation (i) and in situ hybridization image (ii) of 18w expression at S10A, dorsal view. Changes in the 18w pattern in flies with reduced level of EGFR signaling (iii) and DPP signaling (iv). The midline part of the pattern is missing in flies with the weak allele of Ras (iii). The anterior part of the pattern is greatly reduced in flies overexpressing Dad (iv). The observed changes are highly correlated with the corresponding changes in the pattern of BR, expressed in the R domain.
(C) Summary of the expression dynamics of ana, argos, Cad74A, and 18w at four consecutive stages of oogenesis.

(A) ESEM images of eggshell morphologies induced by the perturbations of EGFR and DPP signaling in the follicular epithelium used in the microarray screen: (i) uniform EGFR activation (CY2>caEGFR), (ii) uniform EGFR downregulation (CY2>dnEGFR), (iii) uniform DPP signaling (CY2>caTkv), (iv) uniform repression of DPP signaling (CY2>Dad).
(B) Summary of the transcriptional profiling approach (see text for details). The screen identified 91 new patterns, corresponding to 32 genes expressed in stages 10A through 12.
(C) Venn diagram comparing the sets of genes described in the literature and identified in the transcriptional profiling screen.
(D) Venn diagram comparing the sets of the annotations that were described in the literature and identified in the screen.
(E) In situ hybridization images showing twelve examples of new gene expression patterns identified in a microarray-based screen (see text for details). The arrows mark the location of the dorsal midline.

(A) ESEM image of the Drosophila eggshell (dorsal view, anterior to the left). The dorsal appendages (DA) are tubular structures located on the dorsal side of the eggshell.
(B) Dorsal view of a stage 12 egg chamber. Each of the appendages is formed by the two adjacent groups of cells within the follicular epithelium. The cells expressing a Zn-finger transcription factor Broad (BR, red) form the roof of the future appendage. The floor of the appendage is formed by the cells that express rho (green), a protease in the Drosophila EGFR pathway.
(C) Lateral view of a stage 10B egg chamber. Patterning of the dorsal eggshell structures depends on the localized activation of the EGFR and DPP pathways in the follicular epithelium. The activation of the EGFR pathway is initiated by GRK (green). The early pattern of EGFR activation is distributed as a broad dorsoventral gradient. The DPP pathway is activated by DPP, a BMP2/4-type ligand secreted by the stretch cells and at the anterior border of the follicle cells associated with the oocyte. This generates an anterior-posterior pattern of MAD phosphorylation (P-MAD, red).
(D) Examples of gene expression patterns in the follicular epithelium during the stages of oogenesis corresponding to the dorsoventral patterning of the eggshell. Gene expression is visualized by whole-mount in situ hybridization. Images i-iv show dorsal views, vi-ix show lateral views.

(A) Lateral views of the six geometric building blocks (primitives) used to describe two-dimensional gene expression in the follicular epithelium.
(B) The first three building blocks are connected to the spatial structure of the patterning inputs. The spatial pattern of GRK protein in the oocyte (not shown), which is a proxy for the spatial pattern of ligand secretion, has a concave boundary and potentially explains the origin of the M primitive. The D primitive originates from the convex level-sets of the spatial distribution of secreted GRK in the lateral region of the egg chamber, computed using a biophysical model of GRK secretion, diffusion, binding, and internalization. The A primitive reflects the AP gradient of DPP sinaling, computed using a biophysical model of DPP secretion, diffusion, binding and internalization. (C) Complex patterns are constructed from primitives and the operations of (i) intersection (∩), (ii) difference (\), (iii) union (∪), and (iv) addition (+). The four examples show the construction of the patterns for argos, pip, 18w, and mia.
(D) Schematic showing how the four spatial operations could be realized by the Boolean and arithmetic operations at the regulatory regions of target genes (see text for details). The diagram shows the two hypothetical spatial inputs that are locally processed by the AND, ANDN (AND NOT), OR, and addition operations. I/O refer to input/output, respectively.

(A) Convergence and divergence of co-expression in annotated patterns at different stages. For example, the patterns of CG3074, Dad, and Cct1 coincide at stage 10A, but separate at later stages of oogenesis. On the other hand, vinc and jar, which are differentially expressed at stage 10A, are co-expressed during stage 12. Genes expressed in primitive patterns can transition both into other primitives and into composite patterns (described by 2 or more primitives).
(B) Most of the genes are expressed in more than one stage of oogenesis. 15 genes are expressed only once between stages 10A-12, 22 genes are expressed twice, 24 genes are expressed in three time points, and 20 genes are expressed in all four stages.
(C) Numbers of genes expressed in each of the four analyzed stages of oogenesis.
(D) Dynamic flow chart for the numbers of genes expressed during different stages of oogenesis, including the number of genes appearing at or dissappearing after a given stage (arrows pointing toward or away from a given stage) and the number of genes that continue to the next stage (arrows pointing toward the next stage).
(E) Dynamics of the fractions of the patterns assigned AP, DV, and INT classes, see text for details.
(F) Network-like representation of the AP, DV, and INT classes of genes at four consecutive stages of oogenesis. The number of genes that transition between the classes are indicated. Arrow thickness highlights the frequency of a given transition (thick: ≥10 genes, medium: 4-9 genes, dashed: 1-3 genes).
(G) Early and late expression stages for Ras85D, Shc, and drk (the arrowheads mark the location of the dorsal midline).
(H) Summary of expression patterns Ras85D, Shc, and drk at four consecutive stages of oogenesis.