Since dGRN structure depends on cis-regulatory linkages at nodes: |
1. Change in dGRN structure occurs by co-optive redeployment of cis-regulatory modules controlling regulatory gene expression |
Since co-optive cis-regulatory redeployments are gain of function changes: |
2. Co-optive redeployment of regulatory gene expression will generally be haplosufficient and act dominantly |
Since dGRNs are deeply hierarchical: |
3. Effects of given cis-regulatory mutations (including co-options) depend specifically on their location in dGRN |
Since dGRNs are deeply hierarchical: |
4. Subcircuits operating at upper levels (early in developmental process) preclude certain downstream linkages, and mediate others, i.e., canalize dGRN structure (and developmental process). |
Since dGRNs are deeply hierarchical: |
5. Conserved upper level subcircuits should produce patterns of canalization that reflect phylogenetic distribution of the developmental processes that generate clade specific body parts (prediction of Kernels) |
Since flexibility at given dGRN nodes depends on their upstream and downstream linkages: |
6. dGRN structure should contain information for prediction of evolutionary hotspots vs. evolutionarily conserved structural features |
Since dGRNs are modular, i.e., given functions are executed by given subcircuits: |
7. Evolution of new developmental outcomes must often involve co-optive gain of function changes that cause redeployment of whole dGRN subcircuits |
Since redeployment of dGRN subcircuits is a mechanism of evolution of developmental novelty: |
8. Evolutionary change must occur in dGRN linkages controlling subcircuit deployment, i.e., in signal presentation and reception, regulatory switches, and inter-subcircuit inputs. |