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WormBase Tree Display for Interaction: WBInteraction000525095

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Name Class

WBInteraction000525095Interaction_typePhysicalProteinProtein
InteractorInteractor_overlapping_geneWBGene00003378Interactor_typeBait
WBGene00003510Interactor_typeTarget
Interaction_summaryMlx ortholog, named MXL-2 for Max-like 2, and a protein that has sequence features of both Myc and Mondo proteins, named MML-1 for Myc and Mondo-like 1. MML-1/MXL-2 complexes have a primary function in regulating migration of the ray 1 precursor cells in the male tail... MML-1/MXL-2 complexes control expression of ECM components in the non-migratory epidermis, which we propose contributes to the substratum required for migration of the neighboring ray 1 precursor cells... Pro-migratory Wnt/-catenin and semaphorin signaling pathways interact genetically with MML-1/MXL-2 to determine ray 1 position... MML-1/MXL-2 complexes and semaphorin signaling act in parallel pathways in adjacent cells and synergize to determine ray 1 position... Wnt/BAR-1 and semaphorin/plexin signaling cascades act in distinct, parallel pathways to modulate ray 1 precursor cell migration.
Detection_methodYeast_two_hybrid
ThroughputLow_throughput
WBProcessWBbiopr:00000023
WBbiopr:00000073
PaperWBPaper00031002
Antibody_remarkMML-1 interacts with MXL-2 but NOT with MXL-1.... MML-1/Mondo and MDL-1/Mad did not dimerize with one another nor do they homodimerize
RemarkModel: MML-1/MXL-2 regulation of cell adhesion and migration is consistent with a Myc-like function and broadens the role of Mondo-like proteins to include these processes. The implication of a Myc and Mondo-like factor, Wnt/-catenin, and sema- phorin/plexin signaling in cell migration leads to a model that incorporates extracellular and intracellular components (Fig. 8). MML-1/MXL-2 complexes function in the non-migratory epidermis to activate expression of lectins and collagens. Meanwhile, the combined activity of a PLX-1 pathway and BAR-1/POP-1 complexes is required in ray 1 precursors, converging on UNC-73, CED-10, and MIG-2 to promote their migratory potential. Finally, we propose that activation of all three pathways results in modulation of integrin-mediated adhesion leading to ray 1 precursor cell migration.