Abstract

Despite the sizable number of components that comprise Mapk cascades, Map3k1 is the only element that contains both a kinase domain and a plant homeodomain (PHD) motif, allowing Map3k1 to regulate the protein phosphorylation and ubiquitin proteasome systems. As such, Map3k1 has complex roles in the regulation of cell death, survival, migration and differentiation. Numerous mouse and human genetic analyses have demonstrated that Map3k1 is of critical importance for the immune system, cardiac tissue, testis, wound healing, tumorigenesis and cancer. Recent gene knockin of Map3k1 to mutate the E2 binding site within the Map3k1 PHD motif and high throughput ubiquitin protein array screening for Map3k1 PHD motif substrates provide critical novel insights into Map3k1 PHD motif signal transduction and bring a brand-new understanding to Map3k1 signaling in mammalian biology.

Highlights

  • Are novel Map3k1 plant homeodomain (PHD) motif substrates targeted by the Ubproteasome system during apoptosis?

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Summary

Open Questions

Are divergent roles for the Map3k1 kinase domain and PHD motifs present within human breast cancers?. Does the Map3k1 PHD motif regulate Tabs by noncanonical ubiquitination following CD40, and other Tnfrs, signal transduction?. Are novel Map3k1 PHD motif substrates targeted by the Ubproteasome system during apoptosis?

Discovery and Early Characterization
Downstream targets
Cell Death and Differentiation
Cell Migration and Wound Healing
Lymphocyte Differentiation and Effector Responses
Role in Stem Cells and Cardiac Myocytes
Roles in Cancer
Summary
This work is licensed under a Creative Commons

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