4.3 Review

Structural mechanisms of plexin signaling

Journal

PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY
Volume 118, Issue 3, Pages 161-168

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbiomolbio.2015.03.006

Keywords

Plexin; Rap; GAP; Dimerization; Signaling

Funding

  1. National Institutes of Health, USA (NIH) [GM088197]
  2. Welch foundation, USA [I-1702]
  3. Cancer Prevention and Research Institute of Texas, USA [RP140661]
  4. NIH [GM008203]

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Signaling through plexin, the major cell surface receptor for semaphorin, plays critical roles in regulating processes such as neuronal axon guidance, angiogenesis and immune response. Plexin is normally kept inactive in the absence of semaphorin. Upon binding of semaphorin to the extracellular region, plexin is activated and transduces signal to the inside of the cell through its cytoplasmic region. The GTPase Activating Protein (GAP) domain in the plexin cytoplasmic region mediates the major intracellular signaling pathway. The substrate specificity and regulation mechanisms of the GAP domain have only been revealed recently. Many intracellular proteins serve as either upstream regulators or downstream transducers by directly interacting with plexin. The mechanisms of action for some of these proteins also start to emerge from recent studies. We review here these advances in the mechanistic understanding of plexin intracellular signaling from a structural perspective. (C) 2015 Elsevier Ltd. All rights reserved.

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