| Literature DB >> 27660391 |
Karly L Ackermann1, Rebecca R Florke1, Shannon S Reyes1, Brooke R Tader1, Michael J Hamann2.
Abstract
TCL/RhoJ is a Cdc42-related Rho GTPase with reported activities in endothelial cell biology and angiogenesis, metastatic melanoma, and corneal epithelial cells; however, less is known about how it is inherently regulated in comparison to its closest homologues TC10 and Cdc42. TCL has an N-terminal extension of 18 amino acids in comparison to Cdc42, but the function of this amino acid sequence has not been elucidated. A truncation mutant lacking the N terminus (ΔN) was found to alter TCL plasma membrane localization and nucleotide binding, and additional truncation and point mutants mapped the alterations of TCL biochemistry to amino acids 17-20. Interestingly, whereas the TCL ΔN mutant clearly influenced nucleotide exchange, deletion of the N terminus from its closest homologue, TC10, did not have a similar effect. Chimeras of TCL and TC10 revealed amino acids 121-129 of TCL contributed to the differences in nucleotide loading. Together, these results identify amino acids within the N terminus and a loop region distal to the nucleotide binding pocket of TCL capable of allosterically regulating nucleotide exchange and thus influence membrane association of the protein.Entities:
Keywords: CDC42; GTPase; Rho (Rho GTPase); RhoJ; TCL; allosteric regulation; cell biology; membrane trafficking; small GTPase; vesicles
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Year: 2016 PMID: 27660391 PMCID: PMC5095414 DOI: 10.1074/jbc.M116.750026
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157