Please use this identifier to cite or link to this item: https://doi.org/10.1074/jbc.M113.467407
Title: Control of RhoA methylation by carboxylesterase I
Authors: Cushman, I.
Cushman, S.M.
Potter, P.M.
Casey, P.J. 
Issue Date: 28-Jun-2013
Citation: Cushman, I., Cushman, S.M., Potter, P.M., Casey, P.J. (2013-06-28). Control of RhoA methylation by carboxylesterase I. Journal of Biological Chemistry 288 (26) : 19177-19183. ScholarBank@NUS Repository. https://doi.org/10.1074/jbc.M113.467407
Abstract: A number of proteins that play key roles in cell signaling are post-translationally modified by the prenylation pathway. The final step in this pathway is methylation of the carboxyl terminus of the prenylated protein by isoprenylcysteine carboxylmethyltransferase. Due to the impact of methylation on Rho function, we sought to determine if the process was reversible and hence could control Rho function in a dynamic fashion. Elevating isoprenylcysteine carboxylmethyltransferase activity in cells has profound effects on MDA-MB-231 cell morphology, implying the presence of a pool of unmethylated prenyl proteins in these cells under normal conditions. Using a knockdown approach, we identified a specific esterase, carboxylesterase 1, whose function had a clear impact not only on the methylation status of RhoA but also RhoA activation and cell morphology. These data provide compelling evidence that C-terminal modification of prenyl proteins, rather than being purely a constitutive process, can serve as a point of regulation of function for this important class of protein. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
Source Title: Journal of Biological Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/109987
ISSN: 00219258
DOI: 10.1074/jbc.M113.467407
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