Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/56363
Title: Oncogenic K-Ras segregates at spatially distinct plasma membrane signaling platforms according to its phosphorylation status
Author: Barceló, Carles
Paco, Noelia
Beckett. Alison J.
Alvarez-Moya, Blanca
Garrido, Eduard
Gelabert, Mariona
Tebar Ramon, Francesc
Jaumot i Pijoan, Montserrat
Prior, Ian
Agell i Jané, Neus
Keywords: Transport biològic
Proteïnes
Tumors
Biologia molecular
Biological transport
Proteins
Tumors
Molecular biology
Issue Date: 13-Aug-2013
Publisher: The Company of Biologists
Abstract: Activating mutations in the K-Ras small GTPase are extensively found in human tumors. Although these mutations induce the generation of a constitutively GTP-loaded, active form of K-Ras, phosphorylation at Ser181 within the C-terminal hypervariable region can modulate oncogenic K-Ras function without affecting the in vitro affinity for its effector Raf-1. In striking contrast, K-Ras phosphorylated at Ser181 shows increased interaction in cells with the active form of Raf-1 and with p110α, the catalytic subunit of PI 3-kinase. Because the majority of phosphorylated K-Ras is located at the plasma membrane, different localization within this membrane according to the phosphorylation status was explored. Density-gradient fractionation of the plasma membrane in the absence of detergents showed segregation of K-Ras mutants that carry a phosphomimetic or unphosphorylatable serine residue (S181D or S181A, respectively). Moreover, statistical analysis of immunoelectron microscopy showed that both phosphorylation mutants form distinct nanoclusters that do not overlap. Finally, induction of oncogenic K-Ras phosphorylation - by activation of protein kinase C (PKC) - increased its co-clustering with the phosphomimetic K-Ras mutant, whereas (when PKC is inhibited) non-phosphorylated oncogenic K-Ras clusters with the non-phosphorylatable K-Ras mutant. Most interestingly, PI 3-kinase (p110α) was found in phosphorylated K-Ras nanoclusters but not in non-phosphorylated K-Ras nanoclusters. In conclusion, our data provide - for the first time - evidence that PKC-dependent phosphorylation of oncogenic K-Ras induced its segregation in spatially distinct nanoclusters at the plasma membrane that, in turn, favor activation of Raf-1 and PI 3-kinase.
Note: Versió postprint del document publicat a: http://dx.doi.org/10.1242/​jcs.123737
It is part of: Journal of Cell Science, 2013, vol. 126, num. 20, p. 4553-4559
Related resource: http://dx.doi.org/10.1242/​jcs.123737
URI: http://hdl.handle.net/2445/56363
ISSN: 0021-9533
Appears in Collections:Articles publicats en revistes (Biomedicina)

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