Characterisation of HRas local signal transduction networks using engineered site-specific exchange factors.
Autor: Herrero, Ana; Reis-Cardoso, Mariana; Jiménez-Gómez, Iñaki; Doherty, Carolanne; Agudo-Ibañez, Lorena; Pinto, Adán; Calvo, Fernando; Kolch, Walter; Crespo, Piero; Matallanas, David
Publication year: 2020
Small GTPases
issn:2154-1256 2154-1248
doi: 10.1080/21541248.2017.1406434
Abstract:
Ras GTPases convey signals from different types of membranes. At these locations, different Ras isoforms, interactors and regulators generate different biochemical signals and biological outputs. The study of Ras localisation-specific signal transduction networks has been hampered by our inability to specifically activate each of these Ras pools. Here, we describe a new set of site-specific tethered exchange factors, engineered by fusing the RasGRF1 CDC25 domain to sub-localisation-defining cues, whereby Ras pools at specific locations can be precisely activated. We show that the CDC25 domain has a high specificity for activating HRas but not NRas and KRas. This unexpected finding means that our constructs mainly activate endogenous HRas. Hence, their use enabled us to identify distinct pathways regulated by HRas in endomembranes and plasma membrane microdomains. Importantly, these new constructs unveil different patterns of HRas activity specified by their subcellular localisation. Overall, the targeted GEFs described herein constitute ideal tools for dissecting spatially-defined HRas biochemical and biological functions.
Language: eng
Rights:
Pmid: 29172991
Tags: Humans; Animals; Mice; Cells, Cultured; *Protein Engineering; CDC25 domain; Cell Proliferation; Chlorocebus aethiops; localisation; oncogene; Proto-Oncogene Proteins p21(ras)/*metabolism; Ras; Ras-GEF; ras-GRF1/*metabolism; Signal Transduction; signalling network
Link: https://pubmed.ncbi.nlm.nih.gov/29172991/
