Literature DB >> 21111786

The RasGrf family of mammalian guanine nucleotide exchange factors.

Alberto Fernández-Medarde1, Eugenio Santos.   

Abstract

RasGrf1 and RasGrf2 are highly homologous mammalian guanine nucleotide exchange factors which are able to activate specific Ras or Rho GTPases. The RasGrf genes are preferentially expressed in the central nervous system, although specific expression of either locus may also occur elsewhere. RasGrf1 is a paternally-expressed, imprinted gene that is expressed only after birth. In contrast, RasGrf2 is not imprinted and shows a wider expression pattern. A variety of isoforms for both genes are also detectable in different cellular contexts. The RasGrf proteins exhibit modular structures composed by multiple domains including CDC25H and DHPH motifs responsible for promoting GDP/GTP exchange, respectively, on Ras or Rho GTPase targets. The various domains are essential to define their intrinsic exchanger activity and to modulate the specificity of their functional activity so as to connect different upstream signals to various downstream targets and cellular responses. Despite their homology, RasGrf1 and RasGrf2 display differing target specificities and non overlapping functional roles in a variety of signaling contexts related to cell growth and differentiation as well as neuronal excitability and response or synaptic plasticity. Whereas both RasGrfs are activatable by glutamate receptors, G-protein-coupled receptors or changes in intracellular calcium concentration, only RasGrf1 is reported to be activated by LPA, cAMP, or agonist-activated Trk and cannabinoid receptors. Analysis of various knockout mice strains has uncovered a specific functional contribution of RasGrf1 in processes of memory and learning, photoreception, control of post-natal growth and body size and pancreatic β-cell function and glucose homeostasis. For RasGrf2, specific roles in lymphocyte proliferation, T-cell signaling responses and lymphomagenesis have been described.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21111786     DOI: 10.1016/j.bbcan.2010.11.001

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  45 in total

Review 1.  How to Target Activated Ras Proteins: Direct Inhibition vs. Induced Mislocalization.

Authors:  Ethan J Brock; Kyungmin Ji; John J Reiners; Raymond R Mattingly
Journal:  Mini Rev Med Chem       Date:  2016       Impact factor: 3.862

2.  Ras and Rho GTPases on the move: The RasGRF connection.

Authors:  Piero Crespo; Fernando Calvo; Victoria Sanz-Moreno
Journal:  Bioarchitecture       Date:  2011-07-01

3.  Genetic evidence that β-arrestins are dispensable for the initiation of β2-adrenergic receptor signaling to ERK.

Authors:  Morgan O'Hayre; Kelsie Eichel; Silvia Avino; Xuefeng Zhao; Dana J Steffen; Xiaodong Feng; Kouki Kawakami; Junken Aoki; Karen Messer; Roger Sunahara; Asuka Inoue; Mark von Zastrow; J Silvio Gutkind
Journal:  Sci Signal       Date:  2017-06-20       Impact factor: 8.192

4.  RasGRF suppresses Cdc42-mediated tumour cell movement, cytoskeletal dynamics and transformation.

Authors:  Fernando Calvo; Victoria Sanz-Moreno; Lorena Agudo-Ibáñez; Fredrik Wallberg; Erik Sahai; Christopher J Marshall; Piero Crespo
Journal:  Nat Cell Biol       Date:  2011-06-19       Impact factor: 28.824

5.  Focal adhesions and Ras are functionally and spatially integrated to mediate IL-1 activation of ERK.

Authors:  Qin Wang; Gregory P Downey; Christopher A McCulloch
Journal:  FASEB J       Date:  2011-06-30       Impact factor: 5.191

6.  Differential Role of the RasGEFs Sos1 and Sos2 in Mouse Skin Homeostasis and Carcinogenesis.

Authors:  Pilar Liceras-Boillos; David Jimeno; Rósula García-Navas; L Francisco Lorenzo-Martín; Mauricio Menacho-Marquez; Carmen Segrelles; Carmela Gómez; Nuria Calzada; Rocío Fuentes-Mateos; Jesús M Paramio; Xosé R Bustelo; Fernando C Baltanás; Eugenio Santos
Journal:  Mol Cell Biol       Date:  2018-07-30       Impact factor: 4.272

7.  Parentally imprinted genes regulate hematopoiesis-new evidence from the Dlk1-Gtl2 locus.

Authors:  Gabriela Schneider; Zachariah Payne Sellers; Mariusz Z Ratajczak
Journal:  Stem Cell Investig       Date:  2016-07-22

8.  RasGRF Couples Nox4-Dependent Endoplasmic Reticulum Signaling to Ras.

Authors:  Ru Feng Wu; Chengxu Liao; Hadi Hatoum; Guosheng Fu; Cristhiaan D Ochoa; Lance S Terada
Journal:  Arterioscler Thromb Vasc Biol       Date:  2016-11-17       Impact factor: 8.311

9.  RasGRF2 promotes migration and invasion of colorectal cancer cells by modulating expression of MMP9 through Src/Akt/NF-κB pathway.

Authors:  Peifen Lu; Junjun Chen; Lihong Yan; Lijun Yang; Litao Zhang; Jie Dai; Zixuan Hao; Tao Bai; Yanfeng Xi; Yahui Li; Zhiming Kang; Jun Xv; Gongqin Sun; Tao Yang
Journal:  Cancer Biol Ther       Date:  2018-10-25       Impact factor: 4.742

Review 10.  Neuronal Rho GEFs in synaptic physiology and behavior.

Authors:  Megan B Miller; Yan Yan; Betty A Eipper; Richard E Mains
Journal:  Neuroscientist       Date:  2013-02-11       Impact factor: 7.519

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