Literature DB >> 21779495

Functional specificity of ras isoforms: so similar but so different.

Esther Castellano1, Eugenio Santos.   

Abstract

H-ras, N-ras, and K-ras are canonical ras gene family members frequently activated by point mutation in human cancers and coding for 4 different, highly related protein isoforms (H-Ras, N-Ras, K-Ras4A, and K-Ras4B). Their expression is nearly ubiquitous and broadly conserved across eukaryotic species, although there are quantitative and qualitative differences of expression depending on the tissue and/or developmental stage under consideration. Extensive functional studies have determined during the last quarter century that these Ras gene products are critical components of signaling pathways that control eukaryotic cell proliferation, survival, and differentiation. However, because of their homology and frequent coexpression in various cellular contexts, it remained unclear whether the different Ras proteins play specific or overlapping functional roles in physiological and pathological processes. Initially, their high degree of sequence homology and the observation that all Ras isoforms share common sets of downstream effectors and upstream activators suggested that they were mostly redundant functionally. In contrast, the notion of functional specificity for each of the different Ras isoforms is supported at present by an increasing body of experimental observations, including 1) the fact that different ras isoforms are preferentially mutated in specific types of tumors or developmental disorders; 2) the different transforming potential of transfected ras genes in different cell contexts; 3) the distinct sensitivities exhibited by the various Ras family members for modulation by different GAPs or GEFs; 4) the demonstration that different Ras isoforms follow distinct intracellular processing pathways and localize to different membrane microdomains or subcellular compartments; 5) the different phenotypes displayed by genetically modified animal strains for each of the 3 ras loci; and 6) the specific transcriptional networks controlled by each isoform in different cellular settings.

Entities:  

Keywords:  Ras; Ras isoforms; canonical Ras; functional specificity; redundancy

Year:  2011        PMID: 21779495      PMCID: PMC3128637          DOI: 10.1177/1947601911408081

Source DB:  PubMed          Journal:  Genes Cancer        ISSN: 1947-6019


  217 in total

1.  Ha-ras and N-ras regulate MAPK activity by distinct mechanisms in vivo.

Authors:  M Hamilton; A Wolfman
Journal:  Oncogene       Date:  1998-03       Impact factor: 9.867

2.  Rescue of cells from ras oncogene-induced growth arrest by a second, complementing, oncogene.

Authors:  T Hirakawa; H E Ruley
Journal:  Proc Natl Acad Sci U S A       Date:  1988-03       Impact factor: 11.205

Review 3.  Cellular oncogenes and multistep carcinogenesis.

Authors:  H Land; L F Parada; R A Weinberg
Journal:  Science       Date:  1983-11-18       Impact factor: 47.728

4.  Coexpression of MMTV/v-Ha-ras and MMTV/c-myc genes in transgenic mice: synergistic action of oncogenes in vivo.

Authors:  E Sinn; W Muller; P Pattengale; I Tepler; R Wallace; P Leder
Journal:  Cell       Date:  1987-05-22       Impact factor: 41.582

5.  Evidence for cell-specific differences in transformation by N-, H- and K-ras.

Authors:  J Maher; D A Baker; M Manning; N J Dibb; I A Roberts
Journal:  Oncogene       Date:  1995-10-19       Impact factor: 9.867

6.  Specific and high-affinity binding of inositol phosphates to an isolated pleckstrin homology domain.

Authors:  M A Lemmon; K M Ferguson; R O'Brien; P B Sigler; J Schlessinger
Journal:  Proc Natl Acad Sci U S A       Date:  1995-11-07       Impact factor: 11.205

7.  Differential expression of the ras gene family in mice.

Authors:  J Leon; I Guerrero; A Pellicer
Journal:  Mol Cell Biol       Date:  1987-04       Impact factor: 4.272

8.  Transformation of NIH 3T3 cells by microinjection of Ha-ras p21 protein.

Authors:  D W Stacey; H F Kung
Journal:  Nature       Date:  1984 Aug 9-15       Impact factor: 49.962

9.  Microinjection of the ras oncogene protein into PC12 cells induces morphological differentiation.

Authors:  D Bar-Sagi; J R Feramisco
Journal:  Cell       Date:  1985-10       Impact factor: 41.582

10.  Expression of ras proto-oncogene proteins in normal human tissues.

Authors:  M E Furth; T H Aldrich; C Cordon-Cardo
Journal:  Oncogene       Date:  1987-03       Impact factor: 9.867

View more
  116 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.  The higher level of complexity of K-Ras4B activation at the membrane.

Authors:  Hyunbum Jang; Avik Banerjee; Tanmay S Chavan; Shaoyong Lu; Jian Zhang; Vadim Gaponenko; Ruth Nussinov
Journal:  FASEB J       Date:  2015-12-30       Impact factor: 5.191

Review 3.  Inhibition of Ras-mediated signaling pathways in CML stem cells.

Authors:  Jessika Bertacchini; Neda Ketabchi; Laura Mediani; Silvano Capitani; Sandra Marmiroli; Najmaldin Saki
Journal:  Cell Oncol (Dordr)       Date:  2015-10-12       Impact factor: 6.730

Review 4.  Drugging Ras GTPase: a comprehensive mechanistic and signaling structural view.

Authors:  Shaoyong Lu; Hyunbum Jang; Shuo Gu; Jian Zhang; Ruth Nussinov
Journal:  Chem Soc Rev       Date:  2016-07-11       Impact factor: 54.564

5.  The differential palmitoylation states of N-Ras and H-Ras determine their distinct Golgi subcompartment localizations.

Authors:  Stephen J Lynch; Harriet Snitkin; Iwona Gumper; Mark R Philips; David Sabatini; Angel Pellicer
Journal:  J Cell Physiol       Date:  2015-03       Impact factor: 6.384

6.  Differences in the regulation of K-Ras and H-Ras isoforms by monoubiquitination.

Authors:  Rachael Baker; Emily M Wilkerson; Kazutaka Sumita; Daniel G Isom; Atsuo T Sasaki; Henrik G Dohlman; Sharon L Campbell
Journal:  J Biol Chem       Date:  2013-11-18       Impact factor: 5.157

7.  The small G protein RAS2 is involved in the metabolic compensation of the circadian clock in the circadian model Neurospora crassa.

Authors:  Norbert Gyöngyösi; Anita Szőke; Krisztina Ella; Krisztina Káldi
Journal:  J Biol Chem       Date:  2017-07-20       Impact factor: 5.157

8.  Functional redundancy of Sos1 and Sos2 for lymphopoiesis and organismal homeostasis and survival.

Authors:  Fernando C Baltanás; Martín Pérez-Andrés; Alicia Ginel-Picardo; David Diaz; David Jimeno; Pilar Liceras-Boillos; Robert L Kortum; Lawrence E Samelson; Alberto Orfao; Eugenio Santos
Journal:  Mol Cell Biol       Date:  2013-09-16       Impact factor: 4.272

9.  The differential effects of wild-type and mutated K-Ras on MST2 signaling are determined by K-Ras activation kinetics.

Authors:  David Romano; Helene Maccario; Carolanne Doherty; Niall P Quinn; Walter Kolch; David Matallanas
Journal:  Mol Cell Biol       Date:  2013-03-04       Impact factor: 4.272

Review 10.  Hras helps hippo heterodimerize to evade tumor suppression.

Authors:  Daniela Araiza-Olivera; Jonathan Chernoff
Journal:  Small GTPases       Date:  2016-09-20
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.