Literature DB >> 8035821

Cellular ras activity is required for passage through multiple points of the G0/G1 phase in BALB/c 3T3 cells.

S Dobrowolski1, M Harter, D W Stacey.   

Abstract

Microinjection experiments demonstrated a requirement for cellular ras activity late in G1. In this study, we used two separate methods to identify an additional requirement for cellular ras activity early in the G0/G1 phase of the cell cycle. Quiescent BALB/c cells were injected with anti-ras antibody prior to stimulation with serum. The cells would therefore be inhibited in progression through the cell cycle at the earliest point requiring ras function. Alternatively, cells were inhibited in late G1 as in previous studies by injecting anti-ras several hours after serum addition to quiescent cells. The injected cultures were then treated with chemical cell cycle inhibitors known to function in mid-G1. Cells injected with anti-ras prior to serum stimulation were retained at a point of ras requirement prior to the execution point of the chemical inhibitor, while cells injected 3 to 5 h after serum stimulation were retained at a point of ras requirement downstream of the execution point of the chemical inhibitor. To confirm these results, quiescent BALB/c cells were injected with anti-ras antibody prior to or several hours following serum addition. In this case, however, second injections of oncogenic ras or adenoviral E1A protein were performed to overcome the inhibitory effects of the anti-ras antibody. Cells injected prior to serum addition were clearly inhibited at an early point of Ras requirement since they required 5 or 6 h longer to enter S phase than cells injected with anti-ras antibody after serum addition.

Mesh:

Substances:

Year:  1994        PMID: 8035821      PMCID: PMC359063          DOI: 10.1128/mcb.14.8.5441-5449.1994

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  42 in total

1.  Dominant inhibitory Ras mutants demonstrate the requirement for Ras activity in the action of tyrosine kinase oncogenes.

Authors:  D W Stacey; M Roudebush; R Day; S D Mosser; J B Gibbs; L A Feig
Journal:  Oncogene       Date:  1991-12       Impact factor: 9.867

2.  New stable butyrate derivatives alter proliferation and differentiation in human mammary cells.

Authors:  P Planchon; H Raux; V Magnien; G Ronco; P Villa; M Crépin; D Brouty-Boyé
Journal:  Int J Cancer       Date:  1991-05-30       Impact factor: 7.396

3.  Involvement of p21ras in activation of extracellular signal-regulated kinase 2.

Authors:  A M de Vries-Smits; B M Burgering; S J Leevers; C J Marshall; J L Bos
Journal:  Nature       Date:  1992-06-18       Impact factor: 49.962

4.  Effects of cyclic AMP and butyrate on cell cycle, DNA, RNA, and purine synthesis of cultured astrocytes.

Authors:  J H Bruce; A Ramirez; L Lin; R P Agarwal
Journal:  Neurochem Res       Date:  1992-04       Impact factor: 3.996

5.  An SH3-SH2-SH3 protein is required for p21Ras1 activation and binds to sevenless and Sos proteins in vitro.

Authors:  M A Simon; G S Dodson; G M Rubin
Journal:  Cell       Date:  1993-04-09       Impact factor: 41.582

6.  The jun and fos protein families are both required for cell cycle progression in fibroblasts.

Authors:  K Kovary; R Bravo
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

7.  Flow cytometric and biochemical analysis of dose-dependent effects of sodium butyrate on human endometrial adenocarcinoma cells.

Authors:  S Saito; H A Crissman; M Nishijima; T Kagabu; I Nishiya; L S Cram
Journal:  Cytometry       Date:  1991

8.  The adenovirus E1A 243R protein purified from Escherichia coli under nondenaturing conditions is found in association with dnaK.

Authors:  D M Wang; B Dalie; M L Harter
Journal:  Protein Expr Purif       Date:  1992-02       Impact factor: 1.650

9.  Torso, a receptor tyrosine kinase required for embryonic pattern formation, shares substrates with the sevenless and EGF-R pathways in Drosophila.

Authors:  H J Doyle; J M Bishop
Journal:  Genes Dev       Date:  1993-04       Impact factor: 11.361

10.  Transforming growth factor beta 1 inhibition of p34cdc2 phosphorylation and histone H1 kinase activity is associated with G1/S-phase growth arrest.

Authors:  P H Howe; G Draetta; E B Leof
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

View more
  29 in total

1.  Aiolos transcription factor controls cell death in T cells by regulating Bcl-2 expression and its cellular localization.

Authors:  F Romero; C Martínez-A; J Camonis; A Rebollo
Journal:  EMBO J       Date:  1999-06-15       Impact factor: 11.598

2.  Distinct tyrosine autophosphorylation sites negatively and positively modulate neu-mediated transformation.

Authors:  D L Dankort; Z Wang; V Blackmore; M F Moran; W J Muller
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

Review 3.  The cell cycle: a critical therapeutic target to prevent vascular proliferative disease.

Authors:  Thierry Charron; Nafiseh Nili; Bradley H Strauss
Journal:  Can J Cardiol       Date:  2006-02       Impact factor: 5.223

4.  Nuclear magnetic resonance structure of the N-terminal domain of nonstructural protein 3 from the severe acute respiratory syndrome coronavirus.

Authors:  Pedro Serrano; Margaret A Johnson; Marcius S Almeida; Reto Horst; Torsten Herrmann; Jeremiah S Joseph; Benjamin W Neuman; Vanitha Subramanian; Kumar S Saikatendu; Michael J Buchmeier; Raymond C Stevens; Peter Kuhn; Kurt Wüthrich
Journal:  J Virol       Date:  2007-08-29       Impact factor: 5.103

Review 5.  Cell cycle proliferation decisions: the impact of single cell analyses.

Authors:  Jacob P Matson; Jeanette G Cook
Journal:  FEBS J       Date:  2016-10-05       Impact factor: 5.542

6.  Role of c-fos and E2F in the induction of cyclin A transcription and vascular smooth muscle cell proliferation.

Authors:  A M Sylvester; D Chen; K Krasinski; V Andrés
Journal:  J Clin Invest       Date:  1998-03-01       Impact factor: 14.808

7.  Ras links growth factor signaling to the cell cycle machinery via regulation of cyclin D1 and the Cdk inhibitor p27KIP1.

Authors:  H Aktas; H Cai; G M Cooper
Journal:  Mol Cell Biol       Date:  1997-07       Impact factor: 4.272

8.  Ras activity late in G1 phase required for p27kip1 downregulation, passage through the restriction point, and entry into S phase in growth factor-stimulated NIH 3T3 fibroblasts.

Authors:  N Takuwa; Y Takuwa
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

9.  Ras binding triggers ubiquitination of the Ras exchange factor Ras-GRF2.

Authors:  C L de Hoog; J A Koehler; M D Goldstein; P Taylor; D Figeys; M F Moran
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

10.  Krüppel-like factor 5 mediates the transforming activity of oncogenic H-Ras.

Authors:  Mandayam O Nandan; Hong S Yoon; Weidong Zhao; Lillian A Ouko; Sengthong Chanchevalap; Vincent W Yang
Journal:  Oncogene       Date:  2004-04-22       Impact factor: 9.867

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.