Literature DB >> 11909960

Mutant mouse models reveal the relative roles of E2F1 and E2F3 in vivo.

Jennifer E Cloud1, Catherine Rogers, Tammi L Reza, Ulrike Ziebold, James R Stone, Michael H Picard, Alicia M Caron, Roderick T Bronson, Jacqueline A Lees.   

Abstract

The E2F1, -2, and -3 transcription factors are key downstream targets of the retinoblastoma protein (pRB) tumor suppressor that drive expression of proliferation-associated genes. Here we use mutant mouse strains to investigate E2F3's role in vivo. We show that E2F3 is essential for embryonic viability in the pure 129/Sv background but the presence of C57BL/6 alleles yields some adult survivors. Although growth retarded, surviving E2f3(-/-) animals are initially healthy. However, they die prematurely, exhibiting no obvious tumor phenotype but with the typical signs of congestive heart failure. The defects are completely distinct from those arising in E2f1 mutant mice (S. J. Field et al., Cell 85:549-561; 1996; L. Yamasaki et al., Cell 85:537-548, 1996), supporting the prevailing view that these E2Fs must have some unique biological functions in vivo. To test this model, we examined the phenotypes of E2f1 E2f3 compound mutant mice. Almost all of the developmental and age-related defects arising in the individual E2f1 or E2f3 mice were exacerbated by the mutation of the other E2f. Thus, E2F1 and E2F3 appear to play critical, overlapping roles in the development and maintenance of a variety of tissues. Importantly, this study did identify one major difference in the properties of E2F1 and E2F3: either alone or in combination with E2F1 loss, E2f3 mutation did not increase the incidence of tumor formation. These data strongly suggest that tumor suppression is a specific property of E2F1 and not E2F3.

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Year:  2002        PMID: 11909960      PMCID: PMC133738          DOI: 10.1128/MCB.22.8.2663-2672.2002

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


  60 in total

1.  Target gene specificity of E2F and pocket protein family members in living cells.

Authors:  J Wells; K E Boyd; C J Fry; S M Bartley; P J Farnham
Journal:  Mol Cell Biol       Date:  2000-08       Impact factor: 4.272

2.  Loss of E2F4 activity leads to abnormal development of multiple cellular lineages.

Authors:  R E Rempel; M T Saenz-Robles; R Storms; S Morham; S Ishida; A Engel; L Jakoi; M F Melhem; J M Pipas; C Smith; J R Nevins
Journal:  Mol Cell       Date:  2000-08       Impact factor: 17.970

Review 3.  The Rb/E2F pathway: expanding roles and emerging paradigms.

Authors:  J W Harbour; D C Dean
Journal:  Genes Dev       Date:  2000-10-01       Impact factor: 11.361

4.  E2F3 contributes both to the inappropriate proliferation and to the apoptosis arising in Rb mutant embryos.

Authors:  U Ziebold; T Reza; A Caron; J A Lees
Journal:  Genes Dev       Date:  2001-02-15       Impact factor: 11.361

5.  A role for E2F1 in the induction of ARF, p53, and apoptosis during thymic negative selection.

Authors:  J W Zhu; D DeRyckere; F X Li; Y Y Wan; J DeGregori
Journal:  Cell Growth Differ       Date:  1999-12

6.  E2F4 is essential for normal erythrocyte maturation and neonatal viability.

Authors:  P O Humbert; C Rogers; S Ganiatsas; R L Landsberg; J M Trimarchi; S Dandapani; C Brugnara; S Erdman; M Schrenzel; R T Bronson; J A Lees
Journal:  Mol Cell       Date:  2000-08       Impact factor: 17.970

Review 7.  Genomic circuits and the integrative biology of cardiac diseases.

Authors:  K R Chien
Journal:  Nature       Date:  2000-09-14       Impact factor: 49.962

8.  E2F4 and E2F5 play an essential role in pocket protein-mediated G1 control.

Authors:  S Gaubatz; G J Lindeman; S Ishida; L Jakoi; J R Nevins; D M Livingston; R E Rempel
Journal:  Mol Cell       Date:  2000-09       Impact factor: 17.970

9.  A common E2F-1 and p73 pathway mediates cell death induced by TCR activation.

Authors:  N A Lissy; P K Davis; M Irwin; W G Kaelin; S F Dowdy
Journal:  Nature       Date:  2000-10-05       Impact factor: 49.962

10.  The E2F6 transcription factor is a component of the mammalian Bmi1-containing polycomb complex.

Authors:  J M Trimarchi; B Fairchild; J Wen; J A Lees
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-30       Impact factor: 11.205

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  41 in total

1.  Inactivation of E2F3 results in centrosome amplification.

Authors:  Harold I Saavedra; Baidehi Maiti; Cynthia Timmers; Rachel Altura; Yukari Tokuyama; Kenji Fukasawa; Gustavo Leone
Journal:  Cancer Cell       Date:  2003-04       Impact factor: 31.743

2.  Defective gene expression, S phase progression, and maturation during hematopoiesis in E2F1/E2F2 mutant mice.

Authors:  Feng X Li; Jing W Zhu; Christopher J Hogan; James DeGregori
Journal:  Mol Cell Biol       Date:  2003-05       Impact factor: 4.272

3.  E2F-dependent histone acetylation and recruitment of the Tip60 acetyltransferase complex to chromatin in late G1.

Authors:  Stefan Taubert; Chiara Gorrini; Scott R Frank; Tiziana Parisi; Miriam Fuchs; Ho-Man Chan; David M Livingston; Bruno Amati
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

4.  Unique requirement for Rb/E2F3 in neuronal migration: evidence for cell cycle-independent functions.

Authors:  Kelly A McClellan; Vladimir A Ruzhynsky; David N Douda; Jacqueline L Vanderluit; Kerry L Ferguson; Danian Chen; Rod Bremner; David S Park; Gustavo Leone; Ruth S Slack
Journal:  Mol Cell Biol       Date:  2007-04-23       Impact factor: 4.272

Review 5.  Cardiac myocyte cell cycle control in development, disease, and regeneration.

Authors:  Preeti Ahuja; Patima Sdek; W Robb MacLellan
Journal:  Physiol Rev       Date:  2007-04       Impact factor: 37.312

6.  p110 CUX1 cooperates with E2F transcription factors in the transcriptional activation of cell cycle-regulated genes.

Authors:  Mary Truscott; Ryoko Harada; Charles Vadnais; François Robert; Alain Nepveu
Journal:  Mol Cell Biol       Date:  2008-03-17       Impact factor: 4.272

7.  Antagonism of E2F-1 regulated Bnip3 transcription by NF-kappaB is essential for basal cell survival.

Authors:  James Shaw; Natalia Yurkova; Tong Zhang; Hongying Gang; Floribeth Aguilar; Danielle Weidman; Carly Scramstad; Harvey Weisman; Lorrie A Kirshenbaum
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-16       Impact factor: 11.205

8.  E2f3b plays an essential role in myogenic differentiation through isoform-specific gene regulation.

Authors:  Patrik Asp; Diego Acosta-Alvear; Mary Tsikitis; Chris van Oevelen; Brian David Dynlacht
Journal:  Genes Dev       Date:  2009-01-01       Impact factor: 11.361

9.  E2f3a and E2f3b make overlapping but different contributions to total E2f3 activity.

Authors:  P S Danielian; L B Friesenhahn; A M Faust; J C West; A M Caron; R T Bronson; J A Lees
Journal:  Oncogene       Date:  2008-07-28       Impact factor: 9.867

10.  Ott1 (Rbm15) is essential for placental vascular branching morphogenesis and embryonic development of the heart and spleen.

Authors:  Glen D Raffel; Gerald C Chu; Jonathan L Jesneck; Dana E Cullen; Roderick T Bronson; Olivier A Bernard; D Gary Gilliland
Journal:  Mol Cell Biol       Date:  2008-11-03       Impact factor: 4.272

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