This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Le Cam, L.
Right arrow Articles by Sicinski, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Le Cam, L.
Right arrow Articles by Sicinski, P.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, July 2004, p. 6467-6475, Vol. 24, No. 14
0270-7306/04/$08.00+0     DOI: 10.1128/MCB.24.14.6467-6475.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

The E4F Protein Is Required for Mitotic Progression during Embryonic Cell Cycles

Laurent Le Cam,1,{dagger} Matthieu Lacroix,2 Maria A. Ciemerych,1,{ddagger} Claude Sardet,2 and Piotr Sicinski1*

Department of Cancer Biology, Dana-Farber Cancer Institute, and Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115,1 Institut de Génétique Moléculaire de Montpellier, CNRS UMR 5535, IFR122, 34293 Montpellier, France2

Received 15 January 2004/ Returned for modification 29 February 2004/ Accepted 9 April 2004

The ubiquitously expressed E4F protein was originally identified as an E1A-regulated cellular transcription factor required for adenovirus replication. The function of this protein in normal cell physiology remains largely unknown. To address this issue, we generated E4F knockout mice by gene targeting. Embryos lacking E4F die at the peri-implantation stage, while in vitro-cultured E4F–/– blastocysts exhibit defects in mitotic progression, chromosomal missegregation, and increased apoptosis. Consistent with these observations, we found that E4F localizes to the mitotic spindle during the M phase of early embryos. Our results establish a crucial role for E4F during early embryonic cell cycles and reveal an unexpected function for E4F in mitosis.


* Corresponding author. Mailing address: Dana-Farber Cancer Institute, 44 Binney St., Boston, MA 02115. Phone: (617) 632-5005. Fax: (617) 632-5006. E-mail: peter_sicinski{at}dfci.harvard.edu.

{dagger} Present address: Institut de Génétique Moléculaire de Montpellier, CNRS UMR 5535, IFR122, Montpellier, France.

{ddagger} Present address: Department of Embryology, Institute of Zoology, Warsaw University, 02-096 Warsaw, Poland.


Molecular and Cellular Biology, July 2004, p. 6467-6475, Vol. 24, No. 14
0022-538X/04/$08.00+0     DOI: 10.1128/MCB.24.14.6467-6475.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Wilkinson, M. B., Xiao, G., Kumar, A., LaPlant, Q., Renthal, W., Sikder, D., Kodadek, T. J., Nestler, E. J. (2009). Imipramine Treatment and Resiliency Exhibit Similar Chromatin Regulation in the Mouse Nucleus Accumbens in Depression Models. J. Neurosci. 29: 7820-7832 [Abstract] [Full Text]  
  • Donninger, H., Vos, M. D., Clark, G. J. (2007). The RASSF1A tumor suppressor. J. Cell Sci. 120: 3163-3172 [Abstract] [Full Text]  
  • Chagraoui, J., Niessen, S. L., Lessard, J., Girard, S., Coulombe, P., Sauvageau, M., Meloche, S., Sauvageau, G. (2006). E4F1: a novel candidate factor for mediating BMI1 function in primitive hematopoietic cells. Genes Dev. 20: 2110-2120 [Abstract] [Full Text]  
  • Lee, H., Lee, D. J., Oh, S. P., Park, H. D., Nam, H. H., Kim, J. M., Lim, D.-S. (2006). Mouse emi1 Has an Essential Function in Mitotic Progression during Early Embryogenesis.. Mol. Cell. Biol. 26: 5373-5381 [Abstract] [Full Text]  
  • Artus, J., Vandormael-Pournin, S., Frodin, M., Nacerddine, K., Babinet, C., Cohen-Tannoudji, M. (2005). Impaired Mitotic Progression and Preimplantation Lethality in Mice Lacking OMCG1, a New Evolutionarily Conserved Nuclear Protein. Mol. Cell. Biol. 25: 6289-6302 [Abstract] [Full Text]  
  • Ahmed-Choudhury, J., Agathanggelou, A., Fenton, S. L., Ricketts, C., Clark, G. J., Maher, E. R., Latif, F. (2005). Transcriptional Regulation of Cyclin A2 by RASSF1A through the Enhanced Binding of p120E4F to the Cyclin A2 Promoter. Cancer Res. 65: 2690-2697 [Abstract] [Full Text]