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Molecular and Cellular Biology, March 2008, p. 1713-1723, Vol. 28, No. 5
0270-7306/08/$08.00+0     doi:10.1128/MCB.01360-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

β-Catenin Expression Results in p53-Independent DNA Damage and Oncogene-Induced Senescence in Prelymphomagenic Thymocytes In Vivo{triangledown} ,{dagger}

Mai Xu,1 Qing Yu,1 Ramesh Subrahmanyam,2 Michael J. Difilippantonio,3 Thomas Ried,3 and Jyoti Misra Sen1*

Lymphocyte Development Unit, Laboratory of Immunology,1 Laboratory of Cellular and Molecular Biology, National Institute on Aging, Baltimore, Maryland 21224,2 Section of Cancer Genomics, Genetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 208923

Received 28 August 2008/ Returned for modification 22 October 2007/ Accepted 11 December 2007

The expression of β-catenin, a potent oncogene, is causally linked to tumorigenesis. Therefore, it was surprising that the transgenic expression of oncogenic β-catenin in thymocytes resulted in thymic involution instead of lymphomagenesis. In this report, we demonstrate that this is because the expression of oncogenic β-catenin induces DNA damage, growth arrest, oncogene-induced senescence (OIS), and apoptosis of immature thymocytes. In p53-deficient mice, the expression of oncogenic β-catenin still results in DNA damage and OIS, but the thymocytes survive and eventually progress to thymic lymphoma. β-Catenin-induced thymic lymphomas are distinct from lymphomas that arise in p53–/– mice. They are CD4 CD8, while p53-dependent lymphomas are largely CD4+ CD8+, and they develop at an earlier age and in the absence of c-Myc expression or Notch1 signaling. Thus, we report that oncogenic β-catenin-induced, p53-independent growth arrest and OIS and p53-dependent apoptosis protect developing thymocytes from transformation by oncogenic β-catenin.


* Corresponding author. Mailing address: Lymphocyte Development Unit, Laboratory of Immunology, National Institute on Aging, 5600 Nathan Shock Drive, Room 4B08 GRC, Baltimore, MD 21224. Phone: (410) 558-8163. Fax: (410) 558-8284. E-mail: Jyoti-Sen{at}nih.gov

{triangledown} Published ahead of print on 26 December 2007.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.


Molecular and Cellular Biology, March 2008, p. 1713-1723, Vol. 28, No. 5
0270-7306/08/$08.00+0     doi:10.1128/MCB.01360-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.




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