E2A Deficiency Leads to Abnormalities in αβ T-Cell Development and to Rapid Development of T-Cell Lymphomas

Gretchen Bain(University of California San Diego), Isaac Engel(University of California San Diego), E.C. Robanus Maandag(The Netherlands Cancer Institute), Hein P. J. te Riele(The Netherlands Cancer Institute), Joseph R. Voland(University of California San Diego), Leslie L. Sharp(University of California San Diego), Jerold Chun(University of California San Diego), Bing Huey(Cancer Research Institute), Dan Pinkel(Cancer Research Institute), Cornelis Murre(University of California San Diego)
Molecular and Cellular Biology
August 1, 1997
Cited by 400Open Access
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Abstract

The E2A gene products, E12 and E47, are critical for proper early B-cell development and commitment to the B-cell lineage. Here we reveal a new role for E2A in T-lymphocyte development. Loss of E2A activity results in a partial block at the earliest stage of T-lineage development. This early T-cell phenotype precedes the development of a T-cell lymphoma which occurs between 3 and 9 months of age. The thymomas are monoclonal and highly malignant and display a cell surface phenotype similar to that of immature thymocytes. In addition, the thymomas generally express high levels of c-myc. As assayed by comparative genomic hybridization, each of the tumor populations analyzed showed a nonrandom gain of chromosome 15, which contains the c-myc gene. Taken together, the data suggest that the E2A gene products play a role early in thymocyte development that is similar to their function in B-lineage determination. Furthermore, the lack of E2A results in development of T-cell malignancies, and we propose that E2A inactivation is a common feature of a wide variety of human T-cell proliferative disorders, including those involving the E2A heterodimeric partners tal-1 and lyl-1.


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