Deregulation of c- <i>myc</i> by Translocation of the α-Locus of the T-Cell Receptor in T-Cell Leukemias

Jan Erikson(The Wistar Institute), L R Finger(The Wistar Institute), Lee K. Sun(The Wistar Institute), A ar-Rushdi(The Wistar Institute), Kazuko Nishikura(The Wistar Institute), Jun Minowada(Fujisawa City Hospital), J Finan(University of Pennsylvania), Beverly S. Emanuel(University of Pennsylvania), Peter C. Nowell̀(University of Pennsylvania), Carlo M. Croce(The Wistar Institute)
Science
May 16, 1986
Cited by 197

Abstract

Two human T-cell leukemias carrying a t(8;14)(q24;q11) chromosome translocation were studied for rearrangements and expression of the c-myc oncogene. For one leukemia, rearrangement was detected in a region immediately distal (3') to the c-myc locus; no rearrangements of c-myc were observed in the second case (DeF). However, studies with hybrids between human and mouse leukemic T cells indicated that in the leukemic cells of DeF, the breakpoint in chromosome 14 occurred between genes for the variable (V alpha) and the constant (C alpha) regions for the alpha chain of the T-cell receptor. The C alpha locus had translocated to a region more than 38 kilobases 3' to the involved c-myc oncogene. Since human c-myc transcripts were expressed only in hybrids carrying the 8q+ chromosome but not in hybrids containing the normal chromosome 8, it is concluded that the translocation of the C alpha locus 3' to the c-myc oncogene can result in its transcriptional deregulation.


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