An avian retrovirus expressing chicken pp59(c-myc) possesses weak transforming activity distinct from v-myc that may be modulated by adjacent normal cell neighbors

• Published in: Journal of virology Vol. 65; no. 12
• Main Authors: Filardo, E.J. (Scripps Clinic and Research Foundation, La Jolla, CA), Humphries, E.H
• Format: Journal Article
• Language: English
• Published: 01.12.1991
• Subjects: AVES DE CORRAL; CAILLE; CARCINOGENOS; CODORNIZ; EXPRESION GENICA; EXPRESSION DES GENES; FIBROBLASTE; FIBROBLASTOS; GENE; GENES; NEOPLASMAS; NEOPLASME; ONCOVIRUS AVIAIRE; ONCOVIRUS AVIAR; SUBSTANCE CANCERIGENE; TRANSFORMACION GENETICA; TRANSFORMATION GENETIQUE; VOLAILLE
• ISSN: 0022-538X; 1098-5514

We demonstrate that EF168, an avian retrovirus that expresses the chicken pp59c-myc proto-oncogene, transforms quail embryo fibroblasts in vitro. An EF168-transformed quail clone, EF168-28, containing a single provirus, synthesizes several hundred copies of c-myc RNA and expresses elevated levels of the pp59c-myc gene product. The EF168 provirus in EF168-28 was isolated as a molecular clone, and the nucleotide sequence of its c-myc allele was confirmed as identical to that of exons 2 and 3 of the chicken c-myc proto-oncogene. Extended infection of quail embryo fibroblast cultures with EF168 induced a number of in vitro transformation-associated parameters similar to those elicited by the oncogenic v-myc-encoding retrovirus MC29, including alteration of cellular morphology, anchorage-independent growth, and induction of immortalized cell lines. Despite the fact that EF168 and MC29 shared these biological activities, further analysis revealed that EF168 initiated transformation in quail embryo fibroblasts, bone marrow, or adherent peripheral blood cultures 100- to 1,000-fold less efficiently than did MC29. Further, in contrast to MC29-induced foci, EF168 foci were smaller, morphologically diffuse, and less prominent. Analysis of newly infected cells demonstrated efficient expression of EF168 viral RNA in the absence of transformation. These differences suggest that while the pp59v-myc gene product can exert dominant transforming activity on quail embryo fibroblasts, its ability to initiate transformation is distinct from that of the pp110gag-v-myc gene product encoded by MC29 and may be suppressed by adjacent nontransformed cell neighbors