TY - JOUR
T1 - Development of cellular resistance to pp60(v-src) kinase-induced cell death
AU - Wu, L. W.
AU - Hackett, Perry B
PY - 1995/1/1
Y1 - 1995/1/1
N2 - The v-src gene of Rous sarcoma virus (RSV) encodes pp60(v-src), a tyrosine kinase that can initiate cellular transformation. High levels of v-src gene expression can either be cytotoxic or the cause of altered expression of cellular genes. Examination of cytotoxic thresholds is difficult because cells expressing high levels of a cytotoxic oncogene will die. To evaluate quantitatively the cytotoxicity of pp60(v-src) on growth, we amplified two different v-src genes, under the control of the human hsp70B heat shock promoter to establish cell clones with varying copy numbers of the heat-inducible v-src gene. The viability of cell lines over a prolonged period of time depended on the particular src gene, the expression of v-src mRNA, synthesis of the pp60(v-src) protein and, most importantly, the tyrosine kinase activity of the pp60(v-src) protein. We found a relatively sharp threshold in v-src-encoded tyrosine kinase activity above which cell viability rapidly declines, However, over time, tyrosine kinase activity was exponentially suppressed at about a 10-fold higher rate than pp60(v-src) protein during passage. Our results indicate that homeostasis of tyrosine phosphorylation is important for cell viability, that perturbation of this balance results in cell mortality, and that cells can evolve to accommodate overexpression of oncogene by downregulating the level of tyrosine kinase activity.
AB - The v-src gene of Rous sarcoma virus (RSV) encodes pp60(v-src), a tyrosine kinase that can initiate cellular transformation. High levels of v-src gene expression can either be cytotoxic or the cause of altered expression of cellular genes. Examination of cytotoxic thresholds is difficult because cells expressing high levels of a cytotoxic oncogene will die. To evaluate quantitatively the cytotoxicity of pp60(v-src) on growth, we amplified two different v-src genes, under the control of the human hsp70B heat shock promoter to establish cell clones with varying copy numbers of the heat-inducible v-src gene. The viability of cell lines over a prolonged period of time depended on the particular src gene, the expression of v-src mRNA, synthesis of the pp60(v-src) protein and, most importantly, the tyrosine kinase activity of the pp60(v-src) protein. We found a relatively sharp threshold in v-src-encoded tyrosine kinase activity above which cell viability rapidly declines, However, over time, tyrosine kinase activity was exponentially suppressed at about a 10-fold higher rate than pp60(v-src) protein during passage. Our results indicate that homeostasis of tyrosine phosphorylation is important for cell viability, that perturbation of this balance results in cell mortality, and that cells can evolve to accommodate overexpression of oncogene by downregulating the level of tyrosine kinase activity.
KW - Cytotoxicity
KW - Tyrosine kinase
KW - pp60(v-src) overexpression
UR - http://www.scopus.com/inward/record.url?scp=0028820452&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0028820452&partnerID=8YFLogxK
M3 - Article
C2 - 7478570
AN - SCOPUS:0028820452
SN - 0950-9232
VL - 11
SP - 1459
EP - 1468
JO - Oncogene
JF - Oncogene
IS - 8
ER -