Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P04637 (
p53
)
77,613
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
We have recently shown that human papillomavirus (HPV16) E6 oncoprotein exhibits two separate biological activities in genital keratinocytes (PHKs). E6 protein by itself is capable of inducing colonies of proliferating cells resistant to serum and calcium-induced differentiation, whereas both E6 and E7 are required for immortalization of
PHK
. Using epitope-tagged E6 carboxy-terminal truncation mutants, we mapped the domain between amino acid residues 132 and 141 as being essential for the induction of differentiation resistance (L. Sherman and R. Schlegel, J. Virol. 70, 3269-3279, 1996). To determine whether E6 protein's ability to alter
PHK
response to serum and calcium was associated with its ability to inactivate
p53
, we evaluated each of the above E6 mutants and three E6 natural variants in these respective assays. Our results demonstrate that the E6 region spanning residues 132-141 is required for
p53
degradation and for abrogation of
p53
transactivation, suggesting a possible correlation between E6 biological activity in altering differentiation and loss of
p53
function. To evaluate whether selective inactivation of
p53
is sufficient for altering the response of
PHK
to serum and calcium we investigated the capacity of plasmids encoding a dominant mutant human
p53
and human MDM-2 to functionally substitute for E6 in colony formation in
PHK
. Plasmids were verified for their ability to inactivate wild-type
p53
by testing their capacity to abrogate the
p53
transactivation function. The results obtained showed that vectors encoding human MDM-2 and mutant p53, while active in inhibition of
p53
-dependent transactivation and capable of expressing stable proteins in
PHK
, failed to induce colonies of proliferating cells resistant to serum and calcium differentiation. These data argue that
p53
inactivation may not be the sole E6 function required for altering the response of
PHK
to serum- and calcium-triggered differentiation.
...
PMID:Inhibition of serum- and calcium-induced differentiation of human keratinocytes by HPV16 E6 oncoprotein: role of p53 inactivation. 935 41