Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
1994-9-15
|
pubmed:abstractText |
The degree of phosphorylation of c-Jun, Jun-B, Jun-D and Egr-1 transcription factors was examined during normal growth and during a prolonged period of defined transformation of NIH-3T3 cells which conditionally express v-sis [Mercola, D. et al. (1992) Oncogene, 7, 1793-1803]. During the asynchronous growth of normal cells phosphorylation of all factors was low and constant at all stages of growth from low density (c. 25 x 10(3) cells/cm2) through log-phase of growth to saturation density (c. 100 x 10(3) cells/cm2). Upon induction of v-sis, a marked and coordinate increase in phosphorylation occurred for c-Jun, Jun-B and Egr-1 to approximately 320%, 230% and 420% respectively above basal levels which was stable for the 2.5 day transformation period. The phosphorylation of Jun-D increased to over 600% and, after about 20 h, steadily declined to near basal levels at 54 h post-induction. Moreover, at any time phosphorylation and v-sis expression were fully reversible upon removal of the inducer. It appears that increased phosphorylation of the Jun family members and Egr-1 is not necessary for normal growth of NIH-3T3 but is dependent upon the expression of v-sis. Thus, normal and transformed cells may be distinguished. For c-Jun, the v-sis enhanced phosphorylation occurs at serines 63 and 73 and is required for transformation by several oncogenes [Smeal, T. et al. (1992) Mol. Cell. Biol., 12, 3507-3513]. The results described here show that the phosphorylation of additional factors is a stable and specific correlate of transformation which have have regulatory significance during transformation.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/EGR1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Early Growth Response Protein 1,
http://linkedlifedata.com/resource/pubmed/chemical/Egr1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Immediate-Early Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Oncogene Proteins v-sis,
http://linkedlifedata.com/resource/pubmed/chemical/Platelet-Derived Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-jun,
http://linkedlifedata.com/resource/pubmed/chemical/Retroviridae Proteins, Oncogenic,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0143-3334
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
15
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1667-74
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:8055649-3T3 Cells,
pubmed-meshheading:8055649-Amino Acid Sequence,
pubmed-meshheading:8055649-Animals,
pubmed-meshheading:8055649-Cell Cycle,
pubmed-meshheading:8055649-Cell Line, Transformed,
pubmed-meshheading:8055649-Cell Transformation, Neoplastic,
pubmed-meshheading:8055649-DNA-Binding Proteins,
pubmed-meshheading:8055649-Early Growth Response Protein 1,
pubmed-meshheading:8055649-Humans,
pubmed-meshheading:8055649-Immediate-Early Proteins,
pubmed-meshheading:8055649-Mice,
pubmed-meshheading:8055649-Molecular Sequence Data,
pubmed-meshheading:8055649-Oncogene Proteins v-sis,
pubmed-meshheading:8055649-Oncogenes,
pubmed-meshheading:8055649-Phosphorylation,
pubmed-meshheading:8055649-Platelet-Derived Growth Factor,
pubmed-meshheading:8055649-Proto-Oncogene Proteins c-jun,
pubmed-meshheading:8055649-Retroviridae Proteins, Oncogenic,
pubmed-meshheading:8055649-Transcription Factors
|
pubmed:year |
1994
|
pubmed:articleTitle |
Transformation-specific pattern of phosphorylation of c-Jun, Jun-B, Jun-D and Egr-1 in v-sis transformed cells.
|
pubmed:affiliation |
San Diego Regional Cancer Center, CA 92161.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|