Altered post-translational processing of p21(ras) oncoprotein in a transformation-suppressed cell line

S. Huang, D. E. Axelrod

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

We have isolated a transformation-suppressed cell line, R35, which is altered in the maturation of p21(ras). It was obtained from the transformed cell line NIH3T3( )(ras(EJ)) as a revertant with flat morphology and anchorage dependent growth. Immunoprecipitation of steady state labeled ras proteins reveals that the revertant produces p21(ras) and in addition, accumulates a protein that migrates as 23kD. Fusion of revertant cells with non-transformed rat2 cells yields cell hybrids which are retransformed and do not accumulate p23, suggesting that accumulation of p23 and suppression of transformation may be related. The accumulated p23 appears to be a precursor to p21 because (1) pulse labeling and cell fractionation of revertant cells shows that label chases from cytoplasmic p23 to membrane-associated p21, although at a slower rate, and (2) the p23 of revertant cells is indistinguishable from the p23 precursor of p21 in parent cells by partial V8 protease digestion and two dimensional electrophoresis. R35 cells are slower than their transformed parent in palmitylation and polyisoprenylation, but not in methylation of ras proteins. These results suggest that the transformation-suppressed cell line R35 is defective in the rate at which it post-translationally processes ras proteins, possibly because it is slower in polyisoprenylation of the cytoplasmic p23 precursor protein.

Original languageEnglish (US)
Pages (from-to)1211-1218
Number of pages8
JournalOncogene
Volume6
Issue number7
StatePublished - 1991

All Science Journal Classification (ASJC) codes

  • Genetics
  • Molecular Biology
  • Cancer Research

Fingerprint

Dive into the research topics of 'Altered post-translational processing of p21(ras) oncoprotein in a transformation-suppressed cell line'. Together they form a unique fingerprint.

Cite this