Literature DB >> 1321277

Transforming properties and substrate specificities of the protein tyrosine kinase oncogenes ros and src and their recombinants.

S M Jong1, C S Zong, T Dorai, L H Wang.   

Abstract

To determine the sequences of the oncogenes src (encoded by Rous sarcoma virus [RSV]) and ros (encoded by UR2) that are responsible for causing different transformation phenotypes and to correlate those sequences with differences in substrate recognition, we constructed recombinants of the two transforming protein tyrosine kinases (PTKs) and studied their biological and biochemical properties. A recombinant with a 5' end from src and a 3' end from ros, called SRC x ROS, transformed chicken embryo fibroblasts (CEF) to a spindle shape morphology, mimicking that of UR2. Neither of the two reverse constructs, ROS x SRC I and ROS x SRC II, could transform CEF. However, a transforming variant of ROS x SRC II appeared during passages of the transfected cells and was called ROS x SRC (R). ROS x SRC (R) contains a 16-amino-acid deletion that includes the 3' half of the transmembrane domain of ros. Unlike RSV, ROS x SRC (R) also transformed CEF to an elongated shape similar to that of UR2. We conclude that distinct phenotypic changes of RSV- and UR2-infected cells do not depend solely on the kinase domains of their oncogenes. We next examined cellular proteins phosphorylated by the tyrosine kinases of UR2, RSV, and their recombinants as well as a number of other avian sarcoma viruses including Fujinami sarcoma virus Y73, and some ros-derived variants. Our results indicate that the UR2-encoded receptorlike PTK P68gag-ros and its derivatives have a very restricted substrate specificity in comparison with the nonreceptor PTKs encoded by the rest of the avian sarcoma viruses. Data from ros and src recombinants indicate that sequences both inside and outside the catalytic domains of ros and src exert a significant effect on the substrate specificity of the two recombinant proteins. Phosphorylation of most of the proteins in the 100- to 200-kDa range correlated with the presence of the 5' src domain, including the SH2 region, but not with the kinase domain in the recombinants. This corroborates the conclusion given above that the kinase domain of src or ros per se is not sufficient to dictate the transforming morphology of these two oncogenes. High-level tyrosyl phosphorylation of most of the prominent substrates of src is not sufficient to cause a round-shape transformation morphology.

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Year:  1992        PMID: 1321277      PMCID: PMC241332     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  84 in total

1.  Biological properties of "partial" transformation mutants of Rous sarcoma virus and characterization of their pp60src kinase.

Authors:  D D Anderson; R P Beckmann; E H Harms; K Nakamura; M J Weber
Journal:  J Virol       Date:  1981-01       Impact factor: 5.103

2.  Four Rous sarcoma virus mutants which affect transformed cell morphology exhibit altered src gene products.

Authors:  D J Fujita; J Bechberger; I Nedic
Journal:  Virology       Date:  1981-10-15       Impact factor: 3.616

3.  An avian sarcoma virus mutant which produces an aberrant transformation affecting cell morphology.

Authors:  D J Fujita; C B Boschek; A Ziemiecki; R R Friis
Journal:  Virology       Date:  1981-05       Impact factor: 3.616

4.  Characterization of the transforming gene of Fujinami sarcoma virus.

Authors:  T Hanafusa; L H Wang; S M Anderson; R E Karess; W S Hayward; H Hanafusa
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

5.  The transforming proteins of Rous sarcoma virus, Harvey sarcoma virus and Abelson virus contain tightly bound lipid.

Authors:  B M Sefton; I S Trowbridge; J A Cooper; E M Scolnick
Journal:  Cell       Date:  1982-12       Impact factor: 41.582

6.  Comparison between the viral transforming gene (src) of recovered avian sarcoma virus and its cellular homolog.

Authors:  T Takeya; H Hanafusa; R P Junghans; G Ju; A M Skalka
Journal:  Mol Cell Biol       Date:  1981-11       Impact factor: 4.272

7.  Properties and location of poly(A) in Rous sarcoma virus RNA.

Authors:  L H Wang; P Duesberg
Journal:  J Virol       Date:  1974-12       Impact factor: 5.103

8.  A short sequence in the p60src N terminus is required for p60src myristylation and membrane association and for cell transformation.

Authors:  F R Cross; E A Garber; D Pellman; H Hanafusa
Journal:  Mol Cell Biol       Date:  1984-09       Impact factor: 4.272

9.  High-level expression in Escherichia coli of the carboxy-terminal sequences of the avian myelocytomatosis virus (MC29) v-myc protein.

Authors:  J A Lautenberger; D Court; T S Papas
Journal:  Gene       Date:  1983-07       Impact factor: 3.688

10.  Amino terminal myristylation of the protein kinase p60src, a retroviral transforming protein.

Authors:  A M Schultz; L E Henderson; S Oroszlan; E A Garber; H Hanafusa
Journal:  Science       Date:  1985-01-25       Impact factor: 47.728

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  3 in total

1.  Modulatory effect of the transmembrane domain of the protein-tyrosine kinase encoded by oncogene ros: biological function and substrate interaction.

Authors:  C S Zong; L H Wang
Journal:  Proc Natl Acad Sci U S A       Date:  1994-11-08       Impact factor: 11.205

2.  Distinctive effects of the carboxyl-terminal sequence of the insulin-like growth factor I receptor on its signaling functions.

Authors:  D Liu; C S Zong; L H Wang
Journal:  J Virol       Date:  1993-11       Impact factor: 5.103

3.  Molecular and biochemical bases for activation of the transforming potential of the proto-oncogene c-ros.

Authors:  C S Zong; B Poon; J Chen; L H Wang
Journal:  J Virol       Date:  1993-11       Impact factor: 5.103

  3 in total

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