Avian Sarcoma Virus Transformed Hamster Cells made Resistant to Ethidium Bromide

1974 ◽  
Vol 16 (3) ◽  
pp. 603-621
Author(s):  
C. ALTANER ◽  
J. MATOSKA

Hamster cells transformed with the Schmidt-Ruppin strain of avian sarcoma virus were selected for resistance to ethidium bromide (EB). The resistant cell lines proliferated in the presence of up to 30 µg/ml EB. From avian sarcoma virus-transformed hamster cells already resistant to bromodeoxy-uridine (BrdU), ethidium bromide-resistant cells which were able to grow in 10 µg/ml EB were also prepared. These cells remain deficient in thymidine kinase activity and are suitable for selective preparation of hybrid cells. The EB resistance was genetically stable. The EB-resistant cell lines, and doubly resistant cells (BrdU, EB) showed no differences in mitochondrial ultrastructure compared with the original cell lines. Thymidine incorporation into mitochondrial DNA was not influenced by EB resistance. All resistant cell lines, including the doubly resistant cell line, contained the avian sarcoma virus genome. The number of cells needed for positive rescue experiments for avian sarcoma virus genome by cell fusion with permissive chicken embryo cells was the same as with the original cell lines. The single EB-resistant cell lines contained R-type virus-like particles, while in BrdU-resistant and doubly resistant cells the R-type particles were absent. The possible nature of EB resistance is discussed.

1982 ◽  
Vol 2 (8) ◽  
pp. 890-896 ◽  
Author(s):  
B Adkins ◽  
T Hunter

The primary translation product of the PRC II avian sarcoma virus genome is a protein of 105,000 daltons (P105), and we have previously shown that approximately 50% of the P105 molecules are converted to molecules of 110,000 daltons (P110) by posttranslational modification. Fractionation of PRC II-infected cells showed that P105 was contained primarily in a nonionic detergent-soluble compartment, whereas P110 partitioned almost exclusively with a nonionic detergent-insoluble or crude cytoskeletal fraction. The tyrosine-specific protein kinase activity previously observed in immunoprecipitates which presumably contained both P110 and P105 was found predominantly in the P110-containing immunoprecipitates made from the cytoskeletal fraction and was essentially absent from the P105-containing immunoprecipitates prepared from the soluble fraction. Individual analysis of 32P-labeled P110 and P105 prepared by this fractionation technique revealed that P110 contained more phosphotyrosine per mole of protein than did P105. Examination of the tryptic peptide maps of 32P-labeled P110 and P105 suggested that the additional phosphotyrosine in P110 resulted from phosphorylation at discrete sites within the protein. From these experiments, we conclude that PRC II-infected cells contain two discrete forms, P105 and P110, of the transforming protein and that each of these proteins exhibits distinct structural and functional characteristics.


Nature ◽  
1975 ◽  
Vol 253 (5492) ◽  
pp. 507-511 ◽  
Author(s):  
Ramareddy V. Guntaka ◽  
Brian W. J. Mahy ◽  
J. Michael Bishop ◽  
Harold E. Varmus

1976 ◽  
Vol 19 (2) ◽  
pp. 548-558 ◽  
Author(s):  
B Cordell ◽  
E Stavnezer ◽  
R Friedrich ◽  
J M Bishop ◽  
H M Goodman

1980 ◽  
Vol 8 (13) ◽  
pp. 2967-2984 ◽  
Author(s):  
A.P. Czernilofsky ◽  
W. DeLorbe ◽  
R. Swanstrom ◽  
H.E. Varmus ◽  
J.M. Bishop ◽  
...  

Biochemistry ◽  
1978 ◽  
Vol 17 (17) ◽  
pp. 3627-3632 ◽  
Author(s):  
Kenneth Dimock ◽  
C. Martin Stoltzfus

2020 ◽  
Vol 19 (10) ◽  
pp. 1649-1663
Author(s):  
Svenja Wiechmann ◽  
Elena Saupp ◽  
Daniela Schilling ◽  
Stephanie Heinzlmeir ◽  
Günter Schneider ◽  
...  

Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive cancers and known for its extensive genetic heterogeneity, high therapeutic resistance, and strong variation in intrinsic radiosensitivity. To understand the molecular mechanisms underlying radioresistance, we screened the phenotypic response of 38 PDAC cell lines to ionizing radiation. Subsequent phosphoproteomic analysis of two representative sensitive and resistant lines led to the reproducible identification of 7,800 proteins and 13,000 phosphorylation sites (p-sites). Approximately 700 p-sites on 400 proteins showed abundance changes after radiation in all cell lines regardless of their phenotypic sensitivity. Apart from recapitulating known radiation response phosphorylation markers such as on proteins involved in DNA damage repair, the analysis uncovered many novel members of a radiation-responsive signaling network that was apparent only at the level of protein phosphorylation. These regulated p-sites were enriched in potential ATM substrates and in vitro kinase assays corroborated 10 of these. Comparing the proteomes and phosphoproteomes of radiosensitive and -resistant cells pointed to additional tractable radioresistance mechanisms involving apoptotic proteins. For instance, elevated NADPH quinine oxidoreductase 1 (NQO1) expression in radioresistant cells may aid in clearing harmful reactive oxygen species. Resistant cells also showed elevated phosphorylation levels of proteins involved in cytoskeleton organization including actin dynamics and focal adhesion kinase (FAK) activity and one resistant cell line showed a strong migration phenotype. Pharmacological inhibition of the kinases FAK by Defactinib and of CHEK1 by Rabusertib showed a statistically significant sensitization to radiation in radioresistant PDAC cells. Together, the presented data map a comprehensive molecular network of radiation-induced signaling, improves the understanding of radioresistance and provides avenues for developing radiotherapeutic strategies.


Virology ◽  
1977 ◽  
Vol 79 (1) ◽  
pp. 183-197 ◽  
Author(s):  
Jacov Tal ◽  
Hsing-Jien Kung ◽  
Harold E. Varmus ◽  
J.Michael Bishop

Cell ◽  
1978 ◽  
Vol 15 (1) ◽  
pp. 79-91 ◽  
Author(s):  
Barbara Cordell ◽  
Susan R. Weiss ◽  
Harold E. Varmus ◽  
J.Michael Bishop

Virology ◽  
1977 ◽  
Vol 79 (1) ◽  
pp. 198-215 ◽  
Author(s):  
Roland Friedrich ◽  
Hsing-Jien Kung ◽  
Barbara Baker ◽  
Harold E. Varmus ◽  
Howard M. Goodman ◽  
...  

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