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PMID: 6281890 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Isolation of human oncogene sequences (v-fes homolog) from a cosmid library.

Science (New York, N.Y.) ·Vol. 216 ·No. 4550 ·1982-06-04 ·Pages 1136-8

Groffen J, Heisterkamp N, Grosveld F, Van de Ven W, Stephenson JR

Abstract

To define the human homolog (or homologs) of transforming sequences (v-fes gene) common to Gardner (GA) and Snyder Theilen (ST) isolates of feline sarcoma virus (FeSV), a representative library of human lung carcinoma DNA in a cosmid vector system was constructed. Three cosmid clones were isolated containing GA/ST FeSV v-fes homologous cellular sequences, within 32- to 42-kilobase cellular inserts representing 56 kilobases of contiguous human cellular DNA. Sequences both homologous to, and colinear with, GA or ST FeSV v-fes are distributed discontinuously over a region of up to 9.5 kilobases and contain a minimum of three regions of nonhomology representing probable introns. A thymidine kinase selection system was used to show that, upon transfection to RAT-2 cells, the human c-fes sequence lacked detectable transforming activity.

MeSH Terms
Bacteriophage lambda/genetics Cell Transformation, Viral Cloning, Molecular/methods DNA Restriction Enzymes DNA, Recombinant Escherichia coli/genetics Genes, Viral Humans Retroviridae/genetics
Chemicals
DNA, Recombinant DNA Restriction Enzymes
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Groffen J
Heisterkamp N
Grosveld F
Van de Ven W
Stephenson J R
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1982-06-04
Pages
1136-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCI NIH HHS · N0I-CO-75380 · United States
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