TY - JOUR
T1 - Molecular cloning of chinese hamster dihydrofolate reductase-specific cDNA and the identification of multiple dihydrofolate reductase mRNAs in antifolate-resistant chinese hamster lung fibroblasts
AU - Lewis, John A.
AU - Kurtz, David T.
AU - Melera, Peter W.
N1 - Funding Information:
ACKNOWLEDGEMENTS We thank Dr. J. L. Biedler for supplying cell lines and Dr. M. Wigler for helpful discussions. The excellent technical assistance of Ms. C. A. Hession is gratefully acknowledged. This work was supported in part by grants from the National Cancer Institute to the Sloan-Kettering Institute for Cancer Research and to P.W.M. The data reported here has been submitted
PY - 1981/3/25
Y1 - 1981/3/25
N2 - ds cDNA from the antifolate-resistant Chinese hamster lung fibroblast subline DC-3F/MQ19 was ligated to Eco RI and Sal I oligonucleotide linkers and cloned into Eco RI and Sal I digested pBR322. Transformed colonies containing dihydrofolate reductase (DHFR)-specific recombinant plasmid were identified by Grunstein Hogness assay using a Chinese hamster DHFR-specific cDNA probe. A recombinant plasmid, pDHFR6, containing a 650 bp DHFR insert was isolated and analyzed. This plasmid was used as a molecular probe in a Northern blot analysis of both cytoplasmic and polysomal DHFR, poly A+ mRNAs of the DC-3F/MQ19 subline, which over-produces a 20,000d DHFR 150-fold, and the DC-3F/A3 subline, which over-produces a 21,000d DHFR 170-fold. This analysis revealed the presence of three DHFR mRNA species of 1350, 2200, and 3300 nucleotides in both independently-derived cell lines. The relative abundance of each species however varied strikingly between the two cell lines.
AB - ds cDNA from the antifolate-resistant Chinese hamster lung fibroblast subline DC-3F/MQ19 was ligated to Eco RI and Sal I oligonucleotide linkers and cloned into Eco RI and Sal I digested pBR322. Transformed colonies containing dihydrofolate reductase (DHFR)-specific recombinant plasmid were identified by Grunstein Hogness assay using a Chinese hamster DHFR-specific cDNA probe. A recombinant plasmid, pDHFR6, containing a 650 bp DHFR insert was isolated and analyzed. This plasmid was used as a molecular probe in a Northern blot analysis of both cytoplasmic and polysomal DHFR, poly A+ mRNAs of the DC-3F/MQ19 subline, which over-produces a 20,000d DHFR 150-fold, and the DC-3F/A3 subline, which over-produces a 21,000d DHFR 170-fold. This analysis revealed the presence of three DHFR mRNA species of 1350, 2200, and 3300 nucleotides in both independently-derived cell lines. The relative abundance of each species however varied strikingly between the two cell lines.
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U2 - 10.1093/nar/9.6.1311
DO - 10.1093/nar/9.6.1311
M3 - Article
C2 - 6262725
AN - SCOPUS:0019498242
SN - 0305-1048
VL - 9
SP - 1311
EP - 1322
JO - Nucleic acids research
JF - Nucleic acids research
IS - 6
ER -