Mapping and sequencing of the dihydrofolate reductase gene ( DFR1) of Saccharomyces cerevisiae

The dihydrofolate reductase gene ( DFR1) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated on an 8.8-kb BamHI fragment from a yeast genomic library by screening of Escherichia coli transformants for resistance to trimethoprim. A 1.8-kb SalI- BamHI fragment which was...

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Published inGene Vol. 63; no. 2; pp. 175 - 185
Main Authors Barclay, Barry J., Huang, Tun, Nagel, Michael G., Misener, Virginia L., Game, John C., Wahl, Geoffrey M.
Format Journal Article
LanguageEnglish
Published Lausanne Elsevier B.V 31.03.1988
Amsterdam Elsevier
New York, NY
Subjects
Online AccessGet full text
ISSN0378-1119
1879-0038
DOI10.1016/0378-1119(88)90523-9

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Abstract The dihydrofolate reductase gene ( DFR1) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated on an 8.8-kb BamHI fragment from a yeast genomic library by screening of Escherichia coli transformants for resistance to trimethoprim. A 1.8-kb SalI- BamHI fragment which was able to confer methotrexate resistance in yeast also complemented an E. coli DHFR-deficient ( folA) mutant. Nucleotide sequence analysis revealed that the yeast DFR1 gene encoded a polypeptide with a predicted M r of 24230. The deduced sequence of 211 amino acid residues showed considerable homology with DHFRs from both bacterial and animal sources. The codon bias index of the DFR1 coding region is 0.0083, which indicates a random pattern of codon usage. The upstream region contains two consensus sequences required for binding of the yeast's positive regulatory factor, GCN4, suggesting that the DFR1 gene might be subject to the amino acid general control. Several potential ‘TATA’ boxes are located in the sequence 5' to the gene. Located in the 3' flanking region are homologies with several canonical sequences thought to be required for efficient transcription termination in yeast. We also mapped the DFR1 gene to a position 1.4 cM proximal to the MET7 locus on chromosome XV.
AbstractList The dihydrofolate reductase gene (DFR1) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated on an 8.8-kb BamHI fragment from a yeast genomic library by screening of Escherichia coli transformants for resistance to trimethoprim. A 1.8-kb SalI-BamHI fragment which was able to confer methotrexate resistance in yeast also complemented an E. coli DHFR-deficient (folA) mutant. Nucleotide sequence analysis revealed that the yeast DFR1 gene encoded a polypeptide with a predicted Mr of 24230. The deduced sequence of 211 amino acid residues showed considerable homology with DHFRs from both bacterial and animal sources. The codon bias index of the DFR1 coding region is 0.0083, which indicates a random pattern of codon usage. The upstream region contains two consensus sequences required for binding of the yeast's positive regulatory factor, GCN4, suggesting that the DFR1 gene might be subject to the amino acid general control. Several potential 'TATA' boxes are located in the sequence 5' to the gene. Located in the 3' flanking region are homologies with several canonical sequences thought to be required for efficient transcription termination in yeast. We also mapped the DFR1 gene to a position 1.4 cM proximal to the MET7 locus on chromosome XV.The dihydrofolate reductase gene (DFR1) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated on an 8.8-kb BamHI fragment from a yeast genomic library by screening of Escherichia coli transformants for resistance to trimethoprim. A 1.8-kb SalI-BamHI fragment which was able to confer methotrexate resistance in yeast also complemented an E. coli DHFR-deficient (folA) mutant. Nucleotide sequence analysis revealed that the yeast DFR1 gene encoded a polypeptide with a predicted Mr of 24230. The deduced sequence of 211 amino acid residues showed considerable homology with DHFRs from both bacterial and animal sources. The codon bias index of the DFR1 coding region is 0.0083, which indicates a random pattern of codon usage. The upstream region contains two consensus sequences required for binding of the yeast's positive regulatory factor, GCN4, suggesting that the DFR1 gene might be subject to the amino acid general control. Several potential 'TATA' boxes are located in the sequence 5' to the gene. Located in the 3' flanking region are homologies with several canonical sequences thought to be required for efficient transcription termination in yeast. We also mapped the DFR1 gene to a position 1.4 cM proximal to the MET7 locus on chromosome XV.
The dihydrofolate reductase gene ( DFR1) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated on an 8.8-kb BamHI fragment from a yeast genomic library by screening of Escherichia coli transformants for resistance to trimethoprim. A 1.8-kb SalI- BamHI fragment which was able to confer methotrexate resistance in yeast also complemented an E. coli DHFR-deficient ( folA) mutant. Nucleotide sequence analysis revealed that the yeast DFR1 gene encoded a polypeptide with a predicted M r of 24230. The deduced sequence of 211 amino acid residues showed considerable homology with DHFRs from both bacterial and animal sources. The codon bias index of the DFR1 coding region is 0.0083, which indicates a random pattern of codon usage. The upstream region contains two consensus sequences required for binding of the yeast's positive regulatory factor, GCN4, suggesting that the DFR1 gene might be subject to the amino acid general control. Several potential ‘TATA’ boxes are located in the sequence 5' to the gene. Located in the 3' flanking region are homologies with several canonical sequences thought to be required for efficient transcription termination in yeast. We also mapped the DFR1 gene to a position 1.4 cM proximal to the MET7 locus on chromosome XV.
The dihydrofolate reductase gene (DFR1 ) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated from a yeast genomic library by screening of Escherichia coli transformants for resistance to trimethoprim. Nucleotide sequence analysis revealed that the yeast DFR1 gene encoded a polypeptide with a predicted M sub(r) of 24,230. The deduced sequence of 211 amino acid residues showed considerable homology with DHFRs from both bacterial and animal sources. The upstream region contains two consensus sequences required for binding of the yeast's positive regulatory factor, GCN4, suggesting that the DFR1) gene might be subject to the amino acid general control. Several potential "TATA" boxes are located in the sequence 5' to the gene. The authors also mapped the DFR1 gene to a position 1.4 cM proximal to the MET7 locus on chromosome XV.
The dihydrofolate reductase gene (DFR1) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated on an 8.8-kb BamHI fragment from a yeast genomic library by screening of Escherichia coli transformants for resistance to trimethoprim. A 1.8-kb SalI-BamHI fragment which was able to confer methotrexate resistance in yeast also complemented an E. coli DHFR-deficient (folA) mutant. Nucleotide sequence analysis revealed that the yeast DFR1 gene encoded a polypeptide with a predicted Mr of 24230. The deduced sequence of 211 amino acid residues showed considerable homology with DHFRs from both bacterial and animal sources. The codon bias index of the DFR1 coding region is 0.0083, which indicates a random pattern of codon usage. The upstream region contains two consensus sequences required for binding of the yeast's positive regulatory factor, GCN4, suggesting that the DFR1 gene might be subject to the amino acid general control. Several potential 'TATA' boxes are located in the sequence 5' to the gene. Located in the 3' flanking region are homologies with several canonical sequences thought to be required for efficient transcription termination in yeast. We also mapped the DFR1 gene to a position 1.4 cM proximal to the MET7 locus on chromosome XV.
Author Huang, Tun
Game, John C.
Wahl, Geoffrey M.
Misener, Virginia L.
Barclay, Barry J.
Nagel, Michael G.
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Issue 2
Keywords NADPH
gene cloning
homology
DHF
transcriptional control elements
nt
UAS
trimethoprim and methotrexate resistance
Cm
Recombinant DNA
Chr
codon usage
bp
Ap
Mtx
R
THF
kb
Tp
aa
DFR1 (S. cerevisiae)
DHFR
dUMP
dTMP
TS
Yeast
Nucleotide sequence
Enzyme
Tetrahydrofolate dehydrogenase
Fungi
Resistance
Gene
Restriction map
Regulatory sequence
Ascomycetes
Molecular cloning
Saccharomyces cerevisiae
Thallophyta
Language English
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SSID ssj0000552
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Snippet The dihydrofolate reductase gene ( DFR1) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated on an 8.8-kb BamHI fragment from a...
The dihydrofolate reductase gene (DFR1) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated on an 8.8-kb BamHI fragment from a...
The dihydrofolate reductase gene (DFR1 ) from Saccharomyces cerevisiae has been mapped and sequenced. The gene was isolated from a yeast genomic library by...
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SubjectTerms Amino Acid Sequence
Base Sequence
Biological and medical sciences
Biotechnology
Cloning, Molecular
codon usage
DNA Restriction Enzymes
Escherichia coli - genetics
Fundamental and applied biological sciences. Psychology
gene cloning
Genes
Genes, Fungal
Genes. Genome
Genetic engineering
Genetic technics
homology
Methods. Procedures. Technologies
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
Nucleic Acid Hybridization
Plasmids
Recombinant DNA
Saccharomyces cerevisiae
Saccharomyces cerevisiae - enzymology
Saccharomyces cerevisiae - genetics
Synthetic digonucleotides and genes. Sequencing
Tetrahydrofolate Dehydrogenase - genetics
transcriptional control elements
trimethoprim and methotrexate resistance
Title Mapping and sequencing of the dihydrofolate reductase gene ( DFR1) of Saccharomyces cerevisiae
URI https://dx.doi.org/10.1016/0378-1119(88)90523-9
https://www.ncbi.nlm.nih.gov/pubmed/2838386
https://www.proquest.com/docview/15245599
https://www.proquest.com/docview/78271633
Volume 63
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