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 in | Gene Vol. 63; no. 2; pp. 175 - 185 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Lausanne
Elsevier B.V
31.03.1988
Amsterdam Elsevier New York, NY |
Subjects | |
Online Access | Get full text |
ISSN | 0378-1119 1879-0038 |
DOI | 10.1016/0378-1119(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. |
Author_xml | – sequence: 1 givenname: Barry J. surname: Barclay fullname: Barclay, Barry J. organization: Department of Biological Sciences, Brock University, St. Catharines, OntarioCanada L2S 3A1 – sequence: 2 givenname: Tun surname: Huang fullname: Huang, Tun organization: Department of Biological Sciences, Brock University, St. Catharines, OntarioCanada L2S 3A1 – sequence: 3 givenname: Michael G. surname: Nagel fullname: Nagel, Michael G. organization: Department of Biological Sciences, Brock University, St. Catharines, OntarioCanada L2S 3A1 – sequence: 4 givenname: Virginia L. surname: Misener fullname: Misener, Virginia L. organization: Department of Biological Sciences, Brock University, St. Catharines, OntarioCanada L2S 3A1 – sequence: 5 givenname: John C. surname: Game fullname: Game, John C. organization: Donner Laboratory, Lawrence Berkeley Laboratory, Berkeley, CA 94720 U.S.A. Tel. 642-2810 – sequence: 6 givenname: Geoffrey M. surname: Wahl fullname: Wahl, Geoffrey M. organization: Gene Expression Laboratory, The Salk Institute, San Diego, CA 92138-9216 U.S.A. Tel. 453-4100 |
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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 |
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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 |
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