ArticleMolecular & general genetics : MGG1993
Molecular analysis of the Septoria nodorum beta-tubulin gene and characterization of a benomyl-resistance mutation.
Article in Molecular & general genetics : MGG, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 40 citations in OpenAlex.
- Different Infection Structures and Point Mutation of Diaporthe citri Showing Resistant against Systemic Fungicides.The plant pathology journal · 2024Article
- Chemical Resistance of Diaporthe citri against Systemic Fungicides on Citrus.The plant pathology journal · 2023Article
- Predicting Resistance by Mutagenesis: Lessons from 45 Years of MBC Resistance.Frontiers in microbiology · 2016Article
- Molecular characterization of beta-tubulin from Phakopsora pachyrhizi, the causal agent of Asian soybean rust.Genetics and molecular biology · 2010Article
- Identification and characterization of benzimidazole resistance in Monilinia fructicola from stone fruit orchards in California.Applied and environmental microbiology · 2003Article
- Isolation of a beta-tubulin gene from Fusarium moniliforme that confers cold-sensitive benomyl resistance.Applied and environmental microbiology · 1996Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The complete nucleotide sequence of a benomyl-resistant allele of the Septoria nodorum beta-tubulin gene (tubAR) has been determined including 745 and 1024 nucleotides 5' and 3' to the tubAR coding region, respectively. tubAR encodes a 447 amino acid polypeptide which shows a high degree of homology with other fungal beta-tubulins. The gene contains three introns at codons 4, 12 and 53, uses 48 of the possible 61 sense codons and has a GC content of 59.1% in its coding region. S1 nuclease mapping has identified two transcriptional start sites 80 bp and 83 bp upstream of the translation start, and a transcriptional termination site 192 bp downstream of the stop codon. The two transcriptional start sites lie just 8 bp and 5 bp downstream of a CT motif consisting of 18 pyrimidine nucleotides interrupted by a single adenine. The wild-type allele tubA+ has been cloned using the polymerase chain reaction and the mutation producing the benomyl-resistant phenotype of tubAR mapped to a C to T transition at the first position of codon 6, resulting in a histidine to tyrosine amino acid substitution.
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