Cooley R N, Caten C E
School of Biological Sciences, University of Birmingham, Edgbaston, UK.
Mol Gen Genet. 1993 Feb;237(1-2):58-64. doi: 10.1007/BF00282784.
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.
已确定小麦壳针孢β-微管蛋白基因(tubAR)抗苯菌灵等位基因的完整核苷酸序列,分别包括tubAR编码区5'端的745个核苷酸和3'端的1024个核苷酸。tubAR编码一个447个氨基酸的多肽,与其他真菌β-微管蛋白具有高度同源性。该基因在密码子4、12和53处含有三个内含子,使用了61个可能的有义密码子中的48个,其编码区的GC含量为59.1%。S1核酸酶图谱分析确定了两个转录起始位点,分别位于翻译起始位点上游80 bp和83 bp处,以及一个转录终止位点,位于终止密码子下游192 bp处。这两个转录起始位点分别位于由18个嘧啶核苷酸组成、中间被一个腺嘌呤打断的CT基序下游8 bp和5 bp处。已使用聚合酶链反应克隆了野生型等位基因tubA+,并将导致tubAR抗苯菌灵表型的突变定位到密码子6第一位的C到T转换,导致组氨酸到酪氨酸的氨基酸替换。