首页> 外文期刊>Medical mycology: official publication of the International Society for Human and Animal Mycology >Agrobacterium tumefaciens-mediated transformation of the dermatophyte, Trichophyton mentagrophytes: an efficient tool for gene transfer.
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Agrobacterium tumefaciens-mediated transformation of the dermatophyte, Trichophyton mentagrophytes: an efficient tool for gene transfer.

机译:根癌农杆菌介导的皮肤癣菌,癣菌癣菌的转化:一种有效的基因转移工具。

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摘要

Agrobacterium tumefaciens-mediated transformation (ATMT) was used to facilitate gene transfer into the clinically important dermatophyte, Trichophyton mentagrophytes (teleomorph: Arthroderma vanbreuseghemii). A binary vector containing a hygromycin B resistance cassette was introduced into A. tumefaciens, and the resultant strain was co-cultivated with fungal small conidia. Transformation yielded a large number of hygromycin B-resistant transformants. Hybridization analysis showed that most of the transformants harboured a single copy of T-DNA randomly integrated into the genome. Transformation frequency was increased to more than 200 per 10(7) conidia by optimizing the co-cultivation time and temperature. ATMT was then used for targeted gene disruption mediated by homologous recombination. Using a PCR-based strategy, we isolated the areAit-2-like nitrogen regulatory gene (tnr:Trichophytonnitrogen regulator) from T. mentagrophytes. A binary vector containing two regions of the tnr locus flanking the hygromycin B resistance cassette was constructed and introduced into T. mentagrophytesvia ATMT. Transformants with disruption of the areAit-2-like gene (tnr) were obtained in three of four independent disruption experiments, most of which showed homologous recombination via double crossover without additional ectopic integration of the disruption construct.
机译:根癌农杆菌介导的转化(ATMT)用于促进基因转移到临床上重要的皮肤癣菌,即癣菌癣菌(teleomorph:Arthroderma vanbreuseghemii)中。将含有潮霉素B抗性盒的二元载体引入根癌农杆菌,并将所得菌株与真菌小分生孢子共培养。转化产生大量潮霉素B抗性转化体。杂交分析表明,大多数转化子都带有随机整合到基因组中的单个拷贝的T-DNA。通过优化共培养时间和温度,转化频率提高到每10(7)分生孢子200多个。然后将ATMT用于通过同源重组介导的靶向基因破坏。使用基于PCR的策略,我们从薄荷草(T. mentagrophytes)中分离了areA / nit-2-like氮调节基因(tnr:毛藻氮调节剂)。构建包含潮霉素B抗性盒侧翼的tnr基因座的两个区域的二元载体,并将其通过ATMT引入到薄荷杆菌中。在四个独立的破坏实验中的三个实验中获得了具有areA / nit-2-like基因(tnr)破坏的转化子,其中大多数实验显示通过双重交换实现了同源重组,而没有破坏结构的异位整合。

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