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首页> 外文期刊>Transgenic research >Functional stacking of three resistance genes against Phytophthora infestans in potato.
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Functional stacking of three resistance genes against Phytophthora infestans in potato.

机译:马铃薯中抗疫霉菌的三个抗性基因的功能叠加。

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Functional stacking of broad spectrum resistance (R) genes could potentially be an effective strategy for more durable disease resistance, for example, to potato late blight caused by Phytophthora infestans (Pi). For this reason, three broad spectrum potato R genes (Rpi), Rpi-sto1 (Solanum stoloniferum), Rpi-vnt1.1 (S. venturii) and Rpi-blb3 (S. bulbocastanum) were selected, combined into a single binary vector pBINPLUS and transformed into the susceptible cultivar Desiree. Among the 550 kanamycin resistant regenerants, 28 were further investigated by gene specific PCRs. All regenerants were positive for the nptII gene and 23 of them contained the three Rpi genes, referred to as triple Rpi gene transformants. Detached leaf assay and agro-infiltration of avirulence (Avr) genes showed that the 23 triple Rpi gene transformants were resistant to the selected isolates and showed HR with the three Avr effectors indicating functional stacking of all the three Rpi genes. It is concluded that Avr genes, corresponding to the R genes to be stacked, must be available in order to assay for functionality of each stack component. No indications were found for silencing or any other negative effects affecting the function of the inserted Rpi genes. The resistance spectrum of these 23 triple Rpi gene transformants was, as expected, a sum of the spectra from the three individual Rpi genes. This is the first example of a one-step approach for the simultaneous domestication of three natural R genes against a single disease by genetic transformation.
机译:广谱抗性( R )基因的功能性叠加可能是更持久的抗病性的有效策略,例如,对 Phytophthora infestans Pi )。因此,三个广谱马铃薯 R 基因( Rpi ), Rpi-sto1 ( Solanum stoloniferum ),选择了 Rpi-vnt1.1 (文氏链球菌)和 Rpi-blb3 (球茎沙门氏菌),结合成单个二元载体pBINPLUS,并转化为易感品种Desiree。在550种卡那霉素抗性再生剂中,有28种通过基因特异性PCR进行了进一步研究。所有再生子均对 nptII 基因呈阳性,其中有23个包含三个 Rpi 基因,称为三重 Rpi 基因转化子。分离叶片分析和无毒力( Avr )基因对农杆菌的侵染显示23种三重 Rpi 基因转化株对所选菌株具有抗性,并显示三种的HR Avr 效应物指示所有三个 Rpi 基因的功能堆叠。得出的结论是,与要堆叠的 R 基因相对应的 Avr 基因必须可用,以便分析每个堆叠组件的功能。没有迹象表明沉默或影响插入的 Rpi 基因功能的任何其他负面影响。如所预期的,这23个三联的 Rpi 基因转化体的抗性光谱是来自三个单独的 Rpi 基因的光谱的总和。这是通过遗传转化同时驯化三种天然 R 基因以对抗单一疾病的一步法的第一个示例。

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