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Self-incompatibility in the Iranian Almond Cultivar ‘Mamaei’ Using Pollen Tube Growth, Fruit Set and PCR Technique

机译:花粉管生长,结实和PCR技术在伊朗杏仁品种“ Mamaei”中的自交不亲和性

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Self-incompatibility has been studied by using controlled pollination, pollen tube growth and PCR methods in the Iranian almond ‘Mamaei.’. Pollen tube growth and fruit set following self and cross-pollination treatments were evaluated. The percentage of initial and final fruit set was determined for each treatment at 30 and 60 days after controlled pollination. Pollen germination and pollen tube growth were assessed by fluorescence microscopy at different times after self and cross pollination. Results showed that the percentage of the final fruit set was 0% after self-pollination, while values of 16.34%, 17.22%, 19.12%, and 21.15% were determined after cross-pollination with ‘Azar’, ‘Rabie’, ‘Shahrood-21’, and ‘Sefied’ cultivars as pollen sources, respectively. After 192 hours, observation of pollen tube growth showed that the percentage of reached pollen tubes at the style base from cross-pollination was significant but there were not any reached pollen tubes from self-pollination. According to the results of controlled pollination and pollen tube growth ‘Mamaei’ is self-incompatible. S-RNase assay was used to confirm these results. PCR amplification of genomic DNA from ‘Mamaei’ with EM-PC2consFD and EM-PC3consRD primers revealed the presence of two DNA fragments of sizes around 850 bp and 1250 bp on agarose gels. The size of the smaller fragment is similar to that of S25 almond RNase, while the size of the other fragment is different from all S1-S30 RNase alleles. S-genotype can be regarded as S25S x , with Sx being a new SRNase allele.
机译:在伊朗杏仁“ Mamaei”中,通过控制授粉,花粉管生长和PCR方法研究了自我不相容性。自我和交叉授粉处理后,对花粉管的生长和坐果进行了评估。在控制的授粉后30天和60天,确定每种处理的初始和最终坐果率。在自交和异花授粉后的不同时间,通过荧光显微镜评估花粉的萌发和花粉管的生长。结果显示,自花授粉后最终坐果的百分比为0%,而与“ Azar”,“ Rabie”,“ Shahrood”交叉授粉后确定的值为16.34%,17.22%,19.12%和21.15%。 -21'和'Sefied'品种分别作为花粉来源。 192小时后,对花粉管生长的观察表明,从异花传粉到花粉基部到达的花粉管的百分比是显着的,但是自花粉传粉没有到达任何花粉管。根据控制的授粉和花粉管生长的结果,“ Mamaei”是不相容的。 S-RNase分析用于确认这些结果。用EM-PC2consFD和EM-PC3consRD引物对'Mamaei'的基因组DNA进行PCR扩增,发现琼脂糖凝胶上存在两个大小分别约为850 bp和1250 bp的DNA片段。较小片段的大小与S25杏仁RNase的大小相似,而另一个片段的大小则与所有S1-S30 RNase等位基因不同。 S基因型可被视为S25S x,其中Sx是新的SRNase等位基因。

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