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PEG-mediated symmetric and asymmetric protoplast fusion in sunflower (Helianthus annuus L.)

机译:光伏介导的对称和不对称原生质体融合(Helianthus Annuus L.)

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Symmetric and asymmetric protoplast fusions were evaluated with sunflower ( Helianthus annuus L.) PI441983 and 10A lines. The optimal cytoplasmic inactivation procedure and conditions for induced fusion of protoplasts by using polyethylene glycol (PEG) were developed. The cell division activities of hypocotyl protoplasts of the 10A line with a cytoplasmic male sterile (CMS) trait were inhibited with different concentrations of iodoacetic acid (IOA; 0, 1.5, 3.0 and 4.5 mM) and incubation periods (15 and 20 min) to generate a recipient parent for a normal cytoplasm trait. The optimal inactivation was achieved with 20 min incubation in 1.5 mM IOA, which was the lowest concentration leading to low levels of both cell division (20.41%) and colony formation (3.70%). When various concentrations of PEG 8000 (0, 10, 20 and 30% (w/v)) and fusion periods (10, 15 and 20 min) were used to induce fusion between hypocotyl protoplasts of the 10A line and mesophyll protoplasts with a normal cytoplasm trait of the PI441983 line (donor parent), 20% (w/v) PEG 8000 for 15 min was found to be optimal for induced fusion, giving a high frequency of binary fusion (26.16%) and lowfrequency of multi fusion (12.96%). When both symmetric and asymmetric protoplast fusion procedures were performed, fusion products could develop, divide and form colonies in the culture medium, and also have a tendency to generate microcalli. However, the densities of protoplast-derived colonies in asymmetric fusion were lower than those in symmetric fusion. The efficient procedures developed in this study will be beneficial for future sunflower breeding programs for hybrid production.
机译:用向日葵(Helianthus Annuus L.)PI441983和10A线评估对称和不对称原生质体融合器。开发出通过使用聚乙二醇(PEG)诱导原生质体融合的最佳细胞质灭活程序和条件。用不同浓度的碘乙酸(IOA; 0,1.0和4.5mm)抑制10A线的次胶质基原生质体的细胞分裂活性,抑制了不同浓度的碘乙酸(0,1.5,3.0和4.5mm)和孵育期(15和20分钟)为正常细胞质特征生成受体父母。在1.5mm IOA中孵育最佳灭活,其最低浓度导致细胞分裂(20.41%)和菌落形成(3.70%)。当各种浓度的PEG 8000(0,10,20和30%(w / v))和融合时段(10,15和20分钟)用于诱导10A线和叶片原生质体的胚轴原生质体与正常的融合PI441983线(供体父母)的细胞质性状,20%(w / v)pEG 8000为15分钟的诱导融合是最佳的,得到高频率的二元融合(26.16%)和低频率的多融合(12.96 %)。当进行对称和不对称的原生质体融合程序时,融合产物可以在培养基中发育,分裂和形成菌落,并且还具有产生微加载的趋势。然而,不对称融合中原生质体衍生的菌落的密度低于对称融合中的菌落。本研究中开发的有效手术将有利于对混合生产的未来向日葵育种计划。

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