Kozar Elena V, Domblides Elena A
Federal State Budgetary Scientific Institution Federal Scientific Vegetable Center (FSBSI FSVC), Selektsionnaya St, 14, VNIISSOK, Odintsovo Reg., 143072 Moscow, Russia.
Biol Methods Protoc. 2024 Dec 3;9(1):bpae091. doi: 10.1093/biomethods/bpae091. eCollection 2024.
In this protocol for obtaining doubled haploids plants (DH), we propose a new method for microspore isolation. This method is useful for genotypes of the Brassicaceae family with low responsiveness to DH technology. For such crops, it allows increasing the embryo yield several times and sometimes obtaining embryos for the first time. This method of microspore isolation reduces the mechanical impact on the bud tissue, which minimizes somatic cell destruction and reduces to get it into the preparation through the filter, thus increasing its purity. The new isolation method also increases the relative concentration of embryogenic microspores in the preparation. This is possible because the anther tissues are not destroyed during the isolation process. Therefore, the anther retains its structure and microspores of early and late stages are trapped by the anther tissue, thus the anther acts as a sieve. Late stages are trapped because of their larger size, while early stages are trapped because they are even more tightly bound to the anther tissue. Together, these factors increase the efficiency of the technology for DH production microspore culture. This protocol article provides a detailed experimental protocol to the method presented in the experimental article (E.V. Kozar, E.G. Kozar, E.A. Domblides. Effect of the Method of Microspore Isolation on the Efficiency of Isolated Microspore Culture In Vitro for Brassicaceae Family. Horticulturae. 2022. Vol. 8, No. 10. P. 864. DOI 10.3390/horticulturae8100864) but does not repeat all the results documenting the efficacy of the actual method.
在这个获得双单倍体植株(DH)的方案中,我们提出了一种新的小孢子分离方法。该方法对于对DH技术响应较低的十字花科基因型很有用。对于这类作物,它能使胚产量提高几倍,有时还能首次获得胚。这种小孢子分离方法减少了对花蕾组织的机械冲击,最大限度地减少了体细胞破坏,并减少了通过过滤器进入制剂中的体细胞,从而提高了其纯度。新的分离方法还提高了制剂中胚性小孢子的相对浓度。这是可能的,因为在分离过程中花药组织没有被破坏。因此,花药保持其结构,早期和晚期的小孢子被花药组织捕获,从而花药起到了筛子的作用。晚期小孢子因体积较大而被捕获,而早期小孢子则因与花药组织结合更紧密而被捕获。这些因素共同提高了DH生产小孢子培养技术的效率。本方案文章提供了与实验文章(E.V. 科扎尔、E.G. 科扎尔、E.A. 东布利德斯。小孢子分离方法对十字花科离体分离小孢子培养效率的影响。《园艺学》。2022年。第8卷,第10期。第864页。DOI 10.3390/horticulturae8100864)中提出的方法相关的详细实验方案,但没有重复记录实际方法有效性的所有结果。