Изучен процесс эмбриогенеза и отработаны элементы технологии получения удвоенных гаплоидов брокколи B. oleracea L. convar. botrytis (L.) Alef. var. italica Plenck в культуре микроспор in vitro. Было выявлено, что успешное развитие эмбриоидов происходит из микроспор, изолированных из бутонов длиной 4 и 5 мм, где преимущественно содержатся микроспоры-на поздней вакуолизированной, пыльца-на ранней двухклеточной стадии развития. Оптимальным режимом температурной обработки является обработка 32°С в течение первых 2-х суток после введения в культуру. Эмбриоиды были получены из пяти образцов брокколи: Arcadia F 1 , Everest, Green Valiant, Marathon F 1 , Furio. Наибольший выход эмбриоидов был получен у образца Green Valiant, где он составил до 140 эмбриоидов на чашку Петри, а наименьший-у Furio (до 3 эмбриоидов/чашку Петри). Первые деления в культуре микроспор у всех образцов наблюдали уже на 2-3 сутки культивирования. Дальнейшее развитие эмбриоидов шло по двум направлениямпутем прямого развития или с образованием суспензороподобных структур. Эмбриоиды, содержащие суспензор, развивались медленнее, чем бессуспензорные. Мы наблюдали образование эмбриоида не только на дистальном (по отношению к микроспоре) конце суспензороподобной структуры, но и образование цепочки из эмбриоидов, а также все возможные близнецовые комбинации эмбриоидов. Было показано, что метод получения эмбриоидов в культуре микроспор in vitro может быть использован не только для получения удвоенных гаплоидных растений, но и служить моделью для фундаментальных исследований по изучению этапов развития зиготических эмбриоидов и суспензоров.

Over the recent years the market demand for scaling up the production of European radish (Raphanus sativus L.) varieties and hybrids for open and protected production, varying in ripeness group, root shape and color, has drastically increased. Therefore, the expansion of genetic diversity and acceleration of the selection process are important. Doubled haploid technology considerably curtails the time required for creation of homozygous constant parental cell lines when in vitro microspore culture is used as the most promising method. For the first time, we were able to realize the full production cycle of DH plants of European radish by in vitro microspore culture up to inclusion of the produced material into the selection process. We have selected: preferable flower bud size, heat shock parameters, induction and regeneration media. It was revealed that linear length on the flower buds with the best possible stage of microspore development is genotype-specific: the flower bud length 2.8–3.3 mm is optimal for accessions of Rhodes and 3.7–4.2 mm is optimal for accessions of Teplichny Gribovsky. Heat shock at 32 °C for 48 hours is the most suitable for most genotypes. For the first time Murashige and Skoog based culture medium has been used for embryogenesis induction, and a major dependence of embryogenesis induction on the genotype × medium interaction was found. At regeneration and tiller stage it is advisable to add 1 mg/mL of benzylaminopurine and 0.1 mg/L of gibberellic acid to the medium, and rotting of micro-sprouts is performed with the use of hormone-free medium. Analysis of the produced regenerant plants by chromosome count and cell nucleus flow cytometry showed that 69 % of plants have a diploid chromosome set, 9 % have a haploid chromosome set, and 22 % have mixoploids and aneuploids chromosome sets. The seed progeny from doubled haploids and mixoploids were obtained by self-pollination, where all R1 plants had a doubled set of chromosomes. This study launches the development of an efficient method of radish doubled haploid production to be used in the selection process.

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Relevance. In recent years vegetable crop Brassica rapa ssp. chinensis var. purpuraria (synonyms: Brassica campestris L. var.purpurea Bailey; Brassica rapa L. ssp. chinensis var. purpurea) is gaining popularity as an object of genetic and molecular researches, and as an economically valuable vegetable plant due to the high content of biologically active compounds and distinctive economically valuable traits. Effective technology for development DH-plants to accelerate the breeding process for this culture has not been developed yet, so research in this area is relevant.Materials and methods. The study included two varieties from the collection of Vavilov AllRussian Research Institute of Plant Industry (VIR): No. 1301 (China) and No. 1357(Netherlands). Both protocols standard unmodified and with addition of silver nitrate (AgNO3) in the medium for embryogenesis induction were used in experiments for production of DH plants from isolated microspore in vitro. Direct chromosome counting in meristem cells and flow cytometry were used to determine the ploidy of regenerating plants.Results. As a result of the study embryogenesis in B. purpuraria culture can develop with the use of a standard protocol as well as with the addition of silver nitrate that showed a positive effect on the induction of embryogenesis. The yield of embryoids varied depending on the genotype of the individual plant within the variety accession. The highest yield of embryoids was 40 embryoids/petri dish. The main problem at the stage of regeneration is that about half of the regenerating plants occurred to be albinos and were not viable. We show a high degree of spontaneous chromosome doubling in regenerated plants (all analyzed plants were doubled haploids). In total 38 regenerated plants were obtained from accession No. 1301. It was shown that four DH-plants had self-incompatibility after self-pollination, but seed progeny from other plants was obtained. The created material was taken for genetics study and breeding work.

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