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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">vstisp</journal-id><journal-title-group><journal-title xml:lang="ru">Садоводство и виноградарство</journal-title><trans-title-group xml:lang="en"><trans-title>Horticulture and viticulture</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0235-2591</issn><issn pub-type="epub">2618-9003</issn><publisher><publisher-name>Autonomous non-profit organization Editorial Board of journal «Horticulture and viticulture»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.31676/0235-2591-2022-2-42-55</article-id><article-id custom-type="elpub" pub-id-type="custom">vstisp-863</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ГЕНЕТИКА, СЕЛЕКЦИЯ, СЕМЕНОВОДСТВО</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>GENETICS, BREEDING, SEED PRODUCTION</subject></subj-group></article-categories><title-group><article-title>Интерференционное ингибирование вируса шарки сливы, индуцированное шпилечной конструкцией РНК вирусного происхождения, обеспечивающие длительную устойчивость к инфекции PPV у взрослых растений сорта Стартовая (Prunus domestica L.)</article-title><trans-title-group xml:lang="en"><trans-title>Interference inhibition of Plum pox virus, induced by a hairpin-RNA of viral origin, provides long-term resistance to PPV infection in adult plants of the Startovaya (Prunus domestica L.) variety</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сидорова</surname><given-names>Т. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Sidorova</surname><given-names>T. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Сидорова Т. Н. — младший научный сотрудник</p><p>г. Пущино</p></bio><bio xml:lang="en"><p>Sidorova T. N., Junior Researcher</p><p>Pushchino</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Михайлов</surname><given-names>Р. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Mikhailov</surname><given-names>R. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Михайлов Р. В. — ведущий специалист</p><p>г. Пущино</p></bio><bio xml:lang="en"><p>Mikhailov R. V., Key specialist</p><p>Pushchino</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пушин</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Pushin</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Пушин А. С. — младший научный сотрудник</p><p>г. Пущино</p></bio><bio xml:lang="en"><p>Pushin A. S., Junior Researcher</p><p>Pushchino</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мирошниченко</surname><given-names>Д. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Miroshnichenko</surname><given-names>D. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мирошниченко Д. Н. — кандидат биологических наук, старший научный сотрудник</p><p>г. Пущино</p></bio><bio xml:lang="en"><p>Miroshnichenko D. N., PhD, Senior Researcher</p><p>Pushchino</p></bio><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Долгов</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Dolgov</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Долгов Сергей Владимирович — доктор биологических наук, главный научный сотрудник</p><p>проспект Науки, 6, г. Пущино, Московская область, 142290</p></bio><bio xml:lang="en"><p>Sergey V. Dolgov, Dr. Sci. (Biol.), Chief Researcher</p><p>6, Prospekt Nauki, Pushchino, Moscow region, 142290</p></bio><email xlink:type="simple">dolgov@bibch.ru</email><xref ref-type="aff" rid="aff-5"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Филиал Института биоорганической химии им. М. М. Шемякина и Ю. А. Овчинникова РАН; Никитский ботанический сад − Национальный научный центр Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Branch of the Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences; Nikita Botanical Garden — National Scientific Center of the Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Филиал Института биоорганической химии им. М. М. Шемякина и Ю. А. Овчинникова РАН; ООО “Антерикс”</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Branch of the Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences; LLC «Anterix»</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Филиал Института биоорганической химии им. М. М. Шемякина и Ю. А. Овчинникова РАН; Никитский ботанический сад − Национальный научный центр Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Branch of the Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences;  Nikita Botanical Garden — National Scientific Center of the Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>Филиал Института биоорганической химии им. М. М. Шемякина и Ю. А. Овчинникова РАН; Федеральный научный селекционно-технологический центр садоводства и питомниководства</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Branch of the Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences; Federal Horticultural Research Center for Breeding, Agrotechnology and Nursery</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-5"><aff xml:lang="ru"><institution>Филиал Института биоорганической химии им. М. М. Шемякина и Ю. А. Овчинникова РАН; Никитский ботанический сад − Национальный научный центр Российской академии наук; Федеральный научный селекционно-технологический центр садоводства и питомниководства</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Branch of the Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences;  Nikita Botanical Garden — National Scientific Center of the Russian Academy of Sciences; Federal Horticultural Research Center for Breeding, Agrotechnology and Nursery</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>13</day><month>05</month><year>2022</year></pub-date><volume>0</volume><issue>2</issue><fpage>42</fpage><lpage>55</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Autonomous non-profit organization Editorial Board of journal «Horticulture and viticulture», 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Autonomous non-profit organization Editorial Board of journal «Horticulture and viticulture»</copyright-holder><copyright-holder xml:lang="en">Autonomous non-profit organization Editorial Board of journal «Horticulture and viticulture»</copyright-holder><license xlink:href="https://www.sadivin.com/jour/about/submissions#copyrightNotice" xlink:type="simple"><license-p>https://www.sadivin.com/jour/about/submissions#copyrightNotice</license-p></license></permissions><self-uri xlink:href="https://www.sadivin.com/jour/article/view/863">https://www.sadivin.com/jour/article/view/863</self-uri><abstract><p>В современном садоводстве вирус шарки сливы (PPV) представляет серьезную угрозу для товарных плантаций широкого спектра культур, принадлежащих к роду Prunus. Учитывая отсутствие природных генетических источников, которые обеспечивают надежную устойчивость к инфекции PPV, представляет значительный интерес использование методов биоинженерии для целевой модификации генома косточковых плодовых культур в целях борьбы с болезнью шарки, вызываемой PPV. Рядом исследований показано, что интерференция РНК является наиболее многообещающей стратегией борьбы с вирусными заболеваниями растений. В настоящем исследовании описано получение устойчивой к PPV сливы домашней сорта Стартовая (P. domestica L.) посредством опосредованной агробактериями (Agrobacterium-mediated) трансформации листовых эксплантов in vitro. Благодаря органогенезу из листьев, разработанный протокол позволяет проводить модификацию генома сливы без потери фенотипического соответствия исходному сорту. В результате исследований получено семь независимых линий сливы, содержащих самокомплементарные фрагменты последовательности гена PPV-CP, разделенные интроном PDK картофеля, с использованием гена устойчивости к гигромицину hpt в качестве селективного гена и β-глюкуронидазы uidA в качестве репортерного гена. Трансформацию подтверждали гистохимическим окрашиванием на активность β-глюкуронидазы, ПЦР-амплификацией соответствующих продуктов из выделенной геномной ДНК и саузерн-блотанализом шпилечных фрагментов гена PPV-CP. Для выяснения устойчивости к вирусу почки сливы, инфицированные штаммом PPV-M, прививали на однолетние трансгенные растения, которые в дальнейшем культивировали в теплице. Согласно оценке с помощью RT-PCR, DAS-ELISA, вестерн-блоттинга, теста ImmunoStrip а также визуальных наблюдений, деревья GM сливы оставались незараженными в течение 9 лет. Зараженные ветви, которые развились из привитых почек, на протяжении многих лет проявляли очевидные симптомы болезни шарки и сохраняли высокий уровень накопления вируса, в результате чего трансгенные деревья-хозяева постоянно подвергались инфекционному давлению. Стабильная экспрессия производной от PPV генной конструкции, кодирующей сплайсированные интронами шпилечные РНК, обеспечивала высокоэффективную защиту сливовых деревьев от перманентной вирусной инфекции. В то же время это наблюдение указывает на отсутствие системного распространения устойчивости от ГМ-тканей к инфицированному транспланту сливы даже после нескольких лет совместного роста.</p></abstract><trans-abstract xml:lang="en"><p>In modern horticulture Plum pox virus (PPV) imposes serious threats to commercial plantations of a wide range of fruit species belonging to genera Prunus. Given the lack of natural genetic resources, which display reliable resistance to PPV infection, there has been considerable interest in using genetic engineering methods for targeted genome modification of stone fruit trees to control Sharka disease caused by PPV. Among the many virus defense mechanisms, RNA interference is shown to be the most promising transgenic disease-control strategy in plant biotechnology. The present study describes the production of transgenic PPV resistant European plum `Startovaya` (P. domestica L.) through the Agrobacterium-mediated transformation of in vitro leaf explants. Due to organogenesis from leaves, the established protocol allows the genetic engineering of the plum genome without losing clonal fidelity of original cultivar. Seven independent transgenic plum lines containing the self-complementary fragments of PPV-CP gene sequence separated by a PDK intron were generated using hpt as a selective gene and uidA as a reporter gene. The transformation was verified through the histochemical staining for β-glucuronidase activity, PCR amplification of appropriate vector products from isolated genomic DNA and Southern blot analysis of hairpin PPV-CP gene fragments. To clarify the virus resistance, plum buds infected by PPV-M strain were grafted onto 1-year-old transgenic plants, which further were grown into mature trees in the greenhouse. As evaluated by RT-PCR, DAS-ELISA, Western blot, Immuno Strip test, and visual observations, GM plum trees remained uninfected over 9 years. Infected branches that developed from grafted buds displayed obvious symptoms of Sharka disease over the years and maintained the high level of virus accumulation, whereby host transgenic trees had been constantly challenged with the pathogen. Since the virus was unable to spread to transgenic tissues, the stable expression of PPV-derived gene</p></trans-abstract><kwd-group xml:lang="ru"><kwd>вирус шарки сливы</kwd><kwd>слива домашняя</kwd><kwd>косточковые</kwd><kwd>генетическая трансформация</kwd><kwd>листовой эксплант</kwd><kwd>РНК-интерференция</kwd></kwd-group><kwd-group xml:lang="en"><kwd>plum pox virus</kwd><kwd>European plum</kwd><kwd>stone fruits</kwd><kwd>genetic transformation</kwd><kwd>leaf explant</kwd><kwd>RNA interference</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа частично профинансирована за счет гранта Российского научного фонда № 14-50-00079</funding-statement><funding-statement xml:lang="en">This work was supported by the Russian Science Foundation grant № 14-50-00079</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Scholthof K. 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