EP0362293A1 - Procede de transfert genetique entre des vegetaux - Google Patents

Procede de transfert genetique entre des vegetaux

Info

Publication number
EP0362293A1
EP0362293A1 EP88905828A EP88905828A EP0362293A1 EP 0362293 A1 EP0362293 A1 EP 0362293A1 EP 88905828 A EP88905828 A EP 88905828A EP 88905828 A EP88905828 A EP 88905828A EP 0362293 A1 EP0362293 A1 EP 0362293A1
Authority
EP
European Patent Office
Prior art keywords
grains
pollen
plants
vitro
gene
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP88905828A
Other languages
German (de)
English (en)
Inventor
Erwin Heberle-Bors
Rosa Maria Benito Moreno
Anna Alwen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Agrolinz Agrarchemikalien GmbH
Original Assignee
Chemie Holding AG
Agrolinz Agrarchemikalien GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chemie Holding AG, Agrolinz Agrarchemikalien GmbH filed Critical Chemie Holding AG
Publication of EP0362293A1 publication Critical patent/EP0362293A1/fr
Pending legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
    • A01H4/00—Plant reproduction by tissue culture techniques ; Tissue culture techniques therefor
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8201—Methods for introducing genetic material into plant cells, e.g. DNA, RNA, stable or transient incorporation, tissue culture methods adapted for transformation
    • C12N15/8202—Methods for introducing genetic material into plant cells, e.g. DNA, RNA, stable or transient incorporation, tissue culture methods adapted for transformation by biological means, e.g. cell mediated or natural vector
    • C12N15/8205—Agrobacterium mediated transformation
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/04—Plant cells or tissues

Definitions

  • the invention relates to a method for gene transfer in plants by means of isolated, immature and in vitro cultivated pollen grains as well as seeds and propagation products produced therefrom.
  • Agrobacterium tumefaciens is currently the most common vector. However, it is limited to a certain host range. The use of A. tumefaciens as a vector still depends on the regeneration of in vitro cultivated somatic cells to produce transgenic plants that are capable of producing transgenic progeny. Direct gene transfer through electroporation, liposomes, microinjection, and other physicochemical methods largely depends on the use of protoplasts as target cells. However, regeneration from protopiasts is difficult and even impossible with many species.
  • the poil grain As an alternative to these gene transfer methods, another target line has been proposed, the poil grain. According to Hess D., Plenum Press, New York, 519-537 (1975), it is possible for mature pollen to take up foreign DNA and to introduce this foreign DNA into the egg cell as a "supervector" using natural pollination and fertilization. Similarly, X-ray pollen is said to be able to transport fragments of the irradiated genome into the egg cell (Pandey, Nature 256: 310-313, 1975). DeWet (WO 85/01856) reports that maize poil, which has been treated with exogenous DNA, picks up this DNA when it germinates and transports it into the egg cell after pollination.
  • Pareddy et al in Planta 170: 141-143 (1987) describe the cultivation and ripening of immature maize flags ("tasseis", male inflorescences) in vitro.
  • the isolated ripe pollen was pollinated and seeds were obtained from the pollinated plants. Proof of successful fertilization by means of genetic labeling could not be provided.
  • the present invention accordingly relates to a method for gene transfer into plants, which is characterized in that a) immature pollen grains are removed from stamens in nutrient solution and the surrounding tissue is removed, b) the isolated immature pollen grains are cultivated in a nutrient solution c) foreign gene material is transferred to the pollen grains during in vitro cultivation and ripening d) brings the transformed poile grains to complete ripening in vitro e) pollinates recipient plants with the transformed pollen grains and extracts them from these seeds .
  • a completely new strategy of gene transfer in plants is opened up by gene transfer into isolated, immature pollen grains, in vitro maturation and the use of pollen as a universal supervector. Compared to other methods, it is considerably simplified since the cell culture phase is shortened considerably and the regeneration with the unpleasant side effect of the somaclonal variation is eliminated. This new method can also be used to transform plants that were previously not accessible for successful gene transfer. B. many types of cereals, legumes and trees cannot be regenerated from individual cells or protoplasts.
  • the potential benefit from gene transfer technology is of great economic, ecological and social value.
  • the aim is to genetically modify plants in such a way that the yield is increased, that the plants become resistant to diseases and pests, that they become tolerant of cold, heat, dryness, salinization, lack of nutrients, that they achieve greater nutritional quality that they produce new types of industrial raw materials, or that they fix their own nitrogen or otherwise become independent of fertilizers.
  • poil grains are cultivated without the tissue enveloping them, that is to say isolated, so that the genetic material to be transmitted has direct contact with the pollen grain in a vector or in naked form. If the entire male inflorescence is cultivated, it is not possible to transfer genes into the pollen grains using common transfer methods (A. tumefaciens, electroporation, microinjection and the like) because of the handicap caused by the extensive enveloping tissue.
  • Another essential feature of the invention is the use of immature pollen grains. This means that the entire time of in vitro maturation is available for gene transfer to disposal. The transfer into the unripe pollen can take place in different stages of ripeness, depending on the type of plant. In particular in the case of gene transfer with vectors, it is important that the gene material has to overcome as few cell walls as possible in order to get into the genome of the sperm nuclei and to become part of the zygote genome when fertilized.
  • the transmission occurs preferentially with mononuclear microspores, but can also in the stage during the first pollen mitosis, in the early binuclear stage, as long as the generative line still adheres to the poiien wall, or also in those plants that have trinuclear pollen in the maturation stage (grain) just before or during the second pollen mitosis.
  • the process is carried out as follows, using tobacco (Nicotiana tabacum) as the partial system.
  • tobacco Naturalicotiana tabacum
  • the system can be used on all plants which can be propagated by pollination, in particular on single- and double-leafed crop plants such as wheat, corn, rice, legumes, oilseeds, vegetable plants, fruit and forest plants.
  • the development stage of the pollen of the desired plant is determined in the usual way by isolation from an anther, preparation of a squeeze preparation and observation in a microscope after the addition of e.g. B. Karmin ⁇ acetic acid determined.
  • the poil grains are isolated under aseptic conditions by squeezing them out of the anthers in a nutrient medium, passing through a sieve, washing, centrifuging and resuspending.
  • the cell density should be higher for poile grains in the younger development stage than for poile grains in the older development stage.
  • the nutrient medium used contains all nutrients and growth substances essential for the cultivation and maintenance of the ripeness of the pollen grains. Depending on the plant, different compositions can result, so that it fulfills the function of nutrient tissue (tapetum).
  • the main constituents of the nutrient medium are sugar, nutrients, mineral salts and vitamins, the pH value being around 6.5 to 7.5.
  • the cultivation takes place up to the two-nucleus stage in a sugar-containing z.
  • the additional nutrients can be added in the form of coconut water.
  • the poil grains are obtained for pollination. For this purpose, they are centrifuged, washed and applied in an aqueous medium or dried to flowers from which the anthers have previously been removed for pollination. Seeds which are capable of germinating can be obtained from the plants pollinated with the in vitro ripened polish kernels in a generally customary manner.
  • the foreign genetic material to be transferred can be used in conjunction with a conventional vector, such as e.g. B. A. tumefaciens or as naked DNA by direct transfer using electroporation, microinjection or other physico-chemical methods into the pollen grains.
  • a conventional vector such as e.g. B. A. tumefaciens or as naked DNA by direct transfer using electroporation, microinjection or other physico-chemical methods into the pollen grains.
  • foreign genetic material means any genetic material that has arisen outside of the pollen grain to be transformed. After ripening, the pollen grains are obtained for pollination in the manner described above.
  • poil grains of a tobacco plant with 2 marker genes were ripened in vitro and normal wild type piants were pollinated with these poil grains.
  • the seeds obtained were sterilized and brought to germination in a germination medium containing kanamycin. Mendei's segregation of the marker genes was demonstrated by counting the seedlings in the selective medium. Seedlings that had been germinated on kanamycin-free medium also showed Mendei segregation of the NOS gene after detection of nopaline in high-voltage paper electrophoresis. This is the proof that it was the in vitro-ripened pollen grains that carried out the fertilization and not any pollen contamination from other plants.
  • chloramphenicol acetyitransferase activity was detected in a homogenate from the transformed pollen grains in an enzyme test.
  • a cytochemically detectable gene the beta-glucuronidase gene (GUS gene) was also used. After the cocultivation with the pollen, the agrobacteria were removed or killed by daily washing with the antibiotic Claforan. In the cytochemical test (blue coloring of the pollen) more than 50% blue, in vitro matured pollen could be detected. Non-infected poiles, or pollen, which were infected with agrobacteria without or with a non-functional GUS gene showed no blue coloration after addition of the substrate. A fluorometric test showed strong GUS activity in GUS-transformed poiles, as well as in pollen from GUS-transformed plants, which served as a positive control.
  • GUS gene beta-glucuronidase gene
  • Tobacco flowers were harvested in different lengths, the anthers were isolated aseptically, one of the five anthers was placed on a slide together with a drop of carmine acetic acid (4% carmine in 45% acetic acid) and a squeeze preparation was prepared. The development stage of the pollen grains was determined under the microscope after half an hour.
  • the tobacco pollen grains were isolated by carefully squeezing anthers under aseptic conditions in AMGLU medium (1) with a glass rod and microscope cup, and the resulting pollen suspension was passed through a 75 ⁇ m sieve and washed twice in AMGLU medium. Finally, the pollen suspension was centrifuged off at 6500 rpm in an Eppendorf centrifuge.
  • Example 3 Pollen culture for ripening early binuclear pollen grains
  • Mononuclear tobacco microspores were cultivated in MR24 medium (2) at a cell density of 2.10 Vml. As soon as the poil grains had reached the binuclear stage (after 2 to 5 days depending on the exact age), they were centrifuged off and further cultivated in MIS medium (3) until ripening was complete. Very good results were also achieved when cultivated in MR26 medium (2 '). As soon as the poil grains reached the binuclear stage (after 3 days), the same volume of M2S medium was added. After a further day, the pollen grains were centrifuged off and further cultivated in M2S medium (30 at a line density of 10 Vml until ripening was complete (one day).
  • the tobacco pollen grains were centrifuged off, washed in BK medium (Brewbaker and Kwack 1963) and the cell density set to 1.25.10 ⁇ / ml.
  • the still closed anthers were removed from flowers that were just opening (red flower tip).
  • a 4 ⁇ l drop of the poile suspension was applied to the stigma of the flower using a 20 ⁇ l pipette in such a way that the stigma was completely covered with poile suspension.
  • Example 6 Seed harvest, seed germination and genetic test
  • the transgenic plant contained the Neomyci ⁇ phospho-transferase gene (resistance to kanamycin) and the nopaline synthase gene. Self-fertilization and reciprocal cross-breeding with wild-type ripened in vitro were also carried out.
  • the ripe seed capsules (brown and dry) obtained according to Example 5 were harvested and the seeds isolated by cutting off the tip of the capsule and the seeds were filled directly into an Eppendorf cone.
  • Agrobacteria (A. tumefaciens without tumor genes, with CAT gene coupled to 35S promoter) were preincubated in Luria broth for one day. Pollen grains in the early binuclear stage were isolated and cultivated in AMGLU medium. The bacterial suspension was adjusted to an OD58O of 0.2 using AMGLU medium. After a further dilution with AMGLU medium of 1:10, 20 ⁇ l of the bacterial suspension were added to 1 ml of the pollen suspension. After cocooning for 24 hours, 1 ⁇ l Claforan (1 g / 2 ml) per ml was added to kill the agrobacteria. After two more days, the poil grains were harvested and an extract was made.
  • the CAT test was carried out as described by Sleigh (Anal. Biochem., 56: 251-256, 1986). 30 ul of the extract were mixed with 20 ul chloramphenicol (8mM), 30 ul Tris buffer and 20 ul 14 C-labeled acetyl-CoA (5 uCi / ml in 0.5 mM kaite acetyl-CoA). After incubation at 37 ° C. for 1 hour, the acetylated chloramphenicol was poured out through ethyl acetate (2 ⁇ 100 ⁇ l) and the radioactivity was measured in the scintillation counter.
  • IG ethyl acetate
  • the strong radioactivity signal shows that the agrobacteria have successfully infected the poil grains and that the T-DNA must have reached the cell nucleus of the growing cell for expression (transcription).
  • Agrobacteria of the LBA 4404 strain (A. tumefaciens, disarmed, with beta-glucuronidase (GUS) gene, coupled to the 35S promoter and terminator, (Matzke and Matzke in Plant Moiecuiar Biology 7: 357-365 (1986)) were found in Luribroth was incubated for one day, poil grains in the late mononuclear stage were isolated and adjusted to an OD58Q of 0.2 in MR26 medium, and after a further dilution with 1:26 MR26 medium, 20 ⁇ l of the bacterial suspension became 1 ml of the pollen suspension After 14-20 hours of cocultivation, the centrifuge was centrifuged off and the poiles were washed three times with claforane-containing (1 g / 2 ml) MR26 medium and further perfected, and the claforan-containing medium was changed every day until the poiles matured. 40 ⁇ i of the last medium (M2S
  • the ripened pollen was centrifuged off and a part was taken up in MR26 medium. After adding X-Glu (5-bromo-4-chloro-3-indolyl-glucuronide) to a final concentration of 1 mM and incubation at 37 ° C. for 4-12 hours (Jefferson in Plant Moiecular Biology Reporter, Voi. 5, No. 4, 387-405, (1987)) the formation of indigo (product of beta -Giucuronidase from X-Glu) can be detected using the blue color of the pollen in a light microscope. More than 50% of the living, ripened poiles showed a blue color.
  • GK medium like BK medium, but double the concentration of boric acid. GUS activity was also detected in the pollen tubes of the sprouted poiles.
  • An extract was made from a third part of the pool. For this, 4.10-- 'pollen were centrifuged off and taken up in extraction buffer (6). The poiles were broken up with glass balls and simultaneous ultrasound treatment. The fluorometric GUS test was carried out as described by Jefferson. 50 ⁇ l extract was made up to 1 ml with extraction buffer and MUG (4-methyl umbelliferyl glucuronide) was added to a final concentration of 1 mM. 200 ⁇ l aliquots were removed every 10 or 30 seconds and the enzyme reaction was stopped with 800 ⁇ l Na2CO3 (0.2 M).

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  • Life Sciences & Earth Sciences (AREA)
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Abstract

Selon un procédé de transfert de gènes entre des végétaux a) on prélève des grains de pollen immatures dans des étamines, on les place dans une solution de culture et on enlève le tissu qui les entoure, b) on cultive les grains de pollen immatures ainsi isolés dans une solution de culture, c) on introduit du matériau génétique étranger dans les grains de pollen pendant leur culture et maturation in vitro, d) on féconde des plantes réceptrices avec les grains de pollen ainsi transformés et on recueille les graines de celles-ci. L'invention concerne également des graines transgéniques et des produits de reproduction.
EP88905828A 1987-07-21 1988-07-13 Procede de transfert genetique entre des vegetaux Pending EP0362293A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3724154 1987-07-21
DE3724154 1987-07-21

Publications (1)

Publication Number Publication Date
EP0362293A1 true EP0362293A1 (fr) 1990-04-11

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ID=6332056

Family Applications (2)

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EP88111231A Expired - Lifetime EP0301316B1 (fr) 1987-07-21 1988-07-13 Méthode de transfert de gènes dans des plantes
EP88905828A Pending EP0362293A1 (fr) 1987-07-21 1988-07-13 Procede de transfert genetique entre des vegetaux

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EP88111231A Expired - Lifetime EP0301316B1 (fr) 1987-07-21 1988-07-13 Méthode de transfert de gènes dans des plantes

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EP (2) EP0301316B1 (fr)
JP (1) JP2675114B2 (fr)
CN (1) CN1039031C (fr)
AR (1) AR245216A1 (fr)
AT (1) ATE90963T1 (fr)
AU (1) AU615463B2 (fr)
BR (1) BR8807624A (fr)
CA (1) CA1327173C (fr)
DD (1) DD274234A5 (fr)
DE (2) DE3881977D1 (fr)
ES (1) ES2041286T3 (fr)
HU (1) HU204098B (fr)
MX (1) MX26688A (fr)
NZ (1) NZ225397A (fr)
PL (1) PL158090B1 (fr)
RU (1) RU2054482C1 (fr)
WO (1) WO1989000602A1 (fr)
YU (1) YU48600B (fr)
ZA (1) ZA885302B (fr)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5629183A (en) * 1989-05-08 1997-05-13 The United States Of America As Represented By The Secretary Of Agriculture Plant transformation by gene transfer into pollen
AU643563B2 (en) * 1990-11-01 1993-11-18 Sapporo Breweries Limited Method for preparing transformed plant
EP0737748A1 (fr) * 1995-03-17 1996-10-16 Hoechst NOR-AM AgrEvo Inc. Production effective de plantes transgéniques fertiles homozygènes à partir de microspores fraîches
US5929300A (en) * 1997-07-15 1999-07-27 The United States Of America As Represented By The Secretary Of Agriculture Pollen-based transformation system using solid media
US6812028B1 (en) 1999-12-10 2004-11-02 University Of Guelph Embryogenesis and plant regeneration from microspores
RU2229793C1 (ru) * 2002-11-06 2004-06-10 Научно-исследовательский институт сельского хозяйства Юго-Востока РАСХН Способ получения трансгенных растений сорго
WO2007148926A1 (fr) 2006-06-21 2007-12-27 Snu R & Db Foundation Gène tfla susceptible de dégrader une toxoflavine et ses dérivés chimiques, et organismes transgéniques exprimant le gène tfla
WO2008088161A1 (fr) 2007-01-19 2008-07-24 Myongji University Industry And Academia Cooperation Gène du cytochrome p450 destiné à augmenter la taille de graines ou à améliorer la résistance au stress hydrique d'un végétal
KR100990370B1 (ko) 2008-07-18 2010-10-29 경희대학교 산학협력단 벼 도열병균에 대한 내성을 증진시키는 유전자 및 이의용도
KR101101774B1 (ko) 2009-02-12 2012-01-05 전남대학교산학협력단 토마토 히스티딘 디카르복실라제 유전자 유래 열매 특이적 발현 프로모터 및 이의 용도
WO2010120054A2 (fr) 2009-04-16 2010-10-21 Gendocs, Inc. Promoteur 972 inductible par un stress environnemental isolé à partir de riz et utilisations de celui-ci
US8404827B2 (en) 2009-04-16 2013-03-26 Gendocs, Inc. Environmental stress-inducible 996 promoter isolated from rice and uses thereof
US8237018B2 (en) 2009-08-24 2012-08-07 Myongji University Industry And Academia Cooperation Foundation Promotes and methods thereof
US8987557B2 (en) 2009-08-24 2015-03-24 Myongji University Industry And Academia Cooperation Foundation Promoters and methods thereof
US9677081B2 (en) 2009-08-24 2017-06-13 Seoul National University R&Db Foundation Promoters and methods thereof
KR101300207B1 (ko) 2010-12-03 2013-08-26 서울대학교산학협력단 애기장대 유래의 ｍｙｂ96 유전자 및 이의 용도
KR101541598B1 (ko) 2013-09-24 2015-08-03 포항공과대학교 산학협력단 식물의 체관 발달 및 형성에 관여하는 ｐｈｄ 유전자
KR101526190B1 (ko) 2013-11-28 2015-06-16 제주대학교 산학협력단 시금치 유래의 cyp85 유전자를 이용한 20-히드록시엑디손 함량이 증진된 형질전환 식물체의 제조방법 및 그에 따른 식물체
NL2011980C2 (en) 2013-12-17 2015-06-18 Univ Leiden New effects of plant ahl proteins.
JP2020072645A (ja) * 2017-01-31 2020-05-14 日本たばこ産業株式会社 植物に物質を導入する方法
US11326181B2 (en) 2017-11-02 2022-05-10 Woojung Bio Inc. Method for producing transgenic plant having increased content of 20-hydroxyecdysone using insect-derived gene and plant produced by the same
CN111758550A (zh) * 2020-06-16 2020-10-13 黎铮 杂交水稻商品种子及两系不育系生产用种的生产方法
KR102461600B1 (ko) 2020-07-21 2022-11-02 주식회사 피토맵 N-당질화 돌연변이 벼, 이의 제조방법 및 이를 이용한 단백질 생산용 벼의 제조방법

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0160692A1 (fr) * 1983-11-03 1985-11-13 DE WET, Johannes Martenis Jacob Procede de transfert de genes exogenes dans des plantes en utilisant le pollen comme vecteur
GB2159173B (en) * 1984-05-11 1988-10-12 Ciba Geigy Ag Transformation of hereditary material of plants
EP0257472A3 (fr) * 1986-08-14 1989-10-04 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Plantes monocotylédones transgéniques, leur graines et procédé de préparation des plantes
EP0267159A3 (fr) * 1986-11-07 1990-05-02 Ciba-Geigy Ag Procédé de modification génétique de monocotylédones
IL84459A (en) * 1986-12-05 1993-07-08 Agracetus Apparatus and method for the injection of carrier particles carrying genetic material into living cells
EP0275069A3 (fr) * 1987-01-13 1990-04-25 DNA PLANT TECHNOLOGY CORPORATION (under the laws of the state of Delaware) Transformation génique dans les plantes utilisant le pollen
IL82153A (en) * 1987-04-09 1991-12-15 Yissum Res Dev Co Process for introducing genes into plants

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO8900602A1 *

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Publication number Publication date
AU2073788A (en) 1989-02-13
AR245216A1 (es) 1993-12-30
ZA885302B (en) 1989-04-26
EP0301316A2 (fr) 1989-02-01
RU2054482C1 (ru) 1996-02-20
JP2675114B2 (ja) 1997-11-12
JPH03501802A (ja) 1991-04-25
PL158090B1 (pl) 1992-08-31
CA1327173C (fr) 1994-02-22
YU48600B (sh) 1998-12-23
PL273797A1 (en) 1989-02-20
MX26688A (es) 1994-02-28
CN1039031C (zh) 1998-07-08
NZ225397A (en) 1991-04-26
DE3881977D1 (en) 1993-07-29
YU139888A (en) 1990-08-31
DD274234A5 (de) 1989-12-13
BR8807624A (pt) 1990-08-07
ES2041286T3 (es) 1993-11-16
EP0301316B1 (fr) 1993-06-23
HUT52820A (en) 1990-08-28
ATE90963T1 (de) 1993-07-15
HU204098B (en) 1991-11-28
CN1030788A (zh) 1989-02-01
AU615463B2 (en) 1991-10-03
DE3823712A1 (de) 1989-02-02
EP0301316A3 (en) 1989-03-22
WO1989000602A1 (fr) 1989-01-26

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