• 제목/요약/키워드: Transgenic tomato

검색결과 44건 처리시간 0.025초

Expression of Rice Chitinase Gene in Genetically Engineered Tomato Confers Enhanced Resistance to Fusarium Wilt and Early Blight

  • Jabeen, Nyla;Chaudhary, Zubeda;Gulfraz, Muhammad;Rashid, Hamid;Mirza, Bushra
    • The Plant Pathology Journal
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    • 제31권3호
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    • pp.252-258
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    • 2015
  • This is the first study reporting the evaluation of transgenic lines of tomato harboring rice chitinase (RCG3) gene for resistance to two important fungal pathogens Fusarium oxysporum f. sp. lycopersici (Fol) causing fusarium wilt and Alternaria solani causing early blight (EB). In this study, three transgenic lines TL1, TL2 and TL3 of tomato Solanum lycopersicum Mill. cv. Riogrande genetically engineered with rice chitinase (RCG 3) gene and their R1 progeny was tested for resistance to Fol by root dip method and A. solani by detached leaf assay. All the R0 transgenic lines were highly resistant to these fungal pathogens compared to nontransgenic control plants. The pattern of segregation of three independent transformant for Fol and A. solani was also studied. Mendelian segregation was observed in transgenic lines 2 and 3 while it was not observed in transgenic line 1. It was concluded that introduction of chitinase gene in susceptible cultivar of tomato not only enhanced the resistance but was stably inherited in transgenic lines 2 and 3.

살충성 형질 전환 토마토 식물체의 분자 육종 (Molecular Breeding of Transgenic Tomato Plants Expressing the ${\delta}-Endotoxin$ Gene of Bacillus thuringiensis subsp. tenebrionis)

  • 임성렬
    • Applied Biological Chemistry
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    • 제41권2호
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    • pp.137-140
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    • 1998
  • 딱정 벌레목 유충에 살충성을 나타내는 형질 전환 토마토 식물체를 4세대까지 분자 육종을 하였다. 분자 육종된 4세대 식물체에서 살충성 유전자인 B.t.t. 독소 유전자와 유전자가 발현되는 것을 확인하였다. 이 4세대 형질 전환 식물체는 독소 유전자 발현에 의해 딱정 벌레 유충에 살충성을 나타내고 있음이 확인 되었고, 4세대 형질 전환 식물체는 염색체는 2 배수체로 확인되어 정상적인 토마토 식물체임이 증명 되었다. 이 결과들은 형질 전환에 사용된 독소 유전자가 다음 세대로 안정되게 유전되고 있음을 나타내고 있다는 증거이다. 이러한 형질 전환된 식물체의 분자 육종은 농업에 있어서 현재의 일시적인 해충 방제에 비해 장기적인 해충 구제에 대한 새로운 방법의 가능성을 제시하고 있다고 하겠다.

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The use of SlAdh2 promoter as a novel fruit-specific promoter in transgenic tomato

  • Chung, Mi-Young;Naing, Aung Htay;Vrebalov, Julia;Shanmugam, Ashokraj;Lee, Do-Jin;Park, In Hwan;Kim, Chang Kil;Giovannon, James
    • Journal of Plant Biotechnology
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    • 제47권2호
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    • pp.172-178
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    • 2020
  • Fruit-specific promoters play an important role in the improvement of traits, such as fruit quality through genetic engineering. In tomato, the development of fruit-specific promoters was previously reported, but less attention has been paid to the promoters involved in the fruit development stage. In this study, we characterized the gene expression patterns of tomato alcohol dehydrogenase 2 (SlAdh2) in various tissues of wild-type tomato (cv. Ailsa Craig). Our findings revealed that SlAdh2 expression levels were higher in the developing fruit than in the leaves, stems, and flowers. The ProSlAdh2 region, which is expressed at different stages of fruit development, was isolated from tomato genomic DNA. Following this, it was fused with a β-glucuronidase reporter gene (GUS) and introduced into wild-type tomato using Agrobacterium-mediated transformation to evaluate promoter activity in the various tissues of transgenic tomato. The ProSlAdh2:GUS promoter exhibited strong activity in the fruit and weak activity in the stems, but displayed undetectable activity in the leaves and flowers. Interestingly, the promoter was active from the appearance of the green fruit (1 cm in size) to the well-ripened stage in transgenic tomatoes, indicating its suitability for transgene expression during fruit development and ripening. Thus, our findings suggest that ProSlAdh2 may serve as a potential fruit-specific promoter for genetic-based improvement of tomato fruit quality.

Agrobacterium-mediated transformation of Lycopersicon esculentum (cv. MicroTom) with two pathogen-induced hot pepper transcription factors

  • Seong, Eun-Soo;Oh, Sang-Keun;Eunsook Chung;Park, Doil
    • 한국식물병리학회:학술대회논문집
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    • 한국식물병리학회 2003년도 정기총회 및 추계학술발표회
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    • pp.79.1-79
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    • 2003
  • Two pathogen-induced hot pepper transcription factors (CaNACl and CapIfl) were introduced into‘MicroTom’tomato by Agrobacterium tumefaciens-mediated transformation. We used to nptII containing kanamycin resistance gene as a selection marker. Both transformed and non-transformed plants were transferred to pot after rooting test in vitro. To approximate the levels of caNACl transcript in leaves of wild-type and transgenic plants, RNA blots were hybridized with double-stranded full-length CaNACl probe at moderate stringency, Although the relative signal strength for hybridization fluctuated among the samples on different blots, transgenic plant lines N-1, N-2 and N-3 consistently displayed increased levels of CaNACl transcript relative to other transgenic lines and wild-type plants. Of all the transgenic lines examined, line N-7 had the least amount of CaNACl transcript. Role of these transcription factors in pathogen defense will be examined by overexpression in tomato.

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옥수수 calreticulin 과발현 토마토에서 tobamovirus의 상엽 이동 억제 (Suppression of tobamovirus movement toward upper leaves in the tomato plant over-expressing a maize calreticulin)

  • 한증술
    • Journal of Plant Biotechnology
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    • 제37권4호
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    • pp.567-573
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    • 2010
  • To ascertain the effect of over-expressed maize calreticulin in tomato plant on tobamovirus movement in addition to validating potentiality of the gene (ZmCRT) as a means for the virus-resistance resource, four ZmCRT-expressing homozygous lines were generated from the T0 plants as using an Agrobacterium-mediated transformation, nucleic acid analyses, and a conventional breeding method. Of them, a line was subjected to the bioassay for tolerances to tobacco mosaic virus-U1 (TMV-U1) and tomato mosaic virus (ToMV) followed by RT-PCR and a chlorophyll fluorescence quenching analyses. Both transgenic plants transcribing ZmCRT and wild-type plants showed no symptom by 20 days after viruses inoculation, however the photosystem II quantum yield parameter measured from the upper leaves of ToMV-inoculated plants revealed that ZmCRT transgenic plants have higher photosynthetic ability than wild-type ones at that time, which indirectly implies that over-expressed ZmCRT product acts as a barrier to the cell-to-cell and/or systemic movement of ToMV. Moreover, ZmCRT transgenic plants showed remarkably longer shoot length than wild-type ones in 40 days after TMV-U1 or ToMV inoculation each, which might be resulted from higher photosynthetic ability during the phase not yet showing any external symptoms. Collectively, over-expressed ZmCRT protein in tomato plants is able to interrupt the systemic movement of infected TMV-U1 and ToMV even though not perfect.

Tomato Yellow Leaf Curl China Virus Impairs Photosynthesis in the Infected Nicotiana benthamiana with βC1 as an Aggravating Factor

  • Farooq, Tahir;Liu, Dandan;Zhou, Xueping;Yang, Qiuying
    • The Plant Pathology Journal
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    • 제35권5호
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    • pp.521-529
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    • 2019
  • Tomato yellow leaf curl China virus is a species of the widespread geminiviruses. The infection of Nicotiana benthamiana by Tomato yellow leaf curl China virus (TYLCCNV) causes a reduction in photosynthetic activity, which is part of the viral symptoms. ${\beta}C1$ is a viral factor encoded by the betasatellite DNA ($DNA{\beta}$) accompanying TYLCCNV. It is a major viral pathogenicity factor of TYLCCNV. To elucidate the effect of ${\beta}C1$ on plants' photosynthesis, we measured the relative chlorophyll (Chl) content and Chl fluorescence in TY-LCCNV-infected and ${\beta}C1$ transgenic N. benthamiana plants. The results showed that Chl content is reduced in TYLCCNV A-infected, TYLCCNV A plus $DNA{\beta}$ (TYLCCNV A + ${\beta}$)-infected and ${\beta}C1$ transgenic plants. Further, changes in Chl fluorescence parameters, such as electron transport rate, $F_v/F_m$, NPQ, and qP, revealed that photosynthetic efficiency is compromised in the aforementioned N. benthamiana plants. The presense of ${\beta}C1$ aggravated the decrease of Chl content and photosynthetic efficiency during viral infection. Additionally, the real-time quantitative PCR analysis of oxygen evolving complex genes in photosystem II, such as PsbO, PsbP, PsbQ, and PsbR, showed a significant reduction of the relative expression of these genes at the late stage of TYLCCNV A + ${\beta}$ infection and at the vegetative stage of ${\beta}C1$ transgenic N. benthamiana plants. In summary, this study revealed the pathogenicity of TYLCCNV in photosynthesis and disclosed the effect of ${\beta}C1$ in exacerbating the damage in photosynthesis efficiency by TYLCCNV infection.

Tomato Golden Mosaic Virus(TGMV) AL1 -gene의 antisense RNA 발현 형질 전환 식물체 (Transgenic Plants Expressing an Antisense RNA of ALl-Gene from Tomato Golden Mosaic Virus(TGMV))

  • 임성렬
    • 식물조직배양학회지
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    • 제25권3호
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    • pp.147-152
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    • 1998
  • AL1-gene은 TGMV의 복제에 매우 중요한 역할을 하고 있다. 이 AL1 gene의 발현을 억제하기 위해서는 식물체내에서 AL1 gene의 antisense RNA의 발현에 의한 억제가 효과적 방법 중에 하나로 알려져 있다. 이런 발현을 식물체내에서 실현시키기 위해 hygromycin 저항성 유전자에 antisense AL1-gene을 연결시키고, 연결된 부위를 CaMV35s-promoter와 octopine synthase gene terminator 사이에 연결시켰다. 이 유전자 발현 단위 부분을 다시 kanamycin 저항성 유전자 발현 단위 부분을 지니고 있는 형질 전환 벡터인 pBinAR에 삽입시켜 새로운 형질 전환 벡터인 pAR35-2를 개발하였다. 이 벡터를 Agrobacterium tumefaciens LBA4404에 형질전환 시킨 다음, 토마토와 담배 잎사귀 조직에 감염시켜 식물체들을 kanamycin과 hygromycin이 함유된 배지위에서 배양하여 형질전환된 식물체들을 선발하였다. 형질 전환된 식물체들로부터 antisense AL1-gene 및 antisense RNA를 각각 PCR 및 RT-PCR를 이용한 southern hybridization 방법을 이용하여 증명하였고, 토마토 식물체의 공변세포쌍 내에 있는 엽록체 숫자가 여덟 개라는 것이 확인되어 형질 전환된 토마토 식물체가 2 배수체로서 정상적인 식물체라는 것을 증명하였다. 이러한 형질 전환 식물체는 앞으로 항 바이러스성 형질을 지니는 식물체들을 개발하는 데 많은 도움을 주리라 여겨 진다. 그리고, 본 연구에서 제조된 벡터 pAR35-2는 두 개의 항생제에서 동시 선발 할 수 있도록 되어 있고 promoter가 두 개로 되어 있어 형질 전환 식물체선발 및 유전자 발현 연구에 효과적으로 이용되어 질 수 있으리 라 여겨진다.

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토마토 과실에서 Superoxide Dismutase를 고발현하는 형질전환 식물체 (Transgenic Tomato Plants That Overexpress Superoxide Dismutase in Fruits)

  • 박은정;이행순;권석윤;최관삼;곽상수
    • Journal of Plant Biotechnology
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    • 제29권1호
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    • pp.7-13
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    • 2002
  • Superoxide dismutase (SOD)를 과실에서 고발현시킨 형질전환 토마토 (서광과 꼬꼬)를 개발하였다. 카사바 배양세포에서 분리한 CuZnSOD (mSOD1)를 과실에 우세적으로 발현하는 ascorbate oxidase promoter (ASOp)를 이용하여 ASOp :: mSOD1/pBI101 벡터를 제작한 후 Agrobacterium 매개로 자엽 절편체를 형질전환하였다. Kanamycin 저항성 식물체를 기관발생 경로로 재분화시킨 후 Southern 분석으로 형질전환을 확인하였다. 서광과 꼬꼬 토마토의 형질전환체와 대조구 식물체의 과실을 성숙 단계별로 분류하여 단백질 함량과 SOD 비활성도 (units/mg protein)를 측정한 결과, 단백질 함량은 열매가 익은 단계로 갈수록 점점 감소하여 완전히 익은 단계에서 가장 낮았다. SOD 비활성도는 형질전환 토마토의 열매의 모든 단계에서 대조구보다 높았으며 완전히 성숙한 과실에서 가장 높았다. 성숙한 형질전환 서광과 꼬꼬 과실에서 SOD 비활성도는 비형질전환의 것보다 각각 약 1.6배와 약 2.2배 높았다. SOD isoenzyme gel 분석에서 도입한 mSOD1로 추정되는 CuZnSOD 밴드가 형질전환체에서 과실 성숙에 따라 강하게 발현되었다. 이상의 결과로서 ASO promoter에 의해 SOD 유전자가 토마토 과실에 특이적으로 발현됨이 확인되었다.

Transient and stable expression of hepatitis B surface antigen in tomato (Lycopersicon esculentum L.)

  • Srinivas, L.;Sunil Kumar, G.B.;Ganapathi, T.R.;Revathi, C.J.;Bapat, V.A.
    • Plant Biotechnology Reports
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    • 제2권1호
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    • pp.1-6
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    • 2008
  • Cotyledonary leaves of tomato cv. Megha were transformed with the hepatitis B virus 's' gene, which encodes surface antigen. Six plant expression cassettes (pHBS, pHER, pEFEHBS, pEFEHER, pSHER and pEFESHER) were used to assay the possible expression levels by agroinfiltration. The maximum transient expression level of 489.5 ng/g D.W. was noted in pEFEHER-infiltrated cotyledonary leaves. Transgenic tomato plants with pEFEHBS and pEFEHER expression cassettes were regenerated and characterized by molecular analysis. The expression of the antigen in the fruits was confirmed by RT-PCR and ELISA analysis. This is the first report on the expression of hepatitis B surface antigen in tomato.

Antisense Polygalacturonase 유전자 형질전환 토마토의 후대 발현 분석 (Inheritance and Expression of Antisense Polygalacturonase Gene in Transgenic Tomato)

  • 김영미;한장호;김용환;이성곤;황영수
    • 식물조직배양학회지
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    • 제25권2호
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    • pp.131-134
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    • 1998
  • Antisense PG 유전자 형질전판 토마토로부터 자식시켜 얻은 종자를 kanamycin 내성을 이용하여 5세대까지 분리, 육성하여 antisense PG 유전자가 안정적으로 고정된 식물체를 얻었다. 이들 식물체에는 genomic DNA gel blot 분석으로 antisense PG 유전자가 안정적으로 유전되며 northern blot 분석을 통하여 antisense RNA가 발현됨을 확인하였고, 또한 antisense RNA에 의한 endogenous PG 유전자의 발현 저해를 분석하였다. Antisense PG 유전자 형질전환 성숙 토마토내 PG 효소 활성이 비형질전환 성숙 토마토에 비하여 37-65% 수준으로 저하되었다.

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