• 식물병연구
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• 제18권4호
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• pp.290-297
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• 2012

농업유전자원센터에 보존하고 있는 고추 유전자원 1,941점을 240H02sp6 SNP 마커를 이용하여 Cucumber mosaic virus 저항성 정도를 평가하였다. 1941점의 고추 유전자원에서 89점이 저항성, 162점이 이형접합성, 1270점이 이병성으로 분석되었다. 고추 종별로는 C. annuum은 총 839자원 중 38점이 저항성으로 나타났으며, C. baccatum은 277점 중 23%에 해당하는 자원만 분석이 되었고 분석된 자원 중 20점이 저항성을 나타났다. C. chinense는 21점이 저항성, C. frutescens는 8점이 저항성을 보였다. C. pubescens는 K157779 자원만 이병성을 나타내었으며, Capsicum sp. 자원들 중에는 저항성 자원이 없었다. 야생근연종인 C. chacoense는 15점이 분석되어 1점이 저항성, 4점이 이형접합성, 6점이 이병성을 보였고, C. galapagoense, C. tovarii는 각 한 점씩 분석되었고 모두 이병성으로 나타났다.

• Applied Biological Chemistry
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• 제39권5호
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• pp.355-360
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• 1996

시험관내에서 합성한 오이모자이크 바이러스 RNA단편을 성공적으로 절단한 ribozyme (한국농화학회지 37: 56-63(1994))을 담배 식물체에 발현시켜 바이러스 저항성 식물체를 만들려고 하였다. 해당 ribozyme의 염기서열을 함유한 DNA 단편을 꽃양배추 바이러스 35S promoter와 nopaline 합성효소 terminator에 연결시키고 연결 부위 및 ribozyme의 염기서열을 확인하였다. 염기서열을 확인한 합성유전자를 Agrobacterium tumefaciens LBA4404에 합성유전자를 함유한 E. coli HB101을 E. coli HB101(pRK2073)를 helper로 Agrobacterium tumefaciens LBA4404와 함께 배양하는 tri-parental mating system을 이용하여 도입시켰다. Ribozyme 유전자를 함유한 Agrobacterium 세포를 담배잎 조각과 함께 배양한 후 항생제인 kanamycin을 함유한 MS 배지에서 자란 열개의 작은 식물체를 재분화하였다. 형질전환한 식물체내에 ribozyme 유전자가 존재하는지의 여부는 합성효소증폭반응(PCR)을 이용하였던바, 일곱개체가 예상된 570 염기쌍의 DNA 단편을 가지고 있었다. 이들 중 네 개체로부터 RNA을 분리하여 formamide를 함유한 agarose에서 전기영동한 후 35S-ribozyme-nos의 DNA 단편으로 Northern hybridization을 행하였던 바, 식물세포내의 nuclease에 의해 ribozyme RNA가 분해된 듯 감지 할 수 없었다. 따라서 ribozyme을 이용하여 바이러스 저항성 식물체를 얻으려면 nuclease에 의해 분해되지 않는 ribozyme이 필요할 것으로 사료된다.

• 한국육종학회지
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• 제43권5호
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• pp.464-469
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• 2011

벼 줄무늬잎마름병 저항성 유전자 및 연관 DNA 마커 탐색을 위하여 줄무늬잎마름병에 저항성인 통일형 품종인 신광 벼 이용 여교잡 집단을 육성하였다. 줄무늬잎마름병 저항성 유전자에 대한 QTL을 분석한 결과 11번 염색체에 위치하는 SSR 마커 RM6897이 탐색되었으며 전체 표현형 변이의 44.2%를 설명하였다. DNA 마커 RM6897은 여교잡 집단에서 생물검정과 유전자형이 일치하였다. 또한 자포니카 품종들에서 저항성 27품종과 감수성 23품종에 대해 구분이 가능하였다. 따라서 신광벼 유래의 줄무늬잎마름병 저항성원 및 분자마커는 자포니카 품종의 바이러스 저항성 향상에 효율적으로 활용될 것으로 기대된다.

• 한국작물학회지
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• 제51권5호
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• pp.477-482
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• 2006

보리의 저항성 정도에 따른 바이러스병에 의한 생육 및 수량 피해를 조사하였다. 1. 병징 발생정도에 따라 백동과 새쌀보리가 각각 $7{\sim}9$와 $5{\sim}7$의 이병정도를 보여 감수성과 중도저항성을, 내한쌀보리는 $0{\sim}1$ 정도로 저항성으로 조사되었다. 2. 감수성과 중도저항성 품종에서 Barley yellow mosaic virus와 Barley mild mosaic virus의 감염이 확인되었으나, 저항성인 내한쌀보리는 바이러스 감염이 검정되지 않았다. 3. 월동 후 생육 신장 조사에서 저항성은 지속적인 생육 증가 현상을 나타낸 반면, 중도저항성과 감수성 품종은 $10.5{\sim}11.8cm$ 신장이 억제되는 생육 피해를 보였다. 4. 수량구성 요소의 피해를 건전포장 결과와 비교했을 때 중도저항성과 감수성 품종에서 저항성에 비해 출수기, 수수, 간장 등에서 특히 차이가 큰 것으로 나타났다. 감수성 품종에서 출수기는 7일 늦어졌고, 간장과 수수는 50% 이하의 생육을 보였으며, 중도저항성에서는 수수와 간장의 생육이 일반 포장에 비해 20% 정도 억제되는 피해를 보였다. 5. 품종별 저항성 정도에 따른 수량 피해 정도를 조사 결과, 병 발생이 없는 일반포장에 비해 중도저항성과 감수성 품종에서 10a당 $108{\sim}288kg$ 감소되는 피해를 보인 것으로 조사되었다. 6. 바이러스 감염시 중도저항성인 새쌀보리는 평균 35%의 수량 감소 피해를 보였으며, 감수성인 백동의 경우 평균 63%의 수량 감소 피해를 나타내었다.

• 원예과학기술지
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• 제32권2호
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• pp.235-240
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• 2014

Cucumber mosaic virus (CMV) is one of the most important viral diseases in pepper (Capsicum annuum L.), and several genes for resistance were reported in Capsicum spp. In Korea, a single dominant gene that is resistant to $CMV_{Fny}$ and $CMV_{P0}$ has been used for breeding. Recently, a new strain ($CMV_{P1}$) was reported that could infect cultivars resistant to both $CMV_{Fny}$ and $CMV_{P0}$. Therefore, breeding of more robust CMV-resistant cultivars is required. In this study, we surveyed the inheritance of $CMV_{P1}$ resistance and analyzed the location of the resistance loci. After $CMV_{P1}$ inoculation of various germplasms and breeding lines, one accession (ICPN18-8) showed no visual symptoms at 15 dpi (days post inoculation) but was susceptible after 45 dpi, and one resistant line (I7339) showed resistance until at 45 dpi. The latter line was used for tests of resistance inheritance. A total of 189 $F_2$ plants were examined, with 42 individuals showing resistance at 15 dpi and a phenotype segregation ratio close to 1:3 (resistant:susceptible plants). In a lateral ELISA test at 45 dpi, 11 plants showed resistance, and the segregation ratio was changed to 1:15. These results indicate that resistance in C. annuum 'I7339' is controlled by two different recessive genes; we named these resistance genes 'cmr3E' and 'cmr3L,' respectively. To locate these two resistant loci in the pepper linkage map, various RAPD, SSR, and STS markers were screened; only nine markers were grouped into one linkage group (LG). Only one RAPD primer (OPAT16) was distantly linked with cmr3E (22.3 cM) and cmr3L (20.7 cM). To develop more accurate markers for marker-assisted breeding, enriching for molecular markers spanning two loci will be required.

• 한국연초학회지
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• 제13권2호
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• pp.48-51
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• 1991

A program was initiated to transfer potato virus Y vein-necrosis strain resistance from N. africana to N. tabacum The Fl plants between the above species were self-sterile, but all amphidiploid plants from the Fl plants and backcrossed flowers, that is, the N. tabacum flowers crossed with amphidiploid were self-fertile. The parent, amphidiploid plants of Fl, F2 population of the amphidiploid and the backcrossed generation were screened for a resistance of potato virus Y vein-necrosis strain isolated in Korea. The Chi-square values for the F2 population of the amphidiploid and the backcrossed generation fitted 35: 1 and 5 : 1 ratios of resistant to susceptible for the potato virus Y vein-necrosis strain, respectively. Therefore, it was found that the resistance of N. tabacum for the potato virus Y vein-necrosis strain was controlled by a single dominant gene.

• The Plant Pathology Journal
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• 제16권5호
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• pp.264-268
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• 2000

A fluorescent material was accumulated in inoculated leaves showing necrotic local lesions of tobacco plants with N gene, Nicotiana tabacum cvs. Xanthi-nc NN, Samsun NN, Burley 21 and KF 114, and N. glutinosa, and Datura stramonium at the early growth stages by the inoculation of Tobacco mosaic virus (TMV). It was identified as a coumarin phytoalexin, scopoletin. Although the material was most prominently produced in TMV-inoculated tobacco leaves with local necrotic lesions, its accumulation was also noted in uninoculated leaves of TMV-inoculated plants. Its accumulation was somewhat greater in high resistance-induced leaves than low resistance-induced and intact leaves. Scopoletin treatment induced the expression of a pathogenesis-related protein, PR-1, prominently at the concentration of 500 or 1000 ${\mu}$g/ml. This suggests that scopoletin is a phytoalexin abundantly accumulating in N gene-containing resistant plants in response to TMV infection, and may be related to hypersensitive responses (HR) and systemic acquired resistance (SAR) in the resistant tobacco plants.

• 식물병연구
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• 제8권2호
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• pp.78-83
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• 2002

Tobacco diseases have not been recorded until 1900s in Korea, where tobacco plants were introduced at early 1700s. Practical researches on the disease have been conducted since mid 1960s. Major ten tobacco diseases were mosaic caused by tobacco mosaic virus·potato virus Y·cucumber mosaic virus, bacterial wilt, hollow stalk, wild fire caused by angular leaf spot strain, black shank, brown spot, powdery mildew and fusarium wilt. But their annual occurrences were varied according to changes of tobacco varieties and their cultivating practices. As no useful chemicals, several biological tactics have been developed to control the viral or bacterial diseases that give significant economic damages on sustainable crop yield, but not practicable to field farming condition yet. Transgenic tobacco plants containing foreign disease resistant genes have been developed by current bio-technology, but not released to farmers yet. Though some disease-resistant tobacco varieties have been developed by the conventional breeding technology and currently used by farmers, their disease controlling efficacy have been diminished by occurrence of the new strain or race. Future research on tobacco diseases has been focused on technical development to produce high quality tobacco with less production cost, which leads Korean tobacco industry to keep its competence against foreign industry and decreasing overall market.

• 한국수의병리학회지
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• 제5권2호
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• pp.49-56
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• 2001

Ocular lesions induced in 40 specific-pathogen-free Marek's disease (MD) resistant chicks by inoculation at 1 day of age with very virulent strain of Marek's disease virus (WV) were pathologically examined. Grossly,24/40 (60%) chicks had white gel-like materials in the vitreous body, whereas thickening and discoloration of iris (gray eye) were not observed. Microscopically, characteristic ocular MD lesions were observed in choroid (27/40), ciliary (30/40) and iris (23/40) in which small focal inflammatory to diffuse neoplastic Iymphoid cells were infiltrated. Five out of 40 MDV-inoculated birds revealed necrotizing Iymphomas in choroid. These lesions consisted of necrotic and degenerating Iymphoblasts accompanied by intranuclear inclusion body. There was retinal atrophy and necrosis with inclusion body detected in necrotic ganglion, inner or outer nuclear and infiltrated Iymphoblast cells. Conjunctiva showed lymphoid cell infiltration in 29/40 chicks inoculated with MDV, Vitreous body exhibited mild to severe exudation of eosinophilic proteinaceous material in 24/40 chicks. These lesions were associated with Iymphoid cell infutration, edema and fibrosis of choroid. Pecten (7/40) and optic nerve (13/40) were infiltrated usually mildly with Iymphoid cells. From these results, very virulent strain, Md/5 of MDV caused high incidence of ocular lesions in MD resistant chicks. In addition, Md/5 induced exudation of proteinaceous material into the vitreous body and fibrosis of choroid. Necrotizing ocular Iymphoma lesions in choroid is the first report in the MD literature.

• 한국연초학회지
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• 제21권1호
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• pp.57-63
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• 1999

Pokeweed antiviral protein II (PAP-II) encoding cDNA was synthesized by reverse-transcriptase polymerase chain reaction (RT-PCR) from Phytolacca american a leaf. The PAP-II cDNA fragment of 974bp was subcloned to pBluescript II SK- SmaI site and the inserted PAP-II cDNA fragment was sequenced by dideoxy sequencing method. The number of nucleotides of PAP-II cDNA coding region containing start and stop codon was 933bp. To develop a virus-resistant tobacco plant, PAP-II cDNA fragment was inserted to pKGT101B and the insertion of PAP-II cDNA fragment was confirmed by restriction enzyme analysis and colony PCR.