• Journal of Plant Biotechnology
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• 제42권3호
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• pp.204-214
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• 2015

SHI-RELATED SEQUENCE (SRS) 유전자는 zinc-binding RING finger motif를 갖고있는 식물 특이적 전사인자로서 식물 생장과 발달에서 중요한 역할을 하고 있다. 배추 생장점 부위로부터 분리된 Brassica rapa SHI-RELATED SEQUENCE (BrSRS) 유전자인 BrSRS7과 BrLRP1은 식물 생장과 발달에서 중요한 조절자이다. BrSRS7과 BrLRP1 유전자가 원예작물의 생장과 발달에 미치는 영향을 보고자 35S 프로모터에 유전자를 결합시켜 두 종류의 식물 형질전환 벡터를 제작한 후 아그로박테리움을 이용하여 페튜니아에 형질전환하였다. 형질전환체들은 전체적으로 식물체 크기가 감소되었고 잎은 작으면서 upward-curled된 특성을 나타내었고 줄기 사이의 길이가 줄었다. 페튜니아의 꽃 모양은 도입된 유전자에 따라 오각형, 별 모양, 둥근 모양으로 다르게 나타났다. 이러한 특성들은 $T_2$, $T_3$ 세대진전 후에도 안정적으로 나타났다. RT-PCR로 유전자 발현을 분석한 결과 BrSRS7과 BrLRP1 유전자는 정단 분열 조직에서 형태 형성에 관여하는 지베릴린과 옥신 관련 유전자인 PtAGL15, PtIAMT1 발현을 조절함으로서 페튜니아의 생장과 발달에 중요한 역할을 하는 것으로 추측된다. 따라서 본 연구결과로 BrSRS 계열 유전자는 왜성 특성, 식물 형태 변형을 갖는 화훼 품종을 개발하는데 유용하게 이용될 수 있을 것으로 사료된다.

• Journal of Plant Biotechnology
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• 제31권4호
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• pp.261-266
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• 2004

Agrobacterium을 이용하여 도입된 유전자의 세대진전, 교잡 등에 따른 유전적 안정성을 확인코자, 형질 전환으로부터 얻어진 bar 유전자가 도입된 형질전환 식물체들을 상호 교배, 여교배, T$_4$ 세대까지의 자식의 반복 등에 의해 유전적 안정성을 검토하였다. 조합이나 계통에 따라서는 일부 멘델식 분리를 따르지 않고 제초제 Basta에 대한 저항성이 사라지거나 저항성개체보다 감수성개체가 기대치보다 많은 등의 경우가 있었으나, 대부분 멘델식 분리를 따르고 있어 세대진전, 교배 등에 의해서도 유전적 안정성이 높게 유지됨을 확인할 수 있었다.

• Journal of Plant Biotechnology
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• 제30권2호
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• pp.143-149
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• 2003

This experiment was carried out to confirm the stability of bar gene introduced into petunia plant through Agrobacerium-mediated transformation. Twenty-five transgenic plants T$_{0}$ plants, back cross (BC$_1$) populations to wild type and F$_1$plants between different T$_{0}$ plants were prepared, and polymerase chain reaction(PCR), PCR-Southern blot analysis, and field test with 0.1% Basta treatment were done. The results of PCR, PCR-Southern blot hybridization, and field test indicated that NPTII and bar gene introduced into the genome of petuina plants were stably transmitted to their progenies, and conferred the plants resistance to herbicide, Basta.sta.

• 한국식물학회:학술대회논문집
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• 한국식물학회 1996년도 제10회 식물생명공학심포지움 고등식물 발생생물학의 최근 진보
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• pp.48-60
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• 1996

We previously identified and characterized a predominantly pollen-expressed gene of Petunia inflata that encodes a receptor-like kinase named PRK1. The extracellular domain of PRK1 contains leucine-rich repeats which have been implicated in protein-protein interactions, and the cytoplasmic domain was found to autophosphorylate on serine and tyrosine. To investigate the function PRK1 in pollen development, we transformed P. inflata plants with a construct containing the promoter of a predominantly pollen-expressed gene of tomato, LAT52, fused to an antisense PRK1 cDNA corresponding to part of the extracellular domain of PRK1, There transgenic plants were found to each produce approximately equal amounts of normal and aborted pollen. Analysis of the inheritance of the transgene inserts in two of the transgenic plants, ASRK-13 and ASRK-20, to their progeny revealed that certain transgene inserts cosegregated with the pollen abortion phenotype. Microscopic examination of the aborted pollen grains showed that their outer wall, the exine, was essentially normal, but that their cytoplasm contained only starch-like granules. Staining of the nuclei of the microspores at different stages of uninucleate stage. However, at subsequent stages half of the microspores completed mitosis and developed into normal binucleate pollen, but the other half initially remained uninucleate, then lost their nucleio. Analysis of the amounts of PRK1 mRNA and the antisense PRK1 transcript suggested that the pollen abortion phenotype most likely resulted from down-regulation of the PRK1 gene by the antisense PRK1 transgene. These results suggest that PRK1 plays an essential role in a signal transduction pathway that mediates post-meiotic development of microspores.

• 원예과학기술지
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• 제34권3호
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• pp.510-510
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• 2016

• 원예과학기술지
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• 제34권1호
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• pp.154-162
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• 2016

유전자 집적에 의해 아황산가스 저항성 증진 페튜니아를 개발하고자 비생물적스트레스 저항성 유전자로 널리 알려진 SOD2와 NDPK2유전자가 각각 도입된 SOD2 형질전환 계통 SOD2-2-1-1-35($T_4$)[S($T_4$)]와 NDPK2 형질전환 계통 NDPK2-7-1($T_2$)[N7-1($T_2$)]간 상호교잡을 실시하여 교잡 제1세대를 획득하였다. 교잡 제1세대 중 SOD2와 NDPK2유전자가 모두 집적된 개체 획득율은 32.1-73.0%이었고, SOD2와 NDPK2유전자가 모두 집적된 개체는 SOD2 또는 NDPK2유전자가 단독 도입된 개체에 비해 아황산가스 30ppm처리 피해율이 2.6-5.1배 낮아 아황산가스 저항성이 증진되었음을 확인하였다. 또한 아황산가스 저항성이 증진된 교잡 제1세대를 자가수분에 의해 세대진전 시켜 획득한 교잡 제2세대의 아황산가스 저항성 검정을 통하여 교잡 제1세대에서의 아황산가스 저항성이 후대에서도 안정적으로 발현함을 확인하였다. 또한, 광합성 효율 증진 조사를 통해 아황산가스 저항성이 증진된 SOD2와 NDPK2유전자 집적 후대가 아황산 가스에 대한 스트레스를 덜 받고 있음을 확인하였고, RT-qPCR분석을 통해 SOD2와 NDPK2유전자 집적 후대의 아황산가스 저항성 증진이 SOD2와 NDPK2 유전자 집적에 의한 효과임을 확인하였다.

• 식물조직배양학회지
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• 제21권5호
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• pp.253-275
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• 1994

Many flowering plants possess genetically controlled self -incompatibility (SI) system that prevents inbreeding and promotes outcrosses. SI is usually controlled by a single, multiallelic S-locus. In gametophytically controlled system, SI results when the S-allele of the pollen is matched by one of the two S-alleles in the style, while in the sporophytic system self-incompatible reaction occurs by the interaction between the pistil genotype and genotype of, not the pollen, but the pollen parent In the former system the self-incompatible phenotype of pollen is determined by the haploid genome of the pollen itself but in the latter the pollen phenotype is governed by the genotype of the pollen parent along with the occurrence of either to-dominant or dominant/recessive allelic interactions. In the sporophytic type the inhibition reaction occurs within minutes following pollen-stigma contact, the incompatible pollen grains usually failing to germinate, whereas in gametophytic system pollen tube inhibition takes place during growth in the transmitting tissue of the style. Recognition and rejection of self pollen are the result of interaction between the S-locus protein in the pistil and the pollen protein. In the gametophytic SI the S-associated glycoprotein which is similar to the fungal ribonuclease in structure and function are localized at the intercellular matrix in the transmitting tissue of the style, with the highest concentration in the collar of the stigma, while in the sporophytic SI deposit of abundant S-locus specific glycoprotein (SLSG).is detected in the cell wall of stigmatic papillae of the open flowers. In the gametophytic system S-gene is expressed mostly at the stigmatic collar the upper third of the style length and in the pollen after meiosis. On the other hand, in the sporophytic SI S-glycoprotein gene is expressed in the papillar cells of the stigma as well as in e sporophytic tape is cells of anther wall. Recognition and rejection of self pollen in the gametophytic type is the reaction between the ribonuclease in the transmitting tissue of the style and the protein in the cytoplasm of pollen tube, whereas in the sporophytic system the inhibition of selfed pollen is caused by the interaction between the Sycoprotein in the wall of stigmatic papillar cell and the tapetum-origin protein deposited on the outer wall of the pollen grain. The claim that the S-allele-associated proteins are involved in recognition and rejection of self pollen has been made merely based on indirect evidence. Recently it has been verified that inhibition of synthesis of S$_3$ protein in Petunia inflata plants of S$_2$S$_3$ genotype by the antisense S$_3$ gene resulted in failure of the transgenic plant to reject S$_3$ pollen and that expression of the transgenic encoding S$_3$ protein in the S$_1$S$_2$ genotype confers on the transgenic plant the ability to reject S$_3$ pollen. These finding Provide direct evidence that S-proteins control the s elf-incompatibility behavior of the pistil.