• Journal of Plant Biology
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• 제38권1호
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• pp.25-32
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• 1995

The distribution of RNA in the anther wall of Brassica napus during male gametogenesis was followed by 3H-uridine autoradiography. Silver grain(SG) density was not above background in the anther wall just after microspore was released from tetrad callose wall. Significant accumulation of SGs occurred in tapetum, endothecium, and epidermis before microspore vacuolation. Accumulation of RNA in the tapetal cells was peak before the vaculation occurred in the microspore. With the onset of tapetal senescence at the partially vacuolated microspore stage, SGs decreased and they completely disappeared in the tapetum at the bicelled pollen stage. Accumulation of RNA in the endothecial cells was peak after the microspore mitosis and continued just after the generative cell mitosis. Appreciable SGs also occurred in cells of epidermis from nonvacuolate microspore stage to bicelled pollen stage. During this period, SG density was almost same and was not high as compared with tapetum or endothecium. At tricelled mature pollen stage, no incorporation occurred in anther wall. SGs were found mostly over the nucleouls and chromation of the cell nuclei.

• Journal of Plant Biology
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• 제36권2호
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• pp.183-192
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• 1993

Efficient plant regeneration system was established through the culture of rice (Oryza sativa L.) microspores. Microspores released by anther shedding culture developed into proembryos and calluses in B5 medium within two weeks of culture. The optimal hormone and carbon sources were dependent on the genotypes used. Microspore's viability decreased rapidly in culture time, therefore less than 3% of the total microspores were viable at the 9th day when the first microspore division was observed. Of two types of microspores (pollen dimorphism) observed in culture, only the P-grain, larger microspores than normal one was able to divide. Using 4',6-diamidino-2-phenylindole (DAPI) fluorescence staining, it was confirmed that the symmetrical division of uninucleate microspore was the first step leading to continuous microspore development. Microspore-derived proembryos and calluses were regenerated to plants in N6 medium containing 1 mg/L NAA and 5 mg/L kinetin, and 78.3% of the regenerated plants were haploids.

• 원예과학기술지
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• 제29권5호
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• pp.494-499
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• 2011

Cold pretreatment, washing medium and composition of nutrient media may have marked effects on microspore embryogenesis. When microspores isolated from radish (Raphanus sativus L. cv. Gwanhun) flower buds were washed with Nitsch & Nitsch (NLN) medium liquid medium containing $130g{\cdot}L^{-1}$ sucrose (NLN-13), yields of microspore-derived embryos were greater than when using B5 liquid medium containing $130g{\cdot}L^{-1}$ sucrose. Microspore viability is known to decrease rapidly with storage; however, in this experiment, microspore viability was maintained for 24 h at $4^{\circ}C$ without media. Among the various medium concentrations used ($0.25{\times}$, $0.5{\times}$, $1.0{\times}$, $2.0{\times}$, and $4.0{\times}$ NLN liquid medium), $0.5{\times}$ NLN liquid medium induced the most efficient formation of microspore-derived embryos. In addition, microspore-derived embryos yields were greater when microspores were cultured in $0.5{\times}$ NLN liquid medium supplemented with $0.25{\times}$, $0.5{\times}$, and $1.0{\times}$ NLN microelements, compared to medium not supplemented with microelements. In this study, the highest yield of microspore-derived embryos was observed when the microspores derived from flower buds were washed using NLN-13 liquid medium and then cultured on $0.5{\times}$ NLN liquid medium supplemented with $0.25{\times}$ NLN microelements, followed by incubation at $25^{\circ}C$ for 30 days.

• Journal of Plant Biology
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• 제36권3호
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• pp.241-249
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• 1993

The pattern of RNA synthesis during male gametogenesis of Brassica napus was studied using 3H-uridine autoradiography. No incorporation of isotope occurred in the newly released microspore and the nonvacuolate, furrowed microspore. Peak incorporation of label during male gametogenesis occurred in the uninucleate, furrowed microspores showing various degrees of vacuolation. In this microspore stage, silver grains were localized in the nucleus and cytoplasm. Moderate incorporation of the isotope occurred in the nulceus of the vacuolated microspore. After the microspore mitosis, isotope incorporation occurred predominantly in the nucleus of the vegetative cell with little or no incorporation in the generative cell. In tricellular pollen, no incorporation of isotope was observed in both the vegetative nucleus and the sperms. Silver grains almost completely disappeared from tricellular mature pollen grains ready to germinate.

• 원예과학기술지
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• 제32권3호
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• pp.382-389
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• 2014

Raphanus sativus L. cv. Taebaek, a efficiently microspore-derived embryo (MDE)-forming cultivar, and 'Chungwoon', a non-MDE-forming cultivar were selected as donor plants for isolated microspore culture. Radish flower bud of 2.0 (small, S), 4.0 (medium, M), and 6.0 (large, L) ${\pm}$ 0.5 mm in length were isolated to determine the temporal relationship between flower bud size and MED yield. Anatomical observations revealed no difference in the structure of the flower buds between the two cultivars. In both cultivars, the stigmas were much longer than the floral leaf in M-sized flower buds. The MDE yields for 'Taebaek' per petri dish were 6.6 and 1.3 for M- and L-sized of flower buds, respectively, but MDE formation was not induced in the S flower buds. On the other hand, 'Chungwoon' failed to form MDEs in all flower buds. The microspore density of 'Taebaek' was 1.3 times more than that of 'Chungwoon' for M sized flower buds. Of the M-sized buds from 'Taebaek' and 'Chungwoon', 92.1 and 81.6%, respectively, were in the late uninucleate microspore stage, which is characterized by the highest frequency of MDE formation. Anatomical observations of MDE formation revealed that the microspores were able to divide to form a primordium from which cell division took place continuously in the 'Teabeak' cultivar. However, the microspores of 'Chungwoon' failed to progress beyond the primodium stage, resulting in lack of MDE formation. By contrast, after the formation of the primordium, various developmental stages of embyos from microspore were observed in the 'Taebaek' cultivar. These results can be used to determine MDE forming potentials of radish cultivars.

• 식물조직배양학회지
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• 제26권2호
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• pp.71-76
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• 1999

약배양에 대한 반응이 비교적ㆍ높은 것으로 알려진 고추의 두 품종 계룡산재래와 밀양재래의 약을 2,4-D와 kinetin이 각각 0.1 mg/L씩 첨가된 배지에 치상한 후 4$^{\circ}C$와 32$^{\circ}C$의 온도 전처리가 소포자배 발생에 미치는 영향을 조사하였다. 소포자배의 발생은 사용한 두 품종 중 밀양재래에서 높았다. 고온처리는 저온처리에 비해 소포자 배의 발생이 많았고 캘러스의 발생은 거의 없었으며 발생한 배는 동일 배지에서 또는 호르몬이 없는 배지에 옮겼을 때 대부분이 정상적인 유식물로 발달하였다. 저온처리에서는 캘러스의 발생이 많았고 발생한 배는 대부분이 비정상적으로 발달하였다. 소포자배 발생에 효과적인 고온처리 기간은 밀양재래에서는 3일, 계룡산재래에서는 6일이었다. 고추의 약배양 시 고온처리는 소포자배의 유기뿐만 아니라 유기된 배의 생장에도 중요한 영향을 미치는 것으로 나타났다.

• Journal of Plant Biotechnology
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• 제35권2호
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• pp.109-114
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• 2008

Agrobacterium 공동배양을 적용하여 소포자에 Agrobacterium-mediated genetic transformation이 가능한지를 조사하기 위하여 소포자 형질전환에 대한 조건을 구축하고자 하였다. 선발 배지에서 Kanamycin에 대한 소포자의 배발생율을 조사하였는데 Kanamycin 농도 10 mg/L, 50 mg/L, 100 mg/L를 처리하였을 때 배발생율이 각각 4배, 8배, 10배 이하로 감소하였고 Kanamycin이 형질전환 선발마커로 사용할 경우 형질 전환율이 매우 낮아질 것으로 사려 된다. GFP 유전자 발현을 이용하여 visual reporter로서 활용하고자 Agrobacterium과 공동배양 후 배발생 유도 배지에 치상하고 소포자가 배로 발생하는 과정을 현미경으로 조사하면서 GFP 발현을 관찰하였다. 소포자는 배양 12일째서부터 소포자 분열로 cluster를 형성하였으며 24일째에는 반복되는 분열을 통하여 큰 mass의 배로 발달된 모습을 각각 GFP 발현을 통해 볼 수 있었다. 배양48일째도 GFP발현이 계속 보이며 총 8 개의 배에서 GFP 발현 재현성을 보임으로서 형질전환은 된 것으로 보이지만 더 이상 성숙된 배로 자라지 않아 소포자를 이용한 Agrobacterium 형질전환 조건을 더 개선할 필요가 있다.

• 식물조직배양학회지
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• 제28권5호
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• pp.263-271
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• 2001

고추의 약을 배지에 치상한 후 4$^{\circ}C$와 32$^{\circ}C$의 온도 전처리가 소포자의 활력, 초기분열 및 소포자 배 발생에 미치는 영향을 조사하였다. 활력 있는 소포자의 비율은 모 식물에서 채취하여 치상할 당시에는 62~64%정도였으나 치상 후 온도처리 기간 중에는 매우 급속하게 저하되었다. 소포자의 활력은 4$^{\circ}C$ 처리에 비해 32$^{\circ}C$ 처리 시에 더욱 심하게 감소하였으며 배양 9일이 되면 온도처리와 관계없이 활력 있는 소포자가 거의 없었다. 치상 당시의 소포자는 대부분이 후기 1핵성 소포자기였으며 배양 2일 후부터 핵이 소실된 무핵 소포자들과 함께 다양한 유형의 다핵 소포자들이 나타났다. 배 발생적 소포자의 비율은 고온처리에서 높았으나 균등분열에 의한 동형2핵 소포자의 출현에는 온도처리에 따른 차이가 크지 않았으며 다핵 소포자들은 균등 또는 불균등 분열에 의해 생겨났다. $25^{\circ}C$와 32$^{\circ}C$ 처리에서는 배양 2일 후에 이미 퇴화 소포자들이 50% 이상이 되었는데 4$^{\circ}C$ 처리에서는 14일 동안 대부분의 소포자들에서 핵이 완전하였다. 소포자 배의 발생은 4$^{\circ}C$ 처리에 비해 32$^{\circ}C$ 처리에서 높았으며 가장 효과적인 고온처리 기간은 4일이었다. 이에 비해 4$^{\circ}C$ 처리에서는 2일 처리가 가장 효과적이었으며 처리기간이 길어질수록 소포자 배의 발생이 감소되었다.

• Journal of Plant Biotechnology
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• 제2권3호
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• pp.129-134
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• 2000

Clear visualization of pepper (Capsicum annuum L.) microspore nuclei with common stains such as acetocarmine or propionocarmine is difficult, hindering cytological analysis. The DAPI stain after the addition of ferric chloride solution to fixative resulted in clear visualization of nuclei. For clear visualization of nuclei and slight fluorescence of microspore wall, addition of 40-60 ${mu}ell$ of ferric chloride solution to the 1 $m\ell$ fixative was identified as most effective. At all stages of gametophytic development, the nuclei can be distinctly visualized. Starch granules does not intefere with the fluorochrome, and so the vegetative and generative nuclei were cleary visible in binucleate pollens. With its rapidity and reliability, this technique represents an efficient tool for routine staging or investigation of the nuclear status of the microspore during culture.

• 한국작물학회:학술대회논문집
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• 한국작물학회 1990년도 춘계 학술대회지
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• pp.110-111
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• 1990