• 한국작물학회:학술대회논문집
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• 한국작물학회 2017년도 9th Asian Crop Science Association conference
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• pp.125-125
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• 2017

The roots of Platycodon grandiflorum are commonly used for treating bronchitis, asthma, tuberculosis, diabetes, and other inflammatory diseases. Since the molecular mechanism underlying the roots of the plant is unclear. Therefore, the present study was conducted to profile proteins from liquid cultured tetraploid roots of Platycodon grandi orum fl using high throughput proteome approach. Two-dimensional gels stained with CBB, a total of 659 differentially expressed proteins were identified from the liquid medium cultured tetraploid roots of which 32 proteins spots (${\geq}1.5-fold$) were sorted for mass spectrometry analysis. Out of these 32 proteins, a total of 15 proteins were up-regulated such as Serine carboxypeptidase-like 27, Transcription factor bHLH150, 60 kDa jasmonate-induced protein, Cytosolic Fe-S cluster assembly factor NBP35, Regulatory associated protein of TOR 2 and a total of 17 proteins were down-regulated such as Protein G1-like2, Phenylalanine ammonia-lyase, Fructokinase-2, Trihelix transcription factor GT-3a, Guanine nucleotide-binding protein alpha-1 subunit. However, the frequency distribution of identified proteins was carried out within functional categories based on molecular functions, cellular components, and biological processes. Functional categorization revealed that the most of the identified proteins from the explants were mainly associated with the nucleic acid binding, oxidoreductase, transferase activity, protein binding and hydrolase activity. In addition, the proteomic feedback of tetraploid roots of P. grandiflorum may potentially be used to understand the characteristics of proteins and their functions.

• 한국약용작물학회지
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• 제26권5호
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• pp.362-369
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• 2018

Background: For stable induction of tetraploidy in Fallopia multiflora Haraldson, colchicine was treated to establish the condition of induction and investigated the morphological and cytogenetic traits of the tetraploid plants obtained compared to those of diploid ones. Methods and Results: For the induction of tetraploidy, F. multiflora plants were soaked in aqueous solutions of colchicine at various concentration (0.1, 0.5, and 1.0%). After this, 2% dimethyl sulfoxide (DMSO) was added at room temperature on a shaker set at 150 rpm for periods of 12, 24, and 48 h. The induction rate of tetraploids appeared to be the highest in plants treated with 0.5% colchicine for 24 h. As the colchicine concentration and soaking time increased above these levels, the growing tip of the roots did not develop and they began to rot. When compared to diploid plants, tetraploids differed greatly in various characteristics, including the sizes and shapes of the leaves, fruits, flowers and roots. The induced tetraploid F. multiflora had larger guard cells, and chloroplasts, increased number of chloroplast in the guard cells and decreased stomatal densities. Conclusions: When colchicine induced plants for tetraploid, it can be distinguished from diploids, in various characteristics such as morphological changes as stomatal size, number of chloroplasts per guard cell, number of chromosomes and flow cytometry. Therefore, it proved that these methods are suitable, quick and easy methods for the identification of the ploidy level of F. multiflora.

• Journal of Plant Biology
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• 제6권3호
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• pp.6-14
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• 1963

삼배체 및 사배체 호맥종자를 중성자 및 감마선에 조사해서 파종하고 발아과정, 지상부와 지하부의 성장, 건중량의 배가 등을 조사하였다. 특히 종자함수량이 방사선감수성에 대한 역할을 관찰하였다. 사배체호맥은 이배체의 그것 보다 속중성자의 조사에 대해서 지항성이 더 강했다. 지하부는 이부체호맥에 있어서는 1120 rads, 사배체에 있어서는 1400 rads 이하인데 지하부 보다 중성자조사에 대한 감수성이 높았다. 조사량이 낮을 때는 건중량성장이 촉진되는 효과가 있었다. 종자함수량이 낮을수록 방사선감수성이 배가했으나 함수량이 28%에 달했을 때 다시 회복되어서 높아졌다. 조사시 종자함수량이 23%를 초과하였을 때에는 6 K rads의 조사량에 있어서 지하부의 신장성장이 촉진되는 현상이 나타났고 지하부의 건중량성장과 조사시의 종자함수량과의 관계는 사배체 호맥 보다는 이배체호맥이 더 큰 영향을 받는다는 사질을 보았다. 지하부의 신장량의 반감을 초래하는 조사량단위를 기준으로 할 때 N/X의 effectiveness ratio는 이배체호맥에 있어서는 약 20.0 이였고 사배체호맥은 약 18.2 였다.

• 한국발생생물학회지:발생과생식
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• 제21권4호
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• pp.425-434
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• 2017

Polyploidy is occurred by the process of endomitosis or cell fusion and usually represent terminally differentiated stage. Their effects on the developmental process were mainly investigated in the amphibian and fishes, and only observed in some rodents as mammalian model. Recently, we have established tetraploidy somatic cell nuclear transfer-derived human embryonic stem cells (SCNT-hESCs) and examined whether it could be available as a research model for the polyploidy cells existed in the human tissues. Two tetraploid hESC lines were artificially acquired by reintroduction of remained 1st polar body during the establishment of SCNT-hESC using MII oocytes obtained from female donors and dermal fibroblasts (DFB) from a 35-year-old adult male. These tetraploid SCNT-hESC lines (CHA-NT1 and CHA-NT3) were identified by the cytogenetic genotyping (91, XXXY,-6, t[2:6] / 92,XXXY,-12,+20) and have shown of indefinite proliferation, but slow speed when compared to euploid SCNT-hESCs. Using the eight Short Tendem Repeat (STR) markers, it was confirmed that both CHA-NT1 and CHA-NT3 lines contain both nuclear and oocyte donor genotypes. These hESCs expressed pluripotency markers and their embryoid bodies (EB) also expressed markers of the three embryonic germ layers and formed teratoma after transplantation into immune deficient mice. This study showed that tetraploidy does not affect the activities of proliferation and differentiation in SCNT-hESC. Therefore, tetraploid hESC lines established after SCNT procedure could be differentiated into various types of cells and could be an useful model for the study of the polyploidy cells in the tissues.

• Asian-Australasian Journal of Animal Sciences
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• 제26권7호
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• pp.916-920
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• 2013

The triploid Pacific oyster, which is produced by mating tetraploid and diploid oysters, is favored by the aquaculture industry because of its better flavor and firmer texture, particularly during the summer. However, tetraploid oyster production is not feasible in all oysters; the development of tetraploid oysters is ongoing in some oyster species. Thus, a method for ploidy verification is necessary for this endeavor, in addition to ploidy verification in aquaculture farms and in the natural environment. In this study, a method for ploidy verification of triploid and diploid oysters was developed using multiplex polymerase chain reaction (PCR) panels containing primers for molecular microsatellite markers. Two microsatellite multiplex PCR panels consisting of three markers each were developed using previously developed microsatellite markers that were optimized for performance. Both panels were able to verify the ploidy levels of 30 triploid oysters with 100% accuracy, illustrating the utility of microsatellite markers as a tool for verifying the ploidy of individual oysters.

• 한국어류학회지
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• 제11권2호
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• pp.172-176
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• 1999

한국 동해안으로 유입하는 형산강, 영덕 오십천, 송천천, 죽산천에 서식하는 미꾸리과 Cobitidae의 한국 고유종인 동방종개 Iksookimia yongdokensis의 핵형을 조사하였다. 그 결과 염색체 수는 100이었고 44 meta-submetacentric, 56 subtelo-telocentric chromosome으로 FN은 144이었다. 이러한 사실로 보아 I. yondokensis는 cobitid fishes의 tetraploid species라고 생각된다.

• BMB Reports
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• 제39권5호
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• pp.607-617
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• 2006

A novel calcium-dependent protein kinase gene (designated as IiCPK2) was cloned from tetraploid Isatis indigotica. The full-length cDNA of IiCPK2 was 2585 bp long with an open reading frame (ORF) of 1878 bp encoding a polypeptide of 625 amino acid residues. The predicted IiCPK2 polypeptide included three domains: a kinase domain, a junction domain (or autoinhibitory region), and a C-terminal calmodulin-like domain (or calcium-binding domain), which presented a typical structure of plant CDPKs. Further analysis of IiCPK2 genomic DNA revealed that it contained 7 exons, 6 introns and the length of most exons was highly conserved. Semi-quantitative RT-PCR revealed that the expression of IiCPK2 in root, stem and leaf were much higher in tetraploid sample than that in diploid progenitor. Further expression analysis revealed that gibberellin ($GA_3$), NaCl and cold treatments could up-regulate the IiCPK2 transcription. All our findings suggest that IiCPK2 might participate in the cold, high salinity and GA3 responsive pathways.

• 한국작물학회:학술대회논문집
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• 한국작물학회 2017년도 9th Asian Crop Science Association conference
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• pp.75-75
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• 2017

Rye is cultivated on about 30,000ha domestically for forage and green-manure production in Korea. 'Daegokgreen' has been developed as a good quality rye cultivar for forage and green-manure, which was doubled-chromosome by colchicine treatment of diploid rye cultivar 'Gogu' in 2010. By the colchicine treatment with 0.05% for 12 hours at $2^{nd}$ leaf stage of 'Gogu', 31 tetraploid plants were obtained and they produced 2,470 seeds with 135 spikes. There was 4.4 in the number of spikes per plant, 18.3 in grain number per spike, and 37.6 g in the1,000-grain weight. The heading date of 'Daegokgreen' was April 11, which was two days later on average compared with 'Gogu'. The biomass (fresh weight) of 'Daegokgreen' was 3,701kg, which was similar to 'Gogu'. The average crude protein content of 'Daegokgreen' was 8.9%, which was 1.0% point higher than 'Gogu'. 'Daegokgreen' was found to be strong resistant to winter-kill and can be adapted to before maize cultivation.

• 한국산림과학회지
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• 제7권1호
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• pp.19-27
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• 1968

본(本) 실험(實驗)은 적자(積子) Colchicine 처리(處理)로 획득(獲得)된 10년생(年生) 4배체(倍體) 소나무에 대(對)하여 교잡(交雜)에 의(依)한 유용(有用)한 동이질배수체(同異質倍數體)를 육성(育成)한 목적(目的)으로 세포학적(細胞學的) 관찰(觀察)을 행(行)하는 동시(同時)에 그의 형태적(形態的) 생리적(生理的) 특성(特性)을 연구(硏究) 조사(調査)하여 다음과 같은 결과(結果)를 얻었다. 1. 유엽기부(幼葉基部) 염색체수(染色體數)는 대조목(對照木)은 2n=24 변이체(變異體)는 2n=48로 4배체(倍體)임을 확인(確認)하였다. 2. 침엽(針葉)의 착생밀도(着生密度)는 소(疎)하고 비후(肥厚)하다. 총합엽(總合葉)은 2%가량(可量) 발생(發生)하였다. 3. 침엽중앙부위(針葉中央部位)의 기공대수(氣孔帶數)는 개체(個體)에 따라 차(差)가 있으나 2배체(倍體)와 대차(大差)없고 공변세포(孔邊細胞)의 장경(長徑)은 36% 증대(增大)하고 있다. 4. 웅화(雄花)는 정상적(正常的)으로 발육(發育)하였으며 장경(長徑)의 크기는 2배체(倍體)와 별차(別差)없고 화분립(花粉粒) 크기는 약(約) 20% 증대(增大)하였다. 5. 화분(花粉)의 배양기상(培養基上)에서 발아율(發芽率)은 치상후(置床後) 17시간(時間)까지는 2배체(倍體)에 비(比)하여 증진(增進)하나 26시간후(時間後)에는 저하(低下)하였다. 연(然)이나 각(各) 치상시간별(置床時間別) 화분관(花粉管)의 최장관(最長管)의 길이는 2배체(倍體)보다 장(長)하게 발육(發育)하였다.

• Journal of Plant Biology
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• 제39권3호
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• pp.185-188
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• 1996

Randomly amplified polymorphic DNAs were employed to study the genetic variation and gene introgression in potato dihaploids (2n=24) which were generated after interspecific pollination of tetraploid cultivars (2n=4X=48, Solanum tuberosum cv Irish Cobbler, Superior and Dejima) by haploid inducer clones (2n=2X=24, Solanum phureja 1.22, Hes-5 and Hes-6). Genetic variation and DNA marker segregation among dihaploids were observed. Most dihaploids contain S. tuberosum specific RAPD markers but haploid inducer-specific RAPD markers were also found in some dihaploids. Of six different arbitrary 10-mer oligonucletide primers which showed polymorphism betwen tetraploid cultivars and haploid inducers used, three generated amplification products which seemed to be derived from the S. phureja parent. Our results indicate that chromosomes of dihaploids may not be pure S. tuberosum and the dihaploids may not be produced by parthenogenesis.