Chrysanthemum is one of the most popular and economically important ornamental plants due to its huge diversity in growing habits, wide range of colors, and different patterns of flower. In the present study, we conducted the karyotype analysis in four naturally occurring genotypes of Chrysanthemum boreale. Karyotype studies based on the fluorescence in situ hybridization (FISH) using 5S and 45S rDNAs. Four chrysanthemum genoteyps showed an aneuploid chromosome number of 2n=18+2 (111016 and 111021) or a diploid of 2n=18 (121001 and 121002). All the genoteyps had the same karyotype formula of 14 metacentrics and 4 submetacentrics. In 111016, the chromosome length during somatic metaphase ranged from 3.11 ± 0.26 μm (shortest) to 3.94 ± 0.20 μm (longest), with a total length of 32.94 μm. The chromosome length at the mitotic metaphase ranged from 3.11 to 6.46 μm, with a total length of 32.94 μm in 111016 and 51.05, 32.81, and 46.00 μm in 111021, 121001, and 121002, respectively. The 5S rDNA and 45S rDNA signals recorded different in all four wildly grown genotypes of C. boreale. This information can be useful in cultivar improvement, as well as in elucidation of the evolution of the chrysanthemum.

본 연구에서는 와인제조에 있어 향미 증진과 같은 품질 향상에 도움이 된다고 알려진Pichia anomala JK04와 일반 적으로 와인 양조에 주로 이용되고 있는 Saccharomyces cerevisiae Fermivin을 혼합 발효하여 감와인의 발효 특성을 비교하였다. 감와인의 발효특성 결과 발효 종료 시 대부분 의 실험구에서 pH 4.0~4.2, 총산 0.5~0.6%를 나타내었다. 당도와 환원당 함량 변화는 발효가 진행될수록 점차 감소하 여 S. cerevisiae Fermivin 단독 발효구와 P. anomala JK04 혼합 첨가 발효구에서 발효 종료시점에서 대부분의 당이 소비되었다. 최종 알코올 함량은S. cerevisiae Fermivin 단독 발효구와S. cerevisiae Fermivin과P. anomala JK04의 혼합 첨가 발효구에서 알코올 생성이 빨랐으며 발효 종료 시 모든 구의 알코올 농도는 12~13%를 나타내었다. 각 첨가구 의 총 페놀성 화합물 함량은 0.05 mg/mL 로 초기 페놀성 화합물 함량과 비슷한 수준을 유지하였다. 감와인의 hue value는 발효 초기에 비해 증가하여 4~5의 값을 나타내었 고, intensity value는 발효초기 0.5의 값에서 점차 감소하여 발효 종료 시까지 0.1~0.2의 값을 유지하였으며 휘발성 향 기성분의 경우 P. anomala JK04의 첨가 비율이 높을수록 S. cerevisiae Fermivin 단독발효구 보다 다양한 알코올류, 에스테르류가 생성되었다. 관능검사 결과에서 향기와 맛의 평가에서P. anomala JK04를 첨가한 모든 혼합 발효구에서 S. cerevisiae Fermivin 단독발효구 보다 높은 점수를 얻었다.

While a wealth of genetic diversity can be found from traditional rice varieties, wild rice species and wild relatives of rice, transfer of useful genes to modern varieties are often hampered by linkage drag. In this study, the previously identified blast resistance locus Pi45(t) from a cross between ‘Ilpumbyeo’ and ‘Moroberekan’ was showed to be linked with the spreading-type panicle caused by the SPR3 locus. Using InDel4 and RM17579 linked to the Pi45(t) and the SPR3, respectively, the distance between the two loci was estimated to be 6.9cM. This suggests a tight, yet incomplete linkage and provides the opportunity to utilize Pi45(t) in breeding programs without including SPR3. Two groups based on the genotype at the SPR3 locus were assembled; the CLosed Panicle (CLP) and SPReading panicle (SPR) groups with lines, which were homozygous for the Ilpumbyeo and Moroberekan alleles, respectively. A comparison between the traits of CLP and SPR groups revealed a decrease in 1000-grain weight and length and an increase in spikelets per panicle and secondary branches in the SPR group. This complicates selection against SPR3 as it is not clear whether these quantitative trait loci are linked to either SPR3 or Pi45(t). Re-evaluation of these traits using lines recombinant at the two loci would be necessary to clarify this issue.

We have identified ATTIRTA1 transposon, a kind of mariner-type DNA transposon from Brassica rapa genome. A total of 811 inverted-terminal repeat, ITR consisting of the both terminal on ATTIRTA1 transposon were found from B. rapa v1.1 sequence. Among them 616 ITR were paired by two in each transposon, indicating three quarters of the transposon exists in original form. Around 10 percentage of the transposon, 82 ITR was located in gene, expecially only in intron. Using these ATTRRTA1, we developed a display system modified from AFLP technique and applied for this system to analyze genetic diversity of Korea Brassica rapa core collection. The collection includes 220 accessions representing the different morphotypes and geographical origin. The analysis of population structure revealed five subgroups and the clustering patterns matched well with their morphological traits. ATTIRTA1 transposon display seems useful marker system for studying genetic relationships. Presently we have profiled the components and contents of glucosinolate in the core collection to analyze genome wide association. This collection will be helpful to identify agriculturally desirable traits from other supspecies.

Heading date in rice is a complex trait that is governed by multiple genes and environmental factors, such as day-length, temperature, and soil conditions. The genetic studies using DNA markers have facilitated the genetic dissection of heading date and many quantitative trait loci (QTLs) for heading date have been identified using several mapping population. In a previous study, a new quantitative trait loci (QTLs) for heading date have been identified using several mapping population. In a previous study, a new for heading date was detected near SSR marker RM215 on chromosome 9 using an advanced backcross line, WH29001, developed by introgressing chromosomal segments from an accession of Oryzaminuta (2n=48, BBCC, Acc. No.101141)into the O. sativa subsp. japonica cv. Hwaseongbyeo. The O. minuta allele of QTL contributed to an increase in heading date. To clarify whether dth9 could be dissected genetically, a high-resolution linkage mapping of dth9 was performed using alarge F2 population derived form the cross between one F4 plant which was homozygous for O.minuta in the target region RM5661-RM215 on chromosome9 and Hwaseongbyeo. Days to heading in the F2 population showed continuous variation rang form 102 to 113 days. The dth9 QTL further narrowed down at the interval between the SSR marker RM1553 and RM215 which was approximately 403kb in length based on the physical map of the region. The QTL for heading date(dth9) had not been detected in previous QTL studies between Oryza cultivars, indicating the existence of potentially novel alleles from O. minuta.

Genetic diversity of 31 rice varieties including 25 japonica and 6 indica varieties was evaluated using a combination of 19 microsatellite or simple sequence repeats (SSRs) and 28 random decamer oligonucle-otide primers. All 19 microsatellite primer sets representing 19 loci in the rice genome showed polymorphisms among the 31 varieties and revealed 91 alleles with an average of 4.80 bands per primer. Also all 28 random decamer primers used were informative and generated 114 non-redundant bands with a mean of 4.07 bands. Microsatellite markers detected higher number of alleles than random primers .although the mean difference was not statistically significant. A cluster analysis based on Nei＇s genetic distances calculated from the 205 bands resolved the 31 varieties into two major groups that correspond to indica and japonica subspecies, which is consistent with the genealogical information. As few as six random decamer primers or a combination of one microsatellite and four random decamer primers were sufficient to uniquely differentiate all 31 varieties. These combinations would be potentially useful in rice variety protection and identification considering that 25 out of 31 varieties used in this study are japonica rices with high grain quality and have close make up.