• 식물분류학회지
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• 제52권4호
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• pp.262-268
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• 2022

The complete chloroplast genome (cp genome) sequence of Clematis calcicola J. S. Kim (Ranunculaceae) is 159,655 bp in length. It consists of large (79,451 bp) and small (18,126 bp) single-copy regions and a pair of identical inverted repeats (31,039 bp). The genome contains 92 protein-coding genes, 36 transfer RNA genes, eight ribosomal RNA genes, and two pseudogenes. A phylogenetic analysis based on the cp genome of 19 taxa showed high similarity between our cp genome and data published for C. calcicola, which is recognized as a species endemic to the Korean Peninsula. The complete cp genome sequence of C. calcicola reported here provides important information for future phylogenetic and evolutionary studies of Ranunculaceae.

• Molecules and Cells
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• 제24권1호
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• pp.60-68
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• 2007

Microsatellites, also called simple sequence repeats (SSR), are very useful molecular genetic markers commonly used in crop breeding, species identification and linkage analysis. In the present study, we constructed a microsatellite-enriched genomic library of Panax ginseng, and identified 251 novel microsatellite sequences. Tri-nt repeat units were the most abundant (46.6%), followed by di-nt repeats (35.5%). The $(AG)_n$ motif was most common (23.1%), followed by the $(AAC)_n$ motif (22.3%). From the genotyping of 94 microsatellites using marker-specific primer sets, we identified 11 intraspecific polymorphic markers as well as 14 possible interspecific polymorphic markers differing between P. ginseng and P. quinquefolius. The exact allele structures of the polymorphic markers were determined and the alleles were named. This study represents the first report of the bulk isolation of microsatellites by screening a microsatellite-enriched genomic library in P. ginseng. The microsatellite markers could be useful for linkage analysis, genetic breeding and authentication of Panax species.

• 원예과학기술지
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• 제30권3호
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• pp.278-285
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• 2012

춘란(Cymbidium goeringii)은 동북아시아에서 난류중에서 가장 잘 알려진 중요한 종이다. 본 연구에서는 8개의 simple sequence repeats(SSR) 마커(CG409, CG415, CG709, CG722,CG787, CG1023, CG1210, and CG1281)를 동시증폭할 수 있는 multiplex PCR 시스템을 개발하여, 춘란의 40품종에 대한 유전자형을 분석하하는데 활용하였다. 품종은 모든 품종은 서로 다른 복합 유전자형을 가졌으며, 개체간 평균 복합식별력은 $7.14{\times}10^{-10}$로 매우 높게 나타났다. 관찰 이형접합도(Ho = 0.466)는 한국 내 야생집단과 유사한 값(동해안: 0.438, 서해안: 0.583)을 보였는데, 이 사실은 각 품종이 원래 야생에서 채집되어 품종으로 등록된 후 영양번식을 통해 번식을 하면서 유전적 본질이 변형되지 않았음을 의미한다. 본 연구에서 아울러 확립한 8개의 SSR 마커의 복합 유전자형을 이용하여 SSR DNA ID를 2차원 바코드로 표현하는 프로그램을 개발하였다. 복합 유전자형을 사용하여 개발된 개체별 고유 DNA ID의 개체 식별력은 통계적으로 99.999999% 이상이 되므로 높은 정확도로 개체간 구분이 가능해진다. 본 연구에서 개발한 SSR DNA ID와 2차원 바코드는 춘란 품종간 식별, 유지 등에 유용하게 활용될 수 있을 것이다.

• Journal of Plant Biotechnology
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• 제7권1호
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• pp.17-25
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• 2005

We have mined each of the five A. thaliana chromosomes for the presence of simple sequence repeats (SSRs) and developed custom perl scripts to examine their distribution and abundance in relation to genomic position, local G/C content and location within and around transcribed sequences. The distribution of repeats and G/C content with respect to genomic regions (exons, UTRs, introns, intergenic regions and proximity to expressed genes) are shown. SSRs show a non-random distribution across the genome and a strong association within and around transcribed sequences, while G/C density is associated specifically with the coding portions of transcribed sequences. SSR motif repeat number shows a high degree of variation for each SSR type and a high degree of motif sequence bias reflecting local genome sequence composition. PCR primers suitable for the amplification of identified SSRs have been designed where possible, and are available for further studies.

• Journal of Microbiology and Biotechnology
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• 제34권9호
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• pp.1848-1856
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• 2024

Chlorella sorokiniana green microalga offers many environmentally friendly applications, including wastewater treatment, biofertilizers, animal feed, and biofuel production. Different strains of C. sorokiniana have unique properties that may suit one application but not another. There is a need to distinguish between the many available strains of C. sorokiniana to choose the one that best fits the application. Consequently, our research goal was to develop strain-specific simple sequence repeat (SSR) markers to differentiate between the different strains. Seventeen markers spanning ten out of the twelve chromosomes of the C. sorokiniana genome were developed and validated on eight different strains from culture collections and our lab, and were then analyzed by fragment analysis. The results demonstrate the potential of these polymorphic markers to detect the genetic differences between the strains of C. sorokiniana, and to serve as useful tools for the intra-species population genetic analysis and conservation genetics studies of C. sorokiniana.

• 한국버섯학회지
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• 제14권4호
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• pp.174-178
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• 2016

SSR은 병렬적으로 반복되는 작은 DNA서열을 말하며, 다양한 마커 기반 연구에 활용되고 있다. 국내의 주요 느타리품종인 '흑타리'와 '미소'의 유전체를 Pacbio를 이용하여 해독하였고 이 서열 정보에서 생물정보학을 이용하여 SSR을 분리하여 특성구명을 하였다. '흑타리'와 '미소' 유래 단핵균사의 유전체의 크기는 각각 40.8 Mbp와 40.3 Mbp로 밝혀졌고, 이는 사철느타리의 단핵균사 PC9과 PC15보다 컸으나, 큰느타리보다는 작았다. 총 949개와 968개의 SSR이 '흑타리'와 '미소'의 유전체 분석을 통하여 각각 검출되었다. 5개의 느타리류 유전체의 SSR 분포와 특징을 비교분석한 결과 흑타리와 미소의 SSR 갯수가 가장 많았으며, 이들의 반복서열의 분포는 다른 느타리류와 비슷한 경향을 보였다. 3-mers, 6-mers와 8-mers가 가장 발견빈도가 높은 패턴이었다.

• Molecules and Cells
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• 제39권2호
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• pp.141-148
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• 2016

Oriental melon (Cucumis melo L. var. makuwa) is one of six subspecies of melon and is cultivated widely in East Asia, including China, Japan, and Korea. Although oriental melon is economically valuable in Asia and is genetically distinct from other subspecies, few reports of genome-scale research on oriental melon have been published. We generated 30.5 and 36.8 Gb of raw RNA sequence data from the female and male flowers, leaves, roots, and fruit of two oriental melon varieties, Korean landrace (KM) and Breeding line of NongWoo Bio Co. (NW), respectively. From the raw reads, 64,998 transcripts from KM and 100,234 transcripts from NW were de novo assembled. The assembled transcripts were used to identify molecular markers (e.g., single-nucleotide polymorphisms and simple sequence repeats), detect tissue-specific expressed genes, and construct a genetic linkage map. In total, 234 single-nucleotide polymorphisms and 25 simple sequence repeats were screened from 7,871 and 8,052 candidates, respectively, between the KM and NW varieties and used for construction of a genetic map with 94 F2 population specimens. The genetic linkage map consisted of 12 linkage groups, and 248 markers were assigned. These transcriptome and molecular marker data provide information useful for molecular breeding of oriental melon and further comparative studies of the Cucurbitaceae family.

• Molecules and Cells
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• 제23권3호
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• pp.349-356
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• 2007

Simple Sequence Repeats (SSRs) represent short tandem duplications found within all eukaryotic organisms. To examine the distribution of SSRs in the genome of Brassica rapa ssp. pekinensis, SSRs from different genomic regions representing 17.7 Mb of genomic sequence were surveyed. SSRs appear more abundant in non-coding regions (86.6%) than in coding regions (13.4%). Comparison of SSR densities in different genomic regions demonstrated that SSR density was greatest within the 5'-flanking regions of the predicted genes. The proportion of different repeat motifs varied between genomic regions, with trinucleotide SSRs more prevalent in predicted coding regions, reflecting the codon structure in these regions. SSRs were also preferentially associated with gene-rich regions, with peri-centromeric heterochromatin SSRs mostly associated with retrotransposons. These results indicate that the distribution of SSRs in the genome is non-random. Comparison of SSR abundance between B. rapa and the closely related species Arabidopsis thaliana suggests a greater abundance of SSRs in B. rapa, which may be due to the proposed genome triplication. Our results provide a comprehensive view of SSR genomic distribution and evolution in Brassica for comparison with the sequenced genomes of A. thaliana and Oryza sativa.

• 한국환경생태학회:학술대회논문집
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• 한국환경생태학회 2006년도 정기총회 및 학술논문발표회
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• pp.157-161
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• 2006

• 한국약용작물학회:학술대회논문집
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• 한국약용작물학회 2012년도 심포지엄 및 춘계학술발표회
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• pp.329-330
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• 2012