참진드기과(Ixodidae) 속하는 개피참진드기(Haemaphysalis flava)는 동남아시아에서 남아시아에 걸쳐 분포 하며, 다양한 질병을 매개하는 것으로 알려져 있다. 특히 중국, 일본, 한국에서 개피참진드기의 주요 매개 질병인 중증열성혈소판감소증후군(SFTS)의 감염 사례가 지속적으로 증가하는 것으로 보고되고 있다. 이 연구는 Illumina HiSeq 4000 시퀀싱을 통해 raw 데이터를 획득하고, Trinity를 기반으로 de novo assembly를 수행하여 unigene을 확보하였다. 이 결과, 총 69,822개의 unigene이 생성되었으며, 이 중 46,175개의 unigene이 PANM-DB에 annotation 되었다. 또한 KOG, GO 및 KEGG 분석을 통해 30,000개, 19,074개, 9,333개의 unigene이 annotation 되었 으며, InterProScan 결과를 통해 protein kinase, zinc finger (C2H2-type), reverse transcriptase, RNA recognition motif domain 등과 같은 세포 조절 메커니즘과 관련된 유전자가 확인되었다. RepeatMasker(v4.0.6)와 MISA(v1.0)를 사 용하여 unigene에서 SSR 마커를 확인한 결과, 총 3,480개의 SSR 마커가 확인되었으며 이 중 trinucleotide 반복이 1,907개, dinucleotide 반복이 1,274개로 확인되었다. 이러한 연구 결과는 H. flava 암컷의 유전자 및 유전자 조절 메커니즘을 이해하는데 기초 자료로서 활용 가능하며, 질병 전파 감수성에 대한 후속 연구에 유용한 정보를 제공 할 것으로 사료된다.

Sensory electrophysiological recording techniques such as EAG (electroantennogram), GCEAD (coupled gas chromatograph-electroantennogram detection) and SSR (single sensillum recording) have been useful in the chemical ecology studies of insects and plants. Numerous pheromones and other semiochemicals have been identified through GCEAD analysis, and the response profiles of antennae and individual olfactory receptor neurons have been characterized by using EAG and SSR techniques. In this talk, the practical aspects of these techniques are presented in detail. Standard setup and procedure of each electrophysiological recording technique, and important parameters and proper data analysis methods will be introduced as well as its applications. Common mistakes and limitations of these techniques will also be discussed.

The main purpose of this study was to examine the correlation between the consumption of red ginseng-based ‘SSR’ for 30 days and the reduction in human fatigue, blood component changes, and immune cell activity in 35 human subjects. ‘SSR’ is composed of zinc oxide, folic acid, and D-α-tocopherol with red ginseng as the main component. According to the protocol criteria of the study, 35 subjects who understood the purpose of the study and signed an informed consent form were selected. The fatigue survey was conducted through a questionnaire, and after taking ‘SSR', a decreased tendency of physical, mental, and neurosensory fatigue was observed. In hematological analysis, no significant changes were observed in the levels of WBC, RBC, and hemoglobin; however, AST (SGOT) and ALT (SGPT) levels were statistically significantly decreased. In immunological analysis, it was observed that the proliferative effect of T cells (CD3+CD4+) was greater than that of NK cells (CD16+CD56+). The collected data were subjected to t-test analysis using the SPSS 25.0 statistical program. The result from this study proposes that ‘SSR’ can be used as a functional food material as it reduces human fatigue and enhances immune function.

느타리 품종구분을 위한 마커의 개발을 위하여 곤지7호 의 어버이 일핵 균사중의 하나인 MT07156-97의 전체 유전자 염기서열을 바탕으로 제작한 251개의 SSR 프라이머를 제작하였다. 우선적으로 수한1호, 곤지7호, 흑타리 품종에 다형성 여부를 관찰하여 20개의 SSR을 선발하고, 이를 10개 품종에 적용하였다. 단일의 프라이머로는 일부 품종이 구분되지 않았으므로, 선발된 프라이머 간의 다양한 조합(multiplex 방식)을 적용한 결과 모든 품종을 판별 할 수 있는 분자마커 다형성을 보인 프라이머 "166+115" 조합을 선발하였다. 별도로 프라이머 115와 166가 만들어 낸 산술적인 유전자좌(loci) 31개보다 12개 많은 40개의 유전자좌가 증폭되어 다양한 품종에 특이적인 분자마커를 제공할 수 있었다. 개발된 분자마커는 종균의 품질관리, 품종의 판별, 신품종 보호에 활용될 수 있을 것이다.

본 연구에서는 유럽 양송이 자원들을 SSR marker를 통 해 유전적 다양성과 집단 구조, 유전적 분화에 대하여 분석하였다. 본 연구에서 유럽의 양송이 자원들은 유전적 거리기반의 4개의 그룹으로 나뉘었고 집단구조 분석을 통하여 2개의 subpopulation으로 이루어져 있었다. 본 연구에서 사용한 SSR 마커로 유럽의 양송이 자원들은 지리적 그리고 갓색으로 구분되지 않았다. 유전적 다양성은 유전적 거리기반의 그룹에서는 Group 4, 집단구조 분석을 통한 subpopulation에서는 Pop. 2의 다양성이 높았다. 그리고 양송이 자원들은 유전적 분화가 매우 낮았다. 본 연구의 결과는 차후 양송이의 육종 등에 이용 할 수 있을 것이다.

Electric of using in daily life is always exposed to risk of electrical fire and electric shock. Only degree of risk is different, there is no risk free electrical product. Generally, the higher voltage, the risk of electric shock is high. The much electric current, the risk of electrical fire is high. But, we can’t help using electric because of risk and we effort to reduce the risk of electrical fire and electric shock. This study deal with the fire prevention generated on heating equipment using SSR for current.

Microsatellite SSR markers were developed and utilized to reveal the genetic diversity of 32 strains of Flammulina velutipes collected in Korea, China, and Japan. From the SSR-enriched library, 490 white colonies were randomly selected and sequenced. Among the 490 sequenced clones, 85 (17.35%) were redundant. Among the remaining 405 unique clones, 201 (49.6%) contained microsatellite sequences. We used 12 primer pairs that produced reproducible polymorphic bands for four diverse strains, and these selected markers were further characterized in 32 Flammulina velutipes strains. A total of 34 alleles were detected using the 12 markers, with an average of 3.42 alleles, and the number of alleles ranged from two to seven per locus. The major allele frequency ranged from 0.42 (GB-FV-127) to 0.98 (GB-FV-166), and values for observed (HO) and expected (HE) heterozygosity ranged from 0.00 to 0.94 (mean = 0.18) and from 0.03 to 0.67 (mean = 0.32), respectively. SSR loci amplified with GB-FV-127 markers gave the highest polymorphism information content (PIC) of 0.61 and mean allele number of five, whereas for loci amplified with GB-FV-166 markers these values were the lowest, namely 0.03 and two. The mean PIC value (0.29) observed in the present study with average number of alleles (3.42). The genetic relationships among the 32 Flammulina velutipes strains on the basis of SSR data were investigated by UPGMA cluster analysis. In conclusion, we succeeded in developing 12 polymorphic SSRs markers from an SSR-enriched library of Flammulina velutipes. These SSRs are presently being used for phylogenetic analysis and evaluation of genetic variations. In future, these SSR markers will be used in clarifying taxonomic relationships among the Flammulina velutipes.

Microsatellite SSR markers were developed and utilized to reveal the genetic diversity of 32 strains of Flammulina velutipes collected in Korea, China, and Japan. From SSR-enriched library, 490 white colonies were randomly selected and sequenced. In the 490 sequenced clones, 85 clones (17.35%) were redundant. Among the remaining 405 unique clones, 201 clones (49.6%) contained microsatellite sequences. As a result, 12 primer pairs produced reproducible polymorphic bands within diverse 4 strains and these selected markers were further characterized in 32 Flammulina velutipes strains. A total of 34 alleles were detected using the 12 markers, with an average of 3.42 alleles and the number of alleles ranged from two to seven per locus. The major allele frequency ranged from 0.42 (GB-FV-127) to 0.98 (GB-FV-166), and values for observed (HO) and expected (HE) heterozygosity ranged from 0.00 to 0.94 (mean = 0.18) and from 0.03 to 0.67 (mean = 0.32), respectively. SSR loci amplified with GB-FV-127 markers gave the highest polymorphism information content (PIC) of 0.61 and mean allele number of five, while for loci amplified with GB-FV-166 markers these values were the lowest, namely 0.03 and two. The mean PIC value (0.29) observed in the present study with average number of alleles (3.42). The genetic relationships among 32 Flammulina velutipes strains based on SSR data were generated by UPGMA cluster analysis. In conclusion, we succeeded in developing 12 polymorphic SSRs markers from SSR-enriched library of Flammulina velutipes. These SSRs are presently being used for phylogenic analysis and evaluation of genetic variations. In future, these SSR markers will be used in clarifying taxonomic relationships among the Flammulina velutipes.

Electric of using in daily life is always exposed to risk of electrical fire and electric shock. Only degree of risk is different, there is no risk free electrical product. Generally, the higher voltage, the risk of electric shock is high. The much electric current, the risk of electrical fire is high. But, we can’t help using electric because of risk and we effort to reduce the risk of electrical fire and electric shock. This study deal with the fire prevention generated on heating equipment using SSR for current

Sesame is queen of oil seed crops and widely cultivated in Asia and Africa. The aim of this study was to develop a mini sub core set representing the diverse germplasm of sesame and to assess the genetic diversity, population structure and phylogenetic relationship of the resulted sub core set to be used in whole genome resequencing platform. One hundred twelve accessions out of 277 accessions were selected by the PowerCore program. A total of 155 alleles were captured from the 158 alleles detected in the primary core population, and rare alleles and specific alleles were also maintained in the sub core set accessions representing almost 100% of the primary core population. Among the sub core set accessions, four sub populations were observed with some admixture accessions. Although the genetic diversity of Pop-1 which includes most accessions from Korea is relatively lower than that of other three sub populations, it can maintain maximum number of accessions in the sub core set with the same percentage as in the primary core set probably because of the specific features of these accessions. Based on this framework of genetically defined populations, the effective use and conservation management of Sesamum indicum for crop improvement might be possible.

본 연구는 효율적인 자원보존과 유전자원의 작물육종 활용 성 제고를 위한 기초정보제공을 목적으로, 29개 SSR marker 를 이용하여 아시아지역의 10개 국가에서 수집된 벼 유전자원 에 대해 유전적 다양성 및 집단 구조 분석을 수행하였다. 1. 총 85점의 벼 유전자원이 수집되었으며, 29개 SSR 마커 에 의해 증폭된 allele 수는 총 342개 였다. Allele 수는 2 개에서 28개 범위로 나타났으며, 마커당 평균 allele 수는 11.8 개 였다. 유전적 다양성을 나타내는 genetic diversity와 PIC 값의 범위는 각각 0.12-0.93과 0.11-0.93으로 나타났고, 평균은 각각 0.73과 0.71로 나타났다. 2. 국가별 벼 자원의 유전적 거리를 기초로 유연관계를 분 석한 결과 2개 그룹으로 구분되었다. BⅠ 그룹에는 남아시아 지역에 속하는 스리랑카, 인도, 방글라데시, 파키스탄이 포함 되었고, BII 그룹에는 라오스를 제외한 동남아시아 지역인 미 얀마, 부탄, 베트남, 필리핀, 태국이 포함되었다. 3. 수집 국가별 마커당 평균 allele 수는 미얀마가 1.28개로 가장 낮았고, 필리핀이 7.03개로 가장 높았으며, PIC 값 역시 필리핀이 0.64로 가장 높은 값을 보였고, 미얀마는 가장 낮은 0.15로 관찰됐다. 4. 유전적 거리와 Structure ver2.2를 이용하여 집단의 구조 를 분석한 결과, 75%의 확률에서 85개 자원 중 80개 자원 (64.1%)는 3개의 subpopulation으로 나눌 수 있었으며, 5개 자원(5.9%)은 유전적으로 혼입된 형태를 나타냈다. 5. 각각의 subpopulation은 수집 국가의 특성과 일치하지 않 았으며, 대부분 자원은 각각의 subpopulation에 불규칙적으로 분포되었다.

Pleurotus eryngii, an edible white-rot fungus, is widespread in Eurasia and northern Africa. It has become a major cultivated mushroom in Asia, with a current global production rate of approximately 3 × 10 5 metrictons/yr. To improve the quality or productivity through breeding, a genetic linkage map is an important component. In this study, genetic linkage map of the P. eryngii was constructed using 98 monokaryotic progeny derived from dikaryon of parental KNR2312 strain derived from haploid meiotic spores. The whole genome sequence of P5 monokaryon from P. eryngii KNR2312 strain by Next Generation Sequencing (NGS) strategy was used to design the SSR markers. 484 primers pairs were identified by SSR Locator I and tested polymorphism via PCR. A total of 241 loci were mapped using Joinmap 4.0, comprising 222 SSR markers, 2 mating type factors, and the 13 INDEL markers. The map consisted of 14 linkage groups spanning 1003 cM at an average marker interval of 4.2 cM. The mating loci, A and B were mapped on linkage groups 4 and 11, respectively. The established linkage map and the genetic information based on NGS could be used for QTL mapping of agronomic traits, marker-assisted breeding that may ultimately lead to outstanding phenotypic characteristics. [Supported by a grant from the IPET (213003-04-3-SBY20), MIFAFF, Republic of Korea.]

Differentiation of Pleurotus eryngii is laborious and time-consuming tasks especially in mycelial status. For development of a method for differentiation of P. eryngii cultivars, simple sequence repeats (SSR) from whole genomic DNA sequence analysis was used for genotyping and two multiplex-SSR primer sets were developed. These SSR primer sets were employed to distinguish 12 cultivars and strains. Five polymorphic markers were selected based on the genotypes. PCR with the each primer produced one to four distinct bands ranging in size from 200 to 300 bp. Polymorphism information content (PIC) values of the five markers were in range of 0.6627 to 0.6848 with an average of 0.6775. Unweighted pair-group method with arithmetic mean clustering analysis based on genetic distances using five SSR markers classified 12 cultivars into 2 clusters. Cluster I and II comprised of 4 and 8 cultivars, respectively. Two multiplex sets, Multi-1 (SSR312 and SSR366) and Multi-2 (SSR178 and SSR277) completely discriminated 12 cultivar and strains with 21 allele with a PIC value of 0.9090. These results might be useful to provide an efficient method for the identification of P. eryngii cultivars with separate PCR reactions. (This work was supported by a grant from the Gold Seed Project [Supported by a grant from the IPET (213003-04-3-WTI11), MIFAFF, Republic of Korea.]