• 제목/요약/키워드: ISSR markers

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Inter Simple Sequence Repeat (ISSR) Polymorphism and Its Application in Mulberry Genome Analysis

  • Vijayan Kunjupillai
    • International Journal of Industrial Entomology and Biomaterials
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    • 제10권2호
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    • pp.79-86
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    • 2005
  • Molecular markers have increasingly been used in plant genetic analysis, due to their obvious advantages over conventional phenotypic markers, as they are highly polymorphic, more in number, stable across different developmental stages, neutral to selection and least influenced by environmental factors. Among the PCR based marker techniques, ISSR is one of the simplest and widely used techniques, which involves amplification of DNA segment present at an amplifiable distance in between two identical microsatellite repeat regions oriented in opposite direction. Though ISSR markers are dominant like RAPD, they are more stable and reproducible. Because of these properties ISSR markers have recently been found using extensively for finger printing, pohylogenetic analysis, population structure analysis, varietal/line identification, genetic mapping, marker-assisted selection, etc. In mulberry (Morus spp.), ISSR markers were used for analyzing phylogenetic relationship among cultivated varieties, between tropical and temperate mulberry, for solving the vexed problem of identifying taxonomic positions of genotypes, for identifying markers associated with leaf yield attributing characters. As ISSR markers are one of the cheapest and easiest marker systems with high efficiency in generating polymorphism among closely related varieties, they would play a major role in mulberry genome analysis in the future.

Evaluation of ISSR and RAPD Markers for the Detection of Genetic Diversity in Mulberry (Morus spp.)

  • Venkateswarlu, M.;Nath, B.Surendra;Saratchandra, B.;Urs, S.Raje
    • International Journal of Industrial Entomology and Biomaterials
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    • 제9권2호
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    • pp.207-215
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    • 2004
  • The present study was carried out to evaluate the ISSR and RAPD markers for their efficiency as genetic marker systems to establish the relationships between 18 mulberry genotypes. A total of 36 from 56 (64%) RAPD primers and 12 from 48 (25%) ISSR primers produced reproducible amplification patterns. A high proportion of polymorphic bands ranging from 44 to 91% was observed respectively with RAPD and ISSR markers. The average Resolving Power (Rp) of ISSR primers was higher than RAPD primers. The ISSR primers, UBC 825, 868 and 873, and RAPD primers, UBC 712, 720 and 729, possessed the highest Rp values and could in each instance distinguish all the 18 genotypes. Similarity matrix values were estimated based on Jaccards coefficient, considering 109 polymorphic ISSR and 212 polymorphic RAPD bands and two dendrograms were constructed. The dendrograms obtained with ISSR and RAPD markers distinguished the eight exotic genotypes from the ten indigenous (Indian) genotypes. A significant correlation value (r=0.959; p=0.001) for the cophenetic matrix between the RAPD and ISSR matrices was observed. The results indicated that the ISSR and RAPD markers could assist in the differentiation of genotypes and permit the determination of genetic distances that might be exploited by mulberry breeders in improvement programs.

양송이 품종과 수집 균주간의 Inter-simple sequence repeat (ISSR) 마커 분석 (Analysis of Inter-simple sequence repeat (ISSR) markers in cultivars and collected strains of button mushroom (Agaricus bisporus))

  • 남윤걸;공원식;장갑열;신평균;오민지;임지훈;구창덕;오연이
    • 한국버섯학회지
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    • 제15권3호
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    • pp.139-144
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    • 2017
  • 양송이(Agaricus bisporus)는 국내에서 2015년 약 10,757톤이 생산되어 5번째로 많이 생산되는 버섯이다. 본 연구에서는 ISSR 마커를 사용하여 국내 수집균주와 상업품종간의 유전적 다양성을 분석하였다. 이를 위해 우선, 다양한 마커 중 양송이 속 내 비교 분석이 가능다고 알려진 ISSR마커를 선발하였다. 분석한 마커는 ISSR 807, 808, 809, 810, 811, 834, 835, 836, 841, 842, P3, P8, P17, P22, P30, P38 and P39 총 16종이였고 이들 중 육종에서 모본선발을 위한 효율적인 마커를 선발하기 위하여 양송이 수집균주 ASI 1110, 1114, 1115, 1238, 1246, 1365, 1366, 1369 등 8종을 선발하여 수행하였다. 그 결과 ISSR P31, P38, P39 마커에서 종내 구분이 가능한 다양한 밴드가 나타났다. 이를 바탕으로 선발된 3종의 마커를 이용하여 국내 수집균주와 새아, 새연 등의 상업품종이 포함된 39균주를 UPGMA 프로그램을 통하여 유연관계를 분석하였다. 국내 수집균주와 상업품종간의 계통도를 분석한 결과, 국내 수집균주와 상업품종들이 다른 그룹을 형성하는 것을 확인하였다. 이 결과를 근거로 ISSR P31, P38, P39가 상업품종을 구분할 수 있는 마커로 활용될 것이라 기대된다.

Analysis of the Genetic Relationship among Mulberry (Morus spp.) Cultivars Using Inter-Simple Sequence Repeat (ISSR) Markers

  • Park, Eun-Ju;Kang, Min-Uk;Choi, Myoung-Seob;Sung, Gyoo-Byung;Nho, Si-Kab
    • International Journal of Industrial Entomology and Biomaterials
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    • 제41권2호
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    • pp.56-62
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    • 2020
  • Mulberry (Morus spp. family: Moraceae) has prime importance in the sericulture industry, and its foliage is the only natural feed of the silkworm Bombyx mori L. Traditional classification methods using morphological traits were largely unsuccessful in assessing the diversity and relationships among different mulberry species because of environmental influences on the traits of interest. For these reasons, it is difficult to differentiate between the varieties and cultivars of Morus spp. In the present study, inter-simple sequence repeat (ISSR) markers were used to investigate the genetic diversity of 48 mulberry samples genotyped using nine ISSR primers. The ISSR markers exhibited polymorphisms (53.2%) among mulberry genotypes. Furthermore, similarity coefficient estimated for these ISSR markers was found to vary between 0.67 and 0.99 for the combined pooled data. The phenogram drawn using the UPGMA cluster method based on combined pooled data of the ISSR markers divided the 48 mulberry genotypes into seven major groups. No genetic association was found in the collection area, and there was a mixed pattern between the mulberry lines. The hybridization between different mulberry species is highly likely to be homogenized due to natural hybridization.

Efficiency of RAPD and ISSR Markers in Differentiation of Homo- and Heterokaryotic Protoclones of Agaricus bisporus

  • Mahmudul, Islam Nazrul;Bian, Yin-Bing
    • Journal of Microbiology and Biotechnology
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    • 제20권4호
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    • pp.683-692
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    • 2010
  • Morphologically, nine different slow-growing protoclones were screened from regenerated protoplasts of heterokaryotic Agaricus bisporus. As such, the present study is the first report on differentiating homo- and heterokaryotic protoclones using random amplified polymorphic DNA (RAPD) and inter-simple sequence repeat (ISSR) markers. Among 80 primers tested, the seven ISSR and seven RAPD primers selected for the analysis generated a total of 94 ISSR and 52 RAPD fragments, respectively. The ISSR fingerprinting also detected more polymorphic loci (38.29%) than the RAPD fingerprinting (34.61%). A principal coordinate analysis (PCA) was employed to evaluate the resolving power of the markers as regards differentiating protoclones. As a result, the mean polymorphism information content (PIC) for each marker system (i.e., 0.787 for RAPD and 0.916 for ISSR) suggested that ISSR is more effective for determining polymorphisms. The dendrograms constructed using RAPD, ISSR, and an integrated RAPD and ISSR marker system were highly correlated with one another as revealed by a high Mantel correlation (r= 0.98). The pairwise similarity index values also ranged from 0.64 to 0.95 (RAPD), 0.67 to 0.98 (ISSR), and 0.67 to 0.98 (RAPD and ISSR), whereas the mean similarity index values of 0.82, 0.81, and 0.84 were obtained for the RAPD, ISSR, and combined data, respectively. As there was a good correspondence between the RAPD and ISSR similarity matrices, ISSR would appear to be an effective alternative to RAPD in the genetic diversity assessment and accurate differentiation of homo- and heterokaryotic protoclones of A. bisporus.

Genetic Variability Within and Among Three Ecoraces of the Tasar Silkworm Antheraea mylitta Drury, as Revealed by ISSR and RAPD Markers

  • Vijayan K.;Nair C. V.;Kar P. K.;Mohandas T. P.;Saratchandra B.;Urs S. Raje
    • International Journal of Industrial Entomology and Biomaterials
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    • 제10권1호
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    • pp.51-59
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    • 2005
  • Genetic diversity within and between populations of Antheraea mylitta Drury was studied using thirty individuals from three ecoraces using 12 ISSR and 10 RAPD primers. Rally, Daba and Modal ecoraces were collected from Chattisgarh, Jharkhand and Orissa states of India respectively. The ISSR and RAPD primers generated $94.7\%$ and $95.6\%$ polymorphism among the 30 individuals. The cluster analysis grouped these individuals according to their ecorace. The intra-ecoracial heterozygosity estimated with ISSR markers were $0.123{\pm}0.18,\;0.169{\pm}0.17\;and\;0.214{\pm}0.17$ respectively for Modal, Raily and Daba ecoraces. Like wise, with RAPD markers the intraecoracial heterozygosity was $0.17{\pm}0.22$ in Modal, $0.229{\pm}0.17$ in Raily and $0.23{\pm}0.19$ in Daba ecoraces. However, the significantly low genetic differentiation (GST) (0.182 for ISSR and 0.161 for RAPD) and the high gene flow (Nm) (2.249 for ISSR and 2.60 for RAPD markers) among the ecoraces revealed that the amount of genetic diversity present among the ecoraces is not significant enough to make drastic genetic drifts among these ecoraces in the near future.

ISSR 마커를 이용한 달래와 산달래의 분류 (Classification of Allium monanthum and A. grai by ISSR Markers)

  • 이샛별;김창길;오중열;김경민
    • 원예과학기술지
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    • 제29권6호
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    • pp.600-609
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    • 2011
  • Allium속에 포함된 6종의 122점을 수집하고, 이 종들의 유전적 관계는 ISSR 마커를 이용하여 확인하였다. 형태적 분석은 6개의 양적 형질을 측정하고 1개의 질적 형질은 수치화하였다. SSR 분석은 17개의 primer를 사용하여 총 370개의 다형성 밴드를 얻었다. 형태적 특성 분석은 유전적 거리로 구분할 경우 3개의 그룹으로 분류되었으나, 부분적으로 몇 몇 종들은 분류에 어려움이 있었다. ISSR 결과를 바탕으로 Allium 속의 군집분석은 5개의 그룹으로 분리되었다. 형태적 분석과 SSR분석 간의 상관 관계는 유의성이 매우 낮았다(r = 0.036). 따라서 본 연구에서 개발한 ISSR 마커는 달래와 산달래의 분류와 교배 육종에 유용하게 이용될 수 있을 것이다.

SSR을 이용한 꽃치자와 열매치자의 유전적 관계 (Genetic Relationships between Gardenia jasminoides var. radicans and G. jasminoides for. grandiflora Using ISSR Markers)

  • 허만규
    • 생명과학회지
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    • 제17권1호
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    • pp.24-30
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    • 2007
  • 꽃치자(Gardenia jasminoides var. radicans)와 열매치자(C. jasminoides for. grandiflora)는 Gardenia속으로는 우리나라에 두 분류군밖에 없으며 열매치자는 약용, 식용, 꽃치자는 방향제로 쓰인다. 그런데 꽃이 지고 나면 형태적으로 구분이 거의 되지 않는다 ISSR분석으로 이들 종의 유전적 다양도와 집단구조를 실시하였다. 88개의 DNA 분절에서 한 분류군에만 나타나는 특이밴드가 탐지되었다. 한국의 세 야생 집단은 분리되어 있고 패치 분포를 보이지만 재배종에 비해 높은 유전적 다양성을 유지하친 있었다. 열매치자가 꽃치자보다 유전적 다양성이 높았으며 ISSR 마커로 이들 분류군이 잘 분리되었다. 또한 야생 집단이 재배 집단보다 다양성이 약간 높으나 유의성은 없었다. 이는 재배화과정에서 유전적 다양성의 일부 상실이 있었으나 인위적인 채취와 식재로 야생 집단과 재배 집단의 유전적 교류가 존재하였음을 시사한다.

ISSR을 이용한 음나무속 분류군의 유전적 다양성과 관련성 비교 (Comparison of Genetic Diversity and Relationships of Genus Kalopanax Using ISSR Markers)

  • 허만규
    • 생명과학회지
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    • 제16권5호
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    • pp.740-745
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    • 2006
  • ISSR 마크로 한국내 자생하는 음나무속 4분류군(음나무, 가시없는 음나무, 털음나무, 가는잎음나무)에 대해 유전적 다양성과 계통관계를 조사하였다. 64개의 재현성 높은 ISSR 밴드가 생성되었다. 음나무속의 각 개체별 분석에서 41개 밴드(64.1%)가 다형성을 나타내었다. 네 분류군을 통합하였을 때 그룹내 다양도는 0.115였고 그룹간 다양도는 0.467이였다. 종내 유전자 흐름(Nm)의 측정결과 음나무의 Nm값은 털음나무, 가는잎음나무에 비해 낮았다. 이는 지리적 거리에 따른 생식적 격리가 이 종의 집단구조를 형성하고 있다고 판단된다. 계통도 분석에서 ISSR 마크로 속수준의 네 분류군뿐만 아니라 집단까지도 잘 분리되어 본 연구에 사용한 마크가 분류에 효과적임이 규명되었다.

ISSR을 이용한 고추나물 집단의 유전적 다양성과 계통학적 연구

  • 허홍욱;허만규;강동호
    • 생명과학회지
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    • 제17권6호통권86호
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    • pp.805-810
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    • 2007
  • Inter simple sequence repeat (ISSR) markers were performed in order to analyse the phylogenetic relationships of eight Hypericum electum populations in Korea. The six primers were produced 37 reproducible ISSR bands. Analysis of ISSR from individual plants of Korean H. erectum resulted in 22 polymorphic bands with 59.5%. Across populations, the mean number of alleles per locus was 1.348 and Shannon's information index was 0.203.Population Mt. Gyeryong had the highest expected genetic diversity (0.175) among all populations. When species were grouped by eight populations, within group diversity was 0.140 (Hs), while among group diversity was 0.472 (G$_{ST}$) on a per locus basis. The estimated gene flow (Nm) for H. erectum was very low (0.561). It is suggested that reproductive isolation by the isolation of geographical distance among H. electum populations and genetic drift may have played roles in shaping the population structure of this species. In phonetic tree, all populations were well separated from each other. Thus, ISSR markers are very effective in classifying natural population levels of genus Hypericum in Korea.