• 제목/요약/키워드: Phylogenetic study

검색결과 1,390건 처리시간 0.03초

Phylogenetic Relationship among Several Korean Coastal Red Tide Dinoflagellates Based on their rDNA Internal Transcribed Spacer Sequences

  • Cho, Eun-Seob;Kim, Gi-Yong;Park, Hyung-Sik;Nam, Byung-Hyouk;Lee, Jae-Dong
    • Journal of Life Science
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    • 제11권2호
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    • pp.74-80
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    • 2001
  • The nucleotide sequences of the internal transcribed spacer regions (ITS1 and ITS2) of ribosomal DNA (rDNA), and the 5.85 rRNA gene, have been determined for 13 strains of dinoflagellates in order to analyze the phylo-genetic relationship. The DNA sequences contained considerable variation in the ITS regions, but little in the 5.85 rDNA. In addition, the ITS1 was more variable than the ITS2 in all species examined. The nucleotide length of this region varied from 519 bp to 596 bp depending on the taxa. The investigated taxa were divided into three large groups based on the ITS length, i. e., a group with short ITS region (A. fraterculus and Alexandrium sp.), a with ITS region group (P. micans, P. minimum and P. triestinum) and a with ITS region group (G. impudicum, C. polykrikoides, G. sanguineum, G. catenatum and H. triquetra). The relationship between nucleotide length of ITS1 and that of ITS2 was negative, whereas G+C content and nucleotide length showed positive correlation. In phylogenetic analyses producing NJ trees, the topology was similar cluster and clearly divided the taxa into three groups based on 5.8S rDNA that were similar to those based on morphological characteristics. In particular, G. impudicum was more closely related to G. catenatum than to C. polykrikoides using phylogenetic analysis. From this study, we chew that the length of ITS region contributes to discriminate Korean harmful algal species and ITS analysis is a useful method for resolving the systematic relationships of dinoflagellates.

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Uridylate kinase를 이용한 원핵생물의 분류 (Phylogenetic analysis of procaryote by uridylate kinase)

  • 이동근;김철민;김상진;하배진;하종명;이상현;이재화
    • 생명과학회지
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    • 제13권6호
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    • pp.856-864
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    • 2003
  • 원핵생물 (Procaryote)의 분류에 16S rRNA유전자가 많이 이용되어 있으나 제한된 해상력과 유전자의 수에 차이가 있는 등의 문제가 있어 이를 보완할 수 있는 새로운 생체분자를 찾고 그 분류 결과를 16S rRNA의 결과와 비교하였다. COG (Clusters of Orthologous of protein) 방법을 이용하여 43종의 미생물중에서 진핵생물을 제외한 42종의 원핵생물 (procaryote)에서만 발견되는 3종류의 COG인 Transcription elongation factor인 COG0195과 bacterial DNA primase인 COG0358 그리고 uridylate kinase인 COG0528를 구하였다. 이중 유사도와 유전자 수를 바탕으로 새로운 분류의 키로 uridylate kinase를 설정하여 분석한 결과, 같은 속 (genus)에 속하는 세균들은 아주 높은bootstrap value를 갖고 분류도에서 같은 위치에 분포하고 고세균 (Archaebacteria) 내부의 응집성이 높은 등의 유사성을 보였다. 한편 alpha와 epsilon 그룹의 Proteobacteria가 분류도에서 다르게 위치하고 진정세균 (Eubacteria)의 Spi-rochaetales에 속하는 Treponema pallidum (Tpa)와 Borrelia burgdorferi (Bbu)가 고세균과 유연관계가 높게 나타나는 등 차이점도 보였다. Uridylate kinase를 이용한 분류는, 아주 높은 보존성에 의해서 생기는 16S rRNA 유전자를 이용한 문제점을 보완하여 원핵생물의 정확한 분류에 기여할 수 있을 것으로 사료되었다.

Vegetative Growth and Phylogenetic Relationship of Commercially Cultivated Strains of Pleurotus eryngii based on ITS sequence and RAPD

  • Alam, Nuhu;Shim, Mi-Ja;Lee, Min-Woong;Shin, Pyung-Gyun;Yoo, Young-Bok;Lee, Tae-Soo
    • Mycobiology
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    • 제37권4호
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    • pp.258-266
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    • 2009
  • Pleurotus eryngii, known as king oyster mushroom has been widely used for nutritional and medicinal purposes. This study was initiated to screen the suitable conditions for mycelial growth and to determine the phylogenetic relationship of the selected strains. Optimal mycelial growth was observed at $30{^{\circ}C}$ and minimum mycelial growth observed at $10{^{\circ}C}$. This mushroom tolerates a broad pH range for mycelial growth, with most favorable growth observed at pH 6. Results also indicated that glucose peptone, yeast malt extract and mushroom complete media were favorable growth media, while Hennerberg and Hoppkins media were unfavorable. Dextrin was the best and xylose the least effective carbon sources. Results revealed that inorganic nitrogen sources were less effective than organic sources for the mycelial growth of P. eryngii. Investigation of genetic diversity is necessary to identify the strains. The ITS region of rDNA were amplified using PCR. The size of the ITS1 and ITS2 regions of rDNA from the different strains varied from 214 to 222 bp and 145 to 236 bp, respectively. The sequence of ITS2 was more variable than that of ITS1, and the 5.8S sequences were identical. A phylogenetic tree based on the ITS region sequences indicated that selected strains could be classified into six clusters. Fourteen IUM and ATCC- 90212 strains were also analyzed by RAPD with 20 arbitrary primers. Fourteen of these primers were efficiently amplified the genomic DNA. The number of amplified bands varied with the primers and strains, with polymorphic fragments in the range from 0.2 to 2.3 kb.

Genetic Homogeneity in the Domestic Silkworm, Bombyx, and Phylogenetic Relationship Between B. mori and the Wild Silkworm, B. mandarina Using Mitochondrial COI Gene Sequences

  • Kim, Iksoo;Bae, Jin-Sik;Sohn, Hung-Dae;Kang, Phil-Don;Ryu, Kang-Sun;Sohn, Bong-Hee;Jeong, Won-Bok;Jin, Byung-Rae
    • International Journal of Industrial Entomology and Biomaterials
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    • 제1권1호
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    • pp.9-17
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    • 2000
  • Genetic variation in the domestic silkworm strains (Bombyx mori) and phylogenetic relationships between domestic silkworms and wild silkworms (B. mandarina) were investigated by using a portion of mitochondrial CGI gene sequences. Ten geographic strains of B. mori we sequenced were identical in the 410 bp-section of mitochondrial COI gene. This sequence was also identical to the homologous sequence of the four Gen-Bank-registered strains, but one strain of B. mori differed a single nucleotide (0.2%) from others. MtDNA homogeneity in the B. mori strains appears to be resulted from fixation into the mast frequent mtDNA type during the course of breeding for new strains, in which an extensive indoor rearing and removal of unwanted individuals were accompanied. In the comparisons between domestic and wild silkworms, some wild silkworms were closely related to domestic silkworms (0.2%-1.2% of divergence), but the others were not (2.7%-3.7% of sequence divergence). This result was also reflected in the phylogenetic analyses, showing two independent phylogenetic groups: one including all B. mandarina sequences and the other including both B. mandarina and B. mori sequences. Thus, domestic silkworms may have been derived from the ancestor of B. mandarina, which belongs to this group, alto-ough more extensive study will provide better understanding on this issue.

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Molecular Phylogenetic Relationships Within the Genus Alexandrium(Dinophyceae) Based on the Nuclear-Encoded SSU and LSU rDNA D1-D2 Sequences

  • Kim, Choong-Jae;Sako Yoshihiko;Uchida Aritsune;Kim, Chang-Hoon
    • Journal of the korean society of oceanography
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    • 제39권3호
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    • pp.172-185
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    • 2004
  • LSU rDNA D1-D2 and SSU rDNA genes of 23 strains in seven Alexandrium (Halim) species, A. tamarense (Lebour) Balech, A. catenella (Whedon et Kofoid), A. fraterculus (Balech) Balech, A. affine (Inoue et Fukuyo) Balech, A. insuetum Balech, A. pseudogonyaulax (Biecheler) Horiguchi ex Yuki et Fukuyo and A. tamiyavanichii Balech, were sequenced and the data were used for molecular phylogenetic analysis. The sequence data revealed 11 and 7 ribotypes in the LSU rDNA D1-D2 region and 4 and 17 ribotypes in the SSU rDNA region of A. catenella and A. tamarense, respectively. Other Alexandrium species had also 1 to 5 ribotypes in the two regions. With the exception of CMC2 and CMC3 of A. catenella, all A. tamarense and A. catenella strains had a common ribotype, a functionally expressed rRNA gene (here termed type A), in both gene regions. In addition to the functionally expressed gene, several pseudogenes were obtained that were found to be good tools to analyze the population designation of regional isolates by grouping them according to shared ribotypes. From the phylogenetic analysis of the sequence data determined in this study and retrieved from GenBank, the genus Alexandrium was divided into 14 groups: 1) A. tamarense, 2) A. excavatum, 3) A. catenella, 4) Tasmanian A. tamarense, 5) A. affine (and/or A. concavum), 6) Thai A. tamarense, 7) A. tamiyavanichii, 8) A. fraterculus, 9) A. margalefii, 10) A. andersonii, 11) A. ostenfeldii, 12) A. minutum (or A. lusitanicum), 13) A. insuetum, and 14) A. pseudogonyaulax. The SSU rDNA gene sequence of A. fundyense was so similar to those of A. tamarense used in this study that the two species were difficult to discriminate each other. A. tamiyavanichii was closest to the A. tamarense strain isolated in Thailand and close to the long chain-forming species of A. affine and A. fraterculus. The phylogenetic tree showed that A. margalefii, A. andersonii, A. ostenfeldii, A. minutum and A. insuetum constituted the basal relative complex, and that A. pseudogonyaulax is an ancestral taxon in the genus Alexandrium.

엽록체 DNA 염기서열을 이용한 한약재 지모의 기원 확인 및 유연관계 분석 (Phylogenetic Analysis of Ji-Mo (Anemarrhena asphodeloides) on the Basis of Chloroplast DNA Sequences)

  • 김명겸;베갈마;손화;노종훈;김세영;양덕춘
    • 한국약용작물학회지
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    • 제16권1호
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    • pp.20-26
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    • 2008
  • 지모 (Anemarrhena asphodeloides)는 탁월한 해열작용과 진정작용을 갖는 한약재로 한국, 중국, 일본에서 널리 이용되어 왔다. 본 연구에서는 먼저 국내 연구소에서 형태학적 분류 결과 지모로 확인된 3종의 식물체를 수집하여 엽록체 DNA의 trnL-F 염기서열을 분석하였다. 분석 결과, 국내 연구기관에서 보관중인 지모 식물체들이 모두 동일한 trnL-F의 염기서열을 보여서, 형태학적 분류와 계통유전학적 분류가 동일함을 확인하였다. 최초로 얻어진 지모 trnL-F 염기서열은 NCBI database에 등록하였다. 다음으로 국내 한약재 시장과 중국 한약재 시장에서 유통 중인 지모 한약재를 다량 구입하여 trnL-F의 염기서열을 분석하였다. 그 결과, 유통 중인 지모 한약재들이 모두 기원식물과 동일한 TrnL-F의 염기서열을 보여서 지모 약재의 경우 진품이 유통되고 있음을 알 수 있었다. TrnL-F의 염기서열로 계통수를 작성한 결과 지모는 아스파라거스목 (Asparagales), 용설란과 (agavaceae)에 속한 것으로 보여 졌다. 엽록체 rbcL 유전자 염기서열로 얻은 계통수와 비교한 결과 trnL-F 계통수와 rbcL 계통수가 비슷한 결과를 보여주어서 분자유전학적 분류에 두 유전자가 상호보완적으로 이용될 수 있음을 확인하였다.

동남아시아 4개국 두족류의 분류 및 계통분류학적 연구 (Classification and Phylogenetic Studies of Cephalopods from four countries of South-East Asia)

  • 황희주;강세원;박소영;정종민;송대권;박형춘;박홍석;한연수;이준상;이용석
    • 한국패류학회지
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    • 제32권1호
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    • pp.55-62
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    • 2016
  • In this study, an attempt has been made to analyze the morphology of Cephalopods distributed in Korea and collected samples from South-East Asian countries including Thailand, Indonesia, Vietnam, and China. A phylogenetic analysis was performed using the mitochondrial gene, Cytochrome c oxidase subunit I (COI) to understand the genetic divergences of the species and validate their origins. For achieving the objectives, samples were collected directly from Thailand Hat Yai, Songkhla, Indonesia Medan, Vietnam Ho Chi Minh, and Vung Tau in August 2015 and from China in September 2015. A total of 23 species of Cephalopods were identified falling under three orders, four familyies and nine genus. The species were distributed under Order: Octopoda (1 family, 3 genus, and 9 species), Order: Sepiolioda (1 family, 2 genus, and 8 species), and Order Teuthoidea (2 family, 4 genus, and 6 species). 23 species which is 1 family 3 genus 9 species in Octopoda, 1 family 2 genus 8 species in Sepiolioda, 2 family 4 genus 6 species in Teuthoidea. Phylogenetic analysis using COI gene was conducted for 18 species. For the remaining 5 species sequencing results showed severe variation and hence were not considered further. The COI phylogenetic analysis for the 18 species of Cephalopods were found consistent with the morphological identification. The excluded species will be subjected for a further detailed analysis.

Phylogenetic Analysis of Ruminant Theileria spp. from China Based on 28S Ribosomal RNA Gene

  • Gou, Huitian;Guan, Guiquan;Ma, Miling;Liu, Aihong;Liu, Zhijie;Xu, Zongke;Ren, Qiaoyun;Li, Youquan;Yang, Jifei;Chen, Ze;Yin, Hong;Luo, Jianxun
    • Parasites, Hosts and Diseases
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    • 제51권5호
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    • pp.511-517
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    • 2013
  • Species identification using DNA sequences is the basis for DNA taxonomy. In this study, we sequenced the ribosomal large-subunit RNA gene sequences (3,037-3,061 bp) in length of 13 Chinese Theileria stocks that were infective to cattle and sheep. The complete 28S rRNA gene is relatively difficult to amplify and its conserved region is not important for phylogenetic study. Therefore, we selected the D2-D3 region from the complete 28S rRNA sequences for phylogenetic analysis. Our analyses of 28S rRNA gene sequences showed that the 28S rRNA was useful as a phylogenetic marker for analyzing the relationships among Theileria spp. in ruminants. In addition, the D2-D3 region was a short segment that could be used instead of the whole 28S rRNA sequence during the phylogenetic analysis of Theileria, and it may be an ideal DNA barcode.

ITS 염기서열에 의한 한국산 담배풀속(Carpesium L.)의 계통분류학적 연구 (A Phylogenetic Study of Korean Carpesium L. Based on nrDNA ITS Sequences)

  • 유광필;박선주
    • 한국자원식물학회지
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    • 제25권1호
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    • pp.96-104
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    • 2012
  • 한국산 담배풀속(Carpesium L.) 7분류군과 3개의 외군(Inula britannica L., Inula germanica L., Rhanteriopsis lannginosa(DC.) Rauschert)을 대상으로 유연관계를 파악하기 위하여 nuclear ribosomal DNA(nrDNA) 중 ITS(internal transcribed spacer) 지역의 계통분류학적 분석을 수행하였다. 계통분류학적 연구방법은 maximum parsimony, neighbor-joining와 maximum likelihood 방법을 사용하였다. 정렬된 계통분의 총 길이는 731 bp이며, ITS1, ITS2와 5.8S 부위의 길이는 각각 284~297 bp, 264~266 bp와 164 bp로 나타났다. 계통분류학 변이를 보이는 site는 111개로 확인 되었으며, 그 중 64개의 site가 계통학적으로 유효한 것으로 나타났고, ITS1 지역이 ITS2 지역보다 염기 변이가 다양하게 나타나는 것으로 확인되었다. 그 결과, 한국산 담배풀속은 단계통을 형성하였으며, 담배풀(C. abrotanoides L.)이 가장 기저부에 위치하였다. 여우오줌(C. macrocephalum Franch. & Sav.)와 두메담배풀(C. triste Maxim.)은 가까운 유연관계를 나타냈으며, 애기담배풀(C. rosulatum Miq.)와 천일담배풀(C. glossophyllum Maxim.) 그리고 좀담배풀(C. cernuum L.)와 긴담배풀(C. divaricatum Siebold & Zucc.)도 유연관계가 가깝게 나타났다. 이와 같은 결과로 담배풀속 nrDNA의 ITS 지역 염기서열에 기초한 분자 계통학적 연구는 계통분류를 이해하는데 유용한 방법으로 판단된다.

Study on Origin and Phylogeny Status of Hu Sheep

  • Geng, R.Q.;Chang, H.;Yang, Z.P.;Sun, W.;Wang, L.P.;Lu, S.X.;Tsunoda, K.;Ren, Z.J.
    • Asian-Australasian Journal of Animal Sciences
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    • 제16권5호
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    • pp.743-747
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    • 2003
  • Applying simple random sampling in typical colony methods in the central area of habitat, 14 structural loci and 31 alleles in blood enzyme and other protein variations of Hu sheep population are examined. After collecting the same data of 11 loci about the 22 sheep colonies in China and other countries, it clusters the 23 sheep populations by fuzzy cluster analysis. The study proves that the phylogenetic relationship between Hu sheep population and Mongolia populations is relatively closed. This result obtained is shown to conform to the historical data.