• 제목/요약/키워드: Core Sequence

검색결과 270건 처리시간 0.022초

ITS 영역의 염기서열을 이용한 근류형성 질소고정균의 계통분류 (Phylogenetic analysis of the genera Azorhizobium, Bradyrhizobium, Mesorhizobium, Rhizobum and Sinorhizobium on the basis of internally transcribed spacer region)

  • 권순우;김창영;류진창;고승주
    • 한국토양비료학회지
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    • 제35권1호
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    • pp.12-26
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    • 2002
  • 근류형성에 의한 생물학적 질소고정기능을 갖는 여러종의 근류균을 대상으로 분자생물학적 계통 분류의 기초자료를 얻기 위하여 Azorhizobium, Bradyrhizobium, Mesorhizobium, Rhizobium, Sinorhizobium 속의 33 균주에 대한 ITS 영역의 염기서열을 이용한 계통 분류가 이루어 졌다. 이들 균주중 대부분의 균주는 한 종류의 ITS 영역을 가지는 반면, 일부균주는 2개의 서로 다른 ITS 염기서열을 가지는 것으로 나타났다. 실험에 이용된 모든 균주들간의 ITS 영역의 염기서열 상동성은 28 - 95%로 매우 변이폭가 컸으며, 이들 염기서열의 계통 분석에 의하면 4가지 그룹으로 구분되었다. Sinorhizobium 속의 모든 균주 및 Rhizobium giardinii 는 그룹 I으로 구분되었다 그룹 II는 R. giardinii를 제외한 모든 Rhizibium 속의 균주를 포함하고 있으며, 계통수의 topology는 매우 불안정한 것으로 나타났다. 특히, R. radiobacter와 R. rubi는 계통분류학적 위치가 불명확한 것으로 나타났다. Bradyrhizobium 속의 균주는 Azorhizobium caulinodans 와 함께 그룹 III로 구분되었고, 그룹 IV는 Mesorhizobium 속의 균주로 이루어 ㅈ다. 특히, Mesorhizobium 속균주의 ITS 영역의 염기서열 상동성이 높게 나타났다.

A New Sterol Regulatory Element Binding Protein, SrbB Is Critical for Hypoxia Adaptation and Virulence in the Human Fungal Pathogen Aspergillus fumigatus

  • Chung, Dawoon;Barker, Bridget M.;Carey, Charles C.;Merriman, Brittney;Werner, Ernst R.;Lechner, Beatrix E.;Dhingra, Sourabh;Cheng, Chao;Xu, Wenjie;Blosser, Sara J.;Morohashi, Kengo;Mazurie, Aurelien;Mitchell, Thomas K.;Haas, Hubertus;Mitchell, Aaron P.;Cramer, Robert A.
    • 한국균학회소식:학술대회논문집
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    • 한국균학회 2015년도 춘계학술대회 및 임시총회
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    • pp.15-15
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    • 2015
  • Aspergillus fumigatus is a major cause of invasive aspergillosis (IA), a significant health issue worldwide with high mortality rates up to 95%. Our lab is interested in how A. fumigatus adapts to low oxygen conditions 'hypoxia', which is one of the important host microenvironments. A. fumigatus SrbA is a basic helix-loop-helix (bHLH) transcriptional regulator and belongs to sterol regulatory element binding protein (SREBP) family members. Loss of SrbA completely blocks growth in hypoxia and results in avirulence in murine models of IA suggesting an essential role of SrbA in hypoxia adaptation and virulence in A. fumigatus. We conducted chromatin immunoprecipitation sequencing (ChIP-seq) with A. fumigatus wild type using a SrbA specific antibody, and 97 genes were revealed as SrbA direct targets. One of the 'SrbA regulons' (AFUB_099590) was a putative bHLH transcriptional regulator whose sequence contained a characteristic tyrosine substitution in the basic portion of the bHLH domain of SREBPs. Therefore, we designated AFUB_099590 SrbB. Further characterization of SrbB demonstrated that SrbB is important for radial growth, biomass production, and biosynthesis of heme intermediates in hypoxia and virulence in A. fumigatus. A series of quantitative real time PCR showed that transcription of several SrbA regulons is coordinately regulated by two SREBPs, SrbA and SrbB in hypoxia. This suggests that SrbA and SrbB have both dependent and independent functions in regulation of genes responsible for hypoxia adaptation in A. fumigatus. Together, our data provide new insights into complicated roles of SREBPs in adaptation of host environments and virulence in pathogenic fungi.

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고리 1호기 소형파단 냉각제 상실사고에 의해 개시된 가상 노심용융 사고 해석 (Severe Accident Sequence Analysis - Part 1: Analysis of Postulated Core Meltdown Accident Initiated by Small Break LOCA in Kori-1 PWR Dry Containment)

  • Jong In Lee;Seung Hyuk Lee;Jin Soo Kim;Byung Hun Lee
    • Nuclear Engineering and Technology
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    • 제16권3호
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    • pp.141-154
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    • 1984
  • 고리 1호기의 소형파단냉각재 상실사고에 의해 개시된 중대사고 유형과 그 현상에 대할 분석이 제시되었다. 본 해석에서는 KAERI에서 기존 전산코드의 수정.보완된 MARCH 전산코드가 사용되었다. 특히 고리 1호기의 소형파단 LOCA 해석시 수소 거동과 중기과압에 대한 평가 및 그 응답성에 중점을 두고 검토되었으며, 2-loop 발전소 데이타 분석 및 debris-Water 상호작용 모델에 대한 비교 분석이 수행되었다. 제 1부 중대 사고유형 분석결과, 저농도에서 H$_2$ burning이 이루어지는 경우 계속적인 수소 생성으로 인해 반복 수소 spike가 야기 되나, 격납용기 설계압력치 보다낮게 예측되었다. 또한 debris/water 상호작용시 core debris의 입자크기는 첨두압력의 크기에 미치는 영향은 미세하나 첨두압력의 발생시점은 dryout모델사용에 의해서 상당히 지연시키게 되었다. 완전한 노심용융 사고시 수소연소와 증기과압으로부터 예측된 격납용기 최대압력은 격납용기 건전성에 심각한 위협을 초래하지 않는 것으로 나타났다.

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Cloning and Expression of Human Liver UDP-Glucuronosyltransferase cDNA, UDPGTh2

  • Dong, Misook;Owens, Ida-S.;Sheen, Yhun-Yhong
    • Archives of Pharmacal Research
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    • 제20권5호
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    • pp.459-464
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    • 1997
  • The human liver cDNA clone UDPGTh2, encoding a liver UDP-glucuronosyltransferase (UDPGT) was isolated from a .gamma. gt 11 cDNA library by hybridization to mouse transferase cDNA clone, UDPGTm1. UDPGTh2 encoded a 529 amino acid protein with an amino terminus membrane-insertion signal peptide and a carboxyl terminus membrane-spanning region. There were three potential asparagine-linked glycosylation sites at residues 67, 68, and 315. In order to obtain UDPGTh2 protein encoded from cloned human liver UDP-glucuronosyltransferase cDNA, the clone was inserted into the pSVL vector (pUDPGTh2) and expressed in COS 1 cells. The presence of a transferase with Mr-52,000 in transfected cells cultured in the presence of $[^{35}S]$ methionine was shown by immunocomplexed products with goat antimouse transferase IgG and protein A-Sepharose and analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and autoradiography. The expressed UDPGT was a glycoprotein as indicated by electrophoretic mobility shift in Mr-3,000-4,000 when expressed in the presence of tunicamycin. The extent of glycosylation was difficult to assess, although one could assume that glycosyl structures incorporated at the level of endoplasmic reticulum were always the core oligosaccharides. Thus, it is likely that at least two moieties inserted can account for the shift of Mr-3,000-4,000. This study demonstrates the cDNA and deduced amino acid sequence of human liver UDP-glucuronosyltransferase cDNA, UDPGTh2.

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BULK 선용자동 Ballast Water Management Plan 개발 (Optimized Ballast Water Exchange Management for Bulk Carrier)

  • 홍충유;박제웅
    • 한국해양공학회:학술대회논문집
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    • 한국해양공학회 2004년도 학술대회지
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    • pp.67-72
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    • 2004
  • Many port states such as New Zealand, the USA, Australia and Canada have strict regulations to prevent ships which arrive in their port from discharging polluted ballast water which contain harmful aquatic organism and pathogens. They are notified that transfer of polluted ballast water can cause serious injury to public health and damage to property and environment. For this reason, they perceived that the ballast exchange in deep sea is the most effective method, together with submitting the ballast management plan which contains the effective exchange method, ballast system and safety consideration. In this study, we pursued both nautical engineering analysis and optimization of algorithm in order to generate the sequence of stability and rapidity. Heuristic Algorithm was chosen on the basis of optimality and applicability to a sequential exchange problem. We have built an optimized algorithm, for automatic exchange of ballast water, by redefining core elements of the $A^\ast$ algorithm, such as node, operator and evaluation function. Final version of the optimized algorithm has been applied to existing bulk carrier and the performance of the algorithm has been verified successfully.

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Identification of hRad21-Binding Sites in Human Chromosome

  • Chin Chur;Chung Byung-Seon
    • Genomics & Informatics
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    • 제4권1호
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    • pp.11-15
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    • 2006
  • The aim of this study is to identify hRad21-binding sites in human chromosome, the core component of cohesin complex that held sister chromatids together. After chromatin immunoprecipitation with an hRad21 antibody, it was cloned the recovered DNA and sequenced 30 independent clones. Among them, 20 clones (67%) contained repetitive elements including short interspersed transposable elements (SINE or Alu elements), long terminal repeat (LTR) and long interspersed transposable elements (LINE), fourteen of these twenty (70%) repeats clones had Alu elements, which could be categorized as the old and the young Alu Subfamily, eleven of the fourteen (73%) Alu elements belonged to the old Alu Subfamily, and only three Alu elements were categorized as young Alu subfamily. There is no CpG island within these selected clones. Association of hRad21 with Alu was confirmed by chromatin immunoprecipitation-PCR using conserved Alu primers. The primers were designed in the flanking region of Alu, and the specific Alu element was shown in the selected clone. From these experiments, it was demonstrated that hRad21 could bind to SINE, LTRs, and LINE as well as Alu.

가공 순서 결정과 기계 선택을 위한 모형 개발 (Model Development for Machining Process Sequencing and Machine Tool Selection)

  • 서윤호
    • 대한산업공학회지
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    • 제21권3호
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    • pp.329-343
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    • 1995
  • Traditionally, machining process sequence was influenced and constrained by the design information obtained from CAD data base, i.e., class of operations, geometric shape, tooling, geometric tolerance, etc. However, even though all the constraints from design information are considered, there may exist more than one way to feasibly machine parts. This research is focused on the integrated problem of operations sequencing and machine tools selection in the presence of the product mix and their production volumes. With the transitional costs among machining operations, the operation sequencing problem can be formulated as a well-known Traveling Salesman Problem (TSP). The transitional cost between two operations is expressed as the sum of total machining time of the parts on a machine for the first operation and transportation time of the parts from the first machine to a machine for the second operation. Therefore, the operation sequencing problem formulated as TSP cannot be solved without transitional costs for all operation pairs. When solved separately or serially, their mutual optima cannot be guaranteed. Machining operations sequencing and machine tool selection problems are two core problems in process planning for discretely machined parts. In this paper, the interrelated two problems are integrated and analyzed, zero-one integer programming model for the integrated problem is formulated, and the solution methods are developed using a Tabu Search technique.

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젊은 나이에 발병한 파킨슨병 환자의 건강-질병 전환 경험 과정 (Health-Illness Transition of Patients with Young-Onset Parkinson's Disease)

  • 김성렬;이숙자
    • 대한간호학회지
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    • 제43권5호
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    • pp.636-648
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    • 2013
  • Purpose: The purpose of this study was to explore the health-illness transition of patients with Young-Onset Parkinson's Disease (YOPD). Methods: From June to November 2011, 17 patients with YOPD who visited a neurologic clinic in a tertiary hospital participated in the study. Data were collected through in-depth interviews and analyzed using the grounded theory of Strauss and Corbin. Results: The core category of the participants' health-illness transition emerged as 'reshaping identity following uncontrollable changes'. The participants' health-illness transition process consisted of six phases in sequence: ego withdrawal, loss of role, frustration, change of thought, modification of life tract, and second life. Although most participants proceeded through the six phases chronologically, some returned to the frustration phase and then took up the remaining phases. Conclusion: The study results provide an in-depth understanding of health-illness transition experiences in the participants. These findings suggest a need to develop appropriate nursing intervention strategies according to the different phases in the health-illness transition of patients with YOPD.

Overview of Arabidopsis Resource Project in Japan

  • Kobayashi, Masatomo
    • Interdisciplinary Bio Central
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    • 제3권1호
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    • pp.2.1-2.4
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    • 2011
  • Arabidopsis is well-known to the world's plant research community as a model plant. Many significant resources and innovative research tools, as well as large bodies of genomic information, have been created and shared by the research community, partly explaining why so many researchers use this small plant for their research. The genome sequence of Arabidopsis was fully characterized by the end of the $20^{th}$ century. Soon afterwards, the Arabidopsis research community began a 10-year international project on the functional genomics of the species. In 2001, at the beginning of the project, the RIKEN BioResource Center (BRC) started its Arabidopsis resource project. The following year, the National BioResource Project was launched, funded by the Japanese government, and the RIKEN BRC was chosen as a core facility for Arabidopsis resource. Seeds of RIKEN Arabidopsis transposon-tagged mutant lines, activation-tagged lines, full-length cDNA over-expresser lines, and natural accessions, as well as RIKEN Arabidopsis full-length cDNA clones and T87 cells, are preserved at RIKEN BRC and distributed around the world. The major resources provided to the research community have been full-length cDNA clones and insertion mutants that are suitable for use in reverse-genetics studies. This paper provides an overview of the Arabidopsis resources made available by RIKEN BRC and examples of research that has been done by users and developers of these resources.

Systematic Development of Tomato BioResources in Japan

  • Ariizumi, Tohru;Aoki, Koh;Ezura, Hiroshi
    • Interdisciplinary Bio Central
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    • 제3권1호
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    • pp.1.1-1.6
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    • 2011
  • Recently, with the progress of genome sequencing, materials and information for research on tomato (Solanum lycopersicum) have been systematically organized. Tomato genomics tools including mutant collections, genome sequence information, full-length cDNA and metabolomic datasets have become available to the research community. In Japan, the National BioResource Project Tomato (NBRP Tomato) was launched in 2007, with aims to collect, propagate, maintain and distribute tomato bioresources to promote functional genomics studies in tomato. To this end, the dwarf variety Micro-Tom was chosen as a core genetic background, due to its many advantages as a model organism. In this project, a total of 12,000 mutagenized lines, consisting of 6000 EMS-mutagenized and 6000 gamma-ray irradiated M2 seeds, were produced, and the M3 offspring seeds derived from 2236 EMS-mutagenized M2 lines and 2700 gamma-ray irradiated M2 lines have been produced. Micro-Tom mutagenized lines in the M3 generation and monogenic Micro-Tom mutants are provided from NBRP tomato. Moreover, tomato cultivated varieties and its wild relatives, both of these are widely used for experimental study, are available. In addition to these bioresources, NBRP Tomato also provides 13,227 clones of full-length cDNA which represent individual transcripts non-redundantly. In this paper, we report the current status of NBRP Tomato and its future prospects.