• 제목/요약/키워드: transgenic line

검색결과 199건 처리시간 0.026초

Biochemical and Molecular Analysis of OsPAP1: A Phosphate Starvation Induced Purple Acid Phosphatase Gene from Rice

  • Hur, Yeon Jae;Yi, Young Byung;Kim, Tae Ho;Kim, Doh Hoon
    • 한국육종학회지
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    • 제42권5호
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    • pp.455-462
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    • 2010
  • Purple acid phosphatase is important for phosphorus remobilization in plants, but its role in plant adaptation to low phosphorus availability is not known. The cDNA encoding O. sativa purple acid phosphatase (OsPAP1) has 1008 bp with an open reading frame of 335 amino acid residues. The amino acid sequence of OsPAP1 cDNA shows of 50-51% identity with other plant purple acid phosphatases. OsPAP1 was expressed in rice plants and in cell cultures in the absence of phosphate ($P_i$). The expression was organ-specific with the strongest expression in $P_i$-deprived roots. Functional expression of the OsPAP1 gene in the transgenic Arabidopsis line was confirmed by northern and western blot analysis. OsPAP1 overexpression lines had higher phosphatase activity than wild-type. Overexpression of OsPAP1 in Arabidopsis plants resulted in increased Pi accumulation under Pi sufficient condition. These results show that the OsPAP1 gene represents more efficient $P_i$ uptake and can be used to develop new transgenic dicotyledonous plants.

Cytokinin 합성효소의 도입에 따른 형질전환 식물체의 노화 지연 및 수량의 증가 (Improvement of Forage Crop Yield and Retardation of Leaf Senescence by Introduction of Gene for Cytokinin Synthetase into Plants)

  • 이병현;원성혜;이효신;김기용;김미혜;은석준;조진기
    • 한국초지조사료학회지
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    • 제19권3호
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    • pp.281-290
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    • 1999
  • 토양 미생물 A. tumefaciens로부터 cytokinin 합성효소 (ipt) 유전자를 분리하여 형질전환 식물을 작성하였다. 도입된 ipt 유전자는 모든 조직에서 발현되었으며, 잎에서의 발현량이 서로 다른 3개의 형질전환 식물체를 선발하였다. 선발한 식물체는 도입유전자의 고정을 위하여 2회 자가수정을 거쳐 homozygous 식물체를 작성한 후 해석하였다. 형질전환 식물체는 노화가 지연되어 녹엽을 유지하였으며, 측아로부터 측지가 분얼하여 그 수가 증가하였을 뿐만아니라, 각 마디에서 복수의 본엽이 생성되었다. 식물체의 노화가 가장 많이 진행된 잎에서의 chlorophyll 함량은 형질전환 식물체에서 1.5~4배 정도로 wild-type에 비하여 월등히 높았다. 이러한 결과는 축적된 cytokinin이 식물의 노화를 지연시킬 뿐만 아니라, 분얼 및 잎수를 증가시켜 식물의 수량을 증가시켰음을 나타낸다.

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시토신 탈메틸화 관련 NtROS2a 유전자 발현을 제어한 RNAi 식물의 DNA microarray 분석 (DNA microarray analysis of RNAi plant regulated expression of NtROS2a gene encoding cytosine DNA demethylation)

  • 최장선;이인혜;정유진;강권규
    • Journal of Plant Biotechnology
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    • 제43권2호
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    • pp.231-239
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    • 2016
  • 담배에서 후성유전관련 유전자의 발현연구를 위해 담배유래 시토신 DNA 탈메틸화 관련 NtROS2a 유전자를 과발현 및 RNAi 식물체를 육성하였다. 이들 형질전환체들은 고염 및 산화 스트레스하에서 내성이 증진되었으며, 다양한 표현형변이를 보였다(Lee et al. 2015). 본연구에서는 선발된 과발현 (OX1), RNAi 식물체(RNAi 13) 및 대조식물체(WT)를 이용하여 Agilent Tobacco 4 X 44K Oligo chip으로 microarray분석을 수행하였다. OX1과 RNAi13 계통을 이용하여 WT과 함께 비교 분석한 결과, 대부분 세포 내 이온 수송, 영양 공급 등과 같은 물질대사와 생물적 비생물적 스트레스 및 methylation과 관련되어 영향을 주는 유전자들에서 up-regulation 되었고, 물질대사관련 유전자와 세포 내 기능유전자의 역할을 담당하는 조효소, 그리고 다양한 스트레스 및 메틸레이션 관련 유전자군에서 또한 down-regulation되었다. 각각의 up-, down-regulation된 유전자들을 WT과 비교하여 qRT-PCR을 수행한 결과, KH domain-containing protein, MADS-box protein 및 Zinc phosphodiesterase ELAC protein 유전자들에서 발현이 높게 나타났으며, 반면에 pentatricopeptide (PPR) repeat-containing protein, histone deacetylase HDAC3 protein 및 protein kinase는 0.4 ~ 1.0-fold 발현양이 감소되었다. 따라서 DNA glycosylase를 암호화하는 NtROS2a 유전자는 demethylation과 관련되어 담배 식물체에서 다양한 전사레벨을 조절하는 것으로 판단된다.

Over-Expression of Ephrin-A5 in Mice Results in Decreasing the Size of Progenitor Pool through Inducing Apoptosis

  • Noh, Hyuna;Park, Soochul
    • Molecules and Cells
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    • 제39권2호
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    • pp.136-140
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    • 2016
  • Eph receptors and their ligands, ephrins, mediate cell-to-cell contacts in a specific brain region and their bidirectional signaling is implicated in the regulation of apoptosis during early brain development. In this report, we used the alpha(${\alpha}$)-Cre transgenic line to induce ephrin-A5 over-expression in the distal region of the neural retina. Using this double transgenic embryo, we show that the over-expression of ephrin-A5 was responsible for inducing massive apoptosis in both the nasal and temporal retinas. In addition, the number of differentiated retinal neurons with the exception of the bipolar neuron was significantly reduced, whereas the laminar organization of the mature retina remained intact. Consistent with this finding, an analysis of the mature retina revealed that the size of the whole retina-particularly the nasal and temporal regions-is markedly reduced. These results strongly suggest that the level of ephrin-A5 expression plays a role in the regulation of the size of the retinal progenitor pool in the neural retina.

MUTATION SPECTRUM OF 1,2-DIBROMO-3-CHLOROPROPANE, AN ENDOCRINE DISRUPTOR, IN THE lacI TRANSGENIC BIG BLUE$\circledR$ RAT2 FIBROBLAST CELL LINE

  • Kim, Youn-Jung;Chai, Young-Gyu;Ryu, Jae-Chun
    • 한국독성학회:학술대회논문집
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    • 한국독성학회 2001년도 International Symposium on Dietary and Medicinal Antimutgens and Anticarcinogens
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    • pp.181-181
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    • 2001
  • 1,2-Dibromo-3-chloropropane (DBCP), a soil fumigant against nematodes, is a genotoxic carcinogen and also is classified by World Wildlife Fund as endocrine disruptors. DBCP has been extensively studied on genotoxicity, carcinogenicity, and damage in male reproductive-related organs. However, information on precise mechanism of mutagenesis and carcinogenesis of DBCP is yet unknown. Thus the mutation spectrum and mechanism of DBCP was determined in lacI transgenic Big Blu $e^{R}$ Rat2 fibroblast cell lines.(omitted)d)

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Antisense Polygalacturonase 유전자 형질전환 토마토의 후대 발현 분석 (Inheritance and Expression of Antisense Polygalacturonase Gene in Transgenic Tomato)

  • 김영미;한장호;김용환;이성곤;황영수
    • 식물조직배양학회지
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    • 제25권2호
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    • pp.131-134
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    • 1998
  • Antisense PG 유전자 형질전판 토마토로부터 자식시켜 얻은 종자를 kanamycin 내성을 이용하여 5세대까지 분리, 육성하여 antisense PG 유전자가 안정적으로 고정된 식물체를 얻었다. 이들 식물체에는 genomic DNA gel blot 분석으로 antisense PG 유전자가 안정적으로 유전되며 northern blot 분석을 통하여 antisense RNA가 발현됨을 확인하였고, 또한 antisense RNA에 의한 endogenous PG 유전자의 발현 저해를 분석하였다. Antisense PG 유전자 형질전환 성숙 토마토내 PG 효소 활성이 비형질전환 성숙 토마토에 비하여 37-65% 수준으로 저하되었다.

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Analysis of Semen Parameters in α1,3-Galactosyltransferase-/- Boars

  • Hwang, In-Sul;Lee, Seung-Chan;Kim, Sung Woo;Kwon, Dae-Jin;Park, Mi-Ryung;Yang, Hyeon;Oh, Keon Bong;Ock, Sun-A;Woo, Jae-Seok;Im, Gi-Sun;Hwang, Seongsoo
    • 한국수정란이식학회지
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    • 제32권2호
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    • pp.53-58
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    • 2017
  • It is very difficult to get the information about semen quality analysis in transgenic pigs because of limited numbers and research facilities. Therefore, in the present study, we analyzed the semen quality of transgenic boars generated for xenotransplantation research. Briefly, the semen samples were collected from 5 homozygous ${\alpha}1,3$-Galactosyltransferase knock-out ($GalT^{-/-}$) transgenic boars and immediately transported to the laboratory. These semen samples were decupled with DPBS and conducted to analyze semen parameters by a computer-assisted semen analysis (CASA) system. The boar semen were examined all 12 parameters such as total motility (TM), curvilinear velocity (VCL), straight line velocity (VSL), average path velocity (VAP), and hyperactivated (HYP), etc. In results, among the 5 $GalT^{-/-}$ boars, three boars (#134, 144, and 170) showed normal range of semen parameters, but #199 and 171 boars showed abnormal ranges of semen parameters according to standard ranges of semen parameters. Unfortunately, #171 boar showed azoospermia symptom with rare sperm counts in the original semen. Conclusively, assessment of semen parameters by CASA system is useful to pre-screening of reproductively healthy boar prior to natural mating and artificial insemination for multiplication and breeding.

Identification of a Cancer Stem-like Population in the Lewis Lung Cancer Cell Line

  • Zhang, An-Mei;Fan, Ye;Yao, Quan;Ma, Hu;Lin, Sheng;Zhu, Cong-Hui;Wang, Xin-Xin;Liu, Jia;Zhu, Bo;Sun, Jian-Guo;Chen, Zheng-Tang
    • Asian Pacific Journal of Cancer Prevention
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    • 제13권3호
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    • pp.761-766
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    • 2012
  • Objective: Although various human cancer stem cells (CSCs) have been defined, their applications are restricted to immunocompromised models. Developing a novel CSC model which could be used in immunocompetent or transgenic mice is essential for further understanding of the biomolecular characteristics of tumor stem cells. Therefore, in this study, we analyzed murine lung cancer cells for the presence of CSCs. Methods: Side population (SP) cells were isolated by fluorescence activated cell sorting, followed by serum-free medium (SFM) culture, using Lewis lung carcinoma cell (LLC) line. The self-renewal, differentiated progeny, chemosensitivity, and tumorigenic properties in SP and non-SP cells were investigated through in vitro culture and in vivo serial transplantation. Differential expression profiles of stem cell markers were examined by RT-PCR. Results: The SP cell fraction comprised 1.1% of the total LLC population. SP cells were available to grow in SFM, and had significantly enhanced capacity for cell proliferation and colony formation. They were also more resistant to cisplatin in comparison to non-SP cells, and displayed increased tumorigenic ability. Moreover, SP cells showed higher mRNA expression of Oct-4, ABCG2, and CD44. Conclusion: We identified SP cells from a murine lung carcinoma, which possess well-known characteristics of CSCs. Our study established a useful model that should allow investigation of the biological features and pharmacosensitivity of lung CSCs, both in vitro and in syngeneic immunocompetent or transgenic/knockout mice.

형질전환 고구마에 대한 Glufosinate-ammonium 저항성 간이진단법 (Rapid Diagnosis of Resistance to Glufosinate-ammonium in Transgenic Sweet Potato)

  • 국용인
    • 한국잡초학회지
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    • 제30권4호
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    • pp.380-389
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    • 2010
  • 본 연구는 유전자총기법에 의해 생산된 형질전환 고구마를 사용하여 glufosinate-ammonium에 대한 저항성 유무를 빠르고, 경제적이며, 신뢰할 수 있는 간이분석법을 찾고자 수행되었다. 저항성 진단법은 whole-plant 진단법, one leaf 진단법 및 leaf disk 진단법을 사용하였고, 이들 진단법에 의해 glufosinateammonium을 처리하고 잎의 피해율과 암모늄 축적량을 조사하였다. Leaf disk 진단법에서 glufosinateammonium 처리 후 형질전환 라인 7171의 잎에 대한 약해는 wild type에 비해 1.9배 낮았다. One leaf 진단법과 whole plant 진단법의 경우 glufosinateammonium 처리 후 7171의 잎에 대한 약해는 wild type에 비해 각각 59배와 92배 적었다. Leaf disk, one leaf와 whole plant 진단법에서 0.5-5mM glufosinateammonium 처리 후 암모늄 축적은 wild type이 7171에 비해 각각 2-20, 4-43 및 6-115배 더 많이 축적되었다. 이들 3가지 방법 모두 형질전환 고구마에 대한 glufosinate-ammonium 저항성 유무를 판단하는데 가능한 방법이나 one leaf 진단법이 가장 간편하면서 빠른 진단방법이었다. 그러나 이 방법은 엽령별 내성차이가 존재할 수 있어 고구마 엽이 10개 전개되었을 때 1, 3, 5, 7, 9엽을 각각 채취하여 3mM glufosinateammonium을 처리시 잎의 피해율과 암모늄 축적을 엽령별로 조사한 결과 유의적인 차이를 보이지 않았다. 따라서 분석에 소요되는 기간, 시료량, 정확성 등을 고려할 때 형질전환 고구마의 저항성을 판별하는데 one leaf 진단법이 가장 적합한 것으로 판명 되었다.

체세포 핵치환 기술을 이용한 hGCSF와 GFP 유전자 동시발현 형질전환 소 배아 생산 (Production of hGCSF and GFP Co-Expressed Transgenic Cow Embryo by Somatic Cell Nuclear Transfer Technique)

  • 양정석;조소영;구본철;허영태;이수민;강만종;송혁;고대환;엄상준
    • 한국수정란이식학회지
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    • 제30권3호
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    • pp.219-224
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    • 2015
  • The purpose of this study is to develop transgenic cell line expressing targeted human granulocyte colony stimulating factor (hGCSF) and green fluorescence protein (GFP) genes as well as production of Somatic Cell Nuclear Transfer (SCNT) embryos derived from co-expressed transgenic donor cells. Constructed pPiggy-mWAP-hGCSF-EF1-GFP vector was chemically transfected into bovine fetus cells and then, only GFP expressed cells were selected as donor cells for SCNT. Cleavage and blastocyst rates of parthenogenetic, SCNT embryos using non-TG cell and hGCSF-GFP dual expressed SCNT embryos were examined (cleavage rate: $78.0{\pm}2.8$ vs. $73.1{\pm}3.2$ vs. $70.4{\pm}4.3%$, developmental rate: $27.2{\pm}3.2$ vs. $21.9{\pm}3.1$ vs. $17.0{\pm}2.9%$). Result indicated that cleavage and blastocyst rates of TG embryos were significantly lower (P<0.05) than those of parthenogenetic and non-TG embryos, respectively. In this study, we successfully produced hGCSF-GFP dual expressed SCNT embryos and cryopreserved to produce transgenic cattle for bioreactor system purpose. Further process of our research will transfer of transgenic embryos to recipients and production of hGCSF secreting cattle.