• 제목/요약/키워드: CycD3

검색결과 11건 처리시간 0.02초

Transgenic tobacco plants overexpressing the Nicta; CycD3; 4 gene demonstrate accelerated growth rates

  • Guo, Jia;Wang, Myeong-Hyeon
    • BMB Reports
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    • 제41권7호
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    • pp.542-547
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    • 2008
  • D-type cyclins control the onset of cell division and the response to extracellular signals during the G1 phase. In this study, we transformed a D-type cyclin gene, Nicta;CycD3;4, from Nicotiana tabacum using an Agrobacterium-mediated method. A predicted 1.1 kb cyclin gene was present in all of the transgenic plants, but not in wild-type. Northern analyses showed that the expression level of the Nicta;CycD3;4 gene in all of the transgenic plants was strong when compared to the wild-type plants, suggesting that Nicta;CycD3;4 gene driven by the CaMV 35S promoter was being overexpressed. Our results revealed that transgenic plants overexpressing Nicta;CycD3;4 had an accelerated growth rate when compared to wild-type plants, and that the transgenic plants exhibited a smaller cell size and a decreased cell population in young leaves when compared to wild-type plants.

감자 (Solanum tuberosum L.) CycD3유전자의 분리 및 특성 분석 (Isolation and Characterization of a cDNA Encoding CycD3 Gene from Potato(Solanum tuberosum L.))

  • 강인홍;최승호;이홍근;황현식;이석찬;정태영;임학태;배신철
    • Journal of Plant Biotechnology
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    • 제30권4호
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    • pp.329-334
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    • 2003
  • D-type cyclin은 호르몬과 영양분의 영향을 받아 세포주기의 G1기에서 S기로 전환을 조절하는 인자이다. 우리는 감자에서 이 유전자를 분리 해냈고, 염기서열 분석을 통하여 D3 cyclin으로 분류하였다. 그리고 StCycD3;1이라 명명하였다. 다른 D cyclin유전자가 세포 분열이 활발한 조직에서 발현되는 것과 같이 StCycD3;1은 감자의 괴경, 뿌리, 꽃, 잎, 줄기, 뿌리줄기, 복지에서 다양한 발현 양상을 보였고, 영양분의 하나인 sucrose에 의하여 발현이 유도되는 것을 확인하였다.

Effects of loading frequency and specimen size on the liquefaction resistance of clean sand

  • Sung-Sik Park;Dong-Eun Lee;Dong-Kiem-Lam Tran
    • Geomechanics and Engineering
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    • 제37권2호
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    • pp.123-133
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    • 2024
  • This study investigates the effects of loading frequency (f) and specimen size on the liquefaction resistance of clean sand. A series of cyclic direct simple shear tests were conducted on Jumunjin sand with varying consolidated relative densities (40% and 80%), f values (0.05, 0.10, and 0.20 Hz), and diameter to height (D/H) ratios (3.63, 3.18, 2.82, and 2.54). The results demonstrated the significant influence of f and D/H ratio on the number of cycles to liquefaction (Ncyc-liq) and the cyclic resistance ratio (CRR15). It was observed that increasing f linearly increased Ncyc-liq. Increasing the specimen height also led to higher Ncyc-liq values irrespective of the f or relative density. Moreover, a positive correlation between CRR15 and f indicated that higher f yielded higher CRR15. This relationship was more pronounced in dense sand than in loose sand. Specimen height also significantly affected CRR15, with increasing the specimen height resulting in higher CRR15 values. Furthermore, the effect of f on CRR15 was less significant compared to the influence of specimen height. The effect of f on the normalized cyclic resistance ratio (NCRR) was relatively negligible for loose sand but more substantial for dense sand depending on the D/H ratio. Data analysis revealed that the NCRR generally decreases as the D/H ratio increases. An interpolation formula was provided to calculate the NCRR based on the D/H ratio regardless of the f and relative density.

Effects of Abiotic Stresses on Cell Cycle Progression in Tobacco BY-2 Cells

  • Jang, Su Jin;Shin, Sung Hae;Yee, Sung Tae;Hwang, Baek;Im, Kyung Hoan;Park, Ky Young
    • Molecules and Cells
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    • 제20권1호
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    • pp.136-141
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    • 2005
  • Mild stresses such as high temperature ($30^{\circ}C$) or a low $H_2O_2$ concentration induced transient cell cycle arrest at G1/S or G2/M depending on the cell cycle stage at which the stress was applied. When stresses were introduced during G0 or G1, the G1/S checkpoint was mainly used; when stresses were introduced after S phase, G2/M was the primary checkpoint. The slowing of cell cycle progression was associated with transient delays in expression of A-, B-, and D-type cyclins. The delay in expression of NtcycA13, one of the A-type cyclins, was most pronounced. The levels of expression of Ntcyc29 (a cyclin B gene) and of CycD3-1 differed most depending on the applied stress, suggesting that different cellular adjustments to mild heat and a low concentration of $H_2O_2$ are reflected in the expression of these two cyclins.

Physiological Responses of Oxygen-Tolerant Anaerobic Bifidobacterium longum under Oxygen

  • Ahn, Jun-Bae;Hwang, Han-Joon;Park, Jong-Hyun
    • Journal of Microbiology and Biotechnology
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    • 제11권3호
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    • pp.443-451
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    • 2001
  • In order to investigate what kind of response anaerobic bifidobacteria has on oxygen stress, five oxygen-tolerant bifidobacteria were isolated from human fecal samples. All were temporarily identified as Bifidobacterium longum through an analysis of carbohydrate utilization patterns and cellular fatty acid profiles. In the presence of oxygen, the lag phase became extended and the cell growth was suppressed. Bifidobacterial cell was able to remove dissolved oxygen in an early stage of growth and to overcome oxygen stress to a certain extent. The cell became long n size and showed a rough surface containing many nodes which were derived from abnormal or incomplete cell division. Cellular fatty acid profiled changed remarkably under a partially aerobic condition, so that the carbon chain of cellular fatty acid became short. All the dimethyl acetals originated from plasmalogen were reduced, any cyclopropane fatty acid, 9, 10-methyleneoctadecanoic acid ($C_{19:0}cyc9,10$), was increased remarkably. Oxygen stress induced a 5.5 kD protein in B. longum JI 1 of the oxygen-teolerant bifidobacteria, that was named Osp protein, and its N-terminal amino acid sequence was as follows: unknown amino acid-Thr-Gly-Val-Arg-Phe-Ser-Asp-Asp-Glu. Therefore, the oxygen-tolerant bifidobacteria seemed to defend against oxygen stress byincreasing the content of short fatty acid and cyclopropane fatty acid, and induction of an oxygen stress protein, but not the plasmalogen.

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전조 뿌리의 유리 아미노산과 정유 성분 조성 (Composition of Free Amino Acids and Essential Oils in Root of Anthriscus sylvestylis)

  • 김상국;권태용;민기군;이승필;최부술;이상철
    • 한국작물학회지
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    • 제41권5호
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    • pp.521-525
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    • 1996
  • 본 연구는 우리나라에 자생하는 전조의 근에 대한 조성분, 유리 아미노산, 향기성분 등의 분석을 통하여 향료작물로서의 가능성을 검토하고자 수행하였는 바 얻어진 결과를 요약하면 다음과 같다 1. 전조 뿌리의 조성분가운데 조단백질은 7.69%, 조지방 1.74%, 조섬유 2.44%, 그리고 조회분은 3.76% 였으며 엑스 함량은 27.68%로 나타났다. 2. 유리 아미노산 조성 및 함량에서 종류는 총 16종이었으며 아미노산의 함량에 따른 순위는 phenylalanine>tyrosine>arginine>alanine>glutamic acid>aspartic acid>lysine>isoleucine>proline>glycine>histidine>thereonine>leucine>methionine>valine, serine이었고 유리 아미노산 함량 중 가장 높은 아미노산은 phenylalanlne으로 6.38 mg이었다. 3. 전조의 뿌리에 대한 향기성분은 $\alpha$-pinene, d-1imonene 등의 mono terpene류가 11종이었고 methyl eugenol 등의 phenyl propanoid류가 3종, 기타 8종으로 구성되어 있었으며 식물정유의 수율은 0.58%였다. 4. 종합적으로 볼 때, 한국산 전조에 대한 향료작물로서의 가능성이 있을 것으로 판단되어 금후 향기성분의 수율을 높이기 위한 재배법 연구의 일환으로 차광, 재배거리, 시비량 등의 시험이 필요한 것으로 판단되었다.

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수용성 폴리파라시클로판류와 약물과의 상호작용(제 3보)-수용액 중 수용성 폴리파라시클로판류와 형광 소수 나프탈렌 유도체류와의 복합체 형성- (Interactions between Water-Soluble Polyparacyclophanes and Drugs (III) -Complex Formation of Water-Soluble Polyparacyclophanes with Fluorescent Hydrophobic Naphthalene Derivatives in Aqueous Solution-)

  • 전인구;이민화
    • Journal of Pharmaceutical Investigation
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    • 제19권2호
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    • pp.71-79
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    • 1989
  • Complex formation of water-soluble polyparacyclophanes bearing two diphenylmethane or two diphenyl ether skeletons with l-anilinonaphthalene-8-sulfonate (ANS) and 2-p-toluidinylnaphthalene-6-sulfonate (TNS) was investigated quantitatively to develop useful host compounds comparing with ${\alpha}\;-\;and\;{\beta}-cyc1odextrins$$({\alpha}-\;and\;{\beta}-CyDs$) in aqueous solution. Benesi-Hildebrand type analysis of the fluorescent intensity showed that the dissociation constants (Kd) of paracyclophane-ANS complexes were $1.55\;{\times}\;10^{-4}M$ for 1,6,20,25-tetraaza[6.1.6.1]paracyclophane(CPM 44) and $1.23\;{\times}\;10^{-4}M$ for 1,7,21,27-tetraaza[7.1.7.1]paracyclophane (CPM 55), and those of paracyclophane-TNS complexes were $6.99\;{\times}\;10^{-6}M$ for CPM 44 and $6.23\;{\times}\;10^{-5}M$ for CPM 55, in 1:1 molar ratio. On the other hand, the Kd values of 1,7,21,27-tetraaza-14,34-dioxa[7.1.7.1]paracyclophane (CPE 55)-ANS, 1,8,22,29-tetraaza-15,36-dioxa[8.1.8.1]paracyclophane (CPE 66)-ANS, CPE 55-TNS, CPE 66-TNS complexes were $1.75\;{\times}\;10^{-3}M$, $3.07\;{\times}\;10^{-3}M$, $3.75\;{\times}\;10^{-3}M$ and $2.15\;{\times}\;10^{-3}M$, respectively. On the contrary, the Kd values of ${\alpha}-CyD-ANS$, ${\beta}-CyD-ANS$, ${\alpha}-CyD-TNS$ and ${\beta}-CyD-TNS$ complexes were found to be $3.98\;{\times}\;10^{-2}M$, $1.05\;{\times}\;10^{-2}M$, $1.38\;{\times}\;10^{-2}M$ and $3.52\;{\times}\;10^{-4}M$, respectively. These results mean that the complexation of CPMs with ANS or TNS is by 5.6-1,975 fold stronger than that for ${\alpha}-or\;{\beta}-CyDs$, and the complex formation of CPEs with ANS or TNS is nearly same as or somewhat stronger than that for ${\alpha}-or\;{\beta}-CyDs$. From the Kd values determined at different temperatures, thermodynamic parameters were calculated and the complexation was found to be a spontaneous exothermic reaction. The effects of pH on Kd values of CPM 44-ANS, and CPM 55-ANS complexes were negligible in the range of pH 1.2-1.8. However, the Kd values of these complexes increased significantly with increasing ionic strength.

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밤 저장(貯藏)에 관(關)한 연구(硏究) (Study on the Storage of Chestnut)

  • 임호;김정옥;신동화;서기봉
    • 한국식품과학회지
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    • 제12권3호
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    • pp.170-175
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    • 1980
  • 양산(量産)되는 방의 대량(大量) 장기(長期) 저장(貯藏)을 위(爲)해 숙도별(熟度別) 및 저장(貯藏) 조건(條件) 별(別)로 그 저장성(貯藏性)을 비교(比較) 시험(試驗)하고 출고(出庫)된 저장(貯藏) 밤의 성상변화(性狀變化)를 시험(試驗)한 결과(結果)는 다음과 같다. 1. 부패률(腐敗率) 10% 내외(內外)를 저장(貯藏) 한도(限度)로 볼 때 밤의 저장(貯藏) 가능(可能) 기간(期間)은 정온(定溫) 정습(定濕) 저장(貯藏)$(1{\pm}1^{\circ}C,\:85{\sim}95%\:RH)$ 으로는 $8{\sim}9$개월(個月)이고, 움 저장(貯藏)으로는 $4{\sim}5$개월(個月)이었다. 2. 저장성(貯藏性)은 숙도(熟度)에 크게 영향을 받고 있어서 $5.5^{\circ}$ Baume 의 염수로 선별(選別)된 미숙과(未熟果)는 숙과(熟果)에 비(比)해 최대(最大) 저장(貯藏) 가능(可能) 기간(期間)에서 2개월(個月) 정도(程度) 짧았다. 3. 저장(貯藏) 형태(形態)로 포장(包裝)된 밤의 전열(傳熱) 특성(特性)은 가장 전열(傳熱)이 늦은 중심(中心) 부위(部位)의 대기중(大氣中)에서의 온도상승(溫度上昇)으로 측정(測定)한 결과(結果)에서 j치(値)=1, $f_{h}$치(値)=320분(分)이었으며, 온도(溫度) 예측식(豫測式)은 $T_{\infty}-T=(T_{\infty}-T_0){\cdot}10^{-t/320}$로 표현(表現)될 수 있었다. 4. 정온(定溫) 정습(定濕)으로 4개월(個月) 저장(貯藏)된 밤의 출고후(出庫後) 유통(流通)및 보관(保管)은 보습재(保濕材)가 충진(充塡)된 원내(原來)의 포장(包裝) 형태(形態)가 가장 품질면(品質面)에서 유리(有利)하였다.한 것으로 생각된다.서는 백수발생시 평균 3.4-7.0cm, 부분퇴화가 4.2-5.2cm, 퇴화가 0.4-5.4cm, 줄기 고사가 0.4-0.6cm로 차이를 보였다. 제1절간장은 보리, 밀 각각 0.3-8.4cm, 0.2-24.2cm로 신장정도에서 저온에 따른 변이를 보였고, 지엽-이삭간 거리도 보리 -2.5∼-7.4cm, 밀 -0.6-11.5cm로 신장정도에 차이가 컸다.d from a constant temperature to a temperature cycle under DD. These results suggest that per/sup 01/ and tim/sup 01/ flies have a temperature-entrainable weak oscillatory mechanism. The fact that dClk/sup Jrk/ and cyc/sup 01/ flies did not show any sign of the endogenous oscillation suggests that the per-less oscillatory mechanism may require CLK and CYC.out to investigate the reactants between cement hydrates and chemical ions and some crystalline such as gypsum ettringite and Fridel′s salt were confirmed.ng for others, 3. Virtue of "forgiveness other′s mistakes"(from 3.32 to 3.65 for experimental group and from 3.33 to 3.25 for comparison group) in domain of kindness, concession, forgiveness,

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6-Amino-2-N-(n-propionylamino)selenazolo[4,5-f]indan의 합성 (Synthesis of 6-amino-2-N-(n-propionylamino)selenazolo[4,5-f]indan)

  • 김민겸;마은숙
    • 약학회지
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    • 제52권1호
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    • pp.20-26
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    • 2008
  • 2-Aminothiazole ring as a bioisoster of catechol in dopamine has provided with good oral availability and lipophilic property. Selenium was reported to have an improved antioxidant ability and to reduce the loss of dopamine. 2-Aminoindan, is a rigid form of dopamine, was evaluated as a dopamine agonist with low neurotoxocity. In order to develop a novel dopamine agonist, we tried to synthesize the selenazoloaminoindan derivative that is a hybrid structure of aminoindan and aminoselenazole instead of aminothiazole. 2-Indanone-2-oxime was reduced with $TiCl_4$ and $NaBH_4$ to form 2-aminoindan, which was reacted with propionyl chloride to give 2-N-n-propionylaminoindan (2). Compound 2 was reduced with $TiCl_4$ and $NaBH_4$ to afford 2-N-n-propylaminoindan (3) and it was nitrated and reduced to form 5-amino-2-N-n-propylaminoindan (5), which was reacted with KSeCN, $Br_2$, and glacial acetic acid to give 4,6-dibromo-5- amino-2-N-n-propylaminoindan (7) instead of selenazole ring formation. Otherwise, compound 2 was nitrated and hydrogenated to form 5-amino-2-N-n-propionylaminoindan (9), which was treated with KSeCN, $Br_2$, and glacial acetic acid to give 4,6-dibromo-5-amino-2-N-n-propionylaminoindan (10). Compound 9 was cyc1ized with KSeCN and glacial acetic acid in the absence of $Br_2$ to give 6-amino-2-N-(n-propionylamino)selenazolo[4,5-f]indan (11).

Src Kinase Regulates Nitric Oxide-induced Dedifferentiation and Cyc1ooxygenase-2 Expression in Articular Chondrocytes via p38 Kinase-dependent Pathway

  • Yu, Seon-Mi;Lee, Won-Kil;Yoon, Eun-Kyung;Lee, Ji-Hye;Lee, Sun-Ryung;Kim, Song-Ja
    • IMMUNE NETWORK
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    • 제6권4호
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    • pp.204-210
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    • 2006
  • Background: Nitric oxide (NO) in articular chondrocytes regulates dedifferentiation and inflammatory responses by modulating MAP kinases. In this study, we investigated whether the Src kinase in chondrocytes regulates NO-induced dedifferentiation and cyclooxygenase-2 (COX-2) expression. Methods: Primary chondrocytes were treated with various concentrations of SNP for 24 h. The COX-2 and type II collagen expression levels were determined by immunoblot analysis, and prostaglandin $E_2\;(PGE_2)$ was determined by using a $PGE_2$ assay kit. Expression and distribution of p-Caveolin and COX-2 in rabbit articular chondrocytes and cartilage explants were determined by immunohistochemical staining and immunocytochemical staining, respectively. Results: SNP treatment stimulated Src kinase activation in a dose-dependent manner in articular chondrocytes. The Src kinase inhibitors PP2 [4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo(3,4-d)pyrimidine], a significantly blocked SNP-induced p38 kinase and caveolin-1 activation in a dose-dependent manner. Therefore, to determine whether Src kinase activation is associated with dedifferentiation and/or COX-2 expression and $PGE_2$ production. As expected, PP2 potentiated SNP-stimulated dedifferentiation, but completely blocked both COX-2 expression and $PGE_2$ production. And also, levels of p-Caveolin and COX-2 protein expression were increased in SNP-treated primary chondrocytes and osteoarthritic and rheumatoid arthritic cartilage, suggesting that p-Caveolin may playa role in the inflammatory responses of arthritic cartilage. Conclusion: Our previously studies indicated that NO caused dedifferentiation and COX-2 expression is regulated by p38 kinase through caveolin-1 (1). Therefore, our results collectively suggest that Src kinase regulates NO-induced dedifferentiation and COX-2 expression in chondrocytes via p38 kinase in association with caveolin-1.