• Title/Summary/Keyword: $R_f$

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A Role for Arabidopsis miR399f in Salt, Drought, and ABA Signaling

  • Baek, Dongwon;Chun, Hyun Jin;Kang, Songhwa;Shin, Gilok;Park, Su Jung;Hong, Hyewon;Kim, Chanmin;Kim, Doh Hoon;Lee, Sang Yeol;Kim, Min Chul;Yun, Dae-Jin
    • Molecules and Cells
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    • v.39 no.2
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    • pp.111-118
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    • 2016
  • MiR399f plays a crucial role in maintaining phosphate homeostasis in Arabidopsis thaliana. Under phosphate starvation conditions, AtMYB2, which plays a role in plant salt and drought stress responses, directly regulates the expression of miR399f. In this study, we found that miR399f also participates in plant responses to abscisic acid (ABA), and to abiotic stresses including salt and drought. Salt and ABA treatment induced the expression of miR399f, as confirmed by histochemical analysis of promoter-GUS fusions. Transgenic Arabidopsis plants overexpressing miR399f (miR399f-OE) exhibited enhanced tolerance to salt stress and exogenous ABA, but hypersensitivity to drought. Our in silico analysis identified ABF3 and CSP41b as putative target genes of miR399f, and expression analysis revealed that mRNA levels of ABF3 and CSP41b decreased remarkably in miR399f-OE plants under salt stress and in response to treatment with ABA. Moreover, we showed that activation of stress-responsive gene expression in response to salt stress and ABA treatment was impaired in miR399f-OE plants. Thus, these results suggested that in addition to phosphate starvation signaling, miR399f might also modulates plant responses to salt, ABA, and drought, by regulating the expression of newly discovered target genes such as ABF3 and CSP41b.

ON t-ALMOST DEDEKIND GRADED DOMAINS

  • Chang, Gyu Whan;Oh, Dong Yeol
    • Bulletin of the Korean Mathematical Society
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    • v.54 no.6
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    • pp.1969-1980
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    • 2017
  • Let ${\Gamma}$ be a nonzero torsionless commutative cancellative monoid with quotient group ${\langle}{\Gamma}{\rangle}$, $R={\bigoplus}_{{\alpha}{\in}{\Gamma}}R_{\alpha}$ be a graded integral domain graded by ${\Gamma}$ such that $R_{{\alpha}}{\neq}\{0\}$ for all ${\alpha}{\in}{\Gamma},H$ be the set of nonzero homogeneous elements of R, C(f) be the ideal of R generated by the homogeneous components of $f{\in}R$, and $N(H)=\{f{\in}R{\mid}C(f)_v=R\}$. In this paper, we introduce the notion of graded t-almost Dedekind domains. We then show that R is a t-almost Dedekind domain if and only if R is a graded t-almost Dedekind domain and RH is a t-almost Dedekind domains. We also show that if $R=D[{\Gamma}]$ is the monoid domain of ${\Gamma}$ over an integral domain D, then R is a graded t-almost Dedekind domain if and only if D and ${\Gamma}$ are t-almost Dedekind, if and only if $R_{N(H)}$ is an almost Dedekind domain. In particular, if ${\langle}{\Gamma}{\rangle}$ isatisfies the ascending chain condition on its cyclic subgroups, then $R=D[{\Gamma}]$ is a t-almost Dedekind domain if and only if R is a graded t-almost Dedekind domain.

Insulin Inhibits the Expression of Adiponectin and AdipoR2 mRNA in Cultured Bovine Adipocytes

  • Sun, Y.G.;Zan, L.S.;Wang, H.B.;Guo, H.F.;Yang, D.P.;Zhao, X.L.;Gui, L.S.
    • Asian-Australasian Journal of Animal Sciences
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    • v.22 no.10
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    • pp.1429-1436
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    • 2009
  • Adiponectin is an adipocyte-derived protein that has a regulatory role in energy homeostasis and influences insulin sensitivity. Its effects on glucose utilization and lipid metabolism are mediated by AdipoR1 and AdipoR2. How insulin affects adiponectin gene expression and secretion is still controversial. This study was conducted to determine the expression of adiponectin, AdipRs and $PPAR-\gamma$ during the differentiation of bovine preadipocytes and the effect of insulin on expression of these genes in bovine adipocytes. The bovine preadipocytes started to accumulate lipids three days after differentiation was induced, with increased expression of adiponectin, AdipoR2 and $PPAR-\gamma$ mRNAs. Insulin decreased the expression of adiponectin mRNA in a dose- and time-dependent fashion, and the inhibition was detectable at insulin concentrations as low as 10 nM and as early as 2 h after addition of 100 nM insulin. Insulin also inhibited the expression of AdipoR2 mRNA at concentrations from 1 to 1,000 nM or 24 h after addition of 100 nM insulin, but did not affect the expression of AdipoR1 in bovine adipocytes. Inhibition of PI3K with LY294002 reversed the inhibition of adiponectin and AdipoR2 mRNA expression by insulin. These results suggest that insulin suppresses the expression of adiponectin and AdipoR2 at least partially via the PI3K signal pathway.

A Study of correlation between spherical refractive error and astigmatism (굴절이상도와 난시와의 관계 연구)

  • Lee, Jeung-Young;Kim, Jae-Do;Kim, Dae-Hyun
    • Journal of Korean Ophthalmic Optics Society
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    • v.9 no.2
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    • pp.439-446
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    • 2004
  • Many studies have reported that retinal defocus cause and increase refractive error specially myopia. Uncorrected astigmatism may be one factor of retinal defocus factors. To understand the relationship between myopia and astigmatism 62 college students were participated in this study. Spherical refractive error and astigmatism were measured using N-vision 5001 autorefractor (Shinnippon). Co-relations between spherical refractive error and astigmatism were high both in the with-the-rule astigmatism group(r=0.53; ANOVA F=32.40, N=87, P<0.05) and oblique astigmatism group (r=0.53ANOVA F=5.14, N=15, P<0.001). However it was very low (r=0.09; ANOVA F=0.18, N=22, P<0.001)in the against-the-rule stigmatism group. In the total group co-relation was also high (r=0.56: ANOVA F=77.80, N=173, P<0.001). Uncorrected astigmatism may cause and increase spherical refractive error.

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Linear Free Energy Relationship on the Phosphorylation of Acetylcholinesterase by Insecticidal O,O-Diethylphenylphosphate Derivatives (살충성(殺蟲性) O,O-Diethylphenylphosphate유도체(誘導體)들에 의(依)한 Acetylcholinesterase의 Phosphorylation에 미치는 자유(自由)에너지 관계(關係))

  • Sung, Nack-Do
    • Korean Journal of Agricultural Science
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    • v.11 no.1
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    • pp.176-181
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    • 1984
  • Linear free energy relation ship(LFER) on the insecticidal activity of O,O-diethylphenylphosphate (A) and 3,5-dimethylphenyl-O,O-diethylphosphate (B) derivatives were studied by EHT MO calculation method and regression analysis method. LFER between varying substituent constants and $pI_{50}$ constants of phosphates, (A) & (B) were calculated with applying Hammett, Okamoto-Brown, Taft and Swain-Lupton's DSP equations;percent resonance effect(R) and field effect(F) of (A) were %R=33.5 & %F=66.5 and also that of (B) were %R=2 & %F=98, respectively. On the basis of above findings, the insecticidal activities were similar for both (A) and (B), but (B) have larger field and inductive contribution than (A), due to the 3,5-dimethyl group of (B).

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LINC00174 Facilitates Proliferation and Migration of Colorectal Cancer Cells via MiR-3127-5p/ E2F7 Axis

  • Ma, Yuhong;Li, Yuzhen;Tang, Yuanyuan;Tang, Ning;Wang, Dengke;Li, Xiaofei
    • Journal of Microbiology and Biotechnology
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    • v.31 no.8
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    • pp.1098-1108
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    • 2021
  • The literature indicates that LINC00174 promotes the growth of colorectal cancer (CRC) cells, but its research needs to be enriched. We tried to explore the function and mechanism of LINC00174 in CRC cell proliferation and migration. Bioinformatics analysis predicted the binding relationship and expressions of lncRNA, miRNA and mRNA. Clinical study analyzes the relationship between LINC00174 and clinical data characteristics of CRC patients. The expressions of LINC00174, miR-3127-5p and E2F7 were verified by RT-qPCR, and the combination of the two was verified by dual luciferase analysis and RNA immunoprecipitation as needed. Western blot was used to detect the expression of EMT-related protein and E2F7 protein. Functional experiments were used to evaluate the function of the target gene on CRC cells. LINC00174 was up-regulated in CRC clinical samples and cells and was related to the clinical characteristics of CRC patients. High-expression of LINC00174, contrary to the effect of siLINC00174, promoted cell viability, proliferation, migration and invasion, up-regulated the expressions of N-Cadherin, Vimentin, E2F7, and inhibited the expression of E-Cadherin. MiR-3127-5p was one of the targeted miRNAs of LINC00174 and was down-regulated in CRC samples. In addition, miR-3127-5p mimic partially reversed the malignant phenotype of CRC cells induced by LINC00174. Besides, E2F7 was a target gene of miR-3127-5p, and LINC00174 repressed miR-3127-5p to regulate E2F7. Our research reveals that LINC00174 affected the biological characteristics of CRC cells through regulated miR-3127-5p/ E2F7 axis.

Nature of Suppressiveness and Conduciveness of Some plant pathogens in Soils (토양내(土壤內) 식물(植物) 병원균(病原菌)의 발병억제(發病抑制) 및 유발성질(誘發性質))

  • Shim, Jae-Ouk;Lee, Min-Woong
    • The Korean Journal of Mycology
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    • v.18 no.3
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    • pp.164-177
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    • 1990
  • This study was carried out to obtain some useful data for increasing an effective ginseng production. There was a direct relationship (r=0.2645) between spore germination of Fusarium solani and soil pH, and (r=0.315) between Cylindrocarpon destructans and soil pH. On the other hand, there was a direct relationship (r=0.19) between relative hyphal growth of Rhizoctonia solani and soil pH. There was a direct relationship (r=0.21) between number of total bacteria and F. solani, (r=0.37) between actinomycetes and F. solani and (r=0.20) between celluloytic bacteria and F. solani. However, there was an inverse relationship (r=-0.20) between number of total fungi and F. solani. There was a direct relationship (r=0.24) between number of actinomycetes and R. solani. Each ginseng pathogen-suppressive soil screened was 40 in F. solani, 20 in C. destructans and 9 soil samples in R. solani among 146 soil samples, respectively. The mean contents of K, Ca and Mg were fairly lower in each ginseng pathogen-suppressive soil than conducive soil, whereas Na were somewhat lower. The mean contents of organic matter were over 2 times higher in each ginseng pathogen-suppressive soil than conducive soil. The mean contents of phosphate were fairly lower in F. solani and R. solani-suppressive soil than conducive soil and, on the other hand, were somewhat higher in C. destructans-suppressive soil than conducive soil. The mean soil pH was somewhat lower in each ginseng pathogen-suppressive soil than conducive soil. The mean contents of sand were about 2 times higher in each ginseng pathogen­suppressive soil than conducive soil, whereas silt and clay were somewhat lower. The microbial numbers of total bacteria, total fungi and celluloytic fungi were higher in F. solani-suppressive soil than conducive soil, whereas actinomycetes and celluloytic bacteria were lower. Each microbial number of total bacteria or total fungi indicated a significant difference (p=0.05) between F. solani­suppressive and conducive soil, and the microbial number of actinomycetes was a highly significant difference (p=0.01) between F. solani-suppressive and conducive soil. The microbial numbers of total bacteria, total fungi, actinomycetes and celluloytic fungi were higher in C. destructans-suppressive soil than conducive soil, whereas celluloytic bacteria were about 2 times lower. On the other hand, the microbial numbers of total fungi were higher in R. solani-suppressive soil than conducive soil, whereas total bacteria, actinomycetes, celluloytic bacteria and celluloytic fungi were lower. Fourteen of 16 F. solani-suppressive soils tested were suppressive to ginseng root rot, whereas fifteen of 16 C. destructans-suppressive soils were suppressive. Ginseng root rots of ginseng disease-suppressive soils were in the range of 1.0-17.4% in F. solani-suppressive soil and 0.2-20.4% in C. destructans-suppressive soil, respectively.

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THE ITERATION OF ENTIRE FUNCTION

  • Sun, Jianwu
    • Bulletin of the Korean Mathematical Society
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    • v.38 no.2
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    • pp.369-378
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    • 2001
  • In this paper, we obtain the following results: Let f be a transcendental entire function with log M(r,f)=$O(log r)^\beta (e^{log r}^\alpha)\; (0\leq\alpha<1,\beta>1$). Then every component of N(f) is bounded. This result generalizes the result of Baker.

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Power consumption of skull melting

  • Assmus, W.;Gross, C.;Muiznieks, A.;Raming, G.;Muhlbauer, A.;Stenzel, C.
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.9 no.4
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    • pp.353-359
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    • 1999
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