975 research outputs found

    A multi-dimensional approach from seed-to-seed to understand and improve heat stress tolerance in rice

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    In changing climatic conditions, stress caused by high temperature poses a serious threat to rice cultivation. Physiological, biochemical, and molecular analysis of rice cultivars revealed that Nagina22 (N22) shows lesser reduction in chlorophyll content, net photosynthetic rate, spikelet fertility and grain yield, but increased membrane thermal stability, antioxidant enzymes activity and transpiration rate (E) at high temperature. DREB, RAB, LEA, and genes associated with hormones signalling were induced during germination, while OsFd (an iron sulphur cluster binding protein) and CWIP (cell wall integrity protein) emerged as high priority candidate genes in seedling and reproductive stages. Their function is being analysed by transgene expression and CRISPR/Cas genome editing approaches. Field screening in polyhouse, late sowing and temperature gradient chamber for 20 morpho-physiological traits indicated the importance of both yield and spikelet fertility, and photosynthesis traits. N22 showed the least Heat Susceptibility Index (HSI) for yield/plant, spikelet fertility, flag leaf SPAD and stomatal conductance, while Vandana showed the highest HSI for spikelet fertility and flag leaf temperature. QTLs for HSI of spikelet fertility were identified on chromosome 1 and HSI of yield per plant on chromosomes 1, 2, 3, 4, 7 and 8; and PV of 6% to 57% using 174 F2-3 Vandana x N22 mapping population. Simultaneously, RNAseq was performed to identify the genome wide miRNAs and transcriptome of N22 and Vandana from shoot and root after short and long duration of heat stress treatments; and recovery phase for an eQTL-guided function-related co-expression analysis to identify the putative regulators and gene regulatory networks

    Insilico and Invitro anthelmintic properties of phytocompounds in Rostellularia quinquangularis (J. Koenig ex Roxb.) Nees

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    The present study aimed to evaluate the anthelmintic activity of various extracts of Rostellularia quinquangularis (R. quinquangularis) against adult Indian earthworms (Pheretima posthuma). Petroleum ether extract (PERQ), ethyl acetate extract (RQEA), and ethanol extract (RQEE) of R. quinquangularis were tested at different concentrations (10, 20, 50, and 100 mg/mL), along with the positive control (albendazole) and negative control (normal saline). Anthelmintic activity was assessed based on the duration of paralysis and mortality. The RQEE extract showed significant anthelmintic activity, with the highest activity observed at a concentration of 100 mg/mL, exhibiting paralysis time of 1.62 min and death times of 19.9 min, compared to the standard albendazole. Further, HR LC-MS analysis of the RQEE extract revealed the presence of various phytoconstituents based on m/z signals. Molecular docking analysis using AutoDock Vina indicated that Columbianetin, Dunnione, Cryptochlorogenic acid, Gaylussacin, Luvangetin, and Albendazole showed docking scores of -8.1, -7.9, -7.4, -7.3, -7.2, and -6.8 Kcal/mol, respectively. These results suggest that R. quinquangularis possesses potent anthelmintic activity, supporting its traditional use in medicinal practices.

    Deep sequencing of small RNAs reveals ribosomal origin of microRNAs in Oryza sativa and their regulatory role in high temperature

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    MicroRNAs are small noncoding regulatory RNAs which control gene expression by mRNA degradation or translational repression. They are significant molecular players regulating important biological processes such as developmental timing and stress response. We report here the discovery of miRNAs derived from ribosomal DNA using the small RNA datasets of 16 deep sequencing libraries of rice. Twelve putative miRNAs were identified based on highly stringent criteria of novel miRNA prediction. Surprisingly, 10 putative miRNAs (mi_7403, mi_8435, mi_12675, mi_4266, mi_4758, mi_4218, mi_8200, mi_4644, mi_14291, mi_16235) originated from rDNA of rice chromosome 9. Expression analysis of putative miRNAs and their target genes in heat tolerant and susceptible rice cultivars in control and high temperature treated seedlings revealed differential regulation of rDNA derived miRNAs. This is the first report of rDNA derived miRNAs in rice which indicates their role in gene regulation during high temperature stress in plants. Further studies in this area will open new research challenges and opportunities to broaden our knowledge on gene regulation mechanisms

    Observation of D0ρ0γD^0\to \rho^0\gamma and search for CPCP violation in radiative charm decays

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    We report the first observation of the radiative charm decay D0ρ0γD^0 \to \rho^0 \gamma and the first search for CPCP violation in decays D0ρ0γD^0 \to \rho^0 \gamma, ϕγ\phi\gamma, and K0γ\overline{K}{}^{*0} \gamma, using a data sample of 943 fb1^{-1} collected with the Belle detector at the KEKB asymmetric-energy e+ee^+e^- collider. The branching fraction is measured to be B(D0ρ0γ)=(1.77±0.30±0.07)×105\mathcal{B}(D^0 \to \rho^0 \gamma)=(1.77 \pm 0.30 \pm 0.07) \times 10^{-5}, where the first uncertainty is statistical and the second is systematic. The obtained CPCP asymmetries, ACP(D0ρ0γ)=+0.056±0.152±0.006\mathcal{A}_{CP}(D^0 \to \rho^0 \gamma)=+0.056 \pm 0.152 \pm 0.006, ACP(D0ϕγ)=0.094±0.066±0.001\mathcal{A}_{CP}(D^0 \to \phi \gamma)=-0.094 \pm 0.066 \pm 0.001, and ACP(D0K0γ)=0.003±0.020±0.000\mathcal{A}_{CP}(D^0 \to \overline{K}{}^{*0} \gamma)=-0.003 \pm 0.020 \pm 0.000, are consistent with no CPCP violation. We also present an improved measurement of the branching fractions B(D0ϕγ)=(2.76±0.19±0.10)×105\mathcal{B}(D^0 \to \phi \gamma)=(2.76 \pm 0.19 \pm 0.10) \times 10^{-5} and B(D0K0γ)=(4.66±0.21±0.21)×104\mathcal{B}(D^0 \to \overline{K}{}^{*0} \gamma)=(4.66 \pm 0.21 \pm 0.21) \times 10^{-4}

    Search for CPCP violation in the D+π+π0D^{+}\to\pi^{+}\pi^{0} decay at Belle

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    We search for CPCP violation in the charged charm meson decay D+π+π0D^{+}\to\pi^{+}\pi^{0}, based on a data sample corresponding to an integrated luminosity of 921 fb1\rm 921~fb^{-1} collected by the Belle experiment at the KEKB e+ee^{+}e^{-} asymmetric-energy collider. The measured CPCP violating asymmetry is [+2.31±1.24(stat)±0.23(syst)]%[+2.31\pm1.24({\rm stat})\pm0.23({\rm syst})]\%, which is consistent with the standard model prediction and has a significantly improved precision compared to previous results.Comment: 8 pages, 3 figure

    Evidence for Isospin Violation and Measurement of CPCP Asymmetries in BK(892)γB \to K^{\ast}(892) \gamma

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    We report the first evidence for isospin violation in BKγB \to K^* \gamma and the first measurement of difference of CPCP asymmetries between B+K+γB^+ \to K^{*+} \gamma and B0K0γB^0 \to K^{*0} \gamma. This analysis is based on the data sample containing 772×106BBˉ772 \times 10^6 B\bar{B} pairs that was collected with the Belle detector at the KEKB energy-asymmetric e+ee^+ e^- collider. We find evidence for the isospin violation with a significance of 3.1σ\sigma, Δ0+=(+6.2±1.5(stat.)±0.6(syst.)±1.2(f+/f00))\Delta_{0+} = (+6.2 \pm 1.5 ({\rm stat.}) \pm 0.6 ({\rm syst.}) \pm 1.2 (f_{+-}/f_{00}))\%, where the third uncertainty is due to the uncertainty on the fraction of B+BB^+B^- to B0Bˉ0B^0\bar{B}^0 production in Υ(4S)\Upsilon(4S) decays. The measured value is consistent with predictions of the SM. The result for the difference of CPCP asymmetries is ΔACP=(+2.4±2.8(stat.)±0.5(syst.))\Delta A_{CP} = (+2.4 \pm 2.8({\rm stat.}) \pm 0.5({\rm syst.}))\%, consistent with zero. The measured branching fractions and CPCP asymmetries for charged and neutral BB meson decays are the most precise to date. We also calculate the ratio of branching fractions of B0K0γB^0 \to K^{*0} \gamma to Bs0ϕγB_s^0 \to \phi \gamma.Comment: 11 pages, 7 figures. shown at FPCP2017. accepted by PR

    Angular analysis of B0K(892)0+B^0 \to K^\ast(892)^0 \ell^+ \ell^-

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    We present a measurement of angular observables, P4P_4', P5P_5', P6P_6', P8P_8', in the decay B0K(892)0+B^0 \to K^\ast(892)^0 \ell^+ \ell^-, where +\ell^+\ell^- is either e+ee^+e^- or μ+μ\mu^+\mu^-. The analysis is performed on a data sample corresponding to an integrated luminosity of 711 fb1711~\mathrm{fb}^{-1} containing 772×106772\times 10^{6} BBˉB\bar B pairs, collected at the Υ(4S)\Upsilon(4S) resonance with the Belle detector at the asymmetric-energy e+ee^+e^- collider KEKB. Four angular observables, P4,5,6,8P_{4,5,6,8}' are extracted in five bins of the invariant mass squared of the lepton system, q2q^2. We compare our results for P4,5,6,8P_{4,5,6,8}' with Standard Model predictions including the q2q^2 region in which the LHCb collaboration reported the so-called P5P_5' anomaly.Comment: Conference paper for LHC Ski 2016. SM prediction for P6P_{6}' corrected and reference for arXiv:1207.2753 adde

    Measurement of the τ\tau lepton polarization and R(D)R(D^*) in the decay BˉDτνˉτ\bar{B} \to D^* \tau^- \bar{\nu}_\tau

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    We report the first measurement of the τ\tau lepton polarization Pτ(D)P_\tau(D^*) in the decay BˉDτνˉτ\bar{B} \rightarrow D^* \tau^- \bar{\nu}_\tau as well as a new measurement of the ratio of the branching fractions R(D)=B(BˉDτνˉτ)/B(BˉDνˉ)R(D^{*}) = \mathcal{B}(\bar {B} \rightarrow D^* \tau^- \bar{\nu}_\tau) / \mathcal{B}(\bar{B} \rightarrow D^* \ell^- \bar{\nu}_\ell), where \ell^- denotes an electron or a muon, and the τ\tau is reconstructed in the modes τπντ\tau^- \rightarrow \pi^- \nu_\tau and τρντ\tau^- \rightarrow \rho^- \nu_\tau. We use the full data sample of 772×106772 \times 10^6 BBˉB{\bar B} pairs recorded with the Belle detector at the KEKB electron-positron collider. Our results, Pτ(D)=0.38±0.51(stat.)0.16+0.21(syst.)P_\tau(D^*) = -0.38 \pm 0.51 {\rm (stat.)} ^{+0.21}_{-0.16} {\rm (syst.)} and R(D)=0.270±0.035(stat.)0.025+0.028(syst.)R(D^*) = 0.270 \pm 0.035{\rm (stat.)} ^{+0.028}_{-0.025}{\rm (syst.)}, are consistent with the theoretical predictions of the Standard Model.Comment: 7 pages, 2 figures, submitted to Physical Review Letters; one figure was removed from the first versio
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