2,880 research outputs found

    Floral induction and flower formation : the role and potential applications of miRNAs

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    The multiple regulatory pathways controlling flowering and flower development are varied and complex, and they require tight control of gene expression and protein levels. MicroRNAs (miRNAs) act at both the transcriptional and post-transcriptional level to regulate key genes involved in flowering-related processes such as the juvenile–adult transition, the induction of floral competence and flower development. Many different miRNA families are involved in these processes and their roles are summarized in this review, along with potential biotechnological applications for miRNAs in controlling processes related to flowering and flower development

    Systemic movement of FT mRNA and a possible role in floral induction

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    FLOWERING LOCUS T (FT) protein is known to be part of the mobile flowering inducing “florigen” signal in plants, but it may not be acting alone. This article reviews the data that FT mRNA can also move systemically throughout the plant and into the shoot apical meristem (SAM) independently of the FT protein. There is a promotion of flowering when increased levels of virally expressed FT mRNA are present together with endogenously produced FT protein in inducing conditions, even if the additional FT mRNA is non-translatable and thus not increasing the overall levels of FT protein. A specific sequence, or “zip code” of the FT mRNA is required for systemic movement and this sequence binds a specific protein(s) in plant extracts. This raises the possibility the FT mRNA may be moving systemically through the plant and into the SAM as an RNA–protein complex, whether FT protein is also a component of this mobile complex remains to be determined

    The Lorentz Force and the Radiation Pressure of Light

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    In order to make plausible the idea that light exerts a pressure on matter, some introductory physics texts consider the force exerted by an electromagnetic wave on an electron. The argument as presented is both mathematically incorrect and has several serious conceptual difficulties without obvious resolution at the classical, yet alone introductory, level. We discuss these difficulties and propose an alternate demonstration.Comment: More or less as in AJ

    "Quantum Interference with Slits" Revisited

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    Marcella [arXiv:quant-ph/0703126] has presented a straightforward technique employing the Dirac formalism to calculate single- and double-slit interference patterns. He claims that no reference is made to classical optics or scattering theory and that his method therefore provides a purely quantum mechanical description of these experiments. He also presents his calculation as if no approximations are employed. We show that he implicitly makes the same approximations found in classical treatments of interference and that no new physics has been introduced. At the same time, some of the quantum mechanical arguments Marcella gives are, at best, misleading.Comment: 11 pages, 3 figure

    Spectroscopy of B_c Mesons in the Relativized Quark Model

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    We calculate the spectrum of the charm-beauty mesons using the relativized quark model. Using the wavefunctions from this model we compute the radiative widths of excited c\bar{b} states. The hadronic transition rates between c\bar{b} states are estimated using the Kuang-Yan approach and are combined with the radiative widths to give estimates of the relative branching ratios. These results are combined with production rates at the Tevatron and the LHC to suggest promising signals for excited B_c states. Our results are compared with other models to gauge the reliability of the predictions and point out differences.Comment: 15 pages, 1 fig. uses revtex4. References adde

    Quantum simulation of multiple-exciton generation in a nanocrystal by a single photon

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    We have shown theoretically that efficient multiple exciton generation (MEG) by a single photon can be observed in small nanocrystals (NCs). Our quantum simulations that include hundreds of thousands of exciton and multi-exciton states demonstrate that the complex time-dependent dynamics of these states in a closed electronic system yields a saturated MEG effect on a picosecond timescale. Including phonon relaxation confirms that efficient MEG requires the exciton--biexciton coupling time to be faster than exciton relaxation time

    Radiation from a Charge Uniformly Accelerated for All Time

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    A recent paper of Singal [Gen. Rel. Grav. 27 (1995), 953-967] argues that a uniformly accelerated particle does not radiate, in contradiction to the consensus of the research literature over the past 30 years. This note points out some questionable aspects of Singal's argument and shows how similar calculations can lead to the opposite conclusion.Comment: LaTeX, 9 pages, to appear in General Relativity and Gravitatio

    Selection of reference genes for diurnal and developmental time-course real-time PCR expression analyses in lettuce

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    Background: Real-time quantitative polymerase chain reaction (RT-qPCR) analysis is a low cost and sensitive technique that is widely used to measure levels of gene expression. Selecting and validating appropriate reference genes for normalising target gene expression should be the first step in any expression study to avoid inaccurate results. Results: In this study, ten candidate genes were tested for their suitability for use as reference genes in diurnal and developmental timecourse experiments in lettuce. The candidate reference genes were then used to normalise the expression pattern of the FLOWERING LOCUS T (FT) gene, one of key genes involved in the flowering time pathway whose expression is known to vary throughout the day and at different stages of development. Three reference genes, LsPP2A-1 (PROTEIN PHOSPHATASE 2A-1), LsPP2AA3 (PROTEIN PHOSPHATASE 2A REGULATORY SUBUNIT A3) and LsTIP41 (TAP42-INTERACTING PROTEIN OF 41 kDa), were the most stably expressed candidate reference genes throughout both the diurnal and developmental timecourse experiments. In the developmental experiment using just LsPP2A-1 and LsTIP41 as reference genes would be sufficient for accurate normalisation, whilst in the diurnal experiment all three reference genes, LsPP2A-1, LsPP2AA3 and LsTIP41, would be necessary. The FT expression pattern obtained demonstrates that the use of multiple and robust reference genes for RT-qPCR expression analyses results in a more accurate and reliable expression profile. Conclusions: Reference genes suitable for use in diurnal and developmental timecourse experiments in lettuce were identified and used to produce a more accurate and reliable analysis of lsFT expression levels than previously obtained in such timecourse experiments
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