3 resultados para Its dna barcodes

em Universidad Politécnica de Madrid


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Protein hydrolysis plays an important role during seed germination and post-germination seedling establishment. In Arabidopsis thaliana, cathepsin B-like proteases are encoded by a gene family of three members, but only the AtCathB3 gene is highly induced upon seed germination and at the early post-germination stage. Seeds of a homozygous T-DNA insertion mutant in the AtCathB3 gene have, besides a reduced cathepsin B activity, a slower germination than the wild type. To explore the transcriptional regulation of this gene, we used a combined phylogenetic shadowing approach together with a yeast one-hybrid screening of an arrayed library of approximately 1200 transcription factor open reading frames from Arabidopsis thaliana. We identified a conserved CathB3-element in the promoters of orthologous CathB3 genes within the Brassicaceae species analysed, and, as its DNA-interacting protein, the G-Box Binding Factor1 (GBF1). Transient overexpression of GBF1 together with a PAtCathB3::uidA (β-glucuronidase) construct in tobacco plants revealed a negative effect of GBF1 on expression driven by the AtCathB3 promoter. In stable P35S::GBF1 lines, not only was the expression of the AtCathB3 gene drastically reduced, but a significant slower germination was also observed. In the homozygous knockout mutant for the GBF1 gene, the opposite effect was found. These data indicate that GBF1 is a transcriptional repressor of the AtCathB3 gene and affects the germination kinetics of Arabidopsis thaliana seeds. As AtCathB3 is also expressed during post-germination in the cotyledons, a role for the AtCathB3-like protease in reserve mobilization is also inferred.

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Los enjarjes, jarjas o jarjamentos conforman el comienzo de la bóveda de crucería, el lugar en el que todos los nervios nacen reunidos. Permiten la transición entre el muro y las dovelas que constituyen nervios, resolviendo un encuentro de gran importancia constructiva. Están compuestos por piezas de lechos horizontales que traban con el muro y que, además de conformar el arranque de los nervios, han de proporcionar apoyo a las primeras dovelas. Al construirse a la vez que el muro y antes que el resto de la bóveda, se podría decir que son los encargados de portar su ADN: en ellos queda registrado el número de nervios que tendrá la bóveda, su curvatura, desde qué altura arrancará cada uno, su perfil, etc. El objetivo de este trabajo se centra en estudio de los enjarjes en la obra de Guillem Sagrera abordando su dimensión tecnológica, constructiva y de diseño. Dos características los distinguen de otras soluciones y justifican su interés: los nervios surgen directamente del muro, sin la intermediación de capiteles, ménsulas o pilastras; y se diseñan con la intención de facilitar la aparición de intersecciones entre las molduras de sus perfiles, en algunos casos mediante el cruce de los ejes de los nervios. Sagrera nos acerca a una innovación arquitectónica en la que el esfuerzo no se centra en realizar bóvedas con muchos nervios o con trazados en planta complejos, sino en la cuidada resolución de este encuentro de nervios. En ella se adivina el trabajo minucioso con las plantillas que controlan el trazado del contorno de los lechos de las piezas y la hábil mano de los canteros que son capaces de tallar intersecciones de gran complejidad. Se ha realizado un repaso de los primeros experimentos relativos al modo de relacionarse los nervios entre sí para ilustrar el contexto y origen de las soluciones realizadas por Guillem Sagrera. Mostramos que ante ciertas dificultades, consecuencia de la reunión de nervios, los constructores fueron capaces de desarrollar nuevas soluciones, mediante la experimentación con un sistema constructivo que conocían y manejaban con destreza. Para acercarnos a la comprensión de las estrategias de diseño que permiten el proyecto de estos enjarjes y los procedimientos técnicos y constructivos necesarios para su ejecución, nos vimos en la necesidad de adentrarnos en la problemática general de los enjarjes de la bóveda de crucería. De este modo, lo que empezó siendo una introducción para poder contextualizar la obra del mallorquín acabó convirtiéndose en la primera parte de la tesis, cuyo volumen prácticamente equipara a la segunda. En ella presentamos el proceso de diseño, trazado y talla de los cuatro enjarjes llevados a cabo en el taller de cantería de la ETSAM, en los que hemos podido experimentar de manera práctica los aspectos teóricos desarrollados. Estos ensayos nos han permitido contrastar hipótesis y baremar la dificultad de ciertos procedimientos o procesos, así como acercarnos realmente al elemento constructivo. El trabajo práctico nos ha enseñado a no fiarnos siempre de las hipótesis que se desarrollan modelando con el ordenador o dibujando; a valorar el pensar con las manos. En relación con la obra de Sagrera, la presente investigación realiza aportaciones al conocimiento del cambio proyectual y constructivo llevado a cabo en los arranques de las bóvedas entre los siglos XIII y XV, cuando los nervios comienzan a surgir directamente de los soportes y se dan los primeros cruzamientos. Mostramos que ya no solamente se construyen enjarjes fruto directo de la geometría general de la bóveda, sino que se llevan a cabo cambios deliberados en relación a su resultado, en los que se advierten decisiones proyectuales que, por supuesto, no serían viables sin las posibilidades que ofrece el trabajo con plantillas. ABSTRACT The solid blocks commonly known as tas-de-charge (in Spanish enjarjes, jarjas or jarjamentos) constitute the beginning of the ribbed vault – the place from which all the ribs spring together. They facilitate a transition between the wall and the rib voussoirs, and thus solve a junction of utmost constructive importance. They consist of blocks set in horizontal courses which interlock with the wall and which, as well as constituting the springing of the ribs, serve as a support for their first voussoirs. The tas-de-charge are built simultaneously with the wall and well before the remainder of the vault – thus, they arguably carry itsDNA’, since they register how many ribs the vault will have as well as their curvature, their springing height or their profile. This work is focused on the study of the tas-de-charge in the works of Guillem Sagrera, and will address their technological, constructive and design aspects. Two characteristics set these apart from other solutions and justify their relevance: these are that the ribs spring directly from the wall without the mediation of capitals, corbels or pilasters; and that they are deliberately designed to force the intersection of their mouldings, in some cases by crossing the rib axes. Sagrera’s work tells a story of architectural innovation – one where the effort is not centred on creating vaults with numerous ribs or a sophisticated ground plan, but on carefully solving the rib unions, which evidence a meticulous use of templates to control the tracing of the pieces’ profiles as well as the skill of the stonemasons, able to carve highly complex intersections. An overview of the first experiments with rib relationships will illustrate the context and origin of Guillem Sagrera’s solutions. We show how, faced with difficulties arising from the convergence of ribs into the tas-de-charge, builders were able to develop new solutions by experimenting with a construction system that they were already familiar with and could control easily. In order to gain a better insight into the design strategies behind his tas-de-charge and the technical and constructive procedures required for their execution, we found ourselves facing the need to address the general subject of tas-de-charge in ribbed vaults. This, which began as an introduction meant as context for Sagrera’s work, took on a life of its own and became the first half of the thesis, with a volume practically equal to that of the second. We have devoted a chapter to experimental archaeology. It comprises the design, tracing and carving processes for the four tas-de-charge executed at the ETSAM Stonecutting Workshop, in which we have tested experimentally the theories studied in the previous chapters. These tests have allowed us to contrast hypotheses, assess the difficulty of certain procedures or processes and understand the built element as a real entity. The practical work has taught us not to always trust the hypotheses proposed through computer modelling or drawing – and to recognise the importance of coordinating the hands and the mind. After studying Sagrera’s work and contrasting it with other related or previous tas-de-charge, our research will seek to make a contribution to the study of the shift in the design and construction of vault springers that took place between the 13th and 14th centuries, when ribs began to spring directly from their support and moulding crossings began to appear. We show that, from then on, tas-de-charge would not only depend on the general vault geometry – deliberate modifications would be carried out in order to achieve the desired result. This reveals design decisions that would have been unworkable if not for the effective use of template strategies.

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Plants contain several genes encoding thioredoxins (Trxs), small proteins involved in redox regulation of many enzymes in different cell compartments. Among them, mitochondrial Trxo has been described to have a response in plants grown under salinity but there is scarce information about its functional role in abiotic stress or its gene regulation. In this work, the transcriptional regulation of the mitochondrial AtTrxo1 gene has been studied for the first time, by identifying functionally relevant cis- elements in its promoter: two conserved motives were found as positive and one as negative regulators. Using them as baits for the screening of an arrayed yeast library containing Arabidopsis Transcription Factors (TF) ORFs, two TFs were selected that are now being validated at the molecular level. We have also studied the response of T-DNA insertion mutant plants for AtTrxo1 to salt stress. The K.O. AtTrxo1 mutants presented several phenotypic changes including the time required to reach 50% germination under salinity, without affecting the final germination percentage.