RESUMEN
Protein-DNA interactions are determinant of the regulation of gene expression in living organisms. Luminescence studies have been used in a wide range of techniques to identify how gene transcription can be regulated by proteins such as transcription factors (TFs). Despite the great advances in the use of luciferases as reporters in the performance of this mechanism, some of them still have disadvantages that have been tried to be solved by the generation of new luciferases that induce a more stable and perfectly visualizable reaction. NanoLuc is a recently described luciferase that has been characterized by its efficient, stable, and powerful luminescence. These qualities have been considered to create a new and efficient reporter system to detect protein-DNA interactions. In this chapter, we take advantage of NanoLuc and describe its use in a reliable procedure to detect protein-DNA interactions in Nicotiana benthamiana extracts and entire leaves.
Asunto(s)
Nicotiana , Factores de Transcripción , Activación Transcripcional , Luciferasas/genética , Luciferasas/metabolismo , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Nicotiana/genética , Nicotiana/metabolismoRESUMEN
Plant cell wall remodeling is an important process during plant responses to heat stress. Pectins, a group of cell wall polysaccharides with a great diversity of complex chemical structures, are also involved in heat stress responses. Enzymatic activity of the pectin methyl esterases, which remove methyl groups from pectins in the cell wall, is regulated by DUF642 proteins, as described in different plants, including Arabidopsis thaliana and Oryza sativa. Our results demonstrated that heat stress altered the expression of the DUF642 gene, BIIDXI. There was an important decrease in BIIDXI expression during the first hour of HS, followed by an increase at 24 h. bdx-1 seedlings had less tolerance to heat stress but presented a normal heat stress response; HSFA2 and HSP22 expressions were highly increased, as they were in WT seedlings. Thermopriming triggered changes in pectin methyl esterase activity in WT seedlings, while no increases in PME activity were detected in bdx-1 seedlings at the same conditions. Taken together, our results suggest that BIIDXI is involved in thermotolerance via PME activation.
RESUMEN
Floral patterning is a complex task. Various organs and tissues must be formed to fulfill reproductive functions. Flower development has been studied, mainly looking for master regulators. However, downstream changes such as the cell wall composition are relevant since they allow cells to divide, differentiate, and grow. In this review, we focus on the main components of the primary cell wall-cellulose, hemicellulose, and pectins-to describe how enzymes involved in the biosynthesis, modifications, and degradation of cell wall components are related to the formation of the floral organs. Additionally, internal and external stimuli participate in the genetic regulation that modulates the activity of cell wall remodeling proteins.
Asunto(s)
Pared Celular/genética , Flores/genética , Desarrollo de la Planta/genética , Reproducción/genética , Pared Celular/metabolismo , Celulosa/genética , Flores/crecimiento & desarrollo , Regulación de la Expresión Génica de las Plantas , Pectinas/genética , Polisacáridos/genéticaRESUMEN
The DUF642 protein family is found exclusively in spermatophytes and is represented by 10 genes in Arabidopsis and in most of the 24 plant species analyzed to date. Even though the primary structure of DUF642 proteins is highly conserved in different spermatophyte species, studies of their expression patterns in Arabidopsis have shown that the spatial-temporal expression pattern for each gene is specific and consistent with the phenotypes of the mutant plants studied so far. Additionally, the regulation of DUF642 gene expression by hormones and environmental stimuli was specific for each gene, showing both up- and down-regulation depending of the analyzed tissue and the intensity or duration of the stimuli. These expression patterns suggest that the DUF642 genes are involved throughout the development and growth of plants. In general, changes in the expression patterns of DUF642 genes can be related to changes in pectin methyl esterase activity and/or to changes in the degree of methyl-esterified homogalacturonans during plant development in different cell types. Thus, the regulation of pectin methyl esterases mediated by DUF642 genes could contribute to the regulation of the cell wall properties during plant growth.
Asunto(s)
Pared Celular/metabolismo , Desarrollo de la Planta , Proteínas de Plantas/metabolismo , Regulación de la Expresión Génica de las Plantas , Genes de Plantas , Desarrollo de la Planta/genética , Proteínas de Plantas/genéticaRESUMEN
Auxin is involved in hypocotyl elongation in response to different environmental factors. BIIDXI is a cell wall DUF642 protein that participates in the regulation of the degree of pectin-methylesterification of the cell wall in different tissues, including hypocotyls. Under continuous light, bdx-1 seedlings presented longer hypocotyls than those of WT, while BIIDXI-overexpressed hypocotyls were auxin resistant. Auxin accumulation was observed in epidermal cells from bdx-1 hypocotyls, and the distribution pattern of PIN1 proteins differed. Moreover, the gravitropic response of bdx-1, a process that is highly dependent on auxin flux, was increased. In this study, we determined that BIIDXI is involved in hypocotyl elongation through the regulation of auxin flux.
