ABSTRACT
We investigated the microRNA172 (miR172)-mediated regulatory network for the perception of changes in external and endogenous signals to identify a universally applicable floral regulation system in ornamental plants, manipulation of which could be economically beneficial. Transgenic gloxinia plants, in which miR172 was either overexpressed or suppressed, were generated using Agrobacterium-mediated transformation. They were used to study the effect of altering the expression of this miRNA on time of flowering and to identify its mRNA target. Early or late flowering was observed in transgenic plants in which miR172 was overexpressed or suppressed, respectively. A full-length complementary DNA (cDNA) of gloxinia (Sinningia speciosa) APETALA2-like (SsAP2-like) was identified as a target of miR172. The altered expression levels of miR172 caused up- or down-regulation of SsAP2-like during flower development, which affected the time of flowering. Quantitative real-time reverse transcription PCR analysis of different gloxinia tissues revealed that the accumulation of SsAP2-like was negatively correlated with the expression of miR172a, whereas the expression pattern of miR172a was negatively correlated with that of miR156a. Our results suggest that transgenic manipulation of miR172 could be used as a universal strategy for regulating time of flowering in ornamental plants.
ABSTRACT
We investigated the microRNA172 (miR172)-mediated regulatory network for the perception of changes in external and endogenous signals to identify a universally applicable floral regulation system in ornamental plants, manipulation of which could be economically beneficial. Transgenic gloxinia plants, in which miR172 was either overexpressed or suppressed, were generated using Agrobacterium-mediated transformation. They were used to study the effect of altering the expression of this miRNA on time of flowering and to identify its mRNA target. Early or late flowering was observed in transgenic plants in which miR172 was overexpressed or suppressed, respectively. A full-length complementary DNA (cDNA) of gloxinia (Sinningia speciosa) APETALA2-like (SsAP2-like) was identified as a target of miR172. The altered expression levels of miR172 caused up- or down-regulation of SsAP2-like during flower development, which affected the time of flowering. Quantitative real-time reverse transcription PCR analysis of different gloxinia tissues revealed that the accumulation of SsAP2-like was negatively correlated with the expression of miR172a, whereas the expression pattern of miR172a was negatively correlated with that of miR156a. Our results suggest that transgenic manipulation of miR172 could be used as a universal strategy for regulating time of flowering in ornamental plants.
Subject(s)
Arabidopsis/genetics , Arabidopsis Proteins/metabolism , Cloning, Molecular , DNA, Complementary/metabolism , Flowers/physiology , Gene Expression Profiling , Gene Expression Regulation, Plant , Homeodomain Proteins/metabolism , Lamiales/physiology , MicroRNAs/metabolism , Nuclear Proteins/metabolism , Plants, Genetically Modified/physiology , Plasmids/metabolism , Polymerase Chain Reaction , TransgenesABSTRACT
Background: Phalaenopsis is an important ornamental flowering plant that belongs to the Orchidaceae family and is cultivated worldwide. Phalaenopsis has a long juvenile phase; therefore, it is important to understand the genetic elements regulating the transition from vegetative phase to reproductive phase. In this study, FLOWERING LOCUS T (FT) homologs in Phalaenopsis were cloned, and their effects on flowering were analyzed. Results: A total of five FT-like genes were identified in Phalaenopsis. Phylogenetic and expression analyses of these five FT-like genes indicated that some of these genes might participate in the regulation of flowering. A novel FT-like gene, PhFT-1, distantly related to previously reported FT genes in Arabidopsis and other dicot crops, was also found to be a positive regulator of flowering as heterologous expression of PhFT-1 in Arabidopsis causes an early flowering phenotype. Conclusions: Five FT homologous genes from Phalaenopsis orchid were identified, and PhFT-1 positively regulates flowering.
Subject(s)
Plant Proteins/genetics , Arabidopsis , Orchidaceae/genetics , Flowers/genetics , Polymerase Chain Reaction/methods , Cloning, Molecular , Genes, Plant/genetics , Computational Biology , Orchidaceae/growth & development , Flowers/growth & developmentABSTRACT
Soybean genome sequences were blasted with Arabidopsis thaliana regulatory genes involved in photoperioddependent flowering. This approach enabled the identification of 118 genes involved in the flowering pathway. Two genome sequences of cultivated (Williams 82) and wild (IT182932) soybeans were employed to survey functional DNA variations in the flowering-related homologs. Forty genes exhibiting nonsynonymous substitutions between G. max and G. soja were catalogued. In addition, 22 genes were found to co-localize with QTLs for six traits including flowering time, first flower, pod maturity, beginning of pod, reproductive period, and seed filling period. Among the genes overlapping the QTL regions, two LHY/CCA1 genes, GI and SFR6 contained amino acid changes. The recently duplicated sequence regions of the soybean genome were used as additional criteria for the speculation of the putative function of the homologs. Two duplicated regions showed redundancy of both flowering-related genes and QTLs. ID 12398025, which contains the homeologous regions between chr 7 and chr 16, was redundant for the LHY/CCA1 and SPA1 homologs and the QTLs. Retaining of the CRY1 gene and the pod maturity QTLs were observed in the duplicated region of ID 23546507 on chr 4 and chr 6. Functional DNA variation of the LHY/CCA1 gene (Glyma07g05410) was present in a counterpart of the duplicated region on chr 7, while the gene (Glyma16g01980) present in the other portion of the duplicated region on chr 16 did not show a functional sequence change. The gene list catalogued in this study provides primary insight for understanding the regulation of flowering time and maturity in soybean.
ABSTRACT
A central composite 2 3 full factorial design was used to study the combined effect of ethanol concentration and moistening time on total phenol (TP), flavonoid (TF) and carbohydrates (TC) content, as well as over total soluble substance (TSS) and ashes content (TA) in the Tamarindus indica L. leaves extraction process. Desirability function (0.8377) suggest the 71.73 percent ethanol concentration and 92.37 minutes of moistening time as the best combination variables, predicting values of 25.972 and 2.678 mg/mL for TP and TF; whereas for TSS and TA was predicted 18.417 and 0.566 percent respectively. The TC variable was discarded, because was impossible to find an statistical strong model to describes this variable. The theoretic values predicted were contrasted with new experimental data (n=5) by a hypothesis contrast test and examining the absolute error in the prediction. Results show a good adjustment to the prediction for TP, TSS and TA variables, meanwhile TF exhibit a slight deviation to the predicted value (absolute error over 10 percent). Nevertheless, this study offers a combination of variables when it is intended to prepare a tamarind extract that afford a high extractive capacity and, as a consequence, a larger probability to exhibit some kind of pharmacologic activity.
Un diseño factorial con compuesto central 2 elevado a 3 fue empleado en la evaluación de la influencia de la concentración de etanol y el tiempo de humectación sobre el contenido de fenoles (TP), flavonoides (TF), carbohidratos (TC) sólidos (TSS) y cenizas totales (TA) en el proceso de extracción de hojas de Tamarindus indica L. Valores de 71.73 por ciento de etanol y de 92.37 minutos de tiempo de humectación fue la combinación de factores sugerida por la función deseabilidad (0,8377), la cual predice concentraciones de 25,972 y 2,678 mg/mL para las variables TP y TF; y 18,417 y 0,566 por ciento para TSS y TA respectivamente. La variable TC fue descartada ante la imposibilidad de encontrar modelos predictivos con significación estadística. Estos valores teóricos fueron comparados por contraste de hipótesis y cálculo del error absoluto de la predicción con los obtenidos por réplicas del experimento (n=5). Los resultados mostraron un buen ajuste a la predicción para las variables TP, TSS y TA, mientras que la variable TF muestra una pequeña desviación con un error absoluto ligeramente superior al 10 por ciento. A pesar de ello, el presente estudio ofrece una combinación de variables a la cual se logra una alta capacidad extractiva en hojas de Tamarindus indica L., ofreciendo una mayor probabilidad de actividad farmacológica.
Subject(s)
Carbohydrates/analysis , Phenols/analysis , Flavonoids/analysis , Plant Leaves/chemistry , Tamarindus/chemistry , Ash/analysis , Time Factors , Total Solids , WettabilityABSTRACT
A mamona (Ricinus communis L.) é uma planta oleaginosa anual e, ocasionalmente, bienal em regiões tropicais, com ciclo médio de 150 dias para a maioria das cultivares anuais e de 120 a 130 dias para cultivares anuais precoces. O objetivo deste trabalho foi avaliar características agronômicas de cultivares das mamonas 'Al Guarany 2002', 'IAC 80', 'IAC 226' e 'BRS 188 Paraguaçu'em função do ambiente de cultivo e da época de semeadura. As cultivares foram semeadas entre o primeiro e o quinto dia dos meses de novembro e dezembro, na Embrapa Clima Temperado, em Pelotas, Rio Grande do Sul. Cada época teve 12 unidades experimentais em três blocos casualizados. A emergência, a altura de planta e de inserção do primeiro cacho, o período de florescimento e colheita e o ataque de pragas e doenças foram avaliados e analisados com o programa WinStat Versão 2.0. O comportamento entre as cultivares diferiu entre locais de cultivo e época de semeadura. A inserção do cacho foi mais alta, e as florações e colheitas foram mais tardias em plantas da segunda época de semeadura. Danos por pragas e doenças e os descritores morfológicos da planta de mamona apresentaram diferenças entre os locais de cultivo.
Castor bean (Ricinus communis L.) is an oleaginous plant with annual cycle and occasionally biennial cycle in tropical areas, with mean cycle of 150 days for the majority of annual cultivars and 120 to 130 days for annual early cultivars. The objective of this study was to evaluate the agronomic characteristics of castor cultivars according to environmental crop and sowing season. The experiment was conduced at Embrapa Clima Temperado - Pelotas/RS, in two places. The castor cultivars used in this research were 'Al Guarany 2002', 'IAC 80', 'IAC 226' and 'BRS 188 Paraguaçu', which were sown in two sowing times: the first was in early November (between 1st and 5st) and the second was in early December (between 1st and 5st). Each sowing season was constituted of 12 experimental units, distributed in three random blocks. It was evaluated the emergency, plant height and first spike insertion , flowering and harvest time, pest and disease attacks. The WinStat program Version 2.0 was used for data statistical analysis. There was a significant difference among cultivar behaviors between the environmental crops and sowing seasons. The second sowing season provided a larger plant and first spike insertion was higher. It also promoted retardation in the flowering and harvesting time. The differences among cultivars, between the two environmental crops, were clearer in the pest and disease attacks, but also in morphologic characteristics of castor plant.
ABSTRACT
Floral transition is one the most drastic changes occurring during the life cycle of a plant. The shoot apical meristem switches from the production of leaves with associated secondary shoot meristems to the production of flower meristems. This transition is abrupt and generally irreversible, suggesting it is regulated by a robust gene regulatory network capable of driving sharp transitions. The moment at which this transition occurs is precisely determined by environmental and endogenous signals. A large number of genes acting within these pathways have been cloned in model herbaceous plants such as Arabidopsis thaliana. In this paper, we report the results of our search in the Citrus expressed sequence tag (CitEST) database for expressed sequence tags (ESTs) showing sequence homology with known elements of flowering-time pathways. We have searched all sequence clusters in the CitEST database and identified more than one hundred Citrus spp sequences that codify putative conserved elements of the autonomous, vernalization, photoperiod response and gibberelic acid-controlled flowering-time pathways. Additionally, we have characterized in silico putative members of the Citrus spp homologs to the Arabidopsis CONSTANS family of transcription factors.