26 research outputs found
Selection of reference genes for expression Study in pulp and seeds of Theobroma grandiflorum (Willd. ex Spreng.) Schum
Cupuassu (Theobroma grandiflorum [Willd. ex Spreng.] Schum) is a species of high economic importance in Brazil with great potential at international level due to the multiple uses of both its seeds and pulp in the industry of sweets and cosmetics. For this reason, the cupuassu breeding program focused on the selection of genotypes with high pulp and seed quality—selection associated with the understanding of the mechanisms involved in fruit formation. Gene expression is one of the most used approaches related to such understanding. In this sense, quantitative real-time PCR (qPCR) is a powerful tool, since it rapidly and reliably quantifies gene expression levels across different experimental conditions. The analysis by qPCR and the correct interpretation of data depend on signal normalization using reference genes, i.e. genes presenting a uniform pattern of expression in the analyzed samples. Here, we selected and analyzed the expression of five genes from cupuassu (ACP, ACT, GAPDH, MDH, TUB) to be used as candidates for reference genes on pulp and seed of young, maturing and mature cupuassu fruits. The evaluation of the gene expression stability was obtained using the NormFinder, geNorm and BestKeeper programs. In general, our results indicated that the GAPDH and MDH genes constituted the best combination as reference genes to analyze the expression of cupuassu samples. To our knowledge, this is the first report of reference gene definition in cupuassu, and these results will support subsequent analysis related to gene expression studies in cupuassu plants subjected to different biotic or abiotic conditions as well as serve as a tool for diversity analysis based on pulp and seed quality. (Résumé d'auteur
Genetic characterization of cupuassu theobroma grandiflorum (willd. ex. spreng.) schum. populations by microsatellite markers and botanic-agronomic descriptors.
Este trabalho teve por objetivo caracterizar e comparar a estrutura genética de sete populações de cupuaçuzeiro, Theobroma grandiflorum (Willd. ex Spreng.) Schum., uma fruteira nativa da Amazônia brasileira, utilizando marcadores microssatélites e descritores botânico-agronômicos. Visou também conhecer, preliminarmente, o sistema reprodutivo do cupuaçuzeiro. A estrutura genética das sete populações, sendo três populações naturais, coletadas na suposta área de máxima diversidade da espécie, três populações estabelecidas em Banco Ativo de Germoplasma (BAG), e uma população coletada em plantios comerciais do município de Tomé açu - PA, foi analisada com auxílio de marcadores microssatélites. Foi observada alta variabilidade genética na espécie, ressaltado pelo elevado número de alelos por loco, alto nível de heterozigosidade e divergência entre as populações. A divergência foi mais acentuada entre as populações naturais, em comparação com as populações do Banco de Germoplasma. Essa divergência pode indicar um processo preliminar de diferenciação. Porém, foi mais acentuada entre as populações oriundas de Tucuruí e Nova Ipixuna, corroborando com as indicações que consideram essa região como o centro de máxima diversidade de T. grandiflorum. Estes resultados sugerem, como estratégia de conservação in situ, a necessidade de definição de mais de um local para reserva genética, bem como, em relação a conservação ex situ, as coletas devem ser realizadas em vários locais. A elevada diversidade genética observada nos plantios comerciais, permite recomendar essas plantações como uma fonte alternativa de genes e genótipos ao programa de melhoramento de T. grandiflorum. No BAG foi observada baixa divergência genética entre as populações, sendo que, a maior parte da variabilidade genética encontrava-se dentro das populações. Essa caracterização foi complementada com o emprego de descritores botânico-agronômicos, quando foi observada grande variabilidade para a maioria dos descritores empregados. Houve necessidade, inicialmente, de selecionar dentre as 53 variáveis, aquelas que melhor se prestavam para a caracterização dos acessos. Empregando análises univariada e multivariada por componentes principais, foi possível descartar 64% das variáveis iniciais, sendo sugerida uma lista mínima de 19 descritores para o cupuaçuzeiro. Com base nessa lista e o emprego da distância Euclideana média, foi obtida uma matriz de dissimilaridade entre os 31 acessos avaliados. Esses acessos foram agrupados pelo método de Tocher e UPGMA, tendo sido obtidos seis grupos de similaridade. A comparação entre as duas caracterizações realizadas no BAG, revelou uma correlação positiva e significativa entre distâncias genéticas e fenotípicas. Preliminarmente foi estudado o sistema de reprodução do cupuaçuzeiro, numa população natural de Nova Ipixuna - PA, sendo utilizadas oito progênies de polinização aberta, com dez indivíduos e oito locos microssatélites polimórficos. Baseado na estimativa da taxa de cruzamento multilocos ( t m =1,0) and individual outcrossing rate ( $ t =1.0), the results from this population suggested that T. grandiflorum is a predominatly outbreeding species, with a small percentage (5,4%) of biparental inbreeding. These results have important implications on the in situ conservation strategies and on the use of open-pollinated progenies in breeding programs
Involvement of structurally distinct cupuassu chitinases and osmotin in plant resistance to the fungus Moniliophthora perniciosa
International audienceThe cupuassu tree (Theobroma grandiflorwn) is a crop of great economic importance to Brazil, mainly for its pulp and seeds, which are used in food industry. However, cupuassu fruit production is threatened by witches' broom disease caused by the fungus Moniliophthora perniciosa. As elements of its defense mechanisms, the plant can produce and accumulate pathogenesis-related (PR) proteins such as chitinases and osmotins. Here, we identified three cupuassu PR proteins (TgPR3, TgPR5 and TgPR8) from cupuassu-M. perniciosa interaction RNA-seq data. TgPR3 and TgPR8 corresponded to chitinases, and TgPR5 to osmotin; they are phylogenetically related to cacao and to Arabidopsis PR sequences involved in biotic and abiotic stress. The TgPR proteins' tridimensional structure was obtained through homology modeling, and molecular docking with chitin and chitosan showed that the TgPR proteins can interact with both cell wall molecules and presented a higher affinity for chitosan. TgPR gene expression was analyzed by RT-qPCR on resistant and susceptible cupuassu genotypes infected by M. perniciosa at 8, 24, 48 and 72 h after infection (hai). The TgPR genes showed higher expression in resistant plants compared to the susceptible ones, mainly for TgPR5 at 8 and 24 hai, while the expression was lower in the susceptible cupuassu plants. To our knowledge, this is the first in silico and in vitro reports of cupuassu PR protein. The data suggested that TgPRs could be involved in recognizing mechanisms of the plant's innate immune system through chitin receptors. Our results also suggest a putative role of chitinase/chitosanase for the TgPR5/osmotin
Cupuassu (<i>Theobroma grandiflorum</i> [Willd. ex Sprengel] Schumann) Fruit Development: Key Genes Involved in Primary Metabolism and Stress Response
Cupuassu (Theobroma grandiflorum [Willd. ex Sprengel] Schumann) seeds constitute the raw material for oil extraction and fabrication of cupulate (product similar to chocolate). However, fungal diseases such as witches’ broom caused by Moniliophthora perniciosa have interfered with the large-scale development of cupuassu plantations. Cupuassu genetic breeding programmes focus on a variety of biotechnological tools or approaches to select genes related to quality or resistance mechanisms. In this study, we used expression and interactomics analyses of preselected genes involved in fruit quality and/or resistance to better understand the molecular and physiological mechanisms associated with these plant processes. It was found that (i) resistant and susceptible cupuassu genotypes showed different pulp characteristics as well as gene expression patterns; (ii) monosaccharide and carbohydrate transport pathways were enhanced during fruit maturation; (iii) sugar accumulation participated in signal transduction associated with fruit development and stress response in maturing fruits; and (iv) maturing pulp and seeds showed increased phospholipid metabolism and translocation, as well as immune system activation. The TgSTP1, TgWRKY33, TgCZF1, and TgUBA1 genes in cupuassu and the orthologues of DIN10, CNI1, and TET8 identified by the interactomics approach may be good candidates for marker-assisted selection in breeding programmes focusing on both fruit quality and resistance/tolerance to biotic/abiotic stress
Comparative transcriptomics of cupuassu (<i>Theobroma grandiflorum</i>) offers insights into the early defense mechanism to <i>Moniliophthora perniciosa</i>, the causal agent of witches’ broom disease
Cupuassu (Theobroma grandiflorum) is a fruit tree native to the Amazon region, presenting high social and economic value. Besides, owing to its suitability for agroforestry cultivation, cupuassu is useful for the conservation of the Amazon Forest. Cupuassu plantations are severely affected by Moniliophthora perniciosa. Thus, to gain insights into resistance against M. perniciosa, transcriptomes of susceptible (SG) and resistant (RG) genotypes of cupuassu were analyzed at the early stage of infection using RNA sequencing. A total of 21,441 unigenes were identified, and differentially expressed genes were detected in intra- (440) and inter-genotype (301) analyses. Gene expression was altered at 24 h after inoculation (HAI) in SG. This alteration was prominent at 48 HAI in RG. These datasets allowed the identification of genes potentially involved in defense mechanisms. Phytohormone signature analysis revealed a significant effect of hormones on genotype responses. The present study is the first large-scale transcriptomic analysis of cupuassu.</p
Candidate reference genes, primer characteristics, and efficiency obtained by RT-qPCR.
<p>CV: coefficient of variation, F: forward; R: reverse.</p