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1.
Gene ; 817: 146168, 2022 Apr 05.
Article in English | MEDLINE | ID: mdl-34995731

ABSTRACT

Many studies in the model species Arabidopsis thaliana characterized genes involved in embryo formation. However, much remains to be learned about the portfolio of genes that are involved in signal transduction and transcriptional regulation during plant embryo development in other species, particularly in an evolutionary context, especially considering that some genes involved in embryo patterning are not exclusive of land plants. This study, used a combination of domain architecture phylostratigraphy and phylogenetic reconstruction to investigate the evolutionary history of embryo patterning and auxin metabolism (EPAM) genes in Viridiplantae. This approach shed light on the co-optation of auxin metabolism and other molecular mechanisms that contributed to the radiation of land plants, and specifically to embryo formation. These results have potential to assist conservation programs, by directing the development of tools for obtaining somatic embryos. In this context, we employed this methodology with critically endangered and non-model species Araucaria angustifolia, the Brazilian pine, which is current focus of conservation efforts using somatic embryogenesis. So far, this approach had little success since somatic embryos fail to completely develop. By profiling the expression of genes that we identified as necessary for the emergence of land-plant embryos, we found striking differences between zygotic and somatic embryos that might explain the developmental arrest and be used to improve A. angustifolia somatic culture.


Subject(s)
Araucaria/embryology , Araucaria/genetics , Indoleacetic Acids/metabolism , Plant Somatic Embryogenesis Techniques , Seeds/growth & development , Arabidopsis/genetics , Body Patterning , Evolution, Molecular , Phylogeny , Plant Development/genetics
2.
PLoS One ; 12(7): e0180051, 2017.
Article in English | MEDLINE | ID: mdl-28678868

ABSTRACT

Three zygotic developmental stages and two somatic Araucaria angustifolia cell lines with contrasting embryogenic potential were analyzed to identify the carbohydrate-mediated responses associated with embryo formation. Using a comparison between zygotic and somatic embryogenesis systems, the non-structural carbohydrate content, cell wall sugar composition and expression of genes involved in sugar sensing were analyzed, and a network analysis was used to identify coordinated features during embryogenesis. We observed that carbohydrate-mediated responses occur mainly during the early stages of zygotic embryo formation, and that during seed development there are coordinated changes that affect the development of the different structures (embryo and megagametophyte). Furthermore, sucrose and starch accumulation were associated with the responsiveness of the cell lines. This study sheds light on how carbohydrate metabolism is influenced during zygotic and somatic embryogenesis in the endangered conifer species, A. angustifolia.


Subject(s)
Carbohydrate Metabolism , Seeds/metabolism , Tracheophyta/metabolism , Endangered Species , Gene Expression Regulation, Developmental , Gene Expression Regulation, Plant , Genes, Plant , Seeds/genetics , Seeds/growth & development , Tracheophyta/genetics , Tracheophyta/growth & development , Transcriptome
3.
Tree Physiol ; 37(1): 116-130, 2017 01 31.
Article in English | MEDLINE | ID: mdl-28175909

ABSTRACT

Polyamines (PAs), such as spermidine and spermine, as well as amino acids that are substrates for their biosynthesis, are known to be essential for plant development. However, little is known about the gene expression and metabolic switches associated with the ornithine/arginine and PA biosynthetic pathway during seed development in conifers. To understand these metabolic switches, the enzyme activity of arginine decarboxylase and ornithine decarboxylase, as well as the contents of PAs and amino acids were evaluated in three Araucaria angustifolia (Bertol. Kuntze) seed developmental stages in combination with expression profile analyses of genes associated with the ornithine/arginine and PA biosynthetic pathway. Twelve genes were selected for further analysis and it was shown that the expression profiles of AaADC and AaSAMDC were up-regulated during zygotic embryo development. Polyamines and amino acids were found to accumulate differently in embryos and megagametophytes, and the transition from the globular to the cotyledonary stage was marked by an increase in free and conjugated spermidine and spermine contents. Putrescine is made from arginine, which was present at low content at the late embryogenesis stage, when high content of citrulline was observed. Differences in amino acids, PAs and gene expression profiles of biosynthetic genes at specific seed stages and at each seed transition stage were investigated, providing insights into molecular and physiological aspects of conifer embryogenesis for use in future both basic and applied studies.


Subject(s)
Amino Acids/metabolism , Carboxy-Lyases/genetics , Gene Expression , Ornithine Decarboxylase/genetics , Plant Proteins/genetics , Polyamines/metabolism , Tracheophyta/genetics , Biosynthetic Pathways , Carboxy-Lyases/metabolism , Ornithine Decarboxylase/metabolism , Phylogeny , Plant Proteins/metabolism , Real-Time Polymerase Chain Reaction , Seeds/genetics , Seeds/growth & development , Seeds/metabolism , Sequence Analysis, DNA , Tracheophyta/enzymology , Tracheophyta/growth & development , Tracheophyta/metabolism
4.
PLoS One ; 10(8): e0136714, 2015.
Article in English | MEDLINE | ID: mdl-26313945

ABSTRACT

Quantitative analysis of gene expression is a fundamental experimental approach in many fields of plant biology, but it requires the use of internal controls representing constitutively expressed genes for reliable transcript quantification. In this study, we identified fifteen putative reference genes from an A. angustifolia transcriptome database. Variation in transcript levels was first evaluated in silico by comparing read counts and then by quantitative real-time PCR (qRT-PCR), resulting in the identification of six candidate genes. The consistency of transcript abundance was also calculated applying geNorm and NormFinder software packages followed by a validation approach using four target genes. The results presented here indicate that a diverse set of samples should ideally be used in order to identify constitutively expressed genes, and that the use of any two reference genes in combination, of the six tested genes, is sufficient for effective expression normalization. Finally, in agreement with the in silico prediction, a comprehensive analysis of the qRT-PCR data combined with validation analysis revealed that AaEIF4B-L and AaPP2A are the most suitable reference genes for comparative studies of A. angustifolia gene expression.


Subject(s)
Gene Expression Profiling/methods , Real-Time Polymerase Chain Reaction/standards , Streptophyta/genetics , DNA Primers , DNA, Complementary , Endangered Species , Gene Expression Profiling/standards , Gene Expression Regulation, Plant , Genes, Plant , Real-Time Polymerase Chain Reaction/methods , Reference Standards , Reproducibility of Results , Software
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