Résumé
Background: Plant gene homologs that control cell differentiation can be used as biotechnological tools to study the in vitro cell proliferation competence of tissue culture-recalcitrant species such as peppers. It has been demonstrated that SERK1 homologs enhance embryogenic competence when overexpressed in transformed tissues; therefore, cloning of a pepper SERK1 homolog was performed to further evaluate its biotechnological potential. Results: A Capsicum chinense SERK full-length cDNA (CchSERK1) was cloned and characterized at the molecular level. Its deduced amino acid sequence exhibits high identity with sequences annotated as SERK1 and predicted-SERK2 homologs in the genomes of the Capsicum annuum CM-334 and Zunla-1 varieties, respectively, and with SERK1 homologs from members of the Solanaceae family. Transcription of CchSERK1 in plant tissues, measured by quantitative RT-PCR, was higher in stems, flowers, and roots but lower in leaves and floral primordia. During seed development, CchSERK1 was transcribed in all zygotic stages, with higher expression at 14 days post anthesis. During somatic embryogenesis, CchSERK1 was transcribed at all differentiation stages, with a high increment in the heart stage and lower levels at the torpedo/cotyledonal stages. Conclusion: DNA sequence alignments and gene expression patterns suggest that CchSERK1 is the C. chinense SERK1 homolog. Significant levels of CchSERK1 transcripts were found in tissues with cell differentiation activities such as vascular axes and during the development of zygotic and somatic embryos. These results suggest that CchSERK1 might have regulatory functions in cell differentiation and could be used as a biotechnological tool to study the recalcitrance of peppers to proliferate in vitro.
Sujets)
Capsicum/génétique , Clonage moléculaire , Techniques in vitro , Biotechnologie , Expression des gènes , Différenciation cellulaire , Gènes de plante , ADN complémentaire/génétique , Solanaceae/génétique , Protéines d'Arabidopsis , Prolifération cellulaire , Développement embryonnaire , Réaction de polymérisation en chaine en temps réelRésumé
Background: Capsicum is a genus of an important spice crop that belongs to the chili lineage. However, many Capsicum species (family Solanaceae) are known to be recalcitrant to genetic transformation and in vitro regeneration, thus hampering the effort in using Capsicum species for detailed biological investigation. In this study, we have developed an optimized protocol for the direct transformation of Capsicum frutescens L. cv. Hot Lava using a biolistic particle delivery system. In addition, a procedure for in vitro whole plant regeneration from the hypocotyl explants of C. frutescens was established. Results: In this study on the biolistic system, explant target distance, bombardment helium (He) pressure, and the size of the microcarrier were the key parameters to be investigated. The optimized parameters based on the screening of GFP expression were determined to have a target distance of 6 cm, helium pressure of 1350 psi, and gold particle (microcarrier) size of 1.6 µm. The greatest number of shoots was obtained from hypocotyls as explants using Murashige and Skoog medium supplemented with 5.0-mg/L 6-benzylaminopurine and 0.1-mg/L 1-naphthaleneacetic acid. On an average, five shoots per explant were formed, and of them, one shoot managed to form the root and developed into a whole plant. Conclusions: We obtained an optimized protocol for the biolistic transformation of chili and in vitro regeneration of chili plantlets. The establishment of the protocols will provide a platform for molecular breeding and biological studies of chili plants.
Sujets)
Capsicum/croissance et développement , Régénération , Transformation génétique , Techniques in vitro , Capsicum/génétique , Réaction de polymérisation en chaîne , Biolistique , Protéines à fluorescence verte , Techniques de culture de tissus , Génie métaboliqueRésumé
Long pepper (Piper hispidinervum) is an Amazonian species of commercial interest due to the production of safrole. Drying long pepper biomass to extract safrole is a time consuming and costly process that can also result in the contamination of the material by microorganisms. The objective of this study was to analyze the yield of essential oil and safrole content of fresh and dried biomass of long pepper accessions maintained in the Active Germoplasm Bank of Embrapa Acre, in the state of Acre, Brazil, aiming at selecting genotypes with best performance on fresh biomass to recommend to the breeding program of the species. Yield of essential oil and safrole content were assessed in 15 long pepper accessions. The essential oil extraction was performed by hydrodistillation and analyzed by gas chromatography. A joint analysis of experiments was performed and the means of essential oil yield and safrole content for each biomass were compared by Student's t-test. There was variability in the essential oil yield and safrole content. There was no difference between the types of biomass for oil yield; however to the safrole content there was difference. Populations 9, 10, 12 and 15 had values of oil yield between 4.1 and 5.3%, and safrole content between 87.2 and 94.3%. The drying process does not interfere in oil productivity. These populations have potential for selection to the long pepper breeding program using oil extraction in the fresh biomass.
A pimenta longa (Piper hispidinervum) é uma espécie amazônica de interesse comercial devido à produção de safrol. A secagem da biomassa para extração do óleo essencial demanda tempo e acarreta custos, podendo também resultar em contaminação do material por microorganismos. O objetivo deste estudo foi analisar o rendimento de óleo essencial e teor de safrol da biomassa verde e seca de acessos de pimenta longa mantida no Banco Ativo de Germoplasma da Embrapa Acre a fim de selecionar genótipos com melhor desempenho em biomassa verde para recomendação ao programa de melhoramento genético da espécie. O rendimento do óleo essencial e o teor de safrol foram avaliados em 15 acessos de pimenta longa. Foi realizada uma análise conjunta de experimentos e as médias do rendimento do óleo essencial e do teor de safrol para cada população foram comparadas pelo teste t de Student. Houve variabilidade do rendimento de óleo essencial e do teor de safrol. Não houve diferença entre os tipos de biomassa para o rendimento do óleo, já para o teor de safrol houve diferença. As populações 9, 10, 12 e 15 mostraram valores de rendimento de óleo entre 4,1 e 5,3%, e teor de safrol entre 87,2 e 94,3%. O processo de secagem não interfere na produtividade de óleo. Estas populações têm potencial para seleção para o programa de melhoramento genético de pimenta longa por meio da extração de óleo essencial da biomassa verde.
Sujets)
Biomasse , Capsicum/génétique , Safrole , Huile essentielleRésumé
The gene uidA, codes for beta-glucuronidase, which is one of the reporters more frequently utilized in transgenic plants. However, this can only be use if the selected organism does not present endogenous GUS-like activity. In tissues of C. chinense we found a GUS-like activity showing different levels of intensity. Histochemical screening showed that endogenous GUS-like activity decreased, or reduced significantly, in almost all tissues with exception of stament, when phosphate buffer was adjusted to pH 8. Subsequently, C. chinense zygotic embryo explants were transient transformed with Agrobacterium tumefaciens LBA4404 (pCAMBIA2301) and plantlets regenerated were histochemically stained in phosphate buffer pH 8. Observations of incubated tissues of C. chinense regenerants showed blue staining, suggesting expression of uidA. Incubated tissues of non-transformed regenerants did not show blue staining in phosphate buffer pH 8. The results show that for transformation experiments of C. chinense with uidA gene, pH 8 is recommended for histochemical staining.
Sujets)
Capsicum/physiologie , Capsicum/génétique , Glucuronidase , Agrobacterium tumefaciens/physiologie , Régulation de l'expression des gènes végétaux , Gènes rapporteurs , Histocytochimie , Concentration en ions d'hydrogène , Végétaux génétiquement modifiés/génétique , Régénération , Transformation génétiqueRésumé
Most of the pepper species of the genus Capsicum have been recalcitrant to efficient Agrobacterium tumefaciens-mediated stable or transient, genetic transformation. In the present work, we optimized a protocol for transient transformation of the Habanero pepper (Capsicum chinense Jacq.) through the standardization of several experimental factors. These included the age of the plants, the temperature, the length of co-cultivation, the application of a negative (vacuum) and/or a positive (infiltration) pressure, along with micro injection, the use of acetosyringone during the bacterial culturing, and modification of the pH during the GUS assay to eliminate the endogenous beta-glucuronidase activity. The standardized protocol, which yielded nearly 55 percent fully transformed leaf explants, was used to successfully mobilize two empty binary vectors (pCAMBIA2301 and pCAMex), as well as the C. chinense cDNAs encoding the pathogenesis-related protein 10 and esterase, respectively.
Sujets)
Agrobacterium tumefaciens , Capsicum/génétique , Transformation génétique , Techniques de coculture , Végétaux génétiquement modifiés/génétiqueRésumé
The objective of this work was to study the stress tolerance and regeneration capability of transgenic pepper plants carrying a sod gene, encoding a tomato chloroplast-localized Cu/Zn SOD protein. The expression of the sod gene was confirmed by enzymatic staining following polyacrylamide gel electrophoresis (PAGE), revealing a novel band, which could represent a heterodimeric enzyme. Transgenic T1 and T2 progeny plants were exposed to different oxidative stresses including Methyl viologen (MV) and drought and found to have an increased resistance to oxidative damage. Furthermore, the SOD carrying transgenic pepper plants showed increased levels of regeneration efficiency compared to the wild type pepper plants. Pepper is a recalcitrant species in terms of its in vitro regeneration ability but it could be extremely useful for the development of pharmaceuticals. This approach enables the extent use of pepper for genetic transformation and the production of high valuable products in plants particularly the large fruit varieties.
Sujets)
Animaux , Pousses de plante/croissance et développement , Pousses de plante/enzymologie , Pousses de plante/métabolisme , Capsicum , Capsicum/génétique , Capsicum/métabolisme , Stress oxydatif/génétique , Stress physiologique , Superoxide dismutase/métabolisme , Superoxide dismutase/usage thérapeutique , Électrophorèse bidimensionnelle sur gel , Électrophorèse/méthodes , Végétaux génétiquement modifiés/croissance et développement , Végétaux génétiquement modifiés/enzymologie , Végétaux génétiquement modifiés/métabolisme , Réaction de polymérisation en chaîne/méthodes , Sécheresses/méthodesRésumé
In an attempt to determine a cold defense mechanism in plants, we have attempted to characterize changes occurring in the expression of cold-regulated transcript levels in the hot pepper (Capsicum annum), using cDNA microarray analysis, combined with Northern blot analysis. After analysing a 3.1 K hot pepper cDNA microarray, we isolated a total of 317 cold inducible genes. We selected 42 genes which were up-regulated and three genes which were down-regulated due to cold treatment, for further analysis. Among the 45 genes which appeared to be up-regulated by cold, 19 genes appeared to be simultaneously regulated by salt stress. Among the up-regulated cold-stress genes, we identified a variety of transcription factors, including: a family of 4 ethylene-responsive element binding protein (EREBP, designated CaEREBP-C1 to C4) genes, a bZIP protein (CaBZ1), RVA1, Ring domain protein, HSF1, and the WRKY (CaWRKY1) protein. As mentioned earlier, several genes appeared to be induced not only by cold stress, but also simultaneously by salt stress. These genes included: CaEREBP-C3, CaBZ1, putative trans-activator factor, NtPRp27, malate dehydrogenase, putative auxin-repressed protein, protein phosphatase (CaTPP1), SAR8.2 protein precursor, late-embryogenesis abundant protein 5 (LEA5), DNAJ protein homologue, xyloglucanendo-1,4-beta-D-gucanase precursor, PR10, and the putative non-specific lipid transfer protein StnsLTP.
Sujets)
Séquence d'acides aminés , Technique de Northern/méthodes , Capsicum/génétique , Basse température , Séquence consensus , Protéines de liaison à l'ADN/composition chimique , Déshydratation/génétique , Régulation négative , Congélation , Expression des gènes/génétique , Analyse de profil d'expression de gènes , Régulation de l'expression des gènes végétaux/génétique , Protéines à homéodomaine/composition chimique , Données de séquences moléculaires , Séquençage par oligonucléotides en batterie/méthodes , Phylogenèse , Protéines végétales/composition chimique , Similitude de séquences d'acides nucléiques , Chlorure de sodium , Facteurs de transcription/composition chimique , Régulation positiveRésumé
Root-knot nematodes of the genus Meloidogyne are important pathogens affecting vegetable crop production in Brazil and worldwide. The pepper species Capsicum annuum includes both hot and sweet peppers; very little emphasis has been placed on breeding sweet peppers for nematode resistance. We report on the inheritance of resistance to Meloidogyne incognita (Kofoid & White) Chitwood race 2 in the hot pepper cultivar Carolina Cayenne. The hot pepper cv. Carolina Cayenne was used as seed parent and the sweet pepper cv. Agronômico-8 was used as pollen parent to obtain the F1 and F2 generations and the backcross generations BC11 and BC12. The plants were inoculated with M. incognita race 2 at a rate of 60 eggs/ml of substrate and, after a suitable incubation period, the numbers of root galls and egg masses per root system were evaluated on each plant. Broad- (0.77 and 0.72) and narrow-sense (0.77 and 0.63) heritability estimates were high for both root galls and egg masses, respectively. The mean degree of dominance was estimated as 0.29 and 0.25 for numbers of galls and egg masses, respectively; these estimates were not significantly different from 0, indicating a predominantly additive gene action. The results were consistent with a hypothesis of monogenic resistance in Carolina Cayenne.