ABSTRACT
Background: Jatropha curcas L. (further referred to as Jatropha), as a rapidly emerging biofuel crop, has attracted worldwide interest. However, Jatropha is still an undomesticated plant, the true potential of this shrub has not yet been fully realized. To explore the potential of Jatropha, breeding and domestication are needed. Seed size is one of the most important traits of seed yield and has been selected since the beginning of agriculture. Increasing the seed size is a main goal of Jatropha domestication for increasing the seed yield, but the genetic regulation of seed size in Jatropha has not been fully understood. Results: We cloned CYP78A98 gene from Jatropha,a homologue of CYP78A5 in Arabidopsis.Wefound that CYP78A98 was highly expressed in male flower, female flower, stem apex, leaf and developing seed. However, its transcripts were hardly detected in root and stem. CYP78A98 protein localized in endoplasmic reticulum (ER) and the hydrophobic domain at the N-terminus was essential for the correct protein localization. Furthermore, INNER NO OUTER promoter (pINO) drove specific overexpression of CYP78A98 in transgenic tobacco seeds resulted in increased seed size and weight, as well as improved seed protein and fatty acid content. Conclusions: The results indicated that CYP78A98 played a role in Jatropha seed size control. This may help us to better understand the genetic regulation of Jatropha seed development, and accelerate the breeding progress of Jatropha.
Subject(s)
Cytochrome P-450 Enzyme System/metabolism , Jatropha/genetics , Seeds , Nicotiana , Breeding , Polymerase Chain Reaction , Plants, Genetically Modified , Cloning, Molecular , Sequence Analysis , Gene Expression Regulation, Plant , Fatty Acids/analysis , BiofuelsABSTRACT
Background The classification of diversity in germplasm collections is important for plant breeding. The repetitive element palindromic-polymerase chain reaction (rep-PCR) technique was used to investigate inter-specific diversity within 17 species from the Euphorbiaceae family using REP and BOX primers. Results The agglomerative cluster analysis was used to evaluate the scoring data. BOX and REP gave amplification with polymorphism of 98.84% and 100% respectively. REP marker demarcated between the subgenus peltatae. Both markers confirmed Jatropha tanjorensis as a natural hybrid between Jatropha gossypifolia and Jatropha curcas. Five random sequences from the rep-PCR gels were chosen, cloned and sequenced. The blast results demonstrated that the amplified products were from the mitochondrial genomes. Conclusion The rep-PCR molecular tool can be used to characterize diversity in plants as they are suitable for distinguishing eukaryotic genomes effectively.
Subject(s)
Genetic Variation , Polymerase Chain Reaction/methods , Euphorbiaceae/genetics , Jatropha/genetics , Genome, MitochondrialABSTRACT
O objetivo deste trabalho foi estimar parâmetros genéticos de frutos, sementes e plântulas de Jatropha ribifolia (Pohl) Baill., subsidiando futuros programas de melhoramento e conservação genética. Foram selecionadas 20 matrizes da espécie e os frutos coletados em área de Caatinga, no Município de Jequié - BA / Brasil. Para descrição morfológica foram observadas características de 50 frutos e 50 sementes. Para germinação foi utilizado o delineamento experimental inteiramente casualizado com 20 tratamentos (progênie) e três repetições de 20 sementes. O fruto de J. ribifolia é seco, cápsula loculicida e septicida, endocarpo lenhoso e deiscência explosiva (autocórica). A semente é oval, endospérmica, de testa lisa, com diferentes colorações e carúncula presa na parte ventral. O hilo é visível e a rafe bem marcada longitudinalmente. A germinação é hipógea-criptocotiledonar. O tempo médio para germinação foi de 10 a 40 dias. As matrizes de J. ribifolia estudadas apresentaram variabilidade genética significativa para a maioria dos caracteres estudados.
The aim of this study was to estimate genetic parameters of fruits, seeds and seedlings of Jatropha ribifolia (Pohl) Baill, subsidizing future breeding and genetic conservation programs. Twenty matrices of the species and the fruits collected in the Caatinga area in the city of Jequié - BA / Brazil were selected. For morphological description, the features of 50 fruits and 50 seeds were observed. For germination, completely randomized design was used with 20 treatments (progeny) and three replicates of 20 seeds. J. ribifolia fruit is dry and has loculicidal and septicidal capsule, woody endocarp and explosive dehiscence (autochory). The seed is oval, endospermic and has smooth testa and different colors, with caruncle attached to the ventral part. The hilum is visible and the raphe is longitudinally marked. Germination is hypogeal-cryptocotylar. The average time for germination was from 10 to 40 days. The matrices of J. ribifolia showed significant genetic variability for most of the studied traits.