RÉSUMÉ
Peanut (Arachis hypogaea) is the fifth most produced oil crop worldwide. Besides lack of water, fungal diseases are the most limiting factors for the crop. Several species of Arachis are resistant to certain pests and diseases. This study aimed to successfully cross the A-genome with B-K-A genome wild species previously selected for fungal disease resistance, but that are still untested. We also aimed to polyplodize the amphihaploid chromosomes; cross the synthetic amphidiploids and A. hypogaea to introgress disease resistance genes into the cultivated peanut; and analyze pollen viability and morphological descriptors for all progenies and their parents. We selected 12 A-genome accessions as male parents and three B-genome species, one K-genome species, and one A-genome species as female parents. Of the 26 distinct cross combinations, 13 different interspecific AB-genome and three AA-genome hybrids were obtained. These sterile hybrids were polyploidized and five combinations produced tetraploid flowers. Next, 16 combinations were crossed between A. hypogaea and the synthetic amphidiploids, resulting in 11 different hybrid combinations. Our results confirm that it is possible to introgress resistance genes from wild species into the peanut using artificial hybridization, and that more species than previously reported can be used, thus enhancing the genetic variability in peanut genetic improvement programs.
RÉSUMÉ
The processes of megakaryocyte polyploidization and demarcation membrane system (DMS) formation are crucial for platelet production, but the mechanisms controlling these processes are not fully determined. Inhibition of Rho kinase (ROCK) signalling leads to increased polyploidization in umbilical cord blood-derived megakaryocytes. To extend these findings we determined the effect of ROCK inhibition on development of the DMS and on proplatelet formation. The underlying mechanisms were explored by analysing the effect of ROCK inhibition on the expression of MYC and NFE2, which encode two transcription factors critical for megakaryocyte development. ROCK inhibition promoted DMS formation, and increased proplatelet formation and platelet release. Rho kinase inhibition also downregulated MYC and NFE2 expression in mature megakaryocytes, and this down-regulation correlated with increased proplatelet formation. Our findings suggest a model whereby ROCK inhibition drives polyploidization, DMS growth and proplatelet formation late in megakaryocyte maturation through downregulation of MYC and NFE2 expression.
Sujet(s)
Plaquettes/physiologie , Mégacaryocytes/physiologie , Sous-unité p45 du facteur de transcription NF-E2/génétique , Polyploïdie , Protéines proto-oncogènes c-myc/génétique , rho-Associated Kinases/antagonistes et inhibiteurs , Plaquettes/cytologie , Plaquettes/métabolisme , Techniques de culture cellulaire , Membrane cellulaire/physiologie , Régulation négative , Gènes myc , Transplantation de cellules souches hématopoïétiques/méthodes , Humains , Mégacaryocytes/effets des médicaments et des substances chimiques , Mégacaryocytes/métabolisme , Sous-unité p45 du facteur de transcription NF-E2/biosynthèse , Sous-unité p45 du facteur de transcription NF-E2/sang , Protéines proto-oncogènes c-myc/biosynthèse , Protéines proto-oncogènes c-myc/sang , rho-Associated Kinases/sang , rho-Associated Kinases/génétiqueRÉSUMÉ
The artificial obtaining of duplicate genotypes aims to maximize forage characteristics of agronomic interest, such as nutritional value and forage production, resistance against pests and diseases, abiotic stress tolerance and fertility restoration in sterile hybrids. It also aims to obtain genetic variability in apomictic species through chromosome doubling of the sexual accesses by equaling the ploidy in order to allow crossings and the obtaining of fertile descendents. The polyploidy induction is made using antimitotic substances, and colchicine is the most widely used in forage. However, due to its toxicity, other substances such as herbicides and caffeine has been used successfully for grasses. The efficiency in obtaining the polyploidy artificially depends on various exogenous factors, such as the antimitotic substances used, the kind of explants, the time and the exposure conditions and the antimitotic concentrations. This review aims to present the main methods used to induce polyploidy in grasses and the progress obtained in genetic breeding by the use of artificially duplicate genotypes.
A obtenção artificial de genótipos com duplicação cromossômica em forrageiras busca maximizar características de interesse agronômico, como valor nutricional e produção de forragem, resistência a pragas e doenças, tolerância a estresses abióticos e restauração da fertilidade de híbridos estéreis. Outro objetivo da duplicação cromossômica é a geração de variabilidade genética em espécies apomíticas, por meio da duplicação cromossômica de acessos sexuais igualando a ploidia de modo a permitir a realização de cruzamentos e a obtenção de descendentes férteis. A indução de poliploidia é feita utilizando substâncias antimitóticas, sendo a colchicina a mais amplamente usada em plantas forrageiras. Entretanto, devido a sua toxicidade, outras substâncias como herbicidas e cafeína vem sendo empregadas com sucesso em gramíneas. A eficácia na obtenção de poliploides artificialmente depende de uma série de fatores exógenos, tais como as substâncias antimitóticas utilizadas, o tipo de explante, o tempo e as condições de exposição e as concentrações dos antimitóticos. Esta revisão tem por objetivo apresentar os principais métodos usados para indução de poliploidia em gramíneas forrageiras e os avanços obtidos no melhoramento genético, a partir do uso de genótipos poliploidizados.
RÉSUMÉ
The artificial obtaining of duplicate genotypes aims to maximize forage characteristics of agronomic interest, such as nutritional value and forage production, resistance against pests and diseases, abiotic stress tolerance and fertility restoration in sterile hybrids. It also aims to obtain genetic variability in apomictic species through chromosome doubling of the sexual accesses by equaling the ploidy in order to allow crossings and the obtaining of fertile descendents. The polyploidy induction is made using antimitotic substances, and colchicine is the most widely used in forage. However, due to its toxicity, other substances such as herbicides and caffeine has been used successfully for grasses. The efficiency in obtaining the polyploidy artificially depends on various exogenous factors, such as the antimitotic substances used, the kind of explants, the time and the exposure conditions and the antimitotic concentrations. This review aims to present the main methods used to induce polyploidy in grasses and the progress obtained in genetic breeding by the use of artificially duplicate genotypes.
A obtenção artificial de genótipos com duplicação cromossômica em forrageiras busca maximizar características de interesse agronômico, como valor nutricional e produção de forragem, resistência a pragas e doenças, tolerância a estresses abióticos e restauração da fertilidade de híbridos estéreis. Outro objetivo da duplicação cromossômica é a geração de variabilidade genética em espécies apomíticas, por meio da duplicação cromossômica de acessos sexuais igualando a ploidia de modo a permitir a realização de cruzamentos e a obtenção de descendentes férteis. A indução de poliploidia é feita utilizando substâncias antimitóticas, sendo a colchicina a mais amplamente usada em plantas forrageiras. Entretanto, devido a sua toxicidade, outras substâncias como herbicidas e cafeína vem sendo empregadas com sucesso em gramíneas. A eficácia na obtenção de poliploides artificialmente depende de uma série de fatores exógenos, tais como as substâncias antimitóticas utilizadas, o tipo de explante, o tempo e as condições de exposição e as concentrações dos antimitóticos. Esta revisão tem por objetivo apresentar os principais métodos usados para indução de poliploidia em gramíneas forrageiras e os avanços obtidos no melhoramento genético, a partir do uso de genótipos poliploidizados.
RÉSUMÉ
Some species of Brachiaria, generally tetraploid apomictic varieties, have become important forage grasses in the tropics. Breeding of Brachiaria depends on compatibility with the available apomitic tretraploid cultivars. This paper describes a procedure for chromosome duplication of two Bracharia brizantha diploid sexual accessions, using colchicine treatment of basal segments of in-vitro-grown plants. Explants were cultured on a medium containing 1 mg/l naphthaleneacetic acid, 3 mg/l kinetin and 0.01% colchicine for 48 h and transferred to the same medium without colchicine until shoot regeneration occurred. Regenerated plants were screened by flow cytometry, and chromosome number duplication was confirmed by cytological analysis of root tips.