The aim of this thesis was to investigate morphogenesis in the fruit fly Drosophila melanogaster using three in vitro tissue culture systems. Primary embryonic cultures derived from Drosophila melanogaster were used to study the effect of the moulting hormone ecdysone on cells in culture. The hypothesis was that the effect of ecdysone on these primary embryonic cells would parallel events which occur during metamorphosis in vivo and therefore the primary embryonic cultures could be used as an ‘in vitro’ model system. Transgenic fly lines expressing GFP were used to visualise and identify specific cell types and it was shown that cells in primary embryonic cultures respond to ecdysone morphologically. However due to the variability of cultures it was concluded that this culture system was not suitable for use as a model system. As defined cell types were observed the development of a protocol suitable for use with the primary embryonic culture system using dsRNA in order to demonstrate RNA interference was undertaken. Although this was unsuccessful, as cells in the primary embryonic cultures appeared to be resistant to dsRNA, some technical avenues remain to be explored. The Drosophila melanogaster cell line, Clone 8+, was used to investigate cell adhesion in tissue culture. Statistical analyses were carried out and it was established that derivatives of the parent cell line, Clone 8+, showed differential adhesion and proliferation characteristics. Analysis of microarray data was carried out in order to identify genes which may be responsible for the loss of cell adhesion in Clone 8+ cell lines and the potential roles of these genes in adhesion were discussed. A gene of interest, glutactin, was identified which may be responsible for loss of cell adhesion. Antibody staining was used to establish the expression of the protein glutactin in the Clone 8+ cell lines. The expression of glutactin suggested that the Clone 8+ cell line had maintained properties of the wing disc epithelial cell-type and disruption of cell polarity was considered as a possible mechanism. It was shown that f-actin colocalised with glutactin and the role of the cytoskeleton in glutactin secretion was discussed. It was concluded that glutactin was not responsible for loss of cell adhesion in the Clone 8+ cell lines. Further analysis of the microarray data revealed potential genes that could be responsible for the loss of cell polarity in the Clone 8+ cell lines and the possibility of cellular senescence was considered. It was hypothesised that the properties of adhesion and proliferation related to their ‘in vitro’ age. In the final investigation the movement of epithelial cells in Drosophila melanogaster third instar larval imaginal discs during morphogenesis was investigated. Firstly a lumen was identified in fixed imaginal disc tissue in association with cells expressing f-actin. This result was discussed in relation to the process of dorsal closure and wound healing. Further investigations involved live imaging of the dynamic process of evagination in the imaginal wing disc using transgenic flies expressing moesin-GFP. It was concluded that the lumen was not associated with the process of wound healing and it was concluded that the lumen appeared to be the mechanism directing peripodial epithelium contraction during morphogenesis of the imaginal wing disc. Dorsal closure and the process of invagination in relation to morphogenesis of the imaginal wing disc were discussed.

Konjac glucomannan (KGM), the main biologically active constituent of konjac flour extracted from corms of Amorphophallus konjac (konjac), can be used to prepare functional foods and may also have potential as a pharmaceutical product to combat obesity. The current study employed three experimental approaches to study the biology and chemistry of konjac, namely (1) glasshouse experiments to study the morphogenesis, growth and productivity of konjac plants, (2) a histological and immunocytochemical investigation of the localisation and developmental regulation of the deposition and metabolism of KGM in developing corm tissues, and (3) a comparative study of methodologies for the extraction and analysis of KGM. The current data demonstrated a morphological and functional separation between the ventral and dorsal regions of corms. The ventral region appeared to function as a source during the initial period of shoot development, while the dorsal region appeared to operate as a sink after the development of mature canopy. Once the corm reached maturity, both an inflorescence and a leaf were produced within a single season. It has also been demonstrated that the age of the ‘mother’ corm is an important factor affecting the quality of offsets produced. An anti-mannan antiserum detected a temporally regulated pattern of mannan epitope production within glucomannan idioblasts in developing corm tissues, with increased expression as the corm approached maturity/dormancy. The current observations also suggest that the mobilization of KGM initiates at the periphery of the corm and proceeds inwards towards the centre of the corm. Compositional analysis showed that the purified konjac flour (PKF) produced using a modified extraction procedure contained 92% glucomannan, with a weight average molecular weight (Mw), polydispersity index (PDI) and degree of acetylation (DA) of 9.5 ± 0.6 x 105 gmol-1, 1.2 and 2.8 wt. %. These data, plus Fourier-transform infrared spectral (FTIR) and zero shear viscosity analyses of the extract (PKF) were all consistent with the literature. Comparison of three existing methodologies for the quantitative analysis of the KGM content, namely 3,5-dinitrosalicylic acid (3,5-DNS), phenol-sulphuric acid and enzymatic colorimetric assays; indicated that the 3,5-DNS colorimetric assay was the most reproducible and accurate method, with a linear correlation coefficient of 0.997 and recoveries between 97% and 103% across three spiking levels of starch. In summary, this study has provided a better understanding of aspects of the biology and cultivation of A. konjac and has also produced methodologies which can be used as the basis for an improved good laboratory practice (GLP) for the commercial extraction and analysis of this multifunctional natural polymer.

G proteins coupled receptors (GPCRs) play essential developmental roles with functions in all of the immune, olfactory sensory systems amongst other systems as well as exhibiting essential roles in the central and peripheral nervous system. GPCRs are also major targets of pharmaceutical drugs currently used to treat a vast number of conditions. Despite their clear importance, the function of many GPCRs is still obscure. Identifying the physiological role of more GPCRs provides a niche for more drugs to be developed and thus more conditions to be treated. The C.elegans lat-1 gene encodes the latrophilin vertebrate homolog; it is a member of the adhesion GPCR family and is structurally related to the flamingo/CELSR, an essential component of planar cell polarity pathway. This study aims to phenotypically characterise lat-1 mutants in C.elegans to provide insights into the physiological role of this important member of adhesion GPCRs. lat-1 mutants exhibit several morphological defects throughout development and during vulva development. Analysing the embryonic development of such mutants also identified an anterior-posterior polarity defect. The results implicate a second evolutionary conserved subfamily of adhesion GPCRs in the control of tissue polarity and morphogenesis.

Comment les cellules établissent leurs formes et organisations internes est un problème biologique fondamental. Au cours de cette thèse, j’ai étudié le développement de la forme cellulaire et de la polarité chez la cellule de levure fissipare. Ces études sont fondées sur l’exploration de la façon dont les petites spores symétriques de levures se développent et s’organisent pour briser la symétrie pour la définition de leur tout premier axe de polarité. Dans une première partie, j’ai étudié les couplages entre la mécanique de surface de la paroi cellulaire des spores et la stabilité de domaines de polarité de Cdc42 qui contrôlent les aspects spatio-temporelles de la brisure de symétrie de ces spores. Dans une seconde partie, j’ai étudié les mécanismes par lesquels ces domaines de polarité contrôlent leur taille et l'adapte à la géométrie de la cellule, un processus vraisemblablement pertinents pour comprendre comment des domaines fonctionnels corticaux s’adaptent à la taille des cellules. Globalement, ces nouvelles recherches focalisant sur la façon dont les cellules développent dynamiquement leur forme et polarité de novo, permettent de mettre en évidence des couplages complexes dans la morphogenèse qui ne peuvent pas être testés en regardant les cellules à « l’état stationnaire» ou avec des outils génétiques. / How cells establish their proper shapes and organization is a fundamental biological problem. In this thesis, I investigated the dynamic development of cellular form and polarity in the rod-shape fission yeast cell. These studies are based on monitoring how small symmetric fission yeast spores grow and self-organize to break symmetry for the definition of their very first polarity axis. In a first part, I studied interplays between surface mechanics of the spore cell wall and the stability of Cdc42-based polarity domains which control spatio-temporal aspects of spore symmetry breaking. In a second part, I studied mechanisms by which these polarity domains control their width and adapt it to cell surface geometry, a process likely relevant to understand how functional cortical domains scale to cell size. Overall these novel investigations focusing on how cells dynamically develop their form and polarity de novo highlight complex feedbacks in morphogenesis that cannot be evidenced by looking at cells at “steady state” or with genetics.

Comment les cellules établissent leurs formes et organisations internes est un problème biologique fondamental. Au cours de cette thèse, j’ai étudié le développement de la forme cellulaire et de la polarité chez la cellule de levure fissipare. Ces études sont fondées sur l’exploration de la façon dont les petites spores symétriques de levures se développent et s’organisent pour briser la symétrie pour la définition de leur tout premier axe de polarité. Dans une première partie, j’ai étudié les couplages entre la mécanique de surface de la paroi cellulaire des spores et la stabilité de domaines de polarité de Cdc42 qui contrôlent les aspects spatio-temporelles de la brisure de symétrie de ces spores. Dans une seconde partie, j’ai étudié les mécanismes par lesquels ces domaines de polarité contrôlent leur taille et l'adapte à la géométrie de la cellule, un processus vraisemblablement pertinents pour comprendre comment des domaines fonctionnels corticaux s’adaptent à la taille des cellules. Globalement, ces nouvelles recherches focalisant sur la façon dont les cellules développent dynamiquement leur forme et polarité de novo, permettent de mettre en évidence des couplages complexes dans la morphogenèse qui ne peuvent pas être testés en regardant les cellules à « l’état stationnaire» ou avec des outils génétiques. / How cells establish their proper shapes and organization is a fundamental biological problem. In this thesis, I investigated the dynamic development of cellular form and polarity in the rod-shape fission yeast cell. These studies are based on monitoring how small symmetric fission yeast spores grow and self-organize to break symmetry for the definition of their very first polarity axis. In a first part, I studied interplays between surface mechanics of the spore cell wall and the stability of Cdc42-based polarity domains which control spatio-temporal aspects of spore symmetry breaking. In a second part, I studied mechanisms by which these polarity domains control their width and adapt it to cell surface geometry, a process likely relevant to understand how functional cortical domains scale to cell size. Overall these novel investigations focusing on how cells dynamically develop their form and polarity de novo highlight complex feedbacks in morphogenesis that cannot be evidenced by looking at cells at “steady state” or with genetics.

Les urodèles amphibiens, dont fait partie l’axolotl (Ambystoma mexicanum), ont la capacité de régénérer leurs organes et membres suite à une amputation, tout au long de leur vie. La patte est l’organe dont le processus de régénération est le mieux caractérisé et ce dernier est divisé en deux phases principales. La première est la phase de préparation et commence immédiatement suite à l’amputation. Elle renferme des étapes essentielles au processus de régénération comme la guérison de la plaie et la formation d’une coiffe apicale ectodermique. Par la suite, les fibroblastes du derme et certaines cellules musculaires vont revenir à un état pluripotent via un processus appelé dédifférenciation cellulaire. Une fois dédifférenciées, ces cellules migrent et s’accumulent sous la coiffe apicale pour former le blastème. Lors de la phase de redéveloppement, les cellules du blastème se divisent puis se redifférencient pour régénérer la partie amputée. Fait intéressant, la régénération d’un membre ou la guérison d’une plaie chez l’axolotl ne mène jamais à la formation d’une cicatrice. Afin d’en apprendre plus sur le contrôle moléculaire de la régénération, les gènes Heat-shock protein-70 (Hsp-70) et Transforming growth factor-β1 (Tgf-β1) ont été sélectionnés. Ces gènes jouent un rôle important dans la réponse au stress et lors de la guérison des plaies chez les mammifères. HSP-70 est une chaperonne moléculaire qui est produite pour maintenir l’intégrité des protéines cellulaires lorsqu’un stress se présente. TGF-β1 est une cytokine produite suite à une blessure qui active la réponse inflammatoire et qui stimule la fermeture de la plaie chez les amniotes. Les résultats présentés dans cette thèse démontrent que Hsp-70 est exprimé et régulé lors du développement et de la régénération du membre chez l’axolotl. D’autre part, nos expériences ont mené à l’isolation de la séquence codante pour Tgf-β1 chez l’axolotl. Nos résultats montrent que Tgf-β1 est exprimé spécifiquement lors de la phase de préparation dans le membre en régénération. De plus, le blocage de la voie des Tgf-β avec l’inhibiteur pharmacologique SB-431542, lors de la régénération, mène à l’inhibition du processus. Ceci démontre que la signalisation via la voie des Tgf-β est essentielle à la régénération du membre chez l’axolotl. / Urodele amphibians, such as the axolotl (Ambystoma mexicanum), have the unique ability, among vertebrates, to perfectly regenerate many parts of their body throughout their life. Among the complex structures that can be regenerated, the limb is the most widely studied. Limb regeneration is divided in two main phases. The preparation phase, which begins right after amputation, includes wound healing and the formation of an apical ectodermal cap. During this phase, dermal fibroblasts and muscle cells will lose their characteristics and become pluripotent through a process called cellular dedifferentiation. The dedifferentiated cells migrate and accumulate under the apical ectodermal cap to form the blastema. During the redevelopment phase, the cells in the blastema proliferate and redifferentiate to regenerate the lost structures. It is interesting to highlight the fact that regeneration never leads to scar formation in the axolotl. In order to learn more about the molecular control of limb regeneration, the genes Heat-shock protein-70 (Hsp-70) and Transforming growth factor-β1 (Tgf- β1) were selected for their important roles in stress response and wound healing in mammals. HSP-70 is a molecular chaperone which is produced to protect cellular proteins when the cell faces a stress. TGF-β1 is a cytokine produced after wounding that activates the inflammatory response and stimulates wound closure in amniotes. Results presented in this thesis show that Hsp-70 is expressed and regulated during limb development and regeneration in the axolotl. We were also able to isolate the cDNA coding for axolotl Tgf-β1 and our results show that this gene is expressed specifically during the preparation phase of limb regeneration. Treatment of regenerating axolotls with a specific inhibitor of Tgf-β signalling, SB-431542, led to complete inhibition of regeneration. This directly implies that Tgf-β signalling is essential for limb regeneration in axolotl.

Les tissus épithéliaux présentent deux caractéristiques majeures, ils sont robustes (rôle de barrière) mais également plastiques lors de la morphogénèse. L'homéostasie des tissus épithéliaux repose sur la régulation de la balance prolifération/mort cellulaire. Dans ma thèse, je décris tout d'abord, les mécanismes moléculaires permettant à la cellule épithéliale de se diviser tout en maintenant l'intégrité du tissu. J'ai ensuite altéré cette intégrité, en utilisant le système de génération de clônes mosaïques, afin de comprendre comment la cohésion du tissu est maintenue. Ce travail m'a alors permis de comprendre comment l'adhérence est modulée, puis restaurée, au cours de la division cellulaire. Ainsi, j'ai montré que l'intégrité des tissus est assurée par l'action concomitante des forces d'adhésion et des forces de tension. Enfin, mon travail apporte également des éléments clés pour l'étude de la perte d'adhérence des cellules tumorales responsable en partie, de la progression des tumeurs solides en métastases. / Tissue homeostasis relies on the tight regulation of cell proliferation and cell death. Epithelial tissues are robust tissues that support the structure of developing embryos and adult organs and are effective barriers that physically protect the organism against pathogens. In my thesis, I have first described the molecular mechanisms responsible for maintaining tissue integrity during epithelial cell division. I have then abrogated this integrity by inducing mosaic clones within tissues to understand how tissue cohesion is maintained. This work shows how the continuity of adhesive properties is ensured during cell division. It also reveals new key elements that result in loss of adhesion in tissues and thus may be responsible for the progession from solid cancer to metastasis.

Plantas forrageiras se adaptam ao pastejo por meio de modificações em forma e função alterando seus padrões de expressão morfogênica e, consequentemente, de acúmulo e composição morfológica da forragem produzida. O objetivo deste estudo foi avaliar as respostas morfogênicas e as estruturais de perfilhos em pastos de capim-mulato submetidos a estratégias de pastejo rotativo de fevereiro de 2008 a abril de 2009. Os tratamentos corresponderam combinações entre duas condições pós-pastejo (alturas pós-pastejo de 15 e 20 cm - APP) e duas condições pré-pastejo (95% e máxima interceptação de luz pelo dossel forrageiro - IL), e foram alocados às unidades experimentais (piquetes de 1200 m2) segundo arranjo fatorial 2x2 e delineamento de blocos completos casualizados, com 4 repetições. Foram avaliadas as seguintes variáveis-resposta: taxa de aparecimento de folhas (TApF); filocrono (FIL); taxa de alongamento de folhas (TAlF); taxa de alongamento de colmos (TAlC); taxa de senescência de folhas (TSeF); encurtamento do colmo (EC); duração da vida da folha (DVF); duração do alongamento foliar (DAF); comprimento final da folha (CFF); número de folhas vivas (NFV), em expansão (NFEx), expandidas (NFE) e senescentes (NFS) por perfilho; comprimento do colmo (CC) e relação folha:colmo por perfilho (F:C). Tanto perfilhos basais como aéreos apresentaram sazonalidade de desenvolvimento caracterizada por ritmos morfogênicos mais lentos durante o outono/inverno/início de primavera e mais acelerados durante o final de primavera e verão. No caso de perfilhos basais, pastos manejados a 95% de IL apresentaram maiores valores de TApF no Verão 2. No Verão 1, o EC nesses pastos foi menor, sendo observado comportamento inverso no final da primavera. Menores valores de TAlC e TSeF foram registrados nos pastos manejados a 95% relativamente àqueles manejados com máxima IL (99%). Adicionalmente, pastos manejados com altura pós-pastejo 20 cm apresentaram maiores valores de TAlF, TSeF e DAF que pastos manejados a 15 cm, especialmente na condição pré-pastejo de 95% de IL. Nos perfilhos aéreos, maiores valores de TAlC e TSeF foram registrados nos pastos manejados com máxima IL (99%) relativamente àqueles manejados a 95% de IL. Com relação às características estruturais, a APP afetou apenas aquelas relacionadas com o porte da planta (CFF e CC). Apesar das diferenças estatísticas, o NFV foi relativamente constante para aéreos e basais (2,5 e 4,0 folhas por perfilho, respectivamente), com as diferenças entre categorias de perfilhos refletindo diferenças em NFS e NFE e não em NFEx. Perfilhos basais foram maiores que aéreos, porém com menor F:C. Para perfilhos basais, NFV, NFEx e F:C foram maiores em pastos manejados a 95% de IL e, para aéreos, naqueles manejados com máxima IL, padrão condizente com o fato de perfilhos aéreos serem provenientes de perfilhos basais reprodutivos decapitados. De forma geral, as características estruturais foram mais afetadas pela IL e época do ano do que pela APP, indicando, claramente, importância relativa maior da frequência comparativamente à severidade de desfolhação para controle da estrutura do dossel. Diante do exposto, a condição ideal para interrupção do processo de rebrotação dos pastos de capim-mulato é quando o dossel atinge 95% de IL com uma altura pós-pastejo de 20 cm. / Forage plants adapt to grazing through morphological and physiological changes that modify their morphogenesis and, in turn, herbage accumulation and morphological composition of the produced herbage. The objective of this study was to evaluate the morphogenetic responses and the structural characteristics of individual tillers on mulato grass swards subjected to strategies of rotational stocking management from February 2008 until April 2009. Treatments corresponded to combinations between two post-grazing (post-grazing heights of 15 and 20 cm) and two pre-grazing (95% and maximum light interception by sward canopy LI) conditions, and were allocated to experimental units (1200 m2 paddocks) according to a 2x2 factorial arrangement and a randomised complete block design, with four replications. The following response variables were evaluated: rates of leaf appearance (LAR), leaf elongation (LER), stem elongation (SER), leaf senescence (LSR), reduction in stem length (RSL), phyllochron (PHY), leaf lifespan (LLS), leaf elongation duration (LED), final leaf length (FLL), number of live (NLL), expanding (NExL), expanded (NEL) and senescing (NSL) leaves per tiller, stem length (SL) and the leaf:stem ratio per tiller (L:S). Both basal and aerial tillers showed a clear seasonal pattern of growth characterised by slow morphogenetic rhythms during autumn/winter/early spring and fast rhythms during late spring and summer. For basal tillers, swards managed at 95% LI showed highest values of LAR in summer 2. In Summer 1, RSL on those swards was lowest, the reverse happening in late spring. Lower values of SER and LSR were recorded on swards managed at 95% relative to those managed at maximum LI (99%). Further, swards managed with the postgrazing height of 20 cm showed larger values of LER, LSR and LED than those with 15 cm, particularly for the 95% LI pre-grazing condition. For aerial tillers, larger values of SER and LSR were recorded on swards managed at maximum LI (99%) relative to those managed at 95% LI. In relation to structural characteristics, postgrazing height only influenced those related to plant size (FLL and SL). In spite of the statistical differences, NLL was relatively stable for aerial and basal tillers (2.5 and 4.0 leaves per tiller, respectively), with differences between tiller categories mainly due to differences in NSL and NEL, not NExL. Basal tillers were bigger than aerial tillers, although had lower L:S. For basal tillers, NLL, NExL and L:S were larger on swards managed at 95% LI and, for aerial tillers, larger values were recorded on swards managed at maximum LI, a pattern in line with the fact that aerial tillers are originated from decapitated reproductive basal tillers. Overall, structural characteristics were more influenced by LI and season of the year than by postgrazing height, highlighting the larger importance of frequency relative to severity of defoliation for controlling sward structural characteristics. As a result, the ideal 14 condition for interrupting regrowth of rotationally stocked mulato grass correspond to a pre-grazing condition of 95% LI and a post-grazing height of 20 cm.

A transformação genética possibilita a introdução de genes de interesse agronômico no genoma das plantas e pode ser empregada na tentativa de obter plantas resistentes a doenças. No entanto, para se obter uma planta transgênica é necessário primeiramente estabelecer um procotolo eficiente de regeneração de plantas in vitro. Assim, o objetivo desse trabalho foi estudar a organogênese in vitro e a transformação genética de limão Volkameriano e laranja azeda com um fragmento do gene da capa protéica do CTV. Para a organogênese in vitro utilizou-se, como explante, segmento internodal, obtido de planta cultivada em casa-de-vegetação, segmento de epicótilo, coletado de plântula cultivada in vitro e segmento de cotilédone associado ao hipocótilo obtido de semente introduzida in vitro. Esses explantes foram mantidos em meio de cultura EME suplementado com 6-benzilaminopurina (BAP 0,0; 0,5; 1,0; 1,5; 2,0 mg L- 1), sendo incubados sob fotoperíodo de 16 h de luz ou em condições de escuro por 30 dias e então transferidos para fotoperíodo de 16 h de luz. A avaliação foi realizada após 45 dias de cultivo, determinando-se o número de explantes responsivos e o número de gemas por explante. A caracterização anatômica do processo de regeneração foi realizada por meio de cortes histológicos. Pela análise dos dados foi possível verificar que a organogênese in vitro ocorreu a partir dos três tipos de explantes testados, sendo que, nas duas espécies em estudo, os melhores resultados foram obtidos com o cultivo de segmento de cotilédone associado ao hipocótilo. As concentrações de BAP que estimularam as melhores taxas de regeneração foram de 1,0 e 1,5 mg L-1, para limão Volkameriano, e 0,5 e 1,0 mg L-1 para laranja azeda. A incubação dos explantes em ausência de luz favoreceu a regeneração in vitro. Pela análise histológica foi possível observar que o processo de regeneração, a partir dos três tipos de explantes testados, ocorreu por meio de organogênese indireta. O protocolo de desenvolvimento estabelecido durante os experimentos de organogênese in vitro foi utilizado para a transformação genética dessas espécies via Agrobacterium, contendo o plasmídeo pCAMBIA 2201, com um fragmento do gene da capa protéida do CTV, em uma construção gênica do tipo hairpin. As gemas de limão Volkameriano e laranja azeda identificadas como transgênicas pelo teste histoquímico GUS foram enxertadas in vitro em citrange Carrizo. A confirmação da transformação genética foi realizada pela análise de PCR, a qual mostrou a amplificação de um fragmento de 671 pb, correspondente a parte do gene amplificada. / Genetic transformation permits the introduction of agronomically important genes in plant genome and can be utilized in order to produce disease resistant plants. However for the recovery of transgenic plants is required to establish an efficient in vitro plant regeneration protocol. In this work the aim was to study an in vitro organogenesis and the genetic transformation of Volkamer lemon and sour orange with a sequence of the CTV coat protein gene. For in vitro organogenesis explant internodal segments collected from plants cultivated in greenhouse, epicotyl segments obtained from in vitro cultivated seedlings and cotyledon fragment with hypocotyl attached obtained from in vitro germinated seed were used as explant. These explants were cultured in EME medium supplemented with benzilaminopurine (BAP 0,0; 0,5; 1,0; 1,5; 2,0 mg L-1). Cultures were maintained under a 16 h photoperiod or in the dark for 10 d and then transferred to a 16 h photoperiod. The evaluation was performed 45 d after the incubation determining the number of responsive explant and the number of buds per explant. The anatomical characterization of in vitro regeneration process was carried out through histological analyses. The in vitro organogenesis occurred in the three types of explant tested, however cotyledon fragment with hypocotyl attached showed higher morphogenetic potential in both species. The best responses of regeneration were obtained when the medium was supplementation with 1,0 e 1,5 mg L-1 BAP for the Volkamer lemon and 0,5 e 1,0 mg L-1 BAP for the sour orange. The incubation in darkness favored the in vitro regeneration. The histological analyses showed that the regeneration process occurred through indirect organogenesis in the three types of explants tested. The developed protocol was use for genetic transformation of Volkamer lemon and sour orange with Agrobacterium, containing pCAMBIA 2201 plasmid with a sequence of CTV coat protein gene, in a hairpin construction. Volkamer lemon and sour orange shoots identified as transgenic by histochemical test GUS were micrografted into Carrizo citrange. PCR analysis were performed after micrografted showing the presence of the 671 pb fragment of the transgene.

O capim-braquiária (Brachiaria decumbens Stapf. cv. Basilisk) tem grande importância para sistemas de produção pecuários no Brasil, notadamente em regiões com baixa fertilidade natural do solo. O objetivo do presente trabalho foi estudar efeitos de duas intensidades (5 e 10 cm de altura pós-pastejo) e duas frequências de desfolhação (descanso até 95 e 100% de interceptação luminosa, IL, para início do pastejo) como definidores da estrutura do dossel, da morfogênese e do valor nutritivo da B.decumbens cv. Basilisk sob lotação intermitente. O estudo foi conduzido em Brotas - SP. O período experimental foi de Jan 2007 a Ago 2008, compreendendo sete épocas (Verão/2007, Outono/2007, Inverno/2007, Final de primavera/2007, Verão/2008, Outono/2008 e Inverno/2008) para as variáveis: produção de forragem, composição morfológica, índice de área foliar (IAF), altura de dossel, IL e valor nutritivo de folhas. Para características morfogênicas, densidade e demografia de perfilhos, o período foi de Ago 2007 a Ago 2008 e para valor nutritivo da forragem de Jan 2008 a Ago 2008. Os tratamentos foram quatro combinações possíveis entre as duas intensidades e frequências de desfolhação, em arranjo fatorial, com quatro repetições num delineamento inteiramente casualizado.O manejo com 100% IL resultou em produção total de 17,1 Mg MS ha-1, enquanto que para 95% IL a produção foi de 14,2 Mg MS ha-1. Pastos sob a estratégia 100% IL resultaram em maior produção de colmos e material morto, e maior IAF-pré pastejo. A intensidade de 10 cm promoveu maior produção de forragem e colmos (16,6 e 4,4 Mg MS ha-1), e maior IL e IAF no pós-pastejo. As maiores taxas de aparecimento de folhas (TAPF) e menores taxas de senescência foliar (TSF), alongamento (TALC) e acúmulo de colmo (TAFCM), na primavera de 2007 até outono de 2008 foram obtidas para 95% IL.As maiores taxas de acúmulo de folhas (TAFLM)no final da primavera ocorreram em pastos submetidos a 95% de IL e no verão e outono para o tratamento 10/95 (24,3, 26,8 e 23,3 kg MS ha-1 dia-1). De forma geral, o tratamento 10/95 resultou em altas taxas de aparecimento e de sobrevivência de perfilhos basais nas épocas com maior disponibilidade nos fatores de crescimento, épocas em que também foram encontrados os maiores teoresem proteína bruta (PB) de folhas para 95% IL, enquanto adigestibilidade in vitro da matéria orgânica (DIVMO)de folhas foi maior para a intensidade de 10 cm. As menores DIVMOs da forragem foram encontradas nos pastos que receberam a combinação 5/100, indicando que períodos longos de descanso e intensidades altasde pastejo resultam na produção de forragem de baixo valor nutritivo. A altura de dossel no pré-pastejo para o manejo com 95% IL ficou próximo a 16 cm e para 100% IL em 22 cm. A desfolhação do capim-braquiária deve ser realizada até10 cm uma vez que isto resulta em rebrotações rápidas e, quando associado à frequência de 95% IL, permite que animais em pastejo tenham acesso a forragem com maior participação de folhas e menor de material morto e colmo. / Signalgrass (Brachiaria decumbens Stapf. cv. Basilisk) is an important forage resource in Brazilian livestock systems, mainly where soil natural fertility is low. The objective in this study was to investigate the effects of two intensities (5 and 10 cm stubble) and two frequencies of defoliation (rest periods determined by 95 or 100% light interception LI by the canopy) as determinants of sward structure, morphogenesis, and forage nutritive value of B.decumbens cv. Basilisk under intermittent grazing. The work was carried out in Brotas, SP. The experimental period was from Jan 2007 through Aug 2008, divided in seven seasons (Summer/2007, Autumn/2007, Winter/2007, Late Spring/2007, Summer/2008, Autumn/2008 and Winter/2008) for the response variables: forage production, plant-part composition, leaf area index (LAI), sward height, LI, and leaf nutritive value. For the morphogenetic characteristics, tiller density, and tiller demography, the experimental period was from Aug 2007 through Aug 2008. For forage nutritive value, it was from Jan 2008 through Aug 2008. Treatments included all possible combinations among two grazing frequencies and two intensities, in a factorial arrangement of a completely randomized design. The 100% LI management resulted in total yield of 17.1 Mg DM ha-1, whereas for the 95% LI treatments total production was 14.2 Mg DM ha-1. Pastures under the 100% LI strategy produced more stem and dead material, as well as higher pregraze LAI. The 10-cm stubble resulted in higher forage and stem yield (16.6 and 4.4 Mg DM ha-1, respectively), as well as higher postgraze LI and LAI.The highest leaf appearance rates and lowest rates of leaf senescence, leaf elongation, and stem accumulation from Spring 2007 through Autumn 2008 were recorded for 95%LI. The highest rates of leaf accumulation in late spring were found in pastures under 95% LI, and in the summer and autumn for the 10/95 treatment (24.3, 26.8 and 23.3 kg DM ha-1 d-1, respectively). In general, the 10/95 treatment resulted in high rates of basal tiller appearance and survival, when the environmental conditions were favorable, which was also when crude protein concentration in leaves was highest under 95% LI, whereas in vitroorganic matter digestibility (IVOMD) of leaves was higher for the 10 cm stubble. The lowest IVOMDs were found in pastures receiving the 5/100 treatment combination, indicating that long rest periods combined with high grazing intensities result in forage of low nutritive value. Pregraze sward height for the 95%-LI managements was around 16 cm and for the 100%-LI, around 22 cm. Defoliation of signalgrass should not be lower than 10 cm height, since this results in rapid regrowth and, when associated with the 95%-LI frequency, allows animals to harvest forage with high proportion of leaves and low proportion of stem and dead material.