Brinjal shoot and fruit borer (Leucinodes orbonalis Guenee) is a major limiting factor in commercial cultivation of eggplant in southeast Asia. Extensive use of pesticides as well as the conventional breeding methods have been ineffective in controlling the borer so there is a need for Integrated Pest Management (IPM) strategies for its control. Bacillus thuringiensis (Bt) is known to produce a variety of insecticidal crystal proteins toxic to lepidopteran, dipteran and coleopteran pests. The Cry2Aa protein has been found to be more toxic to brinjal shoot and fruit borer than Cry1Ab. My objective was to develop eggplant cultivars that express a codon-optimized cry2Aa gene, the sequence of which is based on that of an Indian isolate of Bt, with the eventual goal of producing fully resistant cultivars. The cry2Aa gene was modified for optimal expression in eggplant using the codon usage frequencies based on solanaceous sequences (eggplant, tomato and pepper). The GC content was increased from 34.3% in the native gene to 41.3% in the optimized gene, thus removing the AT-rich regions that are typical for Bt cry genes. Also, other mRNA destabilizing and hairpin forming structure sequences were removed. The gene was synthesized in four different parts with complementary restriction sites. A total of 152 oligonucleotides (oligos) was used to assemble the 1.9 kb gene using dual asymmetric (DA) and overlap extension (OE) PCR techniques. The individual parts were subsequently ligated using the complementary restriction sites and inserted into vector pCAMBIA 1302. Also, the transformation efficiency of 12 different eggplant cultivars was tested using plasmid pHB2892 to predict utility for transformation with the synthetic cry2Aa. / Master of Science

Clonal plants may be able to cope with spatial heterogeneity due to the physiological integration of ramets. Previous studies demonstrated that benefits of clonal integration increase with patch contrast between individual ramets. However, the same magnitude of contrast may be perceived differently in rich and poor environments. According to the theoretical work of Caraco and Kelly (1991), I expected these benefits to be the greatest in overall poor conditions and high between-patch contrast. To test this hypothesis, I conducted experiments with pairs of ramets of a stoloniferous grass, Agrostis stolonifera, grown in variously nutrient rich conditions. The experiment with pairs of ramet of similar developmental age showed only very weak effect of integration on growth of ramets, although integration significantly improved survival of ramets and also affected root-shoot ratio of ramets. Nevertheless, there were considerable benefits of integration in the experiment with developmentally older mother ramets and their daughter ramets. Contrary to the predictions, the benefits of integration were bigger in rich conditions and they decreased with increasing between-patch contrast. In addition, effect of integration on root-shoot ratio of ramets was opposite to the expected specialization for acquisition...

Au vu de l’impact croissant du changement climatique global et en particulier de la sécheresse sur les forêts, il est nécessaire de comprendre les mécanismes de réponse des arbres face à des variations de disponibilité en eau. Ces dernières années, des études ont montré un contrôle épigénétique et notamment par la méthylation de l’ADN de la plasticité phénotypique des plantes en réponse aux variations environnementales. Dans ce contexte, cette thèse visait à évaluer le rôle de la méthylation de l’ADN des cellules du méristème apical caulinaire dans la plasticité développementale de la tige feuillée en réponse à des variations de disponibilité en eau chez le peuplier, un arbre modèle. A cette fin, le méthylome de la chromatine non condensée dans le méristème apical caulinaire de Populus trichocarpa a été caractérisé. Ensuite, l’impact de variations de disponibilité en eau sur la méthylation de l’ADN a été étudié dans l’apex caulinaire de différents hybrides (P. × euramericana). Les loci et les réseaux de gènes affectés pour leur expression et leur méthylation ont ainsi été identifiés. Ces travaux ont montré que dans le méristème apical caulinaire, la majorité des gènes étaient dans un état non condensé de la chromatine et méthylés dans leur corps. Ils ont également mis en évidence une forte variation de la méthylation globale de l’ADN selon les génotypes et en réponse à des variations de disponibilité en eau. De plus, des corrélations ont été établies entre les niveaux de croissance des arbres et de méthylation globale de l’ADN dans l’apex caulinaire. Enfin, les variations de la méthylation de l’ADN en réponse aux variations de la disponibilité en eau s’accompagnent de variations d’expression et ont ciblé particulièrement des gènes impliqués dans la signalisation par les phytohormones ou la morphogenèse. Ainsi, les travaux effectués lors de cette thèse suggèrent un rôle de la méthylation de l’ADN dans la plasticité phénotypique en réponse à des variations de disponibilité en eau chez le peuplier via le contrôle de l’expression de réseaux de gènes dans le méristème apical caulinaire. / Predicted climate changes and particularly drought represent a major threat to forest health. Therefore, understanding mechanisms that control trees response to variations in water availability is of great interest. These last years, epigenetic marks such as DNA methylation have been involved in plant phenotypic plasticity in response to environmental stresses. In this context, this work aimed at assessing the role of shoot apical meristem cells DNA methylation in the shoot developmental plasticity towards variations in water availability in poplar, a model tree. For this purpose, the methylome of non condensed chromatin in Populus trichocarpa shoot apical meristem was characterized. Then, the impact of variations in water availability on shoot apex DNA methylation in different hybrids (P. × euramericana) was studied. Loci and gene networks affected by DNA methylation and expression changes were thus identified. This work showed that in shoot apical meristem, most of the genes was in non condensed chromatin state with DNA methylation in their body. A strong variation in DNA methylation depending on genotypes and water availability was highlighted. Moreover, correlations between trees growth and shoot apex DNA methylation levels were established. Lastly, DNA methylation changes in response to variations in water availability correlated to expression variations were identified for genomic loci and gene networks. Thus, the work performed during this thesis suggests a role for DNA methylation in poplar phenotypic plasticity in response to variations in water availability through the control of gene networks transcription in the shoot apical meristem.

Des génotypes adaptés à des environnements contrastés ont de grandes chances de se comporter différemment lorsqu’ils sont placés dans des conditions similaires et contrôlées, notamment si leur sensibilité aux signaux environnementaux et/ou leur croissance intrinsèque sont limitées à différents niveaux. De ce fait, la variabilité observée dans les populations naturelles peut être utilisée comme une source illimitée de nouveaux allèles ou gènes pour l’étude des bases génétiques de la variation des traits quantitatifs. Mon travail de doctorat a consisté en l’analyse de la variabilité naturelle pour la croissance et la réponse à l’environnement chez Arabidopsis thaliana. Le but des approches de génétique quantitative est de comprendre comment la diversité génétique et épigénétique contrôle la variabilité phénotypique observée dans les populations à différentes échelles, au cours du développement et sous différentes contraintes environnementales. De plus, ces analyses ont pour objectif de comprendre comment les processus adaptatifs et démographiques influencent la fréquence de ces variants dans les populations en fonction de leur environnement local. Ainsi, l’étude de la variabilité naturelle peut être appréhendée en utilisant diverses approches, de la génétique et des méthodes de biologie moléculaire aux études écologiques et évolutives. Au cours de mon doctorat, j’ai eu la chance de travailler sur plusieurs de ces aspects au travers de trois projets indépendants qui exploitent tous la variabilité naturelle d’A. thaliana.Le premier projet a consisté en l’analyse du pattern de polymorphisme observé dans des populations d’A. thaliana au gène MOT1 qui code pour un transporteur de molybdate (la forme assimilable du molybdène (Mo), un micro-élément essentiel) et qui est responsable d’une partie des variations de croissance et de fitness observées à l’échelle de l’espèce en fonction de la disponibilité en Mo des sols. J’ai montré à différentes échelles géographiques que le pattern de polymorphisme à MOT1 ne reflète pas une évolution neutre mais présente plutôt des traces de sélection diversifiante. Ce travail a contribué à renforcer l’hypothèse selon laquelle des mutations au niveau du gène MOT1 pourraient avoir été sélectionnées dans certaines populations pour faire face aux niveaux élevés de Mo observés dans certains sols et potentiellement délétères malgré leur effet négatif sur des milieux pauvres en Mo.Le deuxième projet portait sur la caractérisation et l’analyse fonctionnelle de deux récepteur-kinase putatifs (RLK) identifiés de part leurs effets sur la croissance foliaire spécifiquement en réponse à un stress induit par du mannitol mais pas sous d’autres contraintes osmotiques. La fonction de ces récepteurs chez A. thaliana -qui n’est pas connu pour produire du mannitol- peut paraître intrigante. Les différentes expériences réalisées au cours de cette thèse nous ont cependant permis de construire un modèle selon lequel ces récepteurs pourraient être activés par le mannitol produit par certains pathogènes tel que les champignons et participer aux réponses de défense de la plante.Le troisième projet a été réalisé en collaboration avec l’équipe de Michel Vincentz (CBMEG, Brésil) et de Vincent Colot (IBENS, Paris) et consiste en l’analyse de l’occurrence de variants épigénétiques naturels au gène QQS dans différentes populations d’Asie Centrale et de leurs possibles conséquences phénotypique et adaptative.En conclusion, l’analyse des variants génétiques et épigénétiques naturels à l’origine des variations de biomasse en interaction avec l’environnement permet de comprendre comment l’évolution façonne la variabilité naturelle. / Genotypes adapted to contrasting environments are expected to behave differently when placed in common controlled conditions, if their sensitivity to environmental cues or intrinsic growth behaviour are set to different thresholds, or are limited at distinct levels. This allows natural variation to be exploited as an unlimited source of new alleles or genes for the study of the genetic basis of quantitative trait variation. My doctoral work focuses on analysing natural variation for shoot growth and response to the environment in A. thaliana. Natural variation analyses aim at understanding how molecular genetic or epigenetic diversity controls phenotypic variation at different scales and times of plant development and under different environmental conditions, and how selection or demographic processes influence the frequency of those molecular variants in populations for them to get adapted to their local environment. As such, the analysis of A. thaliana natural variation can be addressed using a variety of approaches, from genetics and molecular methods to ecology and evolutionary questions. During my PhD, I got the chance to tackle several of those aspects through my contributions to three independent projects which have in common to exploit A. thaliana natural variation. The first one is the analysis of the pattern of polymorphism from a set of 102 A. thaliana accessions at the MOT1 gene coding for a molybdate transporter (an essential micronutrient) and responsible for contrasted growth and fitness among accessions in response to Mo availability in the soil. I showed at different geographical scales that MOT1 pattern of polymorphisms is not consistent with neutral evolution and shows signs of diversifying selection. This work helped reinforce the hypothesis that in some populations, mutations in MOT1 have been selected to face soils rich in Mo and potentially deleterious despite their negative effect on Mo-limiting soils. The second project consists in the characterisation and functional analysis of two putative receptor-like kinases (RLKs) identified from their effect on shoot growth specifically under mannitol-supplemented media and not in response to other osmotic constraints. The function of such RLKs in A. thaliana, which is not known to synthesize mannitol was intriguing at first but, through different experiments, we built the hypothesis that those RLKs could be activated by the mannitol produced by some pathogens such as fungi and participate to plant defensive response. The third project, in collaboration with Michel Vincentz’s team from CBMEG (Brasil) and Vincent Colot (IBENS, Paris), consists in the analysis of the occurrence of natural epigenetic variants of the QQS gene in different populations from Central Asia and their possible phenotypic and adaptive consequences. Overall, these analyses of the genetic and epigenetic molecular variation leading to the biomass phenotype(s) in interaction with the environment provide clues as to how and where in the pathways adaptation is shaping natural variation.

As bromélias são valorizadas por suas características ornamentais, sendo o gênero Vriesea representativo neste setor. O aprimoramento de métodos de propagação in vitro destas plantas é altamente necessário a fim de suprir as necessidades do mercado, e evitar o extrativismo ilegal. Nesse contexto, o presente trabalho objetivou aprimorar o protocolo de propagação in vitro de espécies do gênero Vriesea, bem como aumentar o conhecimento global das espécies em estudo. Para tanto, sementes das espécies V. carinata, V. friburgensis, V. paraibica e V. simplex foram submetidas a processos de assepsia e introduzidas in vitro sob três temperaturas: 22 °C, 27 °C e 32 °C. Paralelamente, sementes das mesmas espécies foram semeadas em bandejas e mantidas em casa de vegetação. Através da microscopia eletrônica de varredura e ótica foi realizada a descrição morfo-anatômica do desenvolvimento pós-seminal das plântulas das mesmas espécies. Além disso, procurou-se adequar o meio de cultura às necessidades das mesmas espécies e de V. hieroglyphica, sendo testadas 3 doses de nitrogênio e 3 doses de magnésio. Também procurou-se avaliar a taxa de sobrevivência durante o processo de aclimatização de plântulas das espécies de Vriesea mencionadas (com exceção de V. hieroglyphica). Objetivou-se comparar características anatômicas e morfológicas de folhas das referidas espécies cultivadas in vitro e em casa de vegetação. Por fim, com o objetivo de estabelecer um protocolo de micropropagação para as espécies Vriesea carinata, V. paraibica, V. phillipo-coburgii; V. simplex e Aechmea nudicaulis, foram introduzidos in vitro explantes somáticos, após testes de assepsia. A partir dos experimentos citados foi verificado que a temperatura exerce uma forte influência nas taxas de germinação e mortalidade das sementes de Vrieseas in vitro, sendo que a temperatura de 32°C proporcionou as maiores taxas de mortalidade, mostrando-se prejudicial ao sucesso reprodutivo. A germinação em casa de vegetação apresentou altas taxas de mortalidade e taxas de germinação mais baixas do que in vitro. A descrição morfo-anatômica do desenvolvimento pós-seminal permitiu a caracterização de cinco estágios de desenvolvimento. Com relação ao experimento de nutrição mineral, foi evidenciado que as doses de nitrogênio e magnésio testadas acarretaram em menor acúmulo de cálcio e de potássio nas plantas, sendo que esse fato resultou em menor acúmulo de massa fresca. O experimento de aclimatização ficou inviabilizado devido ao ataque às plântulas por praga Fungus Gnats. Com a análise morfo-anatômica das folhas de plantas cultivadas in vitro e em casa de vegetação foi possível observar a presença de estruturas típicas de Bromeliaceae nas plantas cultivadas em ambas as condições: estômatos, tricomas escamiformes, mesofilo com epiderme unisseriada, parênquima aqüífero, feixes colaterais fechados e canais de aeração. Com relação à introdução in vitro a partir de explantes somáticos, pode-se afirmar que o uso de cefotaxima apresentou uma boa eficiência no combate à contaminação bacteriana em cultura de ápices caulinares. A escolha de ápice vegetativo de brotos laterais como explantes iniciais para a cultura das referidas espécies in vitro é uma boa opção. A otimização da propagação destas espécies in vitro poderá diminuir a pressão extrativista que estas vêm sofrendo e, ao mesmo tempo, abastecer o mercado ornamental / Bromeliads are valued for their ornamental characteristics and the genus Vriesea is representative in this sector. The improvement of in vitro propagation of these plants is highly necessary in order to meet market needs, and, at the same time, to prevent illegal extraction of this plants from their natural habitat. In this context, this study aimed to improve the protocol for in vitro propagation of species of Vriesea and increase the global knowledge of these by morpho-anatomical characterization of the development of the seedling and leaf. Seeds of V. carinata, V. friburgensis, V.paraiba and V. simplex were submitted to aseptic procedures and introduced in vitro under three temperatures: 22 ° C, 27 ° C and 32 ° C. Additionaly, seeds of these species were sown in trays and maintained in a greenhouse. The post-seminal development was described by light and scanning electron microscopy. In addition, the adjustment of the culture medium for these four species and V. hieroglyphica was tested, by testing three doses of nitrogen combined with three doses of magnesium. The acclimatization efficiency of these Vriesea species, except for V. hieroglyphica, after a prior culture in the presence and absence of IBA was done, in three commercial substrates to verify IBA effect in rooting and seedling survival. This study also aimed to compare anatomical and morphological characteristics of leaves of the species cultivated in vitro and in the greenhouse. Finally, in order to establish a micropropagation protocol for the species Vriesea carinata, V. paraiba, V. phillipo-coburgii; V. simplex and Aechmea nudicaulis, somatic explants were introduced in vitro after sterilization tests. From all the experiments cited it was observed that the temperature strongly influences germination and mortality rates of Vriesea germinating seeds in vitro. The temperature of 32 ° C provided the highest mortality rates, being harmful to the reproductive success of this species. The germination in the greenhouse showed higher mortality and lower germination rates than in vitro germination. The morpho-anatomical description of the post-seminal development allowed for the characterization of five stages of development. With regard to the mineral nutrition experiment, the doses of nitrogen and magnesium tested resulted in less accumulation of calcium and potassium in plants, resulting in less accumulation of fresh weight. The acclimatization experiment was lost by the attack of Fungus gnats. With the morpho-anatomical analysis of leaves of plants grown in vitro and in the greenhouse it was possible to observe the presence of typical structures of Bromeliaceae such as stomata, scales, mesophyll with uniseriate epidermis, water storage tissue, collateral vascular bundles and air channels. Finally, the use of cefotaxime proved efficient against bacterial contamination in in vitro establishment of shoot apex explants in vitro. The choice of shoot apices from lateral buds as initial explants for in vitro establishment of those species was a good alternative. Optimization of in vitro propagation of bromeliad species can reduce their extractivism pressure and, at the same time, supply the ornamental plant market

No description available.

Protoplast fusion of Lolium perenne and Lotus corniculatus for gene introgression by Sanjeev V. Raikar Lolium perenne is one of the most important forage crops globally and in New Zealand. Lotus corniculatus is a dicotyledonous forage that contains valuable traits such as high levels of condensed tannins, increased digestibility, and high nitrogen fixing abilities. However, conventional breeding between these two forage crops is impossible due to their markedly different taxonomic origin. Protoplast fusion (somatic hybridisation) provides an opportunity for gene introgression between these two species. This thesis describes the somatic hybridisation, the regeneration and the molecular analysis of the putative somatic hybrid plants obtained between L. perenne and L. corniculatus. Callus and cell suspensions of different cultivars of L. perenne were established from immature embryos and plants were regenerated from the callus. Of the 10 cultivars screened, cultivars Bronsyn and Canon had the highest percentage of callus induction at 36% each on 5 mg/L 2,4-D. Removal of the palea and lemma which form the seed coat was found to increase callus induction ability of the embryos. Plant regeneration from the callus was achieved when the callus was plated on LS medium supplemented with plant growth regulators at different concentrations. Variable responses to shoot regeneration was observed between the different cultivars with the cv Kingston having the lowest frequency of shoot formation (12%). Different factors affecting the protoplast isolation of L. perenne were investigated. The highest protoplast yield of 10×106 g-1FW was obtained when cell suspensions were used as the tissue source, with enzyme combination ‘A’ (Cellulase Onozuka RS 2%, Macerozyme R-10 1%, Driselase 0.5%, Pectolyase 0.2%), for 6 h incubation period in 0.6 M mannitol. Development of microcolonies was only achieved when protoplasts were plated on nitrocellulose membrane with a L. perenne feeder layer on PEL medium. All the shoots regenerated from the protoplast-derived calli were albino shoots. The highest protoplast yield (7×106 g-1FW) of L. corniculatus was achieved from cotyledons also with enzyme combination ‘A’ (Cellulase Onozuka RS 2%, Macerozyme R-10 1%, Driselase 0.5%, Pectolyase 0.2%), for 6 h incubation period in 0.6 M mannitol. The highest plating efficiency for L. corniculatus of 1.57 % was achieved when protoplasts were plated on nitrocellulose membrane with a L. perenne feeder layer on PEL medium. The highest frequency of shoot regeneration (46%) was achieved when calli were plated on LS medium with NAA (0.1 mg/L) and BA (0.1 mg/L). Protoplast fusion between L. perenne and L. corniculatus was performed using the asymmetric somatic hybridisation technique using PEG as the fusogen. L. perenne protoplasts were treated with 0.1 mM IOA for 15 min and L. corniculatus protoplasts were treated with UV at 0.15 J/cm2 for 10 min. Various parameters affecting the fusion percentage were investigated. Successful fusions were obtained when the fusions were conducted on a plastic surface with 35% PEG (3350 MW) for 25 min duration, followed by 100 mM calcium chloride treatment for 25 min. A total of 14 putative fusion colonies were recovered. Shoots were regenerated from 8 fusion colonies. Unexpectedly, the regenerated putative hybrid plants resembled L. corniculatus plants. The flow cytometric profile of the putative somatic hybrids resembled that of L. corniculatus. Molecular analysis using SD-AFLP, SCARs and Lolium specific chloroplast microsatellite markers suggest that the putative somatic hybrids could be L. corniculatus escapes from the asymmetric protoplast fusion process. This thesis details a novel Whole Genome Amplification technique for plants using Strand Displacement Amplification technique.

The response of cucumber (Cucumis sativus L.) plants to various root and shoot environments (solution depth, temperature, ionic strength, nitrogen and calcium level and light intensity) were studied. Cucumber plants were grown in continuously circulating-solution in a heated-glasshouse. Dry weights of leaves, stems and roots, leaf area, leaf number, root length and root number were measured as well as uptake of potassium, calcium and nitrogen. The relationship between shoot and root in terms of functional equilibrium equations was also examined. The results presented show that: 1. Shoot growth of cucumber plants was reduced if grown in solutions of less than 50mm in depth; 2. When roots were grown in shallow solution depths at 1 or 5mm the dry weight allocated to the root increased. The ratio of root number/root length(no./cm) also increased. Lowering solution temperature to 12.5±2.5°C enhanced the production of root number relctive to root length, and 5 and 2% of full strength and 5% of full strength nitrogen level solution stimulated the growth of root length relative to root number; 3. Under low solution temperature treatment leaf number was maintained at the expense of leaf area. Under low total ionic strength and low nitrogen solution, enhanced root length growth was at the expense of leaf area growth; 4. Low solution temperature enhanced the dry weight allocated to the stem relative to the leaf. Low total ionic strength and low nitrogen solution increased the dry weight allocated to the leaf relative to the stem; 5. The specific activity of root, represented by specific absorption rate, increased when the shoot was under light stress and, the specific activity of shoot, represented by unit shoot rate, increased when the root was under nitrogen-stress; 6. The form of equation developed by Thornley (∆M = fm∆W, where ∆M is the increment in weight of element M and ∆W the increment in total plant dry weight during a time period ∆t with fm a constant) showed a better relationship than the equation developed by Davidson [root mass x rate(absorption) ∝ leaf mass x rate(photosynthesis)] and subsequently used by Hunt in the form of mass ratio(root/shoot) ∝ l/activity ratio; 7. The equation developed by Chung et al, total plant weight/(leaf number/leaf area) ∝ total "k"/(root number/root length), where k represents the total contents of elements or compounds, showed a good approximation of the relationship between shoot and root under all the environmental stresses imposed with the exception of calcium uptake. The results support the concept that the activity of the root or shoot in carrying out its function is influenced by the demand created by the opposite organ and appears to be a better assumption than that which proposes that the activity of an organ is solely dependent on its own size.

Much is known about how organs acquire their identity, yet we are only beginning to learn how their shape is regulated. Recent work has elucidated the role of coordinated cell division & expansion in determining plant organ shape. For instance, in Antirrhinum, leaf shape is affected in the cincinnata (cin) mutant because of an alteration in the cell division pattern. CIN codes for a TCP transcription factor and controls cell proliferation. It is unclear how exactly CIN-like genes regulate leaf morphogenesis. We have taken biochemical and genetic approach to understand the TCP function in general and the role of CIN-like genes in leaf morphogenesis in Antirrhinum and Arabidopsis. Targets of CINCINNATA To understand how CIN controls Antirrhinum leaf shape, we first determined the consensus target site of CIN as GTGGTCCC by carrying out RBSS assay. Mutating each of this target sequence, we determined the core binding sequence as TGGNCC. Hence, all potential direct targets of CIN are expected to contain a TGGNCC sequence. Earlier studies suggested that CIN activates certain target genes that in turn repress cell proliferation. To identify these targets, we compared global transcripts of WT and cin leaves by differential display PCR and have identified 18 unique, differentially expressed transcripts. To screen the entire repertoire of differentially expressed transcripts, we have carried out extensive micro-array analysis using 44K Arabidopsis chips as well as 13K custom-made Antirrhinum chips. Combining the RBSS data with the results obtained from the micro-array experiments, we identified several targets of CIN. In short, CIN controls expression of the differentiation-specific genes from tip to base in a gradient manner. In cin, such gradient is delayed, thereby delaying differentiation. We also find that gibberellic acid, cytokinin and auxin play important role in controlling leaf growth. Genetic characterization of CIN-homologues in Arabidopsis Arabidopsis has 24 TCP genes. Our work and reports from other groups have shown that TCP2, 4 and 10 are likely to be involved in leaf morphogenesis. These genes are controlled by a micro RNA miR319. To study the role of TCP4, the likely orthologue of CIN, we generated both stable and inducible RNAi lines. Down-regulation of TCP4 transcript resulted in crinkly leaves, establishing the role of TCP4 in leaf shape. To study the function of TCP2, 4 & 10 in more detail, we isolated insertion mutants in these loci. The strongest allele of TCP4 showed embryonic lethal phenotype, indicating a role for TCP4 in embryo growth. All other mutants showed mild effect on leaf shape, suggesting their redundant role. Therefore, we generated and studied various combinations of double and triple mutants to learn the concerted role of these genes on leaf morphogenesis. To further study the role of TCP4 in leaf development, we generated inducible RNAi and miRNA-resistant TCP4 transgenic lines and carried out studies with transient down-regulation and up-regulation of TCP4 function. Upon induction, leaf size increased in RNAi transgenic plants whereas reduced drastically in miR319 resistant lines, suggesting that both temporal & spatial regulation of TCP4 is required for leaf development. Biochemical characterization of TCP domain To study the DNA-binding properties of TCP4, random binding site selection assay (RBSS) was carried out and it was found that TCP4 binds to a consensus sequence of GTGGTCCC. By patmatch search and RT-PCR analysis, we have shown that one among 74 putative targets, EEL (a gene involved in embryo development), was down regulated in the RNAi lines of TCP4. This suggests that EEL could be the direct target of TCP4. We have tested this possibility in planta by generating transgenic lines in which GUS reporter gene is driven by EEL upstream region with either wild type or mutated TCP4 binding site. GUS analysis of embryos shows that transgenic with mutated upstream region had significantly reduced reporter activity in comparison to wild type, suggesting that EEL is a direct target of TCP4. We have further shown that TCP4 also binds to the upstream region of LOX2, a gene involved in Jasmonic acid (JA) biosynthesis (in collaboration with D. Weigel, MPI, Tubingen, Germany). TCP domain has a stretch of basic residues followed by a predicted helix-loop-helix region (bHLH), although it has little sequence homology with canonical bHLH proteins. This suggests that TCP is a novel and uncharacterized bHLH domain. We have characterized DNA-binding specificities of TCP4 domain. We show that TCP domain binds to the major groove of DNA with binding specificity comparable to that of bHLH proteins. We also show that helical structure is induced in the basic region upon DNA binding. To determine the amino acid residues important for DNA binding, we have generated point mutants of TCP domain that bind to the DNA with varied strength. Our analysis shows that the basic region is important for DNA binding whereas the helix-loop-helix region is involved in dimerization. Based on these results, we have generated a molecular model for TCP domain bound to DNA (in Collaboration with Prof. N. Srinivasan, IISc, Bangalore). This model was validated by further site-directed mutagenesis of key residues and in vitro assay. Functional analysis of TCP4 in budding yeast To assess TCP4 function in regulation of eukaryotic cell division, we have introduced TCP4 in S. cerevisiae under the GAL inducible promoter. TCP4 induction in yeast cells always slowed down its growth, indicative of its detrimental effect on yeast cell division. Flow cytometry analysis of synchronized cells revealed that TCP4 arrests yeast cell division specifically at G1→S boundary. Moreover, induced cells showed distorted cell morphology resembling shmoo phenotype. Shmooing is a developmental process which usually happened when the haploid cells get exposed to the cells of opposite mating type and get arrested at late G1 phase due to the inhibition of cdc28-cln2 complex. This suggested that TCP4-induced yeast cells are arrested at late G1 phase probably by the inhibition of cdc28-cln2 complex. To further investigate how TCP4 induce G1→S arrest, we carried out microarray analysis and found expression of several cell cycle markers significantly altered in TCP4-induced yeast cells. Studies on crinkly1, a novel leaf mutant in Arabidopsis To identify new genes involved in leaf morphogenesis, we have identified crinkly1 (crk1), a mutant where leaf shape and size are altered. We observed that crk1 also makes more number of leaves compared to wild type. Phenotypic analysis showed that crk1 leaf size is ~5 times smaller than that of wild type. Scanning electron microscopy (SEM) showed that both cell size and number are reduced in the mutant leaf, which explains its smaller size. We have mapped CRK1 within 3 cM on IV chromosome.

Vegetative propagation allows the amplification of selected genotypes for research, breeding, and commercial planting. However, efficient in vitro regeneration and genetic transformation remains a major obstacle to research and commercial application in many plant species. Our aims are to improve knowledge of gene regulatory circuits important to meristem organization, and to identify genes that might be useful for improving the efficiency of in vitro regeneration. In this thesis, we have approached these goals in two ways. First, we analyzed gene expression during poplar (Populus) regeneration using an AffymetrixGeneChip® array representing over 56,000 poplar transcripts. We have produced a catalog of regulated genes that can be used to inform studies of gene function and biotechnology. Second, we developed a GUS reporter system for monitoring meristem initiation using promoters of poplar homologs to the meristem-active regulatory genes WUSCHEL (WUS) and SHOOTMERISTEMLESS (STM). This provides plant materials whose developmental state can be assayed with improved speed and sensitivity. For the microarray study, we hybridized cDNAs derived from tissues of a female hybrid poplar clone (INRA 717-1 B4, Populus tremula x P. alba) at five sequential time points during organogenesis. Samples were taken from stems prior to callus induction, at 3 days and 5 days after callus induction, and at 3 and 8 days after the start of shoot induction. Approximately 15% of the monitored genes were significantly up-or down-regulated based on both Extraction and Analysis of Differentially Expressed Gene Expression (EDGE) and Linear Models for Microarray Data (LIMMA, FDR<0.01). Of these, over 3,000 genes had a 5-fold or greater change in expression. We found a very strong and rapid change in gene expression at the first time point after callus induction, prior to detectable morphological changes. Subsequent changes in gene expression at later regeneration stages were more than an order of magnitude smaller. A total of 588 transcription factors that were distributed in 45 gene families were differentially regulated. Genes that showed strong differential expression encoded proteins active in auxin and cytokinin signaling, cell division, and plastid development. When compared with data on in vitro callogenesis from root explants in Arabidopsis, 25% (1,260) of up-regulated and 22% (748) of down- regulated genes were in common with the genes that we found regulated in poplar during callus induction. When ~3kb of the 5' flanking regions of close homologs were used to drive expression of the GUSPlus gene, 50 to 60% of the transgenic events showed expression in apical and axillary meristems. However, expression was also common in other organs, including in leaf veins (40% and 46% of WUS and STM transgenic events, respectively) and hydathodes (56% of WUS transgenic events). Histochemical GUS staining of explants during callogenesis and shoot regeneration using in vitro stems as explants showed that expression was detectable prior to visible shoot development, starting 3 to 15 days after explants were placed onto callus inducing medium. Based on microarray gene expression data, a paralog of poplar WUS was detectably up-regulated during shoot initiation, but the other paralog was not. Surprisingly, both paralogs of poplar STM were down-regulated 3- to 6-fold during early callus initiation, a possible consequence of its stronger expression in the secondary meristem (cambium) than in shoot tissues. We identified 15 to 35 copies of cytokinin response regulator binding motifs (ARR1AT) and one copy of the auxin response element (AuxRE) in both promoters. Several of the WUS and STM transgenic events produced should be useful for monitoring the timing and location of meristem development during natural and in vitro shoot regeneration. / Graduation date: 2008