Spermatogenesis is a complex process of male germ cell development in which the diploid spermatogonia undergo series of mitotic divisions and differentiation steps culminating into the preleptotene spermatocytes which then enter into the meiotic prophase following a single replication cycle. This phase is characterized by meiotic recombination and is followed by reduction division resulting in haploid round spermatids. These cells then undergo extensive morphological and nuclear changes to form a unique cell, spermatozoa. This entire germ cell differentiation process occurs in a unique environment present inside the seminiferous tubules which is created by the Sertoli cells, the somatic cells in the tubules by forming junctions with each other thus providing unique milieu to the developing germ cells. Within the tubule, the germ cells are also arranged in an orderly manner called stages of spermatogenesis indicating a complex mechanism of germ cell differentiation. This complex differentiation process is a consequence of developmentally and precisely regulated differential gene expression (Eddy, 2002). Unraveling the molecular mechanisms involved in the male germ cell development is an uphill task due to the complexity of the cyto-architecture existing in the tubules and further complicated by unavailability of established germ cell lines and lack of cell culture systems that facilitate the germ cell differentiation in vitro. Comparative gene expression analysis of spermatogenesis in nematodes, flies and rodents revealed highly conserved transcriptomes and have provided some insights into its regulation (Schlecht and Primig, 2003). However, these data fail to represent the genetic and biological complexity of human spermatogenesis. In the present study, an attempt has been made to identify the genes that are differentially expressed in human tetraploid and haploid germ cells and to investigate the mechanism of regulation of the genes expressed in the post-meiotic germ cells. To identify the cell type specific genes, expression profiling of the human tetraploid and haploid germ cells was carried out using cDNA microarray. These cells were purified by centrifugal elutriation (Meistrich et al., 1981; Shetty et al., 1996) from the human testicular tissues obtained from the patients undergoing orchidectomy as treatment for prostate cancer. Purity of the enriched population of the germ cells was ascertained by DNA flow cytometry and by RT-PCR analysis using the known cell-specific markers and ruling out contamination of the somatic cells such as the Sertoli cells and the Leydig cells. Microarray experiments were carried out with the RNA isolated from each cell type and labeling the cDNA with Cy3/Cy5-dUTP and hybridizing to the human 19K array chip (University Health Network, Toronto, Canada) containing 19,200 ESTs. Two independent hybridizations were carried out using the germ cells isolated from two individuals and the microarray data were analyzed using Avadis 3.1 software (Strand Life Sciences, India). Analysis of the microarray data following normalization revealed that 723 transcripts showed higher expression in the meiotic cells whereas 459 transcripts showed higher expression in the post-meiotic germ cells. Microarray data were validated further by RT-PCR analysis of some of the differentially regulated genes. The DAVID analysis (Database for Annotation, Visualization and Integrated Discovery; http://david.abcc.ncifcrf.gov/) of these genes revealed that many genes associated with diverse functions and pathways appeared to be differentially expressed in both cell types. It is known that many biological systems exhibit distinct temporal gene expression profiles during different processes related to cell cycle, stress response and differentiation. Similarly, there are sets of genes, which respond to specific stimuli, appear to be synchronized in their expression. Such ‘synexpressed’ genes have been shown to be regulated by common transcription regulatory processes and have similar upstream transcription factor binding sites (Niehrs and Pollet, 1999). And therefore, having identified genes that appeared to be differentially expressed in the haploid and the tetraploid germ cells, attempt was made to analyze transcription factor binding sites in the promoter of those genes. In silico promoter analysis of several genes showing higher post-meiotic expression was carried out in order to identify the common regulatory motifs. Analysis of the annotated promoters (available from Eukaryotic Promoter Database; http://www.epd.isb-sib.ch/) of about forty genes highly expressed in the post-meiotic germ cells using TFSEARCH program (http://www.cbrc.jp/ research/db/TFSEARCH.html) confirmed that many genes had common transcription factor binding sites. Interestingly, almost all of the analyzed genes harbored SRY (Sex determining Region in Y)/SOX (SRY-box containing) binding motifs. In addition, the promoters of genes such as Protamine 1 and 2, Transition protein 1 and 2, A kinase (PRKA) anchor protein 4 that are known to be expressed post-meiotically, also harbor SRY binding sites suggesting that SRY may be one of the key regulators of the post-meiotic gene expression. SRY is a HMG-box containing member of Sox-family of architectural transcription factors. SRY is encoded by the Y chromosome and was first discovered as the testis-determining factor in mammals (Koopman et al., 1991). SRY HMG-box is eighty amino acids conserved motif that binds to the minor groove of the DNA in a sequence-dependent manner resulting in its bending and thus regulating the gene expression. The RT-PCR analysis of the human haploid and tetraploid germ cells showed very high expression of SRY in the post-meiotic cells further suggesting key role of SRY in the post-meiotic gene regulation. Role of SRY in the post-meiotic gene expression was investigated by determining the effect of SRY on human Protamine 1 (PRM1) promoter, a gene known to be exclusively expressed in the round spermatids and as indicated above, harbors many SRY binding sites in its promoter. SRY cDNA was cloned into the mammalian expression vector, pcDNA3.1 and the PRM1 promoter was cloned into the promoter-less pGL3 Basic vector upstream of the Luciferase reporter gene. Co-transfection of both constructs led to up-regulation of PRM1 promoter activity in both HeLa cells and LNCaP cells in a dose-dependent manner clearly demonstrating the role of SRY in PRM1 gene expression. Sequential deletion of the SRY binding sites in the PRM1 promoter led to the identification of the critical SRY binding motif important for SRY-mediated upregulation of PRM1 gene expression. This was confirmed by demonstrating in vitro binding of SRY to its critical binding site in the PRM1 promoter by gel shift assay using the nuclear extract of the HeLa cells transfected with FLAG-tagged SRY. The human SRY is an atypical transcription factor that binds DNA through its HMG, but unlike the mouse Sry and other Sox proteins, lacks the trans-activation domain and therefore requires other factors for its actions. Recently, the glutamine-rich, zinc-finger containing transactivator, Specificity protein 1 (Sp1) has been identified as one such interacting partner (Wissmuller et al., 2006). RT-PCR analysis showed that human SP1 is highly expressed in the haploid germ cells and could up-regulate PRM1 expression which harbors two SP1 binding sites in its promoter. When co-transfected, SRY and SP1 up-regulated PRM1 promoter in co-operative manner suggesting that SP1 may act in coordination with SRY in regulating PRM1. All these data taken together clearly signifies a critical role of SRY in post-meiotic germ cell gene expression. Recent reports suggest that SRY is also expressed in the adult human brain and prostate. However, its role in these tissues is not clearly understood. The Y chromosome has been shown to be frequently lost in prostate cancer and has also been shown to suppress the tumorigenicity of the PC-3 prostate cancer cells suggesting that the Y chromosome encoded genes may be involved in tumor suppression. SRY can physically interact with the androgen receptor (AR) and thereby interfere in its downstream signaling (Yuan et al., 2001). Since the prostate tumors show initial androgen-dependency, it was interesting to look at the role of SRY in the prostate cancer. To decipher the effect of SRY on the androgen-responsive LNCaP cells, stable clones of LNCaP expressing human SRY were generated. These clones showed significant decrease in growth in response to 5α-dihydrotestosterone (DHT) compared to the vector transfected or the parental LNCaP cells. In the soft agar colony formation assay, the SRY expressing LNCaP formed smaller colonies as compared to the controls in presence of DHT. Preliminary experiments in male athymic nude mice demonstrated that one of the SRY expressing clones showed reduced tumor growth compared to control cells suggesting that SRY may play a role in prostate cancer progression by decreasing the sensitivity to DHT. To summarize, the present study has identified several genes differentially expressed in the human haploid and tetraploid germ cells and further showed that SRY may be one of the key regulators of the post-meiotic gene expression.

Doctor of Philosophy / Polyphenol oxidase (PPO) catalyses undesirable darkening in wheat products such as Asian noodles. Genetic variation for PPO activity is characterized in bread wheat. Australian wheat breeding programmes recognize that reduced PPO activity is an important quality target. Despite this interest from breeders, no varieties possessing extremely low and null PPO activity exist. The development of null PPO wheat varieties is dependant on an understanding of the genetic control of the null phenotype. Knowledge of these factors will accelerate efforts to develop them. The inheritance of PPO activity was investigated in two populations that were derived from hybrids between a null PPO genotype and Australian wheat varieties Lang and QAlBis. Observed genetic ratios were consistent with two and three gene control, respectively in these populations. QTL mapping was performed in the QALBis x VAW08-A17 population. The Diversity Array Technology (DArT) approach was employed to genotype the QALBis x VAW08-A17 population. Three highly significant QTLs that control PPO activity were identified on chromosomes 2AL, 2BS and 2DL. Close associations between PPO activity and DArT marker loci wPt-7024, wPt-0094 and wPt-2544 were observed, respectively. Collectively, these loci explained 74% of the observed variation in PPO activity across seasons. Significant QTLs on chromosomes 1B and 3B were also identified that together explained an additional 17% of variation in PPO activity. The relationship between PPO activity and yellow alkaline noodles (YAN) colour stability parameters was investigated in a DM5637*B8 x H45 doubled haploid population. PPO activity and changes in YAN brightness (ΔL* 0-24h) and yellowness (Δb* 0-24h) in both seasons were analysed. Quantitative trait analyses of PPO activity, flour yellowness (b*) and YAN colour stability was also conducted in this population. QTL mapping of variation in PPO activity in the DM5637*B8 x H45 DH population identified a highly significant QTL on chromosome 2AL, which explained 52% of the observed variation across seasons. Regression analysis identified that wPt-7024 was highly significantly associated with PPO activity in this population. A highly significant association between this marker and PPO was also identified in the QALBis x VAW08-A17 population. Collectively, the three identified QTLs (on chromosomes 2AL, 7A and 7B) explained 71% of variation in PPO activity across seasons. A highly significant (P<0.001) QTL on chromosome 2B along with significant (P<0.01) QTLs on the chromosomes 1A, 3B, 4B and 5B were found to control flour yellowness. The QTLs on 2B, 4B and 5B were detected in both seasons analysed and accounted for 90% of variation in flour b* across seasons. The study on YAN colour stability located two highly significant (P<0.001) QTLs and two significant (P<0.01) QTLs that controlled the change in brightness of yellow alkaline noodle. The 2A QTL accounted for 64% of observed variation across seasons. It was in the same location as the PPO QTL and shared a common closest marker wPt-7024. Only one significant QTL for YAN a* (0-24h) was identified. It accounted for 12% of variation across seasons and was only detected in one season. One highly significant (P<0.001) QTL and two significant (P<0.01) QTLs were identified that controlled the change in yellowness of yellow alkaline noodle. The 2A QTL accounted for 68% of observed variation across seasons. The location of this QTL corresponded with that of 2A QTLs for PPO activity and L* of YAN in this study. Furthermore, wPt-7024 was also identified as the marker with the most significant association with L*. The identification of a correlation between the characters and a common location of a highly significant QTL for each of these characters indicates that it is likely that PPO activity is directly responsible for a large proportion of the changes in brightness and yellowness of YAN. QTLs for L* and b* of YAN were detected in a common location on chromosome 1A. However, no corresponding QTL was identified that controls PPO activity, highlighting the complexity of the relationship between these traits. Resistance to three rust pathogens (Puccinia graminis, Puccinia striiformis, and Puccinia triticina) was also investigated in the DM5637*B8 x H45 DH population because they are major yield limiting diseases in wheat. Disease response data at the seedling stage were converted to genotypic scores for rust genes Sr24/Lr24, Sr36, Lr13 and Yr7 to construct a genetic linkage map. No recombination was observed between rust resistance genes Sr36, Lr13 and Yr7 in this DH population. Therefore, these genes mapped in the same position on chromosome 2B. The Lr24/Sr24 locus was incorporated into the chromosome 3D map. Interval mapping analysis identified QTLs on chromosomes 2B, 3B, 4B and 5B that control adult plant resistance (APR) to stripe rust. Two QTLs on chromosomes 2B and 3D were identified that controlled APR to leaf rust in this DH population.

O trigo (Triticum aestivum L.) é uma importante cultura no Brasil. Poucas cultivares são recomendadas para produção do tipo sequeiro no Bioma Cerrado onde a escassez de água limita o rendimento de grãos. Aqui reportamos uma análise de transcriptoma do MGS1 Aliança (cultivar de trigo adaptada ao Cerrado) sob estresse de seca. Um grupo de 4.422 transcritos diferencialmente expressos foi encontrado em raízes e folhas. O número de transcritos reprimidos em raiz (1.102) foi menor que os transcritos induzidos (1.706), enquanto o oposto ocorreu em folhas (1,017 induzidos e 647 reprimidos). O número de transcritos comuns entre ambos órgaõs foi 1.249, enquanto 2.124 foram específicos para raíz e 1.049 específicos para folhas. Análises de RT-qPCR de 35 transcritos selecionados ao acaso revelou uma correlação de 0,78 com os dados de transcriptoma. Os transcritos diferencialmente expressos foram distribuídos por todos os cromossomos e componentes do genoma. O número de transcritos no genoma B foi maior do que nos genomas A e D. Ainda, um grande número de transcritos relacionados à seca foi mapeado nos cromossomos 3B, 5B e 2B. Quando consideramos ambos órgãos, 116 diferentes rotas metabólicas foram alteradas. Uma rota em comum, entre as três mais alteradas em ambos órgãos, foi o metabolismo do amido e da sacarose. A comparação de transcritos derivados de raiz e de folha permite a identificação de transcritos importantes relacionados à respota ao estresse de seca em cada um destes órgãos. Os dados obtidos, também, abrem caminho para o desenvolvimento de futuros marcadores e seleção de genes candidatos ligados à característica. Estes resultados são úteis para o entendimento de rotas metabólicas envolvidas na tolerância à seca em trigo. A informação gerada será usada, a mais longo prazo, para propósitos de transgenia. Para isto, a metodologia de duplo-haploides é desejável e uma primeira investigação sobre a eficiência de protocolo se mostrou necessária. Micrósporos são células gaméticas com capacidade de dar origem a uma nova planta via embriogênese in vitro. Plantas duplo-haploides geradas pela cultura de micrósporos isolados são completamente homozigotas e representam uma importante ferramenta para estudos genéticos e melhoramento de plantas O processo androgenético é desencadeado por diferentes pré-tratamentos de estresse, os quais são empregados para mudar os micrósporos da rota gametofítica para a rota esporofítica. Embora a cultura de micrósporos isolados tenha inúmeras vantagens, importantes limitações tem impedido sua apliação em larga escala. Diferenças genotípicas na resposta androgenética e na formação de plantas albinas ainda constituem desafios. Embora o albinismo seja principalmente uma característica genética, pré-tratamentos e meios de cultura apropriados podem evitar este fenômeno até certo ponto. A resposta androgenética de cinco genótipos de trigo brasileiro foi avaliada no presente estudo. Dois pré-tratamentos foram testados: frio (4°C) e ácido 2-hidroxinicotinico (100 mg/L). O frio foi melhor que o pré-tratamento químico, produzindo mais plantas verdes em quatro de cinco genótipos. Somente dois genótipos brasileiros tratados com ácido 2-hidroxinicotinico produziram plantas, e um deles apenas uma única planta albina. Nossos reultados mostram, também, que o meio semilíquido (contendo 10% de Ficoll) promoveu uma maior resposta androgenética que o meio líquido, aumentando o número de embriões e plantas regeneradas. / Wheat (Triticum aestivum L.) is an important crop cultivated in Brazil. Few cultivars are recommended for rainfed production in the Cerrado Biome where water scarcity limits grain yield. Here we report a transcriptome analysis of MGS1 Aliança (a wheat cultivar adapted to the Cerrado) under drought stress. A set of 4,422 differentially expressed transcripts was found in roots and leaves. The number of down-regulated transcripts in roots (1,102) was lower than the up-regulated transcripts (1,706), while the opposite occurred in leaves (1,017 induced and 647 repressed). The number of common transcripts between the two tissues was 1,249, while 2,124 were specific to roots and 1,049 specific to leaves. Quantitative RT-PCR analysis of 35 randomly selected transcripts revealed a 0.78 correlation with the transcriptome data. The differentially expressed transcripts were distributed across all chromosomes and component genomes. The number of transcripts on the B genome was greater than on the A and D genomes. Additionally, a greater number of drought related transcripts was mapped on chromosomes 3B, 5B and 5D. When considering both tissues, 116 different metabolic pathways were changed. One common pathway, among the top three changed pathways in both tissues, was starch and sucrose metabolism. The comparison of root- and leaf-derived transcripts allows the identification of important transcripts related to water stress response in each of these tissues. It also paves the way for future marker development and selection of candidate genes linked to that trait. These results are useful for understanding the metabolic pathways involved in wheat drought response. The information generated will be used for transgenic wheat purposes. For this the doubled-haploid method is desirable and an investigation about the protocol eficiency is needed. Microspores are gametic cells with capacity to give rise to a new plant via in vitro embryogenesis. Doubled haploid plants generated by isolated microspore culture are completely homozygous and represent an important tool for plant genetics and breeding research. This process is triggered by different stress pretreatments, which are employed to switch microspores from gametophytic to a sporophytic pathway. Although isolated microspore culture has innumerous advantages, important limitations have prevented its application on a large scale. Genotypic differences in androgenic response and the formation of albino plants remain great challenges. Although albinism is a major genetic characteristic, appropriated pretreatments and culture medium can avoid this phenomenon to some extent. The androgenic response of five Brazilian wheat genotypes was evaluated in the present study. Two pretreatments were tested: cold (4°C) and 2-hydroxynicotinic acid (100 mg/L). Cold was better than chemical pretreatment, producing more green plants in four out of five genotypes. Only two Brazilian genotypes treated with 2-hydroxynicotinic acid produced plants, and one of them produced a single albino plant. Our results also show that semi-liquid medium (containing 10% Ficoll) promoted a higher androgenic response than did liquid medium, increasing the number of embryos and regenerated plants.

O trigo (Triticum aestivum L.) é uma importante cultura no Brasil. Poucas cultivares são recomendadas para produção do tipo sequeiro no Bioma Cerrado onde a escassez de água limita o rendimento de grãos. Aqui reportamos uma análise de transcriptoma do MGS1 Aliança (cultivar de trigo adaptada ao Cerrado) sob estresse de seca. Um grupo de 4.422 transcritos diferencialmente expressos foi encontrado em raízes e folhas. O número de transcritos reprimidos em raiz (1.102) foi menor que os transcritos induzidos (1.706), enquanto o oposto ocorreu em folhas (1,017 induzidos e 647 reprimidos). O número de transcritos comuns entre ambos órgaõs foi 1.249, enquanto 2.124 foram específicos para raíz e 1.049 específicos para folhas. Análises de RT-qPCR de 35 transcritos selecionados ao acaso revelou uma correlação de 0,78 com os dados de transcriptoma. Os transcritos diferencialmente expressos foram distribuídos por todos os cromossomos e componentes do genoma. O número de transcritos no genoma B foi maior do que nos genomas A e D. Ainda, um grande número de transcritos relacionados à seca foi mapeado nos cromossomos 3B, 5B e 2B. Quando consideramos ambos órgãos, 116 diferentes rotas metabólicas foram alteradas. Uma rota em comum, entre as três mais alteradas em ambos órgãos, foi o metabolismo do amido e da sacarose. A comparação de transcritos derivados de raiz e de folha permite a identificação de transcritos importantes relacionados à respota ao estresse de seca em cada um destes órgãos. Os dados obtidos, também, abrem caminho para o desenvolvimento de futuros marcadores e seleção de genes candidatos ligados à característica. Estes resultados são úteis para o entendimento de rotas metabólicas envolvidas na tolerância à seca em trigo. A informação gerada será usada, a mais longo prazo, para propósitos de transgenia. Para isto, a metodologia de duplo-haploides é desejável e uma primeira investigação sobre a eficiência de protocolo se mostrou necessária. Micrósporos são células gaméticas com capacidade de dar origem a uma nova planta via embriogênese in vitro. Plantas duplo-haploides geradas pela cultura de micrósporos isolados são completamente homozigotas e representam uma importante ferramenta para estudos genéticos e melhoramento de plantas O processo androgenético é desencadeado por diferentes pré-tratamentos de estresse, os quais são empregados para mudar os micrósporos da rota gametofítica para a rota esporofítica. Embora a cultura de micrósporos isolados tenha inúmeras vantagens, importantes limitações tem impedido sua apliação em larga escala. Diferenças genotípicas na resposta androgenética e na formação de plantas albinas ainda constituem desafios. Embora o albinismo seja principalmente uma característica genética, pré-tratamentos e meios de cultura apropriados podem evitar este fenômeno até certo ponto. A resposta androgenética de cinco genótipos de trigo brasileiro foi avaliada no presente estudo. Dois pré-tratamentos foram testados: frio (4°C) e ácido 2-hidroxinicotinico (100 mg/L). O frio foi melhor que o pré-tratamento químico, produzindo mais plantas verdes em quatro de cinco genótipos. Somente dois genótipos brasileiros tratados com ácido 2-hidroxinicotinico produziram plantas, e um deles apenas uma única planta albina. Nossos reultados mostram, também, que o meio semilíquido (contendo 10% de Ficoll) promoveu uma maior resposta androgenética que o meio líquido, aumentando o número de embriões e plantas regeneradas. / Wheat (Triticum aestivum L.) is an important crop cultivated in Brazil. Few cultivars are recommended for rainfed production in the Cerrado Biome where water scarcity limits grain yield. Here we report a transcriptome analysis of MGS1 Aliança (a wheat cultivar adapted to the Cerrado) under drought stress. A set of 4,422 differentially expressed transcripts was found in roots and leaves. The number of down-regulated transcripts in roots (1,102) was lower than the up-regulated transcripts (1,706), while the opposite occurred in leaves (1,017 induced and 647 repressed). The number of common transcripts between the two tissues was 1,249, while 2,124 were specific to roots and 1,049 specific to leaves. Quantitative RT-PCR analysis of 35 randomly selected transcripts revealed a 0.78 correlation with the transcriptome data. The differentially expressed transcripts were distributed across all chromosomes and component genomes. The number of transcripts on the B genome was greater than on the A and D genomes. Additionally, a greater number of drought related transcripts was mapped on chromosomes 3B, 5B and 5D. When considering both tissues, 116 different metabolic pathways were changed. One common pathway, among the top three changed pathways in both tissues, was starch and sucrose metabolism. The comparison of root- and leaf-derived transcripts allows the identification of important transcripts related to water stress response in each of these tissues. It also paves the way for future marker development and selection of candidate genes linked to that trait. These results are useful for understanding the metabolic pathways involved in wheat drought response. The information generated will be used for transgenic wheat purposes. For this the doubled-haploid method is desirable and an investigation about the protocol eficiency is needed. Microspores are gametic cells with capacity to give rise to a new plant via in vitro embryogenesis. Doubled haploid plants generated by isolated microspore culture are completely homozygous and represent an important tool for plant genetics and breeding research. This process is triggered by different stress pretreatments, which are employed to switch microspores from gametophytic to a sporophytic pathway. Although isolated microspore culture has innumerous advantages, important limitations have prevented its application on a large scale. Genotypic differences in androgenic response and the formation of albino plants remain great challenges. Although albinism is a major genetic characteristic, appropriated pretreatments and culture medium can avoid this phenomenon to some extent. The androgenic response of five Brazilian wheat genotypes was evaluated in the present study. Two pretreatments were tested: cold (4°C) and 2-hydroxynicotinic acid (100 mg/L). Cold was better than chemical pretreatment, producing more green plants in four out of five genotypes. Only two Brazilian genotypes treated with 2-hydroxynicotinic acid produced plants, and one of them produced a single albino plant. Our results also show that semi-liquid medium (containing 10% Ficoll) promoted a higher androgenic response than did liquid medium, increasing the number of embryos and regenerated plants.

O desenvolvimento embrionário é o resultado de uma sequência controlada de eventos modulados por sinais ambientais e mecanismos intracelulares. Em Hymenoptera, esse processo tem um caráter especial devido ao sistema de determinação do sexo (Haplodiploide). Neste sistema, os ovos fecundados se desenvolvem em fêmeas (diploides) e os ovos não fecundados em machos (haploides). Assim, eventos importantes, como a ativação do ovo e transição materno-zigótica, eventos iniciais da embriogênese, são elementos-chave para compreender o desenvolvimento de ambos os tipos de embriões. Ativação do ovo é um evento complexo acionado em resposta a estímulos externos, necessários para o início da embriogênese. Em abelhas a ativação ovo ocorre independentemente da fecundação e parece ser desencadeado durante a passagem pelo trato reprodutivo da mãe. Além disso, se o ovócito não for fecundado ele irá se desenvolver em um organismo haploide. No entanto, se o ovo recebe o espermatozóide até 30 minutos depois da ativação, o ovo se desenvolve em um organismo diploide. Em Drosophila, a ativação do ovo é também idependente da fecundação. O estímulo inicial que desencadeia o desenvolvimento é devido tensões mecânicas sofridas pelo ovócito durante a ovulação pela passagem através do trato reprodutivo. Neste modelo, o primeiro sinal de ativação inclui a ativação da via dependente de cálcio. Moléculas maternas que são incorporados no ovócito durante ovogênese, atuam durante a ativação do ovo, bem como no início da embriogênese. Os eventos iniciais da embriogênese também são caracterizados pela ausência de altos níveis de transcrição zigótica. As moléculas depositadas atuam na ativação do ovo, quebrando a dormência da divisão celular permitindo a ocorrência do início do desenvolvimento embrionário. Mas, o embrião em desenvolvimento gradualmente degrada e substitui essas moléculas herdadas da mãe, em um processo conhecido como transição materno-zigótica. Nosso principal objetivo foi o entendimento da comunicação entre as moléculas herdadas e as recém produzidas durante os primeiros passos do desenvolvimento de Apis mellifera. Para alcançar nosso objetivo, 16 bibliotecas de RNAseq (mRNA e miRNA) foram construídas utilizando amostras de RNA total de embriões diploides e haploides de diferentes idades e ovócitos maduros. A análise do transcriptoma mostrou que existem genes diferencialmente expressos entre os dois tipos de embriões já em 1 h de desenvolvimento. Além disso, nossa análise permitiu a identificação de mRNAs e miRNAs maternos e zigóticos, além de processos com que estas moléculas se relacionam. As análises mostraram também que um mesmo miRNA pode atingir diferentes mRNAs em cada tipo de embrião, na mesma fase de desenvolvimento. Além disso, um mesmo gene pode ser diferentemente regulado nos dois tipos de embriões. Por exemplo, broad/GB48272, que é classificado como materno em embriões dipoides é regulado por quatro miRNAs diferentes e em embriões haploides é classificado como zigótico, regulado por apenas um miRNA. Análise das bibliotecas de RNAseq e hibridação in situ mostrou o padrão de expressão de zelda em embriões jovens de abelhas. Zelda é um ativador chave do genoma zigótico em Drosophila e regula eventos importantes na embriogênese se ligando a um motivo conservado, TAGteam. Em A. mellifera, encontramos um motivo TAGteam putativo que tem sido relacionado à transcrição zigótica precoce. Além disso, a hibridização in situ e PCR mostraram três primiRNAs (ame-mir-375-3p, ame-mir-34-5p e ame-mir-263b-5p) que se expressam durante a clivagem. A presença de pri-miRNAs evidenciou a início da transcrição zigótica durante a clivagem. Em suma, podemos dizer que este é o primeiro trabalho em Apis mellifera a descrever os eventos de iniciais do desenvolvimento embrionário comparando embriões haploides e diploides usando os recentes protocolos de bioinformática e os avanços da biologia molecular. / Embryonic development is the result of a precisely controlled sequence of events modulated by environmental signals and intracellular mechanisms. In Hymenoptera, this process takes a special character due the sex-determination system (haplodiploidy). In this system, fertilized eggs develop in females (diploid) and unfertilized eggs in males (haploid). Thus, important events such as egg activation and maternal-zygotic transition, events of the early embryogenesis are key elements to understand the development of both types of embryos. Egg activation is a complex event triggered in response to external stimuli and necessary for the onset of embryogenesis. In honeybees egg activation occurs independently of fertilization and seems to be triggered during the passage through mother\'s reproductive tract. Furthermore, if the egg is not fertilized it will develop into haploid organism. However, if the egg receives the sperm up to 30min after activation, this egg develops into a diploid organism. In Drosophila, the egg activation is also fertilization independent. Initial stimulus that triggers the development is due mechanical stresses suffered by the egg during ovulation and passage through the reproductive tract. In this model, the first activation signal includes activation of calciumdependent pathway. Maternal molecules that are incorporated into the oocyte during ovogenesis, act during egg activation, as well as in early embryogenesis. Early embryogenesis events are also characterized by absence of high levels of zygotic transcription. The deposited molecules drive egg activation, breaking cell division dormancy permitting the beginning of embryonic development. But, the developing embryo gradually degrades and substitutes these mother-inherited molecules, in a process known as mother-to-zygote transition. Our main objective was the understanding of the deep crosstalk among the inherited molecules and the newly ones produced during the first steps of Apis mellifera embryogenesis. To achieve our objective 16 deep sequenced RNA (mRNA, miRNA) libraries were constructed using different age diploid and haploid embryos, and mature oocytes. Genome-wide transcriptome analysis was performed and interactive regulatory networks were constructed. Our analysis permitted the identification of maternal and zygotic mRNAs and miRNAs and related processes. Based on expression profiles of mRNAs and miRNAs in mature oocytes and haploid and diploid embryos of 2, 6 and 18-24 h of development, we constructed integrative regulatory networks (miRNA:mRNA) showing that the same miRNA could target different mRNAs in each type of embryo, in the same phase of development. As example we cite broad/GB48272, which is classified as maternal in diploid embryos and regulated by four different miRNAs. However, in haploid embryos it is zygotic and regulated by only one miRNA. Analysis of RNAseq and in situ hybridization showed the expression pattern of zelda in early honeybee embryos. Zelda is a key activator of Drosophila early zygotic genome and regulates important events in early embryogenesis binding to TAGteam motif. In A. mellifera, we found a putative TAGteam motif that has been implicated in early zygotic transcription. Moreover, in situ hybridization and PCR assay showed three pri-miRNAs (ame-mir-375-3p, ame-mir-34-5p and ame-mir-263b-5p) expressed during cleavage. The presence of pri-miRNAs is the first evidence of early zygotic transcription during cleavage. In short, we could say that this is the first work on Apis mellifera describing the early embryonic developmental events comparing haploid and diploid embryos using modern bioinformatics tools and advanced molecular analysis.

Le genre Ectocarpus Lyngbye (Ectocarpales, Phaeophyceae) regroupe des algues marines filamenteuses caractérisées par un cycle haploïde-diploïde. L'objectif de la thèse était de délimiter les espèces et d'étudier la spéciation dans ce genre. Nous avons commencé par clarifier le nombre d'espèces cryptiques en utilisant deux loci indépendants et une approche intégrative associant une analyse de détection de " barcode gap " avec des reconstructions phylogénétiques. Nos résultats montrent l'existence d'au moins 15 espèces qui se répartissent en un groupe monophylétique composé d'E. crouaniorum (Ecro) et de deux espèces proches ainsi que d'un mélange paraphylétique composé des 12 autres espèces incluant E. siliculosus (Esil). Deuxièmement, les analyses de séquençage Rad et de phylogénomique ont permis de résoudre les relations au sein du groupe paraphylétique. Les espèces se regroupent maintenant en deux clades divergents (Ecro and Esil). Des niveaux de divergence variables entre espèces sont révélés au sein du clade Esil. Des phénomènes d'hybridation entre les espèces les plus apparentées, et trouvées en sympatrie, sont suspectés. Finalement, l'importance de l'isolement reproducteur a été étudié entre les espèces Esil et Ecro, les plus communes, mais les plus divergentes, en utilisant des marqueurs spécifiques de chacune des espèces. Nos résultats indiquent que la méiose agit comme une forte barrière reproductive entre ces espèces et démontrent que les espèces du genre Ectocarpus sont d'excellents systèmes pour étudier les conséquences évolutives de l'hybridation et de l'introgression pour le maintien ou la divergence des espèces grâce à leur cycle haploïde-diploïde. / The genus Ectocarpus Lyngbye (Ectocarpales, Phaeophyceae) comprises marine filamentous algae characterized by an alternation between two independent multicellular organisms of different ploidy. The general objective of the thesis was to study species delineation and speciation within this genus. We started clarifying the number of cryptic species using two unlinked loci (COI-5P and ITS1) and an integrative approach associating barcode gap detection analyses with phylogenetic reconstructions. We showed the presence of at least 15 species partitioned within a monophyletic group composed of E. crouaniorum (Ecro) and two closely related species and a paraphyletic assemblage composed of the remaining 12 other species including E. siliculosus (Esil). Second, Rad sequencing and phylogenomics analyses allowed to resolve the relationships within the paraphyletic assemblage. The different species becomes well separated into two divergent clades (Ecro and Esil). A diversity of taxa with various levels of divergence was revealed within the clade Esil and hybridization between the closest and sympatric species was suggested. Finally, the importance of reproductive isolation among the two commonest but most divergent species Esil and Ecro was studied using species-specific nuclear and cytoplasmic markers jointly with 9 microsatellites. We showed that meiosis acts as a strong reproductive barrier among these two species and demonstrates that the species of the genus Ectocarpus are excellent systems to study evolutionary consequences of hybridization and introgression for the maintenance or breakdown of species because of their haploid diploid life cycle.

La reproduction sexuée conduit à l'alternance d'une phase haploïde et d'une phase diploïde, dont la durée relative est très variable entre taxons. La proportion du cycle de vie passée en phase haploïde et en phase diploïde a d'importantes conséquences sur de nombreux processus adaptatifs. Cette thèse combine des approches théoriques qui explorent l'effet de facteurs génétiques et écologiques sur l'évolution des cycles de vie, et un travail expérimental sur l'effet de la ploidy sur l'évolution de l'isolement reproducteur entre populations. La partie théorique a consisté à intégrer des composantes écologiques dans des modèles génétiques pour l'évolution des cycles de vie. En particulier, j'ai exploré l'interaction entre la différenciation de niche entre haploïdes et diploïdes (qui favorise le maintien de cycles biphasiques, impliquant le développement des deux phases) et l'effet d'allèles délétères (qui favorisent soit l'haploïdie, soit la diploïdie). Tandis que la différentiation de niche (ou plus simplement, une différence de valeur sélective intrinsèque entre phases) stabilise les cycles intermédiaires, la présence d'allèles délétères conduit souvent à un branchement évolutif, avec la coexistence stable d'allèles codant pour l'haploïdie et la diploïdie. Cependant, des fluctuations temporelles de l'habitat permettent d'empêcher ce branchement et de stabiliser les cycles biphasiques. La partie expérimentale a consisté à comparer la dynamique de l'isolement reproducteur entre petites populations de levure haploïdes et de diploïdes avec de taux de mutations élevés. Les résultats montrent que tandis que les hybrides haploïdes ont une valeur sélective plus faible que leurs parents, les hybrides diploïdes bénéficient du phénomène d'hétérosis en génération F1, et ont encore une valeur sélective plus élevée que leurs parents en génération F2. La variance de la valeur sélective des hybrides était cependant beaucoup plus élevée chez les haploïdes, avec la production de certains génotypes très performants. / Sexual reproduction leads to an alternation between haploid and diploid phases, whose relative length varies widely across taxa. The proportion of the life cycle spent in the haploid and diploid phase has important consequences on a number of adaptive processes. This thesis combines theoretical approaches exploring the effect of genetic and ecological factors on the evolution of life cycles, and experimental work on the effects of ploidy on the evolution of reproductive isolation between populations. The theoretical part consisted in integrating ecological components into genetic models for the evolution of life cycles. In particular, I explored the interplay between niche differentiation between haploids and diploids (known to favour the maintenance of biphasic life cycles, involving development in both phases) and the effect of deleterious alleles (known to favour either haploid or diploid life cycles). While niche differentiation (or more simply intrinsic fitness differences between phases) stabilizes biphasic cycles, the presence of deleterious alleles often lead to evolutionary branching and to the stable coexistence of alleles coding for haploid and diploid cycles. Branching is prevented, however, when temporal environmental fluctuations are included into the model. The experimental part consisted in comparing the dynamics of reproductive isolation between small populations of haploid and diploid yeasts with elevated mutation rate. The results show that while haploid hybrids tend to have a lower fitness than their parents, diploid hybrids benefit from heterosis in the F1 generation, and still have a higher fitness than the diploid homozygous parents in the F2 generation. However, the variance of hybrid fitness was much higher in haploids, with the production of some highly fit genotypes.

ABSTRACT Triticum sphaerococcum (AABBDD, 2n = 6x = 42) is a land race of wheat known from the Indian subcontinent. It has several favourable characters including short and strong culms, hemispherical grains with a shallow crease (that may increase the yield of white flour), higher protein content compared to bread wheat (T. aestivum), and resistance to drought, and yellow rust caused by Puccinia striiformis. However, an unfavourable characteristic of T. sphaerococcum is its lower yield compared to bread wheat. Being a land race, the sphaerococcum wheat is poorly studied. This study was undertaken to increase knowledge of the physiology and genetics of this land race and determine if it may be possible to separate the favourable characters of T. sphaerococcum from its unfavourable characters. Plant height in bread wheat is controlled by many genes. ‘Reduced Height’ (Rht) genes which differ in their response to externally applied gibberellic acid (GA3) are responsible for the short stature of modern bread wheat varieties. Therefore, GA3 was used to probe the relationship between the semidwarf sphaerococcum phenotype and the Rht gene. T. sphaerococcum variety Sp5 showed a unique “seedling response” to externally applied GA3 when compared with T. aestivum varieties harbouring Rht1, Rht2, Rht8, Rht12, Rht13 or Rht18 alleles. A mapping population of doubled haploids was generated through wide hybridisation of F1 (Sp5 x Otane) with Zea mays. A genome-wide scan of Sp5 and Otane (parents) using 348 microsatellite (SSR) markers showed that only 169 of these markers (49%) were polymorphic between the parents. A DArT profiling yielded 348 markers that were polymorphic between the parents. Microsatellite markers and DArT markers were used to create a genetic map. The mapping population was phenotyped and a quantitative trait loci (QTL) analysis was performed for component traits of the complex sphaerococcum trait including plant height, spike length, awn length, yield, grain shape and crease size. Results of the QTL analysis indicated that it may be difficult to separate the favourable characters of T. sphaerococcum from its unfavourable characters through mutation because the component traits of the complex sphaerococcum trait may be under pleiotropic control of the Sp gene. The hypothesis that T. sphaerococcum originated through a mutation in T. aestivum was tested through induced mutation using gamma rays. Mutants from sphaerococcum-type to aestivum-type were isolated and phenotyped. Sphaerococcum-type mutants also were isolated and characterised from mutated aestivum-type wheat suggesting a possible origin of T. sphaerococcum through a mutation in T. aestivum.

ABSTRACT Triticum sphaerococcum (AABBDD, 2n = 6x = 42) is a land race of wheat known from the Indian subcontinent. It has several favourable characters including short and strong culms, hemispherical grains with a shallow crease (that may increase the yield of white flour), higher protein content compared to bread wheat (T. aestivum), and resistance to drought, and yellow rust caused by Puccinia striiformis. However, an unfavourable characteristic of T. sphaerococcum is its lower yield compared to bread wheat. Being a land race, the sphaerococcum wheat is poorly studied. This study was undertaken to increase knowledge of the physiology and genetics of this land race and determine if it may be possible to separate the favourable characters of T. sphaerococcum from its unfavourable characters. Plant height in bread wheat is controlled by many genes. ‘Reduced Height’ (Rht) genes which differ in their response to externally applied gibberellic acid (GA3) are responsible for the short stature of modern bread wheat varieties. Therefore, GA3 was used to probe the relationship between the semidwarf sphaerococcum phenotype and the Rht gene. T. sphaerococcum variety Sp5 showed a unique “seedling response” to externally applied GA3 when compared with T. aestivum varieties harbouring Rht1, Rht2, Rht8, Rht12, Rht13 or Rht18 alleles. A mapping population of doubled haploids was generated through wide hybridisation of F1 (Sp5 x Otane) with Zea mays. A genome-wide scan of Sp5 and Otane (parents) using 348 microsatellite (SSR) markers showed that only 169 of these markers (49%) were polymorphic between the parents. A DArT profiling yielded 348 markers that were polymorphic between the parents. Microsatellite markers and DArT markers were used to create a genetic map. The mapping population was phenotyped and a quantitative trait loci (QTL) analysis was performed for component traits of the complex sphaerococcum trait including plant height, spike length, awn length, yield, grain shape and crease size. Results of the QTL analysis indicated that it may be difficult to separate the favourable characters of T. sphaerococcum from its unfavourable characters through mutation because the component traits of the complex sphaerococcum trait may be under pleiotropic control of the Sp gene. The hypothesis that T. sphaerococcum originated through a mutation in T. aestivum was tested through induced mutation using gamma rays. Mutants from sphaerococcum-type to aestivum-type were isolated and phenotyped. Sphaerococcum-type mutants also were isolated and characterised from mutated aestivum-type wheat suggesting a possible origin of T. sphaerococcum through a mutation in T. aestivum.

Diplodia ear rot caused by the fungus Stenocarpella maydis (Berkeley) and Stenocarpella macrospora (Earle) have become one of the most important limiting factors for the production of Corn (Zea mays L.) in Brazil. The fungus can attack the stalks, leaves and the grain causing significant reductions on yield and the overall quality of the grain, since it can produce micotoxinas that are dangerous to livestock. Resistance to ear rot by Stenocarpella sp in corn is quantitative and highly influenced by the environment and even that artificial inoculation techniques are available to screen for the disease the overall cost is very expensive. The objective of this study was the identification of quantitative trait loci (QTL s) associated with ear rot resistance by Stenocarpella sp in one breeding population composed of 141 doublehaploid progenies resulted from the cross among the resistant inbred MONDR1 and the susceptible inbred MONDS1 in testcrosses with the susceptible tester MONDS5. Testcrosses were evaluated at harvest time after artificial inoculation for ear rot at three different locations in the central region of Brazil during the 2005/06 summer season. Thru Composite interval mapping (CIM), a total of three QTL s (LOD>2.5) for ear rot resistance were identified at chromosomes 2, 3 and 5, all together accounting for up 26% of total phenotypic variation for this character. The identification of two QTL s for ear rot resistance coming from the susceptible parent MONDS1 appear to indicate the presence of the phenomena of transgressive segregation. Additionally we were able to identify six double-haploid progenies with high level of resistance to ear rot by Stenocarpella (MDH15, MDH443, MDH95, MDH2, MDH120 e MDH81), being those recommended for their incorporation into the breeding program as new breeding sources for the Central Brazil regions. / Grãos ardidos causados pelos fungos Stenocarpella maydis (Berkeley) e Stenocarpella macrospora (Earle) tem se constituído num dos maiores fatores limitantes para a produção de milho (Zea mays L.) no Brasil. Estes fungos podem causar infecções no colmo, folhas e grãos, podendo ocasionar reduções significativas na produtividade e na qualidade do grão, pela produção de micotoxinas daninhas para aves e bovinos. A resistência para podridão de grão por Stenocarpella sp apresenta herança quantitativa e pode ser altamente influenciada pelo meio ambiente, e embora existam técnicas de inoculação que facilitam a discriminação de materiais suscetíveis, isto requer de grande quantidade de recursos. O objetivo do presente trabalho foi à identificação de locos de caracteres quantitativos (QTL) associados à resistência para podridão de grãos ( grãos ardidos ) ocasionados por Stenocarpella sp numa população de 141 progênies duplo-haplóides derivadas do cruzamento entre a linhagem resistente MONDR1 e a linhagem susceptível MONDS1 em testcross com o testador susceptível MONDS5. A porcentagem de espigas infectadas por Stenocarpella sp foi registrada para cada uma das testcrosses apos da inoculação artificial em três localidades na região Central de Brasil durante a Safra agrícola 2005/06. Mediante a análise de mapeamento por intervalo composto foram identificados três QTL s com LOD>2.5 para resistência à grãos ardidos nos cromossomos 2, 3 e 5, sendo estes em conjunto, responsáveis por ate 26% de variação fenotípica para este caráter. A identificação de dois QTL s para resistência a grãos ardidos por Stenocarpella sp com origem no progenitor susceptível parece indicar a presença do fenômeno de segregação transgressiva. Adicionalmente foram identificadas seis progênies duplohaplóides com alto nível de resistência a grãos ardidos (MDH15, MDH443, MDH95, MDH2, MDH120 e MDH81), sendo estas recomendadas para sua incorporação no programa de melhoramento para a região central do Brasil. / Mestre em Genética e Bioquímica