The process of translation initiation is the most highly regulated step of protein synthesis. In bacteria, three initiation factors (IF1, IF2 and IF3) play crucial roles during initiation. IF3 acts as an anti-association factor for the two ribosomal subunits. Eubacterial IF3 also permits initiator tRNA (i-tRNA) selection at the P site of the ribosome. Two features of i-tRNA, i. e. the characteristic 3GC base pairs in the anticodon stem and the cognate interaction of the anticodon sequence with the initiation codon of the mRNA contribute to IF3 based selection and/or proofreading. However, the exact mechanism of this discrimination and the contribution of the individual domains towards this process of selection/ proofreading are unclear. Further, there are exceptional instances in the natural world where either the codon-anticodon interaction or the anticodon stem composition deviates from the norm. For instance, in mammalian mitochondria, non-AUG codons such as AUU and AUA are present in the genome although they are notoriously poor initiation codons. In addition, some species of Mycoplasma have i-tRNAs with variations in the typically conserved 3GC base pairs of the anticodon stem. In this study, we have investigated the mechanism of proofreading activity of IF3 of E. coli, mitochondrial and mycoplasmal origins. Part I: Proofreading function of IF3 in E. coli IF3 is composed of N and C terminal domains joined by a flexible linker region. By means of complete and partial IF3 knockouts, we show that the C-terminal domain (CTD) is essential for the survival of E. coli while the N-terminal (NTD) is required for cellular fitness. Using reporter assays, we have established the role of the NTD in proofreading, while polysome profile analyses reaffirm that the CTD alone can bind to the 30S and carry out ribosome anti-association. Therefore, we show that the CTD is the ribosome binding and anti-association domain, while the NTD is the major proofreading domain. Unpublished cryoEM structures from Prof. Ramakrishnan’s lab indicate that the NTD of IF3 pushes the i-tRNA at its elbow and helps in P site accommodation of the i-tRNA. We propose that when the codon-anticodon interaction is non-cognate or if the 3GC base pairs of the anticodon stem are not intact, then the dynamic action of the NTD destabilises the tRNA at the P site and leads to its rejection. Part II: Proofreading function of mitochondrial IF3 (IF3mt) Of the 13 protein-coding genes in mammalian mitochondria, 3 utilise the non-canonical AUA codon and one utilises the non-canonical start codon AUU. Since IF3mt does not possess many of the generally conserved residues implicated in proofreading, we decided to characterise the proofreading function of IF3mt and its role in initiation with non-canonical start codons. Structurally, IF3mt is similar to EcoIF3 with its N and C terminal domains joined by a linker region. However, IF3mt additionally possesses N- and C-terminal extensions which are generally disordered in structure. In vivo studies of mitochondrial translation factors have been mired by the lack of methodologies to manipulate mitochondria. We have developed an E. coli strain to study the proofreading functions of mitochondrial IF3 (IF3mt) with the help of reporter genes. Consistent with its function in mitochondria, IF3mt allowed promiscuous initiation from non-AUG codons. However, IF3mt avoided initiation with i-tRNAs lacking evolutionarily conserved 3GC pairs in anticodon stems. Interestingly, expression of IF3mt N-terminal domain or IF3mt devoid of its typical N-, and C-terminal extensions significantly improved its proofreading activity. Our immunoblot assays from polysome profile fractions indicate that the IF3mt derivative lacking extensions is capable of superior 30S ribosome binding. The two derivatives of IF3mt missing the Next (IF3mtΔNext) or both the Next and Cext (IF3mtΔNextCext) display an affinity for the 50S ribosome. We propose that the extensions of IF3mt may have evolved to reduce the affinity of IF3mt to the ribosome and thereby permit initiation with non-canonical start codons like AUU and AUA. Our studies suggest that E. coli provides an excellent heterologous model to study distinctive features of mitochondrial factors. Part III: Fidelity of translation initiation in mycoplasma One of the many singular features of mycoplasma is the presence of many anticodon stem variants of the i-tRNA across different species. In general, i-tRNAs are characterized by the presence of the typical feature of the conserved 3 consecutive GC base pairs (GC/GC/GC) in the anticodon stem. However, many mycoplasmal species have i-tRNAs with AU/GC/GC, GC/GC/GU or AU/GC/GU sequences. Interestingly, the mycoplasmal species which harbour the AU/GC/GU i-tRNA are also human pathogens. Therefore, we decided to investigate whether these organisms possess any unique features to accommodate the i-tRNA variants, by investigating the usage of Shine Dalgarno sequences and by carrying out multiple sequence alignments of genes encoding initiation factors, ribosomal proteins S9 and S13 and 16S rRNA. Since IF3 plays a crucial role in i-tRNA selection, we carried out computational analysis of mycoplasmal IF3 sequences, which revealed many interesting features. Most striking amongst them was the variation of the highly conserved R at position 131 in some species. Interestingly, these were the very mycoplasmal species which possessed the anticodon stem variant AU/GC/GU, suggesting a strong correlation between these two features. It is known that the R131P mutation of EcoIF3 is characterised by an enormous loss of proofreading activity. It seemed unusual that such compromised proofreading would be tolerated in the cell, so we decided to investigate other components of the translational machinery as well. The C-terminal SKR tail of the ribosomal protein S9, which contacts the P-site tRNA, is highly conserved across bacteria. Analysis of the C-terminal sequences of S9 proteins in various mycoplasmal species revealed a surprising variation- the presence of a TKR tail in strains with the AU/GC/GU tRNA. In this study we have investigated the co-occurrence of S9 and IF3 variations in i-tRNA selection in E. coli. We see that the R131P polymorphism of IF3 leads to a tremendous loss of proofreading, but this loss is significantly tempered by the presence of the S9 TKR variation. Our bioinformatics studies revealed that the mycoplasmal species which are sustained on AU/GC/GU i-tRNAs also tend to use a higher percentage of non-AUG codons. By means of our reporter assays in E. coli, we have shown once again that the R131P polymorphism of IF3 leads to a tremendous increase in initiation with the non-canonical start codon AUA, but this increase is significantly tempered by the presence of the S9 TKR variation.

No description available.

Deoxyhypusine synthase (DHS) catalyzes the first step in the hypusination of eukaryotic translation initiation factor 5A (eIF5A). In human cells, two eIF5A isoforms are present, eIF5A-1 and eIF5A-2, and DHS catalyzes the hypusination of both. Since both eIF5As are substrates for DHS, the biological functions of DHS are likely to be exerted through the various post-translational forms of these two eIF5As. The lysine form of eIF5A-1 has been associated with apoptosis, while the hypusinated form of eIF5A-1 has been associated with cell viability and proliferation. eIF5A-2 has been found to be over-expressed in certain cancers and has been proposed to function as an oncogene. Dhs is also over-expressed in certain human cancers and is a metastatic signature gene. The purpose of the present study was to investigate the role of DHS in cancer cell invasiveness, cell proliferation, and apoptosis using RNA interference. The main finding of the study is that DHS siRNA treatment decreases invasiveness of PC3 cells in vitro. Both DHS 0 siRNA treatment and DHS 1/b siRNA treatment significantly reduced cell invasiveness of PC3 cells as measured by the Matrigel invasion assay. Potential confounding variables, such as differences in cell proliferation or differences in apoptosis in response to DHS siRNA treatment, were assessed using the XTT cell proliferation assay and the Annexin V/Pi apoptosis assay, and they were found not to have an effect. In the absence of serum, DHS siRNA treatment did not result in significant decrease in cell proliferation compared to the control siRNA treatment. Furthermore, DHS siRNA treatment did not induce apoptosis in PC3 cells under the present experimental conditions. In conclusion, depletion of DHS with RNAi reduces invasiveness, but does not induce apoptosis in PC3 cells. The significance of the research is that the anti-invasiveness effect of DHS depletion in metastatic cancer cells is shown for the first time in the present study. Thus, DHS depletion may be useful to combat cancer in conjunction with L-eIF5A-1 over-expression.

Deoxyhypusine synthase (DHS) catalyzes the first step in the hypusination of eukaryotic translation initiation factor 5A (eIF5A). In human cells, two eIF5A isoforms are present, eIF5A-1 and eIF5A-2, and DHS catalyzes the hypusination of both. Since both eIF5As are substrates for DHS, the biological functions of DHS are likely to be exerted through the various post-translational forms of these two eIF5As. The lysine form of eIF5A-1 has been associated with apoptosis, while the hypusinated form of eIF5A-1 has been associated with cell viability and proliferation. eIF5A-2 has been found to be over-expressed in certain cancers and has been proposed to function as an oncogene. Dhs is also over-expressed in certain human cancers and is a metastatic signature gene. The purpose of the present study was to investigate the role of DHS in cancer cell invasiveness, cell proliferation, and apoptosis using RNA interference. The main finding of the study is that DHS siRNA treatment decreases invasiveness of PC3 cells in vitro. Both DHS 0 siRNA treatment and DHS 1/b siRNA treatment significantly reduced cell invasiveness of PC3 cells as measured by the Matrigel invasion assay. Potential confounding variables, such as differences in cell proliferation or differences in apoptosis in response to DHS siRNA treatment, were assessed using the XTT cell proliferation assay and the Annexin V/Pi apoptosis assay, and they were found not to have an effect. In the absence of serum, DHS siRNA treatment did not result in significant decrease in cell proliferation compared to the control siRNA treatment. Furthermore, DHS siRNA treatment did not induce apoptosis in PC3 cells under the present experimental conditions. In conclusion, depletion of DHS with RNAi reduces invasiveness, but does not induce apoptosis in PC3 cells. The significance of the research is that the anti-invasiveness effect of DHS depletion in metastatic cancer cells is shown for the first time in the present study. Thus, DHS depletion may be useful to combat cancer in conjunction with L-eIF5A-1 over-expression.

MAGALHÃES, Vladimir Gonçalves. Prospecção bioquímica e molecular de fatores possivelmente envolvidos na defesa de feijão-de-corda [Vigna unguiculata (L.) Walp] ao vírus do mosaico severo do caupi (CPSMV). 2011. 109 f. : Dissertação (Mestrado em Bioquímica)-Universidade Federal do Ceará, Fortaleza-CE, 2011. / Submitted by Eric Santiago (erichhcl@gmail.com) on 2016-07-15T14:36:03Z No. of bitstreams: 1 2011_dis_vgmagalhaes.pdf: 4392892 bytes, checksum: 571bbf928e7a06498a9e935694d2ab1d (MD5) / Approved for entry into archive by José Jairo Viana de Sousa (jairo@ufc.br) on 2016-08-02T20:26:15Z (GMT) No. of bitstreams: 1 2011_dis_vgmagalhaes.pdf: 4392892 bytes, checksum: 571bbf928e7a06498a9e935694d2ab1d (MD5) / Made available in DSpace on 2016-08-02T20:26:15Z (GMT). No. of bitstreams: 1 2011_dis_vgmagalhaes.pdf: 4392892 bytes, checksum: 571bbf928e7a06498a9e935694d2ab1d (MD5) Previous issue date: 2011 / Cowpea [(Vigna unguiculata (L.) Walp.)] has a major socioeconomic importance in Northeastern Brazil. However, its production is low due abiotic and biotic factors. Amongst the biotic factors the cowpea severe mosaic virus (CPSMV, Secoviridae family) has a great importance because it causes the most prevalent and serious virus disease that affects this crop in the country. Although there are resistant cultivars to CPSMV, the defense mechanisms involved is not understood. For this reason, a comparative study was conducted between resistant and susceptible cultivars, using two experimental approaches. In the first one, the biochemical approach, possible differences of enzyme activities related to oxidative stress (superoxide dismutase, ascorbate peroxidase, guaiacol peroxidase) and pathogenesis (β-1,3-glucanase and chitinase), in addition of phenyl amonium lyase, and H2O2 generation in the leaves of the cultivars Pitíuba (susceptible) and Macaibo (resistant) were analyzed. The secondary leaves were harvested at 6, 12, 24, 48, 72 h after treatment with CPSMV or carborundum (controls) and these above parameters were measures in the protein extracts obtained. It was shown that, in general, the response amongst the cultivars did not differ significantly, suggesting that the defense mechanisms of cowpea are different from the classic response of defense observed for several plant species. In the second approach, molecular, the nucleotide sequences of the genes that code for the translation initiation factors (eIF4E, eIF(iso)4E, eIF4G, eIF(iso)4G and nCBP) and the primary strucuture of the correspondent putative proteins were analyzed in order to search patterns of polymorphis between the studied cowpea cultivars that could be related to a constitutive defense conferred by recessive genes. After sequence analysis, it was found that eIF4E showed polymorphisms between cultivars, and, in at least two positions (68 and 108), there were differences between susceptible and resistant cultivars (Arg68/Pro68; Val108 or Pro108/Ala108). The molecular modeling revealed that differences in amino acid are located in two external loops close to the cap (m7G) binding domain, well reported in cases of recessive resistance within the Potyviridae family. Through immunodetection studies with the leaf extracts and the protein fractions obtained after the affinity chromatography on a Sepharose-7-metil-guanosina column, it was found that the amino acid mutations found did not impair the ability of eIF4E to bind to M7G in vitro. However, as it was observed two variants for eIF4E comparing the resistant and susceptible cultivars to CPSMV, at spatially neighboring regions, it could not be ruled out the hypothesis that this constitutive/recessive resistant trait is correlated with these mutations detected, which could impair, consequently, the in vivo interaction of eIF4E with the viral VPg. / O feijão-de-corda [Vigna unguiculata (L.) Walp.] tem grande importância socioeconômica no Nordeste brasileiro. Entretanto, sua produção é baixa devida a diversos fatores abióticos e bióticos. Dentre os fatôres bióticos, o vírus do mosaico severo do caupi (CPSMV, família Secoviridae) apresenta grande destaque, por causar a virose que mais acomete essa cultura no país. Embora existam cultivares resistentes ao vírus, não se sabe quais os mecanismos de defesa envolvidos. Por essa razão, foi elaborado um estudo comparativo entre cultivares resistentes e susceptíveis, utilizando duas abordagens experimentais. Na abordagem bioquímica, possíveis diferenças de atividades de enzimas relacionadas ao estresse oxidativo (dismutase do superóxido, peroxidase do ascorbato, peroxidase) e à patogênese (β-1,3-glucanase e quitinase), além da fenilamônia liase, e teores de H2O2 foram estudadas nos cultivares Pitiúba (susceptível) e Macaibo (resistente). Após tratamento com o CPSMV ou com apenas carborundum (plantas controles), foram realizadas coletas nos tempos de 6, 12, 24, 48 e 72 h, tendo sido realizadas as análises bioquímicas nos extratos protéicos obtidos das folhas secundárias. Foi verificado que, de maneira geral, a resposta entre os cultivares não diferiram significamente, sugerindo que os mecanismos de defesa de feijão-de-corda sejam diferentes da resposta clássica de defesa. Na segunda abordagem, molecular, as sequências nucleotídicas dos genes codificantes para os fatores de iniciação de tradução (eIF4E, eIF(iso)4E, eIF4G, eIF(iso)4G e nCBP) e as sequências primárias putativas das proteínas correspondentes foram analisados, no intuito de se averiguar a existência de padrões de polimorfismos entre cultivares resistentes e susceptíveis, que pudessem estar relacionados à defesa constitutiva conferida por genes recessivos. Após análise das sequências, foi observado que eIF4E apresentava polimorfismos entre os cultivares, sendo que, em pelo menos duas posições nas sequências primárias putativas do fator (68 e 108), existiram diferenças entre cultivares susceptíveis e resistentes (Arg68/Pro68; Val108 ou Pro108/Ala108). A modelagem molecular revelou que as diferenças em aminoácidos situam-se em dois loops externos, próximos ao domínio de ligação ao capacete (m7G), bastante relatados em casos de resistência recessiva para a família Potyviridae. Através de estudos de imunodectecção posterior ao passo cromatográfico em coluna de afinidade, foi observado que as mudanças de aminoácidos não comprometiam, a capacidade de eIF4E em se ligar ao m7G in vitro. Entretanto, como foram observadas duas variantes para eIF4E, entre cultivares resistentes e susceptíveis ao CPSMV, em regiões próximas espacialmente, não se pode descartar a hipótese de que a resistência recessiva constitutiva esteja associada com essas mutações detectadas nessas sequências, que iriam modificar, consequentemente, a interação da VPg viral com eIF4E in vivo.

Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico / O feijÃo-de-corda [Vigna unguiculata (L.) Walp.] tem grande importÃncia socioeconÃmica no Nordeste brasileiro. Entretanto, sua produÃÃo à baixa devida a diversos fatores abiÃticos e biÃticos. Dentre os fatÃres biÃticos, o vÃrus do mosaico severo do caupi (CPSMV, famÃlia Secoviridae) apresenta grande destaque, por causar a virose que mais acomete essa cultura no paÃs. Embora existam cultivares resistentes ao vÃrus, nÃo se sabe quais os mecanismos de defesa envolvidos. Por essa razÃo, foi elaborado um estudo comparativo entre cultivares resistentes e susceptÃveis, utilizando duas abordagens experimentais. Na abordagem bioquÃmica, possÃveis diferenÃas de atividades de enzimas relacionadas ao estresse oxidativo (dismutase do superÃxido, peroxidase do ascorbato, peroxidase) e à patogÃnese (β-1,3-glucanase e quitinase), alÃm da fenilamÃnia liase, e teores de H2O2 foram estudadas nos cultivares PitiÃba (susceptÃvel) e Macaibo (resistente). ApÃs tratamento com o CPSMV ou com apenas carborundum (plantas controles), foram realizadas coletas nos tempos de 6, 12, 24, 48 e 72 h, tendo sido realizadas as anÃlises bioquÃmicas nos extratos protÃicos obtidos das folhas secundÃrias. Foi verificado que, de maneira geral, a resposta entre os cultivares nÃo diferiram significamente, sugerindo que os mecanismos de defesa de feijÃo-de-corda sejam diferentes da resposta clÃssica de defesa. Na segunda abordagem, molecular, as sequÃncias nucleotÃdicas dos genes codificantes para os fatores de iniciaÃÃo de traduÃÃo (eIF4E, eIF(iso)4E, eIF4G, eIF(iso)4G e nCBP) e as sequÃncias primÃrias putativas das proteÃnas correspondentes foram analisados, no intuito de se averiguar a existÃncia de padrÃes de polimorfismos entre cultivares resistentes e susceptÃveis, que pudessem estar relacionados à defesa constitutiva conferida por genes recessivos. ApÃs anÃlise das sequÃncias, foi observado que eIF4E apresentava polimorfismos entre os cultivares, sendo que, em pelo menos duas posiÃÃes nas sequÃncias primÃrias putativas do fator (68 e 108), existiram diferenÃas entre cultivares susceptÃveis e resistentes (Arg68/Pro68; Val108 ou Pro108/Ala108). A modelagem molecular revelou que as diferenÃas em aminoÃcidos situam-se em dois loops externos, prÃximos ao domÃnio de ligaÃÃo ao capacete (m7G), bastante relatados em casos de resistÃncia recessiva para a famÃlia Potyviridae. AtravÃs de estudos de imunodectecÃÃo posterior ao passo cromatogrÃfico em coluna de afinidade, foi observado que as mudanÃas de aminoÃcidos nÃo comprometiam, a capacidade de eIF4E em se ligar ao m7G in vitro. Entretanto, como foram observadas duas variantes para eIF4E, entre cultivares resistentes e susceptÃveis ao CPSMV, em regiÃes prÃximas espacialmente, nÃo se pode descartar a hipÃtese de que a resistÃncia recessiva constitutiva esteja associada com essas mutaÃÃes detectadas nessas sequÃncias, que iriam modificar, consequentemente, a interaÃÃo da VPg viral com eIF4E in vivo. / Cowpea [(Vigna unguiculata (L.) Walp.)] has a major socioeconomic importance in Northeastern Brazil. However, its production is low due abiotic and biotic factors. Amongst the biotic factors the cowpea severe mosaic virus (CPSMV, Secoviridae family) has a great importance because it causes the most prevalent and serious virus disease that affects this crop in the country. Although there are resistant cultivars to CPSMV, the defense mechanisms involved is not understood. For this reason, a comparative study was conducted between resistant and susceptible cultivars, using two experimental approaches. In the first one, the biochemical approach, possible differences of enzyme activities related to oxidative stress (superoxide dismutase, ascorbate peroxidase, guaiacol peroxidase) and pathogenesis (β-1,3-glucanase and chitinase), in addition of phenyl amonium lyase, and H2O2 generation in the leaves of the cultivars PitÃuba (susceptible) and Macaibo (resistant) were analyzed. The secondary leaves were harvested at 6, 12, 24, 48, 72 h after treatment with CPSMV or carborundum (controls) and these above parameters were measures in the protein extracts obtained. It was shown that, in general, the response amongst the cultivars did not differ significantly, suggesting that the defense mechanisms of cowpea are different from the classic response of defense observed for several plant species. In the second approach, molecular, the nucleotide sequences of the genes that code for the translation initiation factors (eIF4E, eIF(iso)4E, eIF4G, eIF(iso)4G and nCBP) and the primary strucuture of the correspondent putative proteins were analyzed in order to search patterns of polymorphis between the studied cowpea cultivars that could be related to a constitutive defense conferred by recessive genes. After sequence analysis, it was found that eIF4E showed polymorphisms between cultivars, and, in at least two positions (68 and 108), there were differences between susceptible and resistant cultivars (Arg68/Pro68; Val108 or Pro108/Ala108). The molecular modeling revealed that differences in amino acid are located in two external loops close to the cap (m7G) binding domain, well reported in cases of recessive resistance within the Potyviridae family. Through immunodetection studies with the leaf extracts and the protein fractions obtained after the affinity chromatography on a Sepharose-7-metil-guanosina column, it was found that the amino acid mutations found did not impair the ability of eIF4E to bind to M7G in vitro. However, as it was observed two variants for eIF4E comparing the resistant and susceptible cultivars to CPSMV, at spatially neighboring regions, it could not be ruled out the hypothesis that this constitutive/recessive resistant trait is correlated with these mutations detected, which could impair, consequently, the in vivo interaction of eIF4E with the viral VPg.

Les résistances génétiques permettent une lutte efficace contre les maladies des plantes cultivées mais sont limitées par les capacités d’évolution des bioagresseurs ciblés. Chez le piment, le fonds génétique peut améliorer la durabilité de la résistance au PVY conférée par le gène majeur pvr23. L’objectif de ma thèse était de caractériser les facteurs génétiques de l’hôte conditionnant la durabilité du gène majeur en répondant aux questions suivantes : (i) Quels sont leurs actions sur l’évolution des populations virales ? (ii) Correspondent-ils aux QTL (quantitative trait loci) de résistance partielle ? (iii) Sont-ils répandus au sein des ressources génétiques du piment ? Différentes expérimentations incluant des tests de résistances, d’évolution expérimentale et de compétition entre différents variants viraux, ont montré que les facteurs du fonds génétique augmentant la durabilité de pvr23 agissaient en : (i) diminuant la concentration virale dans la plante, (ii) en réduisant les probabilités de mutations du PVY vers le contournement du gène pvr23 et (iii) en ralentissant la sélection des variants viraux contournants. La détection de QTL et la cartographie des facteurs génétiques affectant la fréquence de contournement de pvr23 (QTL de durabilité) a mis en évidence quatre régions du génome du piment qui, par des effets additifs ou épistatiques, expliquent 70% de la variabilité phénotypique observée. La cartographie comparée montre que trois des quatre QTL de durabilité co-localisent avec des QTL affectant la résistance partielle, suggérant que les QTL de résistance partielle ont un effet pléiotropique sur la durabilité d’un gène majeur de résistance. L’étude d’une collection de 20 accessions de piment, porteuses de pvr23 ou pvr24(allèle très proche de pvr23) dans des fonds génétiques variés, a montré que les fonds génétiques favorables à la durabilité de ces allèles de résistance sont fréquents dans les ressources génétiques du piment. Ces résultats mettent en évidence que la durabilité d’un gène majeur de résistance peut-être fortement augmentée lorsqu’il est associé à des facteurs génétiques réduisant la multiplication du pathogène. De plus, la fréquence de contournement du gène majeur s’est révélée être un caractère très héritable (h²=0.87) et la détection de QTL affectant ce caractère est possible. La sélection directe pour de tels QTL est donc envisageable et ouvre de nouvelles perspectives pour préserver la durabilité des gènes majeurs de résistance utilisés en sélection variétale. / Genetic resistances provide an efficient control of crop diseases but are limited by pathogen adaptation.In pepper, the durability of the pvr23 allele, conferring resistance to Potato virus Y (PVY), was demonstrated todepend on the plant genetic background. The aim of my PhD thesis was to characterize the host genetic factorsaffecting the durability of the major resistance gene pvr23 and to answer to the following question s: (i) What istheir action on the evolution of the viral population? (ii) Is there identity between the QTLs (quantitative traitloci) controlling the partial resistance and the QTLs affecting the durability of pvr23? (iii) Are these genetic factorswidespread among the genetic resources of pepper? Various experiments including resistance testing,experimental evolution and competition between various PVY variants, enabled to show that the genetic factorsaffecting the durability of pvr23 acted in: (i) decreasing the viral accumulation, (ii) decreasing the probability ofacquisition of resistance breaking (RB) mutations by PVY and (iii) slowing down the selection of RB variants. QTLdetection and mapping of genetic factors affecting the frequency of pvr23 RB showed that four loci actingadditively and in epistatic interactions explained together 70% of the variance of pvr23 breakdown frequency.Comparative mapping between these QTLs and QTLs affecting partial resistance showed that three of the fourQTLs controlling the frequency of pvr23 RB are also involved in quantitative resistance, suggesting that QTLs forquantitative resistance have a pleiotropic effect on the durability of the major resistance gene. Analysis of acollection of 20 pepper accessions, carrying pvr23 or pvr24 (allele closely related to pvr23) in various geneticbackgrounds, showed that genetic backgrounds favorable to the durability of the pvr2-mediated resistance arewidespread in the genetic resources of pepper. These results highlight that the durability of a major resistancegene can be strongly increased when associated with genetic factors decreasing the pathogen multiplication.Moreover, the frequency of a major gene RB is a highly heritable trait and QTLs detection for this trait isachievable. The direct selection for such QTLs opens new prospects to preserve the durability of major resistancegenes used by breeders.

[ES] Las poliaminas son metabolitos esenciales para el crecimiento de las células eucariotas y su metabolismo está frecuentemente desregulado en cáncer. Una de las dianas moleculares de las poliaminas es el factor de elongación de la traducción eIF5A, una proteína esencial y conservada evolutivamente. eIF5A es la única proteína conocida que contiene el aminoácido hipusina, que deriva de la poliamina espermidina. En humanos existen dos isoformas, eIF5A1 y eIF5A2. EIF5A2 se encuentra en el cromosoma 3q26, una región frecuentemente amplificada en muchos tumores y que está altamente expresada en varios tipos de cáncer, incluyendo el cáncer de pulmón no microcítico (CPNM). eIF5A2 es esencial para el mantenimiento de la proliferación celular y su inhibición la suprime en algunos tumores. Recientemente se ha correlacionado la sobreexpresión de eIF5A2 con la invasión y como biomarcador de mal pronóstico en algunos cánceres, y se ha observado que eIF5A2 induce la transición epitelio-mesenquimal (EMT) en CPNM. La EMT es un proceso complejo y reversible que induce la diferenciación de las células epiteliales a células mesenquimales migrantes con capacidad de invasión. Numerosos estudios han demostrado que la EMT está relacionada con la progresión del cáncer, metástasis y mal pronóstico en tumores. Por tanto, la determinación de un método eficaz para inhibir la EMT en CPNM podría mejorar significativamente los tratamientos actuales. La naturaleza altamente selectiva de la hipusinación de eIF5A2 y su susceptibilidad a la inhibición farmacológica sugieren que eIF5A2 es una diana terapéutica muy atractiva. Actualmente, se dispone de un análogo de poliamina, GC7, que se utiliza para inhibir la hipusinación y se ha demostrado que frena el crecimiento de células cancerosas. El presente trabajo de tesis doctoral tiene como objetivo caracterizar el papel patológico de eIF5A2 en el desarrollo del CPNM. Para ello, hemos estudiado, mediante modificaciones genéticas por silenciamiento y sobreexpresión, el papel de eIF5A2 en la proliferación, motilidad e invasión celular utilizando líneas celulares de CPNM. Así mismo, se ha estudiado el efecto del inhibidor GC7 en líneas celulares de CPNM y modelos murinos para determinar si previene o revierte la EMT, y reduce la migración y la invasión de células de CPNM. Por último, se ha analizado la correlación entre la expresión de eIF5A2, las variables clínico-patológicas y la supervivencia de los pacientes en una colección de muestras de pacientes con CPNM. Los resultados obtenidos sugieren la existencia de una regulación entre las isoformas eIF5A1 y eIF5A2 para compensar la expresión de ambos homólogos. Además, nuestros datos apuntan a una coordinación temporal y posicional entre las vías de TGFß1 y eIF5A2 para impulsar la traducción de proteínas requerida para el reordenamiento del citoesqueleto y la motilidad de las células cancerosas invasivas. Hemos demostrado con modelos de ratón in vivo, que los tumores generados mediante xenotrasplante de células que sobreexpresan eIF5A2 tienen mayor capacidad invasiva. Finalmente, mostramos la existencia de una correlación positiva entre la expresión de eIF5A2 y el marcador de proliferación Ki67 en tejido de tumores de CPNM, y que la tasa de supervivencia es menor en aquellos pacientes que expresan niveles elevados de eIF5A2. Los resultados obtenidos en este trabajo confirman que eIF5A2 podría ser empleado como un biomarcador de mal pronóstico en CPNM y su inhibición farmacológica podría emplearse como una posible herramienta terapéutica, sola o en combinación con otros fármacos, en aquellos casos en los que eIF5A2 se encuentre sobreexpresado. / [CA] Les poliamines són metabòlits essencials per al creixement de les cèl·lules eucariotes i el seu metabolisme està frequentment desregulat en càncer. Una de les dianes moleculars de les poliamines és el factor d'elongació de la traducció eIF5A, una proteïna essencial i conservada evolutivament. eIF5A és l'única proteïna cel·lular coneguda que conté l'aminoàcid hipusina, que deriva de la poliamina espermidina. En humans hi ha dues isoformes, eIF5A1 i eIF5A2. EIF5A2 es troba al cromosoma 3q26, una regió freqüentment amplificada en molts tumors, i que està altament expressada en diferent tipus de càncer, incloent el càncer de pulmó no microcític (CPNM). eIF5A2 és essencial per al manteniment de la proliferació cel·lular i la seva inhibició la suprimeix en alguns tumors. Recentment s'ha correlacionat la sobreexpressió d'eIF5A2 amb la invasió i com a biomarcador de mal pronòstic a alguns càncers i s'ha observat que eIF5A2 indueix la transicició epiteli-mesenquima (EMT) en CPNM. L'EMT és un procés complex i reversible que indueix la diferenciació de les cèl·lules epitelials a cèl·lules mesenquimals migrants amb capacitat d'invasió. Nombrosos estudis han demostrat que l'EMT està relacionada amb la progressió del càncer, la metàstasi i el mal pronòstic en molts tumors. Per tant, la determinació d'un mètode eficaç per inhibir l'EMT a CPNM podria millorar significativament els règims dels tractaments actuals. La naturalesa altament selectiva de la hipusinació d'eIF5A2 i la susceptibilitat a la inhibició farmacològica fan d'aquesta proteina una diana terapèutica molt atractiva. Actualment, es disposa d'un anàleg de poliamina, anomenat GC7, que s'utilitza per inactivar la reacció d'hipusinació i s'ha demostrat que inhibeix el creixement de cèl·lules canceroses. Aquest treball de tesi doctoral té com a objectiu caracteritzar el paper patològic d'eIF5A2 en el desenvolupament del CPNM. Per això, hem estudiat, mitjançant modificacions genètiques per silenciament i sobreexpressió, el paper d'eIF5A2 en la proliferació, la motilitat i la invasió cel·lular utilitzant línies cel·lulars de càncer de pulmó. Així mateix, s'ha estudiat l'efecte de l'inhibidor GC7 en línies cel·lulars de CPNM i models murins per determinar si augmenta la quimiosensibilitat de les cèl·lules, prevé o reverteix l'EMT i redueix la migració i la invasió de cèl·lules de CPNM. Finalment, s'ha analitzat la correlació entre l'expressió d'eIF5A2, les variables clinicopatològiques i la supervivència dels pacients en una col·lecció de mostres de pacients amb CPNM. Els resultats obtinguts suggereixen que hi ha una regulació entre les isoformes eIF5A1 i eIF5A2 per compensar l'expressió dels dos homòlegs. A més, les nostres dades apunten a una coordinació temporal i posicional entre les vies de TGFß1 i eIF5A2 per impulsar la traducció requerida de proteïnes per als reordenaments del citosquelet i les característiques de motilitat de les cèl·lules canceroses invasives. Hem demostrat amb models de ratolí in vivo que els tumors generats mitjançant xenotrasplantament de cèl·lules que sobreexpressen eIF5A2 tenen més capacitat invasiva. Finalment, mostrem l'existència una correlació positiva entre l'expressió d'eIF5A2 i el marcador de proliferació Ki67 en teixit de tumors de CPNM, i que la taxa de supervivència és menor en aquells pacients que expressaven alts nivells d'eIF5A2. Els resultats obtinguts en aquest treball confirmen que eIF5A2 podria ser emprat com un biomarcador de mal pronòstic a CPNM i la seva inhibició farmacològica podria utilitzar-se com una possible eina terapèutica, sola o en combinació amb altres fàrmacs, en aquells casos en què eIF5A2 es trobe sobreexpressat. / [EN] Polyamines are essential metabolites for eukaryotic cells growth, and their metabolism is frequently deregulated in cancer. One of the molecular targets of polyamines is the translation elongation factor eIF5A, an essential and evolutionarily conserved protein. eIF5A is the only protein known that contains the amino acid hypusine, which is derived from the polyamine spermidine. In humans there are two isoforms, eIF5A1 and eIF5A2. EIF5A2 is located on chromosome 3q26, a region frequently amplified in different types of cancer, including non-small cell lung cancer (NSCLC). eIF5A2 is essential for the maintenance of cell proliferation and its inhibition suppresses it in many tumors. Recently, eIF5A2 overexpression has been correlated with invasion and as a biomarker of poor prognosis in some cancers, and it has been observed that eIF5A2 induces epithelial-mesenchymal transition (EMT) in NSCLC. EMT is a complex and reversible process that induces the differentiation of epithelial cells into migrant mesenchymal cells with invasive capacity. Numerous studies have shown that EMT is related to cancer progression, metastasis, and poor prognosis in many tumors. Therefore, the determination of an effective method to inhibit EMT in NSCLC could significantly improve current treatment regimens. The highly selective nature of eIF5A2 hypusination and its susceptibility to pharmacological inhibition make this process a very attractive therapeutic target. Currently, a polyamine analog, called GC7, is available and is used to inactivate the hypusination reaction and has been shown to inhibit cancer cell growth. The objective of this doctoral thesis is to characterize the pathological role of eIF5A2 in the development of NSCLC. For this, we have studied, through genetic alterations by silencing and overexpression, the role of eIF5A2 in cell proliferation, motility and invasion using lung cancer cell lines. Likewise, the effect of the GC7 inhibitor in NSCLC cell lines and murine models has been studied to determine if it increases the chemosensitivity of cells, prevents or reverses EMT, and reduces migration and invasion of NSCLC cells. Finally, the correlation between the expression of eIF5A2, clinicopathological variables and patient survival has been analyzed in a collection of samples from patients with NSCLC. The results obtained suggest the existence of a regulation between the eIF5A1 and eIF5A2 isoforms to compensate the expression of both homologues. Furthermore, our data point to a temporal and positional coordination between the TGFß1 and eIF5A2 pathways to drive the required translation of proteins for cytoskeletal rearrangements and motility characteristics of invasive cancer cells. We have demonstrated with in vivo mouse models that tumors generated by xenotransplantation of cells that overexpress eIF5A2 have a greater invasive capacity. Finally, we show the existence of a positive correlation between the expression of eIF5A2 and the proliferation marker Ki67 in NSCLC tumor tissue, and that the survival rate is lower in those patients who expressed high levels of eIF5A2. The results obtained in this work confirm that eIF5A2 could be used as a biomarker of poor prognosis in NSCLC and its pharmacological inhibition could be used as a possible therapeutic tool, alone or in combination with other drugs, in those cases in which eIF5A2 is found overexpressed. / Martínez Férriz, A. (2023). Funciones del factor de inicio de la traducción eucariota 5A2 en el cáncer de pulmón [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/193293

From RNA-to-protein, translation initiation and protein synthesis is mediated by trans-acting factors that recognize mRNA features common to almost all eukaryotes. Eukaryotic translation initiation factor 3 complex (eIF3) is a highly conserved protein complex that recognizes 5'-CAP elements of the mRNA to initiate translation. eIF3 consists of nine subunits, three of them having two isoforms: eIF3A, eIF2B1, eIF3B2, eIF3C1, eIF3C2, eIF3D, eIF3E, eIF3F, eIF3G1, eIF3G2, eIF3H and eIF3K. This work deals with functional characterization, expression and subcellular localization of eIF3B1, eIF3B2 and eIF3E in Arabidopsis thaliana male gametophyte and interaction of eIF3E with the Constitutive photomorphogenesis 9 (COP9) complex as a regulatory complex of eIF3E post-translational control. Here we show that depletion of eif3b1 or eif3b2 is not gametophytic lethal and that the two protein might function redundantly, whereas, knockout of eIF3E causes male gametophyte lethality. Interestingly, eif3b1 show post-fertilization defects during embryogenesis, suggesting that its redundancy with eIF3B2 is restricted to the gametophyte. Gene expression studies revealed high expression of eIF3 subunits in actively dividing zones of leaf primordia, root meristem and root elongation zones as well as in the vegetative...