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N6-methyladenosine (m6A) is the most ubiquitous post-transcriptional RNA modification and has an important role in determining the fate of mRNA transcripts. Among the key proteins of the m6A pathway are methyltransferases (METTL family enzymes), demethylases (FTO, ALKBH family enzymes), and m6A binding proteins (e.g., YTHDF family) which recognize RNA sequences depending on the amount and localization of m6A in target transcripts and subsequently influence the fate of mRNA transcripts. The role of methyltransferases and demethylases is to provide a dynamic balance of m6A levels and possibly to convey mechanisms of specificity for these so-called epitranscriptomic marks, which are not yet fully understood. The main objective of this work was to determine the relative changes in the expression of key m6A pathway proteins during early postnatal development and adulthood in the rat brain. We found that the level of expression of key m6A pathway proteins decreases from birth to adulthood, with the exception of a transient increase between postnatal days 10 and 18. During this period, we also found significant changes in the expression of respiratory chain complexes. However, further research is needed to provide evidence of a mechanistic link between the m6A pathway and brain energy homeostasis during...

Le contrôle de l’expression des gènes est un processus crucial pour le développement, la reproduction ou les mécanismes d’acclimatation aux stress environnementaux et met en jeu des voies de régulation post-transcriptionnelles agissant sur les ARN messagers (ARNm). Ces molécules portent des modifications chimiques dont l’une des plus abondantes est la N6-méthyladénosine ou m6A. Cette modification permet notamment d’attirer des protéines spécifiques qualifiées de « lecteurs » qui, chez les mammifères, agissent principalement pour favoriser la dégradation et/ou la traduction des ARNm. Mes travaux de thèse ont eu pour objectif de caractériser les fonctions d’un de ces lecteurs, nommé ECT2, chez la plante modèle Arabidopsis thaliana. Dans un premier temps, sa fonction de liaison aux ARNm méthylés ainsi que son rôle dans le développement de la plante ont été démontrés. Au niveau moléculaire, une approche de protéomique a permis d’identifier de nombreux partenaires d’ECT2 dont la majorité est impliquée dans le métabolisme des ARNm parmi lesquels des facteurs inhibiteurs de traduction. Les résultats d’une analyse de translatomique permettent de proposer un modèle où ECT2 jouerait un rôle de répresseur de la traduction d’ARNm en coopération avec ses partenaires LARP1 et DCP5, deux facteurs évolutivement conservés qui agissent dans le contrôle de la traduction des ARNm. Enfin, j’ai également découvert que la protéine ECT2 est dynamiquement modifiée via des phosphorylations en réponse à un stress thermique, ce qui semble notamment affecter sa capacité à reconnaitre les résidus m6A. Ces travaux suggèrent pour la première fois que l’activité d’un lecteur peut être régulée par des phosphorylations en réponse à des variations environnementales. / Control of gene expression is a crucial process for development, reproduction or acclimation to environmental stresses and involves post-transcriptional regulatory pathways acting on messenger RNAs (mRNAs). These molecules carry chemical modifications of which N6-methyladenosine (m6A) is one of the most abundant. This modification allows notably the recruitment of specific proteins qualified as “readers” which, in mammals, mostly act to promote decay and/or translation of mRNAs. My thesis aimed to characterize the functions of one of these readers, named ECT2, in the model plant Arabidopsis thaliana. First, its binding function to methylated mRNAs and its role in plant development was demonstrated. At the molecular level, a proteomic approach identified numerous ECT2’s protein partners, mainly involved in mRNA metabolism including translation inhibition factors. Results obtained from a translatome analysis suggest a model where ECT2 could play a repressive role on the translation of methylated mRNAs cooperatively with its partners LARP1 and DCP5, two evolutionarily conserved factors acting in translational control of mRNAs. Finally, I also discovered that ECT2 is dynamically modified with phosphorylations in response to heat stress affecting especially its ability to recognize m6A residues. These works suggests for the first time that the activity of an m6A reader could be regulated by phosphorylations in response to environmental changes.

In the yeast Saccharomyces cerevisiae, the IME4 methyltransferase, interacts genetically with methyl binding protein, Pho92, to affect the expression of PHO regulon target genes. Cells mutant in IME4 or PHO92 show increases in the RNA abundance of PHO regulon target genes. The increase in the RNA abundance of the PHO regulon target genes is not additive in the cells double mutant in IME4 and PHO92. Hence, Ime4 and Pho92 interact in a single pathway in PHO regulon. Surprisingly, cells overexpressing IME4 and MUM2 shows increase in some PHO regulon target genes, indicating that IME4 affects the PHO regulon target genes through multiple mechanisms in different conditions. A promoter swap experiment revealed that one of the PHO regulon mRNAs that codes for phosphatase, PHO5, is a direct target of Ime4. Further experiments are required to examine whether the same is true for all PHO regulon mRNAs.

The extent and nature of physio-chemical changes that take place in detached leaves after harvest and during storage have been reviewed and discussed by Osborne (1962) and Rogers (1955). These changes include loss of moisture (Wittwer et al., 1962), chlorophyll degredation (Person et al., 1957), Protein loss (Thimann and Manmahan, 1960), and result in subsequent appearance of the visual manifestations of senescence of plant tissues. As lettuce, like most leafy vegetables, deteriorates rapidly and steadily after harvest. Loss of quality is inevitable and can only be minimized by rapid handling and with the best possible storage conditions (Pratt et al., 1954). In recent years, abundant work has been done to delay senescence by the use of various chemicals. Among the investigated chemicals, kinetin (6-furfurylarninopurine) and its related c ompounds show some promise. Van Overbeek et al. (1941) reported a potent new growthpromoting factor (kinetin) in coconut milk. This chemical is active in causing many of the growth reactions of c oconut milk at exceedingly small dosages. Subsequently several arninopurine compounds were synthesized. One of which is SD 4901 (Verdan), N6-benzyladenine, an experimental senescence inhibitor, was developed by Shell Development Company, Modesto, California in 1960. Many reports showed that this chemical is capable of delaying senescence of plant tissues on the basis of restoring protein molecules and respiration inhibition. On the other hand, others have shown stimulation of respiration and delaying of senescence. Paucity of scientific literature on the stability of those chemicals on leafy vegetables gave impetus to a study of the comparative influence of pre- and post-harvest applications of 6-furfurylaminopurine and N6-benzyladenine as related to successive harvest times. Such studies may have considerable economic bearing upon storing and shipping leafy vegetables to distant markets. This thesis presents effects of different concentrations (5, 10, and 20 ppm.) of pre- and post-harvest applications of 6-furfurylaminopurine and N6-benzyladenine as related to three successive harvest times (at one week intervals) on chlorophyll content, moisture content, total nitrogen, insoluble and soluble nitrogen, oxygen uptake, 0 and co2 production during storage (at 40 Fo and 85 percent RH) of "Great Lakes" variety of lettuce.

tRNA molecules contain more than 80 chemically unique nucleotide base modifications that contribute to the chemical and physical diversity of RNAs as well as add to the overall fitness of the cell. For instance, base modifications have been shown to play a critical role in tRNA molecules by improving the fidelity and efficiency of translation. Most of this work has been carried out extensively in Gram-negative bacteria, however, the role of modified bases in tRNAs as they relate to thermostability, structure, and transcriptional regulation in Gram-positive bacteria, such as Bacillus subtilis and Bacillus anthracis, are not well characterized. Infections by Gram-positive bacteria that have become more resistant to established drug regiments are on the rise, making Gram-positive bacteria a serious threat to public safety. My thesis work examined what role partial base modification of the tyrosyl-anticodon stem-loops (ASLTyr ) of B. subtilis and B. anthracis have on thermostability, structure, and transcriptional regulation. The ASLTyr molecules have three modified residues which include Queuine (Q34), 2-thiomethyl-N6-dimethylallyl (ms2i6A37), and pseudouridine (Y39). Differential Scanning Calorimetry (DSC) and UV melting were employed to examine the thermodynamic effects of partial modification on ASLTyr stability. The DSC and UV data indicated that the Y39 and i6A37 modifications improved the molecular stability of the ASL. To examine the effects of partial base modification on ASLTyr structure, NMR spectroscopy was employed. The NMR data indicated that the unmodified and [Y39]-ASLTyr form a protonated C-A+ Watson-Crick-like base pair instead of the canonical bifurcated C-A+ interaction. Additionally, the loop regions of the unmodified and [Y39]-ASLTyr molecules were well ordered. Interestingly, the [i6A37]- and [i6A37; Y39]- ASLTyr molecules did not form a protonated C-A+ base pair and the bases of the loop region were not well ordered. The NMR data also suggested that the unmodified and partially modified molecules do not adopt the canonical U-turn structure. The structures of the unmodified, [Y39]-, and [i6A37;Y39]-ASLTyr molecules did not depend on the presence of Mg2+, but the structure of the [i6A37]-ASLTyr molecule did depend on the presence of multivalent cations. Finally, to determine the repercussions that partial modification has on physiology and tRNA mediated transcriptional regulation in B. anthracis, antibiotic sensitivity tests, growth curves, and quantitative real-time polymerase chain reaction (qRT-PCR) were employed. Strains deficient in ms2 showed comparable growth to the parent strain when cultured in defined media, but Q deficient strains did not. The loss of ms2i6A37 conferred resistance to spectinomycin and ciprofloxacin, whereas the loss of Q34 resulted in sensitivity to erythromycin. Changes in the ratio full-length to truncated transcripts of the tyrS1 and tyrS2 genes were used to monitor tRNA mediated transcriptional regulation. The qRT-PCR data suggested that tyrS1 and tyrS2 are T-box regulated and that the loss of ms2i6A37 and Q34 might affect the interaction of the tRNATyr molecule with the specifier sequence, which is located in the 5’-untranscribed region (UTR) of the messenger RNA (mRNA).

A new series of N6,5'-bis-ureido-5'-amino-5'-deoxyadenosine derivatives was prepared and evaluated for anticancer activities using the NCI 60 panel of human cancers. Certain of the derivatives showed promising activities (low micromolar GI50's) against several of the representative cancers. These included cell lines from the following general cell types in the NCI 60: Leukemia, Breast, Central Nervous System, Non-Small Cell Lung, Ovarian, Prostate, Renal, and Colon cancers. Select compounds were also screened for their affinities for protein kinases. The synthesis of the compounds was straightforward and involved N6 acylation with arylisocyanates, preceded by activation and nucleophilic substitution of the 5'-position to give the desired 5'-azido-5'-deoxyadenosine derivatives. Reduction of the 5'-azido function with either H2/Pd-C, or Ph3P/H2O, gave the desired 5'-amino-5' deoxyadenosine products. Acylation of the 5'-amino group with N-methyl 4-nitrophenylcarbamate gave the N6,5'-bis-ureido-5'-amino-5' deoxyadenosine products. Yields ranged from good (50–75%) to excellent (75–95%) for all synthetic transformations.

Recently the Peterson lab discovered a promising anticancer adenosine derivative-- 2´,3´-bis-O-tert-butyldimethylsilyl-5´-deoxy-5´-[N-(methylcarbamoyl)amino]-N6-(N-phenylcarbamoyl)adenosine. This compound showed selective toxicity against human colon cancer cells in vitro with LC50's = 6--10 µM. It was hypothesized that the lead compound exerted its cytotoxic effects by interacting with a protein kinase. A systematic Structure Activity Relationship (SAR) was undertaken in an attempt to increase the kinase-binding affinity of the lead compound. Many regions of the lead compound were examined: the N6-phenyl urea moiety, the 5´-N-methyl urea group, the 2´,3´-bis-O-TBS groups, the nucleobase, and the ribose sugar. Results of these studies produced some promising new derivatives. In particular, one analogue exhibited potent cancer cell growth inhibition with an average GI50 of 0.58 μM (NCI-60). In addition, another compound showed selective toxicity for the non-small cell adenocarcinoma cell line NCI-H522 with an LC50 of 10 nM. Efficient methods for the preparation of a wide variety of N6-aryl and -alkyl substituted derivatives were developed. One versatile route involved the installation of an N6-ethoxy carbonyl and subsequent displacement with an alkly- or arylamine. Synthetic routes for the preparation of of a variety of 2´,3´-bis-O-acylated analogues were also developed. Nucleoside mono-, di-, and triphosphate bioisosteres in which the phosphoester or phosphoanhydride have been replaced by an unnatural functional group have been extensively investigated. A simple and efficient method was developed for the preparation of carbamoyl analogues of nucleoside mono-, di-, and triphosphate surrogates. This method uses a modified version of the Kočovský reaction to install mono-, di-, and triphosphate mimics in good to excellent yields (ave = 75%).

Följande studie behandlar hur den kommunala och regionala platsmarknadsföringen i norra Sverige fungerar och om det finns en koppling mellan dem. För att undersöka detta har Umeå- och Örnsköldsvik kommun valts ut för att företräda både kommunerna i sig och som representanter för N6-initiativet. Initiativet består av de fem största städerna i norra Sverige som tillsammans vill ändra bilden av norra Sverige. Metoden består av intervjuer med tjänstepersoner inom kommunerna, samt inom N6-initiativets verksamhet. Det kombineras med en innehållsanalys av de berörda kommunernas webbplatser, samt av initiativets hemsida och tillhörande informationsvideo. Resultatet består av en sammanställning av intervjuer och innehållsanalyser, samt en koppling till tidigare forskning som presenterats i studien. Det som framgår av undersökningen är att både Umeå och Örnsköldsvik kommun använder sig av olika strategier för att marknadsföra sig, däremot finns det flera likheter mellan kommunernas val av marknadsföring, såsom kultur och idrott. Det framgår även hur de aktivt anstränger sig för att behålla platsens identitet och unikhet i arbetet med platsmarknadsföring, vilket ofta kan influeras av trender. Ett genomgående tema under intervjuerna är konkurrens, där slutsatsen är att konkurrensen inte färgat N6-initiativets samarbeten. Däremot används initiativet inte direkt i kommunernas arbete, trots att det bidragit med flertalet positiva aspekter.

L’épigénétique se rapporte à un ensemble de mécanismes qui modifient l'expression des gènes sans modifier la séquence nucléotidique sous-jacente, produisant une large gamme de variations phénotypiques et répondant aux fluctuations de l'environnement externe ou interne. La méthylation de l'ADN est le processus épigénétique le plus étudié dans les génomes nucléaires des mammifères. Il existe toutefois des lacunes significatives dans la littérature concernant la méthylation de l'ADN mitochondrial (ADNmt), surtout chez les invertébrés. Les bivalves constituent un modèle particulièrement intéressant pour étudier l’épigénétique mitochondriale ou « mitoépigénétique » puisqu’ils possèdent un système de transmission uniparentale double (DUI) de leur mitochondrie, par lequel les mâles héritent des ADNmt paternel (ou mâle ; M) et maternel (ou femelle ; F). La présente étude avait pour objectif de confirmer l’existence de méthylation dans l’ADNmt de la moule bleue (Mytilus edulis), une espèce à DUI. Notre étude a permis de localiser, par immunofluorescence, des cytosines (5mC) et des adénines (6mA) méthylées, ainsi que des méthyltransférases spécifiques aux adénines et aux cytosines, au sein des mitochondries de cette espèce. Ces résultats sont appuyés par une détection de 5mC et de 6mA dans l’ADNmt par digestions enzymatiques, et confirment la présence de méthylation de l'ADNmt chez M. edulis. Nos résultats en immunofluorescence ont également dévoilé un lien entre la présence de 5mC et le stade de développement des gamètes mâles, c’est-à-dire que les gamètes immatures (spermatides) étaient tous méthylés (au niveau mitochondrial) alors qu’une faible proportion de gamètes matures (spermatozoïdes) présentait ce statut de méthylation. Ceci vient corroborer nos résultats enzymatiques, lesquels ont démontré une plus grande variabilité de méthylation entre les mâles qu’entre les femelles. Enfin, nous avons détecté, par séquençage du méthylome de l’ADNmt, un pic de 5mC en contexte non-CpG conservé entre les ADNmt M et F chez les mâles au sein de la région de contrôle de la réplication, soutenant les résultats d’études antérieures chez les vertébrés. Notre étude est la première à démontrer la présence de méthylation dans l’ADNmt d’une espèce DUI, et met en lumière le rôle potentiel de la méthylation de l'ADN dans leur système de transmission mitochondriale. / Epigenetics refers to a set of mechanisms that modify gene expression without altering the underlying nucleotide sequence, producing a wide range of phenotypic variations, and responding to the external or internal environmental fluctuations. DNA methylation is the most extensively studied epigenetic process in mammalian nuclear genomes. However, there are significant gaps in the literature concerning mitochondrial DNA (mtDNA) methylation, especially in invertebrates. Bivalves are a particularly interesting model for studying mitochondrial epigenetics or “mitoepigenetics”, as they possess a doubly uniparental inheritance (DUI) system of their mitochondria, whereby males inherit both paternal and maternal mtDNAs. The aim of this study was to confirm the existence of methylation in the mtDNA of the blue mussel (Mytilus edulis), a DUI species. Using immunofluorescence, we localized methylated cytosines (5mC) and adenines (6mA), as well as adenine- and cytosine-specific methyltransferases, in mitochondria of this species. These results are supported by the detection of 5mC and 6mA in mtDNA by enzymatic digestions, and confirm the presence of mtDNA methylation in M. edulis. Our immunofluorescence results also revealed a link between the presence of 5mC and the developmental stage of male gametes, i.e. immature gametes (spermatids) were all methylated in their mitochondria while only a small proportion of mature gametes (spermatozoa) showed this methylation status. This corroborates our enzymatic results, which demonstrated greater variability in cytosine methylation status among males than among females. Finally, we detected, by mtDNA methylome sequencing, a 5mC peak in non-CpG context conserved between the paternal and maternal mtDNA in males in the region responsible for control of replication (control region), supporting the results obtained in previous studies on vertebrate. Our study is the first to demonstrate the presence of mtDNA methylation in a DUI species, and highlights the potential role of DNA methylation in their mitochondrial transmission system.