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Analyse des PEX1-Gens bei Patienten mit Zellweger-Syndrom: Identifikation einer neuen Deletion und Untersuchung von Polymorphismen in der 5'-untranslatierten Region / Analysis of the PEX1 gene of patients with Zellweger syndrome: Identification of a novel deletion and characterization of polymorphisms in the 5' untranslated regionRabenau, Jana 19 July 2011 (has links)
No description available.
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Studies on the Evolution and Function of Introns in 5' Untranslated RegionsCenik, Can January 2011 (has links)
The function and evolution of introns have been topics of great interest since introns were discovered in the 1970s. Introns that interrupt protein-coding regions have the most obvious potential to affect coding sequences; therefore, their evolution have been studied most intensively. Splicing of introns within untranslated regions does not contribute directly to the diversity of proteins, yet ~35% of human transcripts contain introns within the 5' untranslated region (UTR). The evolution and possible functions of 5'UTR introns (5UIs) remain largely unexplored. Here we undertook a genome-wide functional analysis of 5UIs. Our main results are as follows: First, the distribution of these introns in the human genome is nonrandom. While genes with regulatory roles are enriched in having 5UIs, genes encoding proteins that are targeted to the endoplasmic reticulum and mitochondria are surprisingly depleted of these introns. Second, we offered and supported a model whereby gene encoding secretory and nuclear-encoded mitochondrial proteins share a common regulatory mechanism at the level of mRNA export, which is dependent on the absence of 5'UTR introns. Specifically, the upstream element in a given transcript, be it an intron or RNA elements near the 5' end of coding sequences (CDS), dictates the mRNA export pathway used. Finally, we discovered a strong correlation between existence of 5'UTR introns and sequence features near the 5' end of CDS. We developed an integrated machine-learning framework that can predict absence of 5UIs using solely the sequence near the 5' end of CDS. Our model achieved >80% accuracy when validated against nuclear-encoded mitochondrial transcripts. Specific RNA elements predictive of 5UI absence are found in ~40% of human transcripts spanning a wide spectrum of functions. By analyzing hundreds of large-scale datasets, we functionally characterized the transcripts with these RNA elements; revealing their association with translational regulation. These RNA elements were bound by proteins interacting with the Exon Junction Complex in vivo suggesting a molecular mechanism that links these elements to their downstream effects in mRNA export and translational regulation. While some 5'UTR introns might be evolving neutrally, our results, taken together, suggest that complex evolutionary forces are acting on this distinct class of introns.
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Evaluation of 5´- and 3´-UTR Translation Enhancing Sequences to Improve Translation of Proteins in CHO CellsEinarsson, Ellen January 2018 (has links)
The purpose of this project was to identify and evaluate nucleotide sequences enhancing translation of proteins in Chinese hamster ovary (CHO) cells. Candidate sequences were placed in the 5´-untranslated region (UTR) or 3´ UTR respectively and evaluated in a CHO-based expression system with a fluorescent Fc-fusion protein as a model protein.Five plasmid vectors were constructed, two of which designed to have a randomized nucleotide library in their 5´ and 3´ UTR respectively, and three of which designed to hold varying repeats of a known enhancing translation (ET) sequence in their 5´ or 3´ UTR. The plasmid constructs were transfected into CHO cells and the protein expression was analyzed both by fluorescence intensity in single cells using flow cytometry and in bulk by monoclonal antibody titer analysis based on Protein A affinity.The main result is that both flow cytometry and titer analysis indicate that insertion of five repeats of the ET in the 5´UTR has a negative effect on protein expression as compared to the control which had no ET repeats. Results related to the insertion of three ETs in the 5´ UTR were ambiguous. The titer analysis indicated that it had a negative effect on the protein expression compared to the control which had no ET repeats, whereas the flow cytometry results suggest that the effect is negligible. Transfection of library plasmids was unsuccessful; hence no library expression analysis results were achieved. Due to the time constraints of the project, the reason for the unsuccessful transfection of library plasmids was not investigated, but the LTX transfection method is stated as a highly plausible cause.Based on the outcome of this study, two recommendations for future work are suggested. The first one is to continue the focus on UTR sequences in terms of library screening, and to improve the method of transfecting library plasmid constructs into CHO cells using lipofection. The second suggestion for further studies is to test different UTR sequence lengths without involving potential ETs, to rule out the effect and positions of the ETs and investigate the expressional effect of UTR length solely.
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Identification et caractérisation d'ARN régulateurs impliqués dans la réponse au stress et la virulence chez Enterococcus faecalis / Identification and characterization of regulatory RNA involved in stress response and virulence in Enterococcus faecalisSalze, Marine 09 May 2019 (has links)
E. faecalis est une bactérie à gram positif, responsable d’infections nosocomiales. Dans cette étude, nous avons identifié par RNA-seq 65 ARN régulateurs potentiels induits en conditions de stress et/ou d’infection chez ce pathogène opportuniste. Parmi ceux-ci, trois ARN surexprimés in vivo, en présence de sels biliaires et à pH acide ont fait l’objet d’une étude approfondie.Le premier, SRC65, s’est avéré être un petit ARN (sARN) agissant probablement en trans. Il présenterait des fonctions redondantes avec son homologue SRC90. Différentes cibles potentielles ont été identifiées et des expériences de physiologie ont révélé un rôle de SRC65 dans le déclenchement de la phase exponentielle de croissance.Le 2ème ARN étudié est une région 5’ régulatrice non traduite (5’UTR), appelée 5’1515. Elle formerait un atténuateur et agirait de manière répressive sur le gène ef1515. EF1515 est un antiterminateur de la famille BglG/SacY capable de se fixer sur 5’1515 pour réguler son expression et celle du gène ef1516 localisé en aval et codant un système de transport des sucres de type PTS. L’antiterminateur EF1515 contrôle aussi l’expression du gène ef3023 codant une protéine impliquée dans la virulence d’E. faecalis.Le dernier ARN régulateur étudié est également une 5’UTR. Celle-ci participerait à la régulation d’une hélicase à motif DEAD (CshA) codée en aval de la 5’UTR. Sa caractérisation s’inscrit dans une étude plus large concernant les éléments du métabolisme des ARN, impliquant les ribonucléases et les autres hélicases à motif DEAD d’E. faecalis. CshA aurait un rôle prépondérant pour la bactérie, en étant impliquée dans la réponse au stress, le fitness et la virulence. L’identification de l’interactome de CshA a notamment permis d’identifier l’énolase comme partenaire privilégié. / E. faecalis is a gram-positive bacterium responsible for nosocomial infections. Using RNA-seq, we identified 65 putative regulatory RNA induced under stress and/or during infection. Of these, three RNA overexpressed in vivo, in the presence of bile salts and at acidic pH have were more deeply studied.The first, SRC65, was found to be a small RNA (sRNA) probably acting in trans. It would present redundant functions with its homologous sRNA SRC90. Different potential targets were identified and physiology experiments revealed a role for SRC65 in triggering the exponential growth phase.The 2nd studied RNA is a 5’ untranslated region (5'UTR), called 5'1515 which would form an attenuator and act repressively on the ef1515 gene. EF1515 is an antiterminator of the BglG/SacY family capable of binding at 5'1515 to regulate its expression and that of the downstream gene ef1516 encoding a PTS-type sugar transporter. The EF1515 antiterminator also controls the expression of the ef3023 gene encoding a protein involved in E. faecalis virulence.The last regulatory RNA studied is also a 5'UTR. It would participate in the regulation of a DEAD-box helicase (CshA) encoded downstream of the 5'UTR. Its characterization is part of a broader study of the elements of RNA metabolism, involving ribonucleases and other DEAD-box helicases of E. faecalis. CshA would have a prominent role for the bacteria, being involved in stress response, fitness and virulence. The identification of the CshA interactome made it possible to identify enolase as a preferred partner.
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Translation Control to Improve Oncolytic Virus Efficacy and Regulate Inflammatory DiseasesHoang, Huy-Dung 14 July 2021 (has links)
Translation control is crucial during virus-host interaction, in which the host relies on the translation machinery to mount an antiviral response or induce the inflammation response to reduce virus spread, while the virus aims to take control of this system to thwart the host defense while producing viral progeny. The field of oncolytic virus (OV) therapy relies on replicating, engineered viruses that preferentially infect tumor cells to induce direct oncolysis or promote an antitumor immune response. Despite the importance of translation control in virus-host interaction, not much has been described on the interaction at the translation level between OV and cancer cells. I propose that this knowledge gap could reveal significant improvements in OV efficacy in treating cancer. In my first study, I set out to characterize the translatome of an infection-resistant breast cancer cell line infected by three clinically advanced OVs to identify residual antiviral activity in cancer cells regulated by translation control. I found the inositol phosphatase Inpp5e to be a novel antiviral gene that is translationally induced during infection via a transcript variant shift. Mechanistically, I showed that the majority of Inpp5e transcripts in uninfected cells contain a long 5’ UTR that harbor four translationally inhibitory upstream reading frames (uORF). Yet, OV infection induced the expression of a shorter 5’ UTR with a spliced intron that removes three uORFs, derepressing the translation of Inpp5e mRNA. CRISPR-Cas9 knockout of Inpp5e also enhanced the infectivity of oncolytic HSV1 and VSV. My study suggests the existence of a class of translationally regulated antiviral genes in cancer cells. In my second study, I sought to adapt the translation of transgenes to the unique translation condition imposed by the infecting virus via the incorporation of a viral 5’UTR. I identified HSV1 5’UTRs by locating the transcription start site of most HSV1 genes using RNA-seq data, then determined the 5’UTR of US11 as a potent translation enhancer during HSV1 infection. Incorporation of this 5’UTR into the transgene expression cassette inserted into the HSV1 genome enhanced transgene expression significantly at the translation level. In my third study, I set out to explore the mechanism of miR-223 mediated inflammation inhibition. miR-223 is a protective miRNA in the context of atherogenesis via suppressing inflammatory signaling. Using transcriptome and translatome profiling (RNA-seq and Ribo-seq), I found that the inhibitory effect of miR-223 on inflammation occurs primarily at the translation level. Overall, my work highlights the importance of translation control in OV-cancer cells interaction, as well as in inflammation-related diseases.
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Diagnosis and Characterization of Bovine Viral Diarrhea VirusYan, Lifang 12 May 2012 (has links)
Bovine viral diarrhea virus (BVDV) is an important viral pathogen affecting all ages of cattle, resulting in significant economic losses worldwide. BVDV infection is associated with a diverse array of symptoms including gastrointestinal disorder, respiratory distress, fetal malformation, stillbirth, abortions, and mucosal disease (MD). Transplacental infections of fetuses between 42 and 125 days of gestation can result in immune-tolerance and the surviving fetuses become persistently infected (PI). PI animals are major reservoir of BVDV and it becomes problematic to control the disease. The objectives of this dissertation were to: 1) develop a cost-effective testing scheme to detect BVDV PI animals from exposed herds, 2) characterize two virulent BVDV-2 Mississippi isolates associated with severe hemorrhagic diseases, and 3) perform phylogenetic analysis based on sequences of 5'UTR, E2, and NS5B regions. First, we developed a BVDV testing scheme by combining pooled real-time RT-PCR with antigen capture enzyme-linked immunosorbent assay (ACE) to screen cattle herds. From positive pools individual positives were identified using ACE. Data from a three year period indicated that 92.94% PI animals were infected with BVDV-1, 3.53% with BVDV-2, and 3.53% with both BVDV-1 and BVDV-2. Analysis of the 5'UTR of 22 isolates revealed the predominance of BVDV-1b followed by BVDV-2a. Second, two virulent BVDV isolates, M10-3432 and M10-5347, were successfully recovered from an adult beef breeding cow and feedlot calf respectively. When compared to the reference strain BVDV-2 125c, five and three unique amino acids in E2 regions were different from M10-5347 and M10-3432 respectively. Phylogenetic analysis of E2 region grouped both Mississippi isolates in BVDV-2a, a subtype containing high virulent strains. M10-3432 was clustered with high virulent strain 890 while M10-5347 was clustered with high virulent strain CD87. Third, we compared the phylogenetic analyses of BVDV based on the sequences of 5'UTR, E2, and NS5B at either nucleotides or amino acids level. Although slight differences were observed, the virulent BVDV isolates were consistently classified into BVDV-2a cluster regardless of region of sequences used. Furthermore, phylogenetic tree constructed using combined two or more regions had higher posterior probability and bootstrap value than phylogenetic trees constructed using a single region
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Analysis of the cryptic promoter in the 5'-UTR of P27Francis, Zachary T. 19 March 2012 (has links)
Indiana University-Purdue University Indianapolis (IUPUI) / Cyclin Dependent Kinase regulation is often manipulated by cancer cells to promote unlimited proliferation. P27 is an important regulator of Cyclin E/CDK 2, which has been found in low amounts in many types of malignant cancers. Lovastatin has been shown to cause cell cycle arrest in the G1 phase of the cell cycle by increasing the P27 protein. There has been some question, however, if lovastatin regulates P27 at the transcriptional or translational level. Although it has been claimed that P27 expression regulation is due to an IRES located in its 5’UTR, other studies suggested that P27 expression is regulated at the level of transcription. To further investigate the regulation mechanism of P27 expression, the 5’-UTR of P27 and its deletion mutants were examined using a luciferase reporter gene in HeLa cells following exposure to lovastatin. It was found that lovastatin stimulated a significant 1.4 fold increase in its promoter activity of the full length 5’UTR (575). Deletion of 35 nucleotides from the 5’ end of the UTR eliminated the lovastatin-induced increase in promoter activity. Further mapping analyses of the first 35 bases showed that two regions, M1 (575-559) and M3 (543-527), were less sensitive to lovastatin than the other mutated constructs.
Since M1 and M3 still showed some activity, a construct was created with deletions in both the M1 and M3 regions. This showed no increase in luciferase activity when exposed to lovastatin. Looking at RNA levels, there was a 1.5 fold increase in RNA when the full length 5’UTR was inserted into HeLa cells and exposed to 81 µM of lovastatin. In contrast, there was no increase in RNA when M1/M3 (575-559; 543-527) was inserted into HeLa cells and exposed to 81 µM of lovastatin. In addition, there was a 1.6 fold increase in endogenous P27 RNA levels after HeLa cells were exposed to 81 µM of lovastatin. In all of these experiments, there seems to be two promoters that work cooperatively: M1 (575-559) and M3 (543-527).
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Topologie und Regulation der Manduca sexta V-ATPaseReineke, Stephan 22 November 2002 (has links)
Topologie und Regulation der Manduca sexta V-ATPase
Die V-ATPase im Mitteldarm der Tabakschwärmerraupen von Manduca sexta besteht aus zwölf Untereinheiten, von denen vier den membranständigen Vo- und acht den cytosolischen V1-Komplex bilden. Das Enzym energetisiert unter ATP-Verbrauch eine Protonentranslokation über die Gobletzellapikalmembran, wobei eine Potentialdifferenz von etwa 250 mV aufgebaut wird. Durch diese Spannung wird ein elektrogener K+/2H+-Antiport getrieben und indirekt ein K+/Aminosäure-Symport, wodurch die Nährstoffversorgung der Raupen gesichert wird. Da die V-ATPase sehr viel ATP verbraucht, erscheint es ökonomisch, diese in Hungerperioden durch die Dissoziation des Enzyms in den cytosolische V1- und den Vo-Komplex, abzuschalten.
In der vorliegenden Arbeit wurde untersucht, ob auch die Biosynthese der V-ATPase Untereinheiten in Hungerperioden reduziert wird und was eventuellen Änderungen von Transkriptionsraten zugrunde liegt. Mit Ausnahme der Untereinheit D waren die Transkriptmengen aller V-ATPase Untereinheiten in Hungerperioden erniedrigt. Am stärksten betraf dies die Untereinheit G, was auch für den Anstieg der Transkriptmengen nach erneuter Futterzufuhr galt. Da Hungerperioden auch in der Entwicklung von Raupen während der Häutungen vorkommen, wurde exemplarisch die Biosynthese von drei, die verschiedenen Bereiche der V-ATPase (V1-Kopf: Untereinheit B, V1-Stiel: Untereinheit G, Vo-Komplex: Untereinheit d) repräsentierenden Untereinheiten, untersucht.
In allen drei Fällen konnte eine Reduktion der Transkriptmengen in der Mitte der Häutungsphase festgestellt werden, welche zu ihrem Ende hin wieder aufgehoben wurde. Der Abfall und Anstieg der mRNA-Mengen korrelierte mit den Titern der beiden Häutungshormone der Insekten: negativ mit dem Titer des Ecdysons und positiv mit dem des Juvenilhormons. Die Injektion von 20-Hydroxyecdyson in fressende Raupen hatte die Reduktion der Transkriptmengen zur Folge, während Juvenilhormon III fast keinen Einfluss ausübte. Darüberhinaus war zu beobachten, dass sich nach Injektion von 20-Hydroxyecdyson die V1-Komplexe von den apikalen Gobletzellmembranen ablösten.
Um auch den Einfluss der Häutungshormone auf die Promotoraktivität zu untersuchen, und dadurch auf Unterschiede in der RNA-Stabilität zu schließen, wurden ca. 1 kb lange 5`-Bereiche stromaufwärts vom Startcodon der drei verwendeten Gene mvB, mvG und mvd in Reportergenassays getestet. Hierbei wurde als Reportergen eine Luciferase verwendet, die unter der Kontrolle der jeweiligen 5`-Region der V-ATPase Untereinheit stand. Nach Transfektion von Sf21-Zellen konnte wie auch in den vorangegangenen Experimenten gezeigt werden, dass 20-Hydroxyecdyson die Promotoraktivität aller drei V-ATPase-Gene nach einem kurzzeitigen Anstieg bei den Genen mvB und mvG über einen längeren Zeitraum negativ beeinflusst und nach 48 h zu einer Reduktion auf 30-50% gegenüber der Kontrolle führt.Im Gegensatz dazu führte die Anwesenheit von Juvenilhormon III zur Aktivitätssteigerung von mvG um den Faktor 3, während die Aktivität der anderen 5`-Bereiche nicht signifikant verändert wurde.Zusammen mit den Daten der Transkriptmengen unter Juvenilhormon III Einfluss könnte dies der erste Hinweis auf eine reduzierte Stabilität der mRNA der Untereinheit G sein.
Des Weiteren wurde in der vorliegenden Arbeit die Nukleotidsequenz der bei der Insekten V-ATPase lange Zeit nicht nachweisbaren Untereinheit a des Vo-Komplexes aufgeklärt. Neben einer ubiquitär vorkommenden Isoform konnte auch eine Teilsequenz einer Malpighigefäß spezifischen Isoform nachgewiesen werden. Antikörper gegen den in dieser Arbeit exprimierten cytoplasmatischen N-Terminus wurden eingesetzt, um die Untereinheit in der Immunhistochemie sowie in den gebildeten Komplexen der Vernetzungsexperimente nachzuweisen. Die durch Kupfer(II)-chlorid induzierte Vernetzung von Cysteinresten der Untereinheiten des V1Vo-Holoenzyms führte zu der Identifizierung von drei Banden, wobei diese wahrscheinlich aus verschiedenen Subkomplexen der Untereinheiten a, A, B, C, E und G aufgebaut waren. Durch diese Ergebnisse und den Daten aus dem Verdau des V1Vo-Holoenzyms mit Trypsin konnte ein neues Modell der V-ATPase erstellt werden, dass sich erheblich von den bisherigen Modellen unterscheidet, insbesondere in der Lokalisation der Untereinheiten des Stators.
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TRANSLATIONAL REGULATORY MECHANISMS OF THE RAT AND HUMAN MULTIDRUG RESISTANCE PROTEIN 2Zhang, Yuanyuan 01 January 2008 (has links)
Multidrug resistance protein 2 (MRP2) is the second member the C subfamily in the superfamily of adenosine triphosphate (ATP)-binding cassette (ABC) efflux transporters. MRP2 is a critical player for generation of bile acidindependent bile flow and biliary excretion of glutathione, glucuronate and sulfate conjugates of endo- and xenobiotics. Dysfunctional expression of MRP2 is associated with Dubin-Johnson Syndrome.
Pathological and physiological states or xenobiotics change the MRP2 expression level. Under some conditions, expression of the human MRP2 and rat Mrp2 proteins are regulated at the translation level. There are several transcription initiation sites in MRP2/Mrp2 gene. The 5’ untranslated regions (5’UTRs) of MRP2/Mrp2 contains multiple translation start codons. The focus of this study, therefore, was investigation of the translational regulatory mechanisms mediated by the upstream open reading frames (uORF) of MRP2/Mrp2.
Using in vitro translation assays and transient cotransfection assays in HepG2 cells, we showed that the rat uORF1 starting at position -109 (relative to the ATG of Mrp2) and the human uORF2 starting at position -105 (relative to the ATG of MRP2) are two major cis-acting inhibitors of translation among the rat and human multiple uORFs, respectively. Translational regulation mediated by the uORFs in the rat Mrp2 mRNA is a combined effect of the leaky scanning model and the reinitiation model, and also results from interaction of the multiple uORFs. In addition, by Ribonuclease Protection Assays (RPA), we detected multiple transcription initiation sites of MRP2/Mrp2 gene in tissues. We also found that the relative abundance of the rat Mrp2 mRNA isoforms with different 5’UTRs differed in the rat liver, kidney, jejunum, ileum, placenta, and lung. This is the first study on the translational regulatory mechanisms of the MRP2/Mrp2 gene.
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Étude de la traduction IRES-dépendante du VIH-1Gendron, Karine 05 1900 (has links)
Le virus de l’immunodéficience humaine de type 1 (VIH-1) est responsable de la pandémie du SIDA (syndrome de l’immunodéficience acquise). Des souches virales résistantes aux antirétroviraux actuellement utilisés apparaissent rapidement. Il est donc important d’identifier de nouvelles cibles dans le cycle de réplication du VIH-1 pour développer de nouveaux agents contre ce virus. La traduction des protéines de structure et des enzymes du VIH-1 est une étape essentielle du cycle de réplication virale. Ces protéines sont exprimées à partir de l’ARN messager (ARNm) pleine-longueur (ARNmPL) à la fin du cycle de réplication. L’ARNmPL du VIH-1 peut utiliser un mode d’initiation de la traduction coiffe-dépendant, comme la majorité des ARNm cellulaires, mais peut aussi utiliser un mode d’initiation alternatif, car sa région 5’ non-traduite (5’UTR) contient un site interne d’entrée du ribosome (IRES), ce qui lui permet d’initier la traduction suivant un mode IRES-dépendant. L’initiation IRES-dépendante permet à l’ARNmPL d’être traduit quand l’initiation coiffe-dépendante est inhibée. L’activité de l’IRES de la région 5’UTR de l’ARNmPL du VIH-1 (IRES5’UTR) est faible dans des conditions physiologiques, mais est stimulée lorsque la cellule est arrêtée à la transition G2/M du cycle cellulaire, un arrêt qu’induit l’infection par le VIH-1. Une grande portion de l’IRES5’UTR, que nous nommons IRES5’UTRc, est présente dans tous les ARNm viraux et a une activité semblable à celle de l’ IRES5’UTR, ce qui indique que le mode IRES-dépendant peut être utilisé par tous les messagers du VIH-1.
Lors de mes études doctorales, j’ai caractérisé le fonctionnement de l’IRES5’UTR du VIH-1. J’ai transfecté des cellules lymphocytaires Jurkat T, dérivées des cibles naturelles du VIH-1, avec un vecteur dual-luciférase contenant les séquences codantes des luciférases de la Renilla (Rluc) et de la luciole (Fluc) séparées par la région 5’UTR de l’ARNmPL du VIH-1. La traduction de la Rluc est coiffe-dépendante alors que celle de la Fluc dépend de l’IRES5’UTR. J’ai d’abord effectué une analyse mutationnelle et j’ai identifié trois régions qui stimulent l’activité de l’IRES5’UTR et une tige-boucle qui réprime l’activité de cet IRES, que j’ai nommée IRENE (IRES negative element). J’ai montré que l’effet répresseur d’IRENE est aboli lorsque les cellules sont soumises à un stress oxydatif, un type de stress induit lors d’une infection par le VIH-1. Nous proposons que IRENE maintiendrait l’IRES5’UTR dans une conformation peu active dans des conditions physiologiques. On sait que les IRES sont activés par divers facteurs cellulaires, appelés ITAF (IRES trans-acting factors). Nous proposons que l’IRES5’UTR adopterait une conformation active suite à la liaison d’un ITAF exprimé ou relocalisé lors d’un stress oxydatif. Ces travaux ont fait l’objet d’une publication (Gendron et al., 2011, Nucleic Acids Research, 39, 902-912). J’ai ensuite étudié l’effet de la protéine virale Tat sur l’activité de l’IRES5’UTR. En plus de son rôle essentiel dans la transactivation de la transcription des ARNm viraux, Tat stimule leur traduction coiffe-dépendante, en empêchant l’inhibition d’un facteur d’initiation canonique, eIF2, induite par la protéine kinase modulée par l’ARN double-brin (PKR) et en déroulant la structure TAR présente à l’extrémité 5’ de tous les ARNm du VIH-1. Elle affecte aussi l’expression de plusieurs gènes cellulaires. J’ai montré que les isoformes Tat86 et Tat72, mais non Tat101, stimulent l’activité de l’IRES5’UTR. Cet effet est indépendant de PKR et de TAR, mais dépendrait de la conformation de Tat. Nous proposons que Tat activerait un facteur de transcription cellulaire qui déclenche l’expression d’un ITAF de l’IRES5’UTR ou encore qu’elle activerait directement un tel ITAF. J’ai de plus montré que PKR stimule l’activité de l’IRES5’UTR, ce qui est surprenant puisque PKR est une protéine antivirale. Cet effet est indépendant de l’inhibition d’eIF2 par PKR et pourrait résulter de l’activation d’un ITAF. Sachant qu’une portion active de l’IRES5’UTR, IRES5’UTRc, est présente dans tous les ARNm viraux, notre hypothèse est que la stimulation de cet IRES par PKR permettait de traduire l’ARNm de Tat au début du cycle de réplication, ce qui permettrait ensuite la traduction coiffe-dépendante des ARNm du VIH-1, qui est stimulée par Tat. Ces travaux font l’objet d’un manuscrit (Gendron et al., soumis à RNA).
Mes résultats, couplés aux données de la littérature, me conduisent à la conclusion que, à la fin du cycle de réplication du VIH-1, l’activité de l’IRES5’UTR est stimulée par le stress oxydatif, l’arrêt en G2/M et la présence de quantités élevées de Tat, alors que la traduction coiffe-dépendante est compromise. L’initiation IRES-dépendante serait alors indispensable pour que le VIH-1 traduise l’ARNmPL. L’IRES5’UTR constituerait donc une cible très intéressante pour développer des agents anti-VIH. / The human immunodeficiency virus type 1 (HIV-1) is the causative agent of AIDS (acquired immunodeficiency syndrome). Viral strains that are resistant to antiretroviral agents used for the treatment of HIV-1 infected patients rapidly emerge. It is thus important to study the viral replication cycle in order to discover new targets for the development of novel agents against HIV-1. Translation of structural proteins and viral enzymes is a key step of the viral replication cycle. These proteins are translated from the HIV-1 full-length mRNA during late stages of the replication. This mRNA can be translated by a cap-dependent mode which is used by the majority of cellular mRNAs. However, since its 5’ untranslated region (5’UTR) contains an internal ribosome entry site (IRES) that we call IRES5’UTR, it can also be translated by an IRES-dependent mode. The IRES-dependent mode enables the full-length mRNA to be translated when the cap-dependent mode is impaired. The activity of the IRES5’UTR is weak in physiological conditions, but it is stimulated when the cell cycle is arrested at the G2/M transition, an arrest induced by HIV-1 infection. A large portion of this IRES, which we name IRES5’UTRc, is present in all HIV-1 mRNAs and its activity is similar to the activity of the complete IRES, which indicates that the IRES-dependent mode can be used by all HIV-1 mRNAs.
During my doctoral studies, I investigated how the HIV-1 IRES5’UTR functions. I transfected Jurkat T cells, a lymphocytic cell line derived from the natural target cells of HIV-1, with a dual-luciferase reporter containing the coding sequences of the Renilla luciferase (Rluc) and the firefly luciferase (Fluc) separated by the complete 5’UTR of the HIV-1 full-length mRNA. Translation of Rluc is cap-dependent while translation of Fluc depends on HIV-1 IRES5’UTR. First, I performed a mutational analysis and I discovered three regions that stimulate the activity of IRES5’UTR and a stem-loop that represses its activity, which we named IRENE (IRES negative element). I showed that the repression induced by IRENE is relieved when cells are exposed to oxidative stress, a type of stress caused by HIV-1 infection. We propose that IRENE maintains the IRES5’UTR in a weakly active conformation in physiological conditions. It is known that IRESes are activated by cellular factors, called ITAFs (IRES trans-acting factors). We propose that the IRES5’UTR adopts an active conformation triggered by the binding of an ITAF that is expressed or relocalized during oxidative stress. These results generated a publication (Gendron et al. Nucleic Acids Research, 2011, 39, 902-912). I then decided to study the effect of the viral protein Tat on the IRES5’UTR activity. In addition to its essential role in the transcription of HIV-1 mRNAs, Tat stimulates the cap-dependent translation of HIV-1 mRNAs by interfering with the inhibition of a canonical initiation factor, eIF2, induced by the protein kinase modulated by double-stranded RNA (PKR) and by unwinding the TAR structure present at the 5’end of all HIV-1 mRNAs. Tat also affects the expression of several cellular genes. I showed that the Tat86 and Tat72 isoforms, but not Tat101, stimulate the activity of the IRES5’UTR. This effect is independent of PKR and TAR, but appears to be dependent upon the conformation of Tat. We suggest that Tat could activate a transcription factor that controls the expression of an ITAF of the IRES5’UTR or else that Tat could directly activate such an ITAF. I also showed that PKR stimulates the IRES5’UTR activity, which is surprising since PKR is an antiviral protein. This effect is independent of the inhibition of eIF2 by PKR and could result from the activation of an ITAF. Knowing that IRES5’UTRc, an active portion of IRES5’UTR is present in all HIV-1 RNAs, our hypothesis is that the stimulation of the IRES activity by PKR would allow Tat mRNA to be translated in the beginning of the replication cycle. This would subsequently allow the cap-dependent translation of HIV-1 mRNAs to proceed, which is stimulated by Tat. These results generated a manuscript that is submitted for publication to RNA.
Altogether, my results, coupled to data from literature, lead me to conclude that, in the late phases of the replication cycle, the activity of the HIV-1 IRES5’UTR is stimulated by oxidative stress, by the cell cycle arrest in G2/M and by the presence of high amounts of Tat, while cap-dependent translation is impaired. The IRES5’UTR would thus be critical to translate the HIV-1 full-length mRNA. Consequently, the IRES5’UTR would constitute a very interesting target for the development of novel anti-HIV agents.
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