Die homodimere Typ IIE Restriktionsendonuklease EcoRII erfordert im Gegensatz zu den orthodoxen Typ II Restriktionsendonukleasen die simultane Wechselwirkung mit zwei Kopien ihrer DNA-Erkennungssequenz 5'CCWGG, um die spezifische endonukleolytisch Spaltung der DNA zu katalysieren. In der vorliegenden Arbeit wurde mittels Transmissionselektronenmikroskopie bewiesen, daß EcoRII die Bildung von DNA-Schlaufen an einem linearen DNA-Substrat mit zwei DNA-Erkennungsorten induziert - ähnlich wie andere DNA prozessierende Enzyme und Transkriptionsfaktoren. Kinetische Untersuchungen der DNA-Spaltreaktion von EcoRII mit superhelikaler Plasmid-DNA, die entweder einen oder zwei DNA-Erkennungsorte für EcoRII enthielt, zeigten, daß EcoRII pro Spaltereignis nur an einem der beiden involvierten doppelsträngigen DNA-Erkennungsorte spaltet. Die Studie, in der EcoRII photochemisch mit den Basen der DNA-Erkennungssequenz vernetzt wurde, ergab ein asymmetrisches Vernetzungsmuster, das durch die partielle Asymmetrie an der A/T-Position der ansonsten palindromischen Erkennungssequenz hervorgerufen wird. Wir konnten zeigen, daß die Aminosäure Tyr41 von EcoRII das 5'C des 5'CCAGG-Stranges der Erkennungssequenz kontaktiert. Durch Aufklärung der Domänenorganisation von EcoRII konnten wir das Modell der EcoRII-DNA-Interaktion verbessern. Wir zeigten, daß für die simultane Interaktion des Enzyms EcoRII mit zwei Kopien der Erkennungssequenz zwei verschiedene Domänen verantwortlich sind. Die C-terminale Domäne ist eine neue Restriktionsendonuklease, die effizienter als das vollständige EcoRII an einzelnen Erkennungsorten spaltet. Die N-terminale Domäne bindet spezifisch an die DNA und reduziert die Aktivität des vollständigen Enzyms, indem sie die Spaltung von einem zweiten Erkennungsort abhängig macht. Daher nehmen wir an, daß EcoRII in der Evolution in Form der N-terminalen Domäne eine zusätzliche DNA-Bindungsfunktion akquiriert hat, um eine neue Proteinfunktion zu entwickeln, die die Spaltung von DNA und die Interaktion mit zwei DNA-Erkennungsorten einschließt. Solche Interaktionen sind z.B. Voraussetzung für die DNA-Rekombination oder Transposition. Daher könnte die gegenwärtige EcoRII Restriktionsendonuklease eine evolutionärer Übergang von ortsspezifischen Endonukleasen zu einem neuen Protein sein, das spezifisch mit zwei DNA-Orten interagiert. / The homodimeric type IIE restriction endonuclease EcoRII requires the cooperative interaction with two copies of the recognition sequence 5'CCWGG for DNA cleavage. This is in contrast to the orthodox type II restriction endonucleases which interact with single recognition sequences. We have proven by transmission electron microscopy that EcoRII simultaneously binds two recognition sites on a linear DNA-substrate by looping out the intervening DNA. This DNA-loop formation is similar to that of other DNA processing enzymes and transcription factors. Kinetic investigations of the DNA cleavage of supercoiled DNA-plasmids containing either one or two recognition sites for EcoRII showed that EcoRII cleaves only at one of the two involved double-stranded DNA recognition sites. Photocross-linking of EcoRII to the bases of the recognition sequence revealed an asymmetric cross-linking pattern. This asymmetry is due to the partial asymmetry of the recognition sequence at the central A/T position. Furthermore, we found that amino acid Tyr41 of EcoRII specifically contacts the 5'C of the 5'CCAGG strand of the recognition sequence. We found by limited proteolysis that a two-domain structure enables EcoRII to interact cooperatively with two recognition sites. The C-terminal domain is a new restriction endonuclease that, in contrast to the complete EcoRII, specifically cleaves at single 5'CCWGG recognition sites. Moreover, this new restriction endonuclease cleaves much more efficiently than EcoRII. The N-terminal domain specifically binds the DNA-substrate and reduces the activity of EcoRII by making the enzyme dependent on a second recognition site. Therefore, we assume that a precursor EcoRII enzyme acquired another DNA binding domain to develop a new protein function that includes DNA cleavage and specific interaction with two DNA sites. The current EcoRII protein could be an evolutionary intermediate between a site-specific endonuclease and a protein that functions specifically with two DNA sites such as DNA recombinases and transposases.

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No description available.

Mémoire numérisé par la Division de la gestion de documents et des archives de l'Université de Montréal

Objectives: The aim of this study was to determine if exposure to volatile organic compounds can lead to DNA damage and impaired DNA repair capacity. Nail cosmetics is a fast growing industry around the world where employees and clients are subjected to various chemical substances which may be harmful to their health: such as formaldehyde, toluene, acetone, xylene, ethylmethacrylate, methylmethacrylate and n–buthyl acetate. These chemicals have the potential to be harmful to their health and exposure to these chemicals should be actively controlled. Formaldehyde is classified as a human carcinogen by the IARC, whereas, toluene and xylene are group three carcinogens, classified in 1999 (not classified as carcinogenic to humans), and various studies have linked DNA damage and impaired DNA repair to the above mentioned substances. Methods: Fifteen nail technicians were monitored by means of personal air sampling, measuring formaldehyde, toluene, xylene, acetone and ethylmethacrylate exposure. Fifteen unexposed subjects were chosen and matched for age and smoking habits with the exposed group. Heparinised blood samples were obtained from each test subject with which the Comet Assay was performed on lymphocytes to determine DNA damage and repair ability. Results: Exposure to ethylmethacrylates and methylmethacrylates leads to DNA damage. Methylmethacrylate causes DNA damage by specifically targeting pyrimidine (fpg) bases. N–buthyl acetate, xylene and acetone exposure impaired DNA repair capacity. The exposed group showed signs of Class III and Class IV DNA damage, whereas the control group had little Class III damage and no indication of Class IV damage. The overall DNA repair ability of the nail technicians was slightly impaired when compared to that of the control group, which is in concurrence with previous studies. Smoking habits and age did not show significant influences on the level of DNA damage and repair when compared with the control group. Conclusion: Exposure to volatile organic compounds such as ethylmethacryale and methylmethacrylate may lead to DNA damage and altered DNA repair in some individuals, although further studies are recommended. / Thesis (M.Sc. (Occupational Hygiene))--North-West University, Potchefstroom Campus, 2011.

Objectives: The aim of this study was to determine if exposure to volatile organic compounds can lead to DNA damage and impaired DNA repair capacity. Nail cosmetics is a fast growing industry around the world where employees and clients are subjected to various chemical substances which may be harmful to their health: such as formaldehyde, toluene, acetone, xylene, ethylmethacrylate, methylmethacrylate and n–buthyl acetate. These chemicals have the potential to be harmful to their health and exposure to these chemicals should be actively controlled. Formaldehyde is classified as a human carcinogen by the IARC, whereas, toluene and xylene are group three carcinogens, classified in 1999 (not classified as carcinogenic to humans), and various studies have linked DNA damage and impaired DNA repair to the above mentioned substances. Methods: Fifteen nail technicians were monitored by means of personal air sampling, measuring formaldehyde, toluene, xylene, acetone and ethylmethacrylate exposure. Fifteen unexposed subjects were chosen and matched for age and smoking habits with the exposed group. Heparinised blood samples were obtained from each test subject with which the Comet Assay was performed on lymphocytes to determine DNA damage and repair ability. Results: Exposure to ethylmethacrylates and methylmethacrylates leads to DNA damage. Methylmethacrylate causes DNA damage by specifically targeting pyrimidine (fpg) bases. N–buthyl acetate, xylene and acetone exposure impaired DNA repair capacity. The exposed group showed signs of Class III and Class IV DNA damage, whereas the control group had little Class III damage and no indication of Class IV damage. The overall DNA repair ability of the nail technicians was slightly impaired when compared to that of the control group, which is in concurrence with previous studies. Smoking habits and age did not show significant influences on the level of DNA damage and repair when compared with the control group. Conclusion: Exposure to volatile organic compounds such as ethylmethacryale and methylmethacrylate may lead to DNA damage and altered DNA repair in some individuals, although further studies are recommended. / Thesis (M.Sc. (Occupational Hygiene))--North-West University, Potchefstroom Campus, 2011.

Les sites apuriniques/apyrimidinique (AP) représentent une forme de dommage à l’ADN hautement mutagène et ce type de dommage peut survenir spontanément ou être induit par une variété d’agents. Afin de préserver la stabilité génomique, deux familles d’endonucléases de type AP, endo-IV et exo-III, sont nécessaires pour contrecarrer les effets mutagènes des sites AP. Malgré l’identification de membres des deux familles dans plusieurs organismes unicellulaire tels que E.coli et S. cerevisiae, aucun membre de la famille endo-IV n’a été identifié chez les organismes multicellulaires à l’exception de C. elegans et de C. briggsae. Nous avons donc décidé d’investiguer l’importance biologique de APN-1 chez C. elegans par l’utilisation d’une approche de knockdown du gène. Dans notre étude, nous avons montré que le knockdown du gène apn-1 chez C. elegans, en utilisant des ARN d’interférence (ARNi), cause une accumulation de mutations spontanées et induites par des drogues résultant en un délai de l’éclosion des œufs ainsi que par une diminution de la survie et de la longévité des vers adultes. De plus, nous avons montré que cette accumulation de mutations mène à un délai dans la progression du cycle cellulaire durant l’embryogénèse, représentant possiblement une explication du délai dans l’éclosion des œufs. Nous avons montré qu’il y avait une augmentation du niveau de mutations dans la gorge des vers, sans toutefois pouvoir confirmer la distribution de APN-1 qui possède une étiquette GFP. Les animaux transgéniques APN-1-GFP n’exprimaient pas suffisamment de la protéine de fusion pour permettre une visualisation à l’aide d’un microscope à fluorescence, mais la protéine a été détectée par immunobuvardage de type western. Les animaux transgéniques APN-1-GFP étaient instables et avaient des phénotypes concordants avec les défauts génétiques. En conclusion, il semble que C. elegans aie évolué afin de retenir un niveau de base de APN-1 jouant ainsi un rôle versatile afin de maintenir l’intégrité génétique d’autant plus que cet organisme semble manquer plusieurs enzymes de la voie de réparation par excision de base. / Apurinic/apyrimidinic (AP) sites are a form of highly mutagenic DNA damage that arise either spontaneously or by a variety of DNA damaging agents. To preserve genomic stability two AP endonuclease families, endo-IV and exo-III, evolved to counteract the mutagenic effect of AP sites. While members of both families were identified in multiple unicellular organisms, notably E. coli and S. cerevisiae, no members of the endo-IV family were identified in multicellular ones, with the exception of C. elegans and its close relatives, particularly C. briggsae. We set out to investigate the biological importance of APN-1 in C. elegans using gene knockdown approach. In our study, we showed that the knockdown of C. elegans apn-1 gene, using RNAi causes the accumulation of spontaneous and drug induced mutations, resulting in a delay in egg hatching, decreased survival and longevity. Furthermore, we have showed that the accumulated mutations lead to delays in cell cycle progression during early embryogenesis, thus providing a possible explanation for the observed delay in hatching. Although we showed increased mutations in the gut of the worm, we were unable to confirm APN-1 distribution tagged with GFP. The transgenic APN-1-GFP animal did not express enough of this fusion protein to be visualized by fluorescent microscopy, although it was detected by Western blot analysis. The transgenic animals over-expressing APN-1-GFP were unstable and showed phenotypes consistent with genetic defects. In conclusion, it would seem that C. elegans has evolved to retain a balanced level of APN-1, which plays a versatile role in maintaining genetic integrity, since this organism lacks a full complement of the enzymes in the base-excision repair pathway.

Les sites apuriniques/apyrimidinique (AP) représentent une forme de dommage à l’ADN hautement mutagène et ce type de dommage peut survenir spontanément ou être induit par une variété d’agents. Afin de préserver la stabilité génomique, deux familles d’endonucléases de type AP, endo-IV et exo-III, sont nécessaires pour contrecarrer les effets mutagènes des sites AP. Malgré l’identification de membres des deux familles dans plusieurs organismes unicellulaire tels que E.coli et S. cerevisiae, aucun membre de la famille endo-IV n’a été identifié chez les organismes multicellulaires à l’exception de C. elegans et de C. briggsae. Nous avons donc décidé d’investiguer l’importance biologique de APN-1 chez C. elegans par l’utilisation d’une approche de knockdown du gène. Dans notre étude, nous avons montré que le knockdown du gène apn-1 chez C. elegans, en utilisant des ARN d’interférence (ARNi), cause une accumulation de mutations spontanées et induites par des drogues résultant en un délai de l’éclosion des œufs ainsi que par une diminution de la survie et de la longévité des vers adultes. De plus, nous avons montré que cette accumulation de mutations mène à un délai dans la progression du cycle cellulaire durant l’embryogénèse, représentant possiblement une explication du délai dans l’éclosion des œufs. Nous avons montré qu’il y avait une augmentation du niveau de mutations dans la gorge des vers, sans toutefois pouvoir confirmer la distribution de APN-1 qui possède une étiquette GFP. Les animaux transgéniques APN-1-GFP n’exprimaient pas suffisamment de la protéine de fusion pour permettre une visualisation à l’aide d’un microscope à fluorescence, mais la protéine a été détectée par immunobuvardage de type western. Les animaux transgéniques APN-1-GFP étaient instables et avaient des phénotypes concordants avec les défauts génétiques. En conclusion, il semble que C. elegans aie évolué afin de retenir un niveau de base de APN-1 jouant ainsi un rôle versatile afin de maintenir l’intégrité génétique d’autant plus que cet organisme semble manquer plusieurs enzymes de la voie de réparation par excision de base. / Apurinic/apyrimidinic (AP) sites are a form of highly mutagenic DNA damage that arise either spontaneously or by a variety of DNA damaging agents. To preserve genomic stability two AP endonuclease families, endo-IV and exo-III, evolved to counteract the mutagenic effect of AP sites. While members of both families were identified in multiple unicellular organisms, notably E. coli and S. cerevisiae, no members of the endo-IV family were identified in multicellular ones, with the exception of C. elegans and its close relatives, particularly C. briggsae. We set out to investigate the biological importance of APN-1 in C. elegans using gene knockdown approach. In our study, we showed that the knockdown of C. elegans apn-1 gene, using RNAi causes the accumulation of spontaneous and drug induced mutations, resulting in a delay in egg hatching, decreased survival and longevity. Furthermore, we have showed that the accumulated mutations lead to delays in cell cycle progression during early embryogenesis, thus providing a possible explanation for the observed delay in hatching. Although we showed increased mutations in the gut of the worm, we were unable to confirm APN-1 distribution tagged with GFP. The transgenic APN-1-GFP animal did not express enough of this fusion protein to be visualized by fluorescent microscopy, although it was detected by Western blot analysis. The transgenic animals over-expressing APN-1-GFP were unstable and showed phenotypes consistent with genetic defects. In conclusion, it would seem that C. elegans has evolved to retain a balanced level of APN-1, which plays a versatile role in maintaining genetic integrity, since this organism lacks a full complement of the enzymes in the base-excision repair pathway.

Ophiostoma novo-ulmi is the causal agent of Dutch elm disease (DED) which has had a severe impact on the urban landscape in Canada. This research program focused on developing molecular genetic strategies to control this pathogenic fungus. The first strategy involved the development of RNA interference (RNAi) for the down-regulation of genes involved in pathogenicity. An efficient RNAi cassette was developed to suppress the expression of the endopolygalacturonase (epg1) locus which encodes a cell-wall degrading enzyme. This epg1-RNAi cassette significantly reduced the amount of polygalacturonase activity in the fungus and resulted in almost complete degradation of epg1 mRNA. The need for a native promoter to selectively down-regulate specific gene loci was addressed by developing a carbon-catabolite regulated promoter (alcA) to drive the expression of the epg1-RNAi cassette. The expression of an alcA-driven epg1-RNAi cassette resulted in the down-regulation of epg expression under glucose starvation but normal levels of expression in high glucose. The expression could therefore be controlled by culture conditions. The second strategy explored the potential of using dsRNA viruses to vector disruptive RNAi cassettes. An isolate of O. novo-ulmi strain 93-1224 collected in the city of Winnipeg, was infected by two dsRNA mitoviruses which upon sequence characterization were named OnuMV1c and OnuMV7. To assess the transmissibility of this dsRNA virus the infected isolate 93-1224 was paired with three naive isolates of the related fungi O. ulmi and O. himal-ulmi. Through the use of nuclear and mitochondrial markers it was determined that the virus OnuMV1c may not rely on mitochondrial fusion for transmission but may have a cytoplasmic transmission route. This investigation of gene expression and manipulation has provided tools to help understand gene regulation in O. novo-ulmi. It has also added to our knowledge of mitoviruses, their transmission and potential use as a biological control. By enhancing our understanding of transmissible hypovirulence this work contributes to efforts to develop a new approach to target DED as well as a potential model for the control of other fungal diseases. / Graduate / 0307 / 0306 / 0369 / jscarneiro@hotmail.com