Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos

Detalhes bibliográficos
Autor(a) principal: Feltrin, Rayana dos Santos
Data de Publicação: 2020
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
Texto Completo: http://repositorio.ufsm.br/handle/1/22076
Resumo: Nucleotide excision repair (NER) is the most versatile DNA repair pathway as it removes different kinds of bulky lesions. Due to its essential role for genome integrity, it appeared early in the evolution of species. However, most published studies are focused on humans, mice, yeast or bacteria. Considering the large amount of information on genome databases, it is currently possible to retrieve sequences from NER components in many organisms. Therefore, we attempted to characterize the potential orthologs of 10 critical components of the human NER pathway in 12 eukaryotic species by using similarity and structural criteria through the use of bioinformatical tools. This approach has allowed us to characterize gene and protein structures comparatively, taking a glance at some evolutionary aspects of the NER pathway. We obtained significant search results for the majority of the proteins in most of the organisms studied, mainly for factors that play a pivotal role in the pathway. However, we revisited significant differences and found new aspects that may imply a distinct functioning of this pathway in different organisms. Through the demonstration of the heterogeneity of the gene structures and a variety in the protein architecture of the NER components evaluated, our results highlight important differences between human NER and evolutionarily distant eukaryotes.
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spelling 2021-08-26T17:58:39Z2021-08-26T17:58:39Z2020-10-21http://repositorio.ufsm.br/handle/1/22076Nucleotide excision repair (NER) is the most versatile DNA repair pathway as it removes different kinds of bulky lesions. Due to its essential role for genome integrity, it appeared early in the evolution of species. However, most published studies are focused on humans, mice, yeast or bacteria. Considering the large amount of information on genome databases, it is currently possible to retrieve sequences from NER components in many organisms. Therefore, we attempted to characterize the potential orthologs of 10 critical components of the human NER pathway in 12 eukaryotic species by using similarity and structural criteria through the use of bioinformatical tools. This approach has allowed us to characterize gene and protein structures comparatively, taking a glance at some evolutionary aspects of the NER pathway. We obtained significant search results for the majority of the proteins in most of the organisms studied, mainly for factors that play a pivotal role in the pathway. However, we revisited significant differences and found new aspects that may imply a distinct functioning of this pathway in different organisms. Through the demonstration of the heterogeneity of the gene structures and a variety in the protein architecture of the NER components evaluated, our results highlight important differences between human NER and evolutionarily distant eukaryotes.A via de reparo por excisão de nucleotídeos (NER) é o mais versátil mecanismo de reparo de DNA, já que está envolvido na remoção de diferentes tipos de lesões que causam grandes distorções na dupla-hélice. Devido à sua grande importância na manutenção da integridade genômica, essa via apareceu cedo na evolução das espécies. Além disso, a maioria dos estudos relacionados ao NER está focada em humanos, camundongos, leveduras e bactérias. Considerando a grande quantidade de dados disponíveis em bancos de dados genômicos, é possível obter sequências de componentes do NER em diferentes organismos. Dessa forma, visamos caracterizar potenciais ortólogos de componentes-chave da via NER em organismos eucarióticos usando diferentes critérios estruturais e de similaridade, através do uso de ferramentas de bioinformática. Essa metodologia nos permitiu caracterizar a estrutura de genes e proteínas de maneira comparativa, bem como esclarecer alguns aspectos evolutivos da via NER. Diante disso, foram obtidos resultados de busca significativos para a maioria das proteínas em grande parte dos organismos analisados, principalmente para aquelas que têm um papel essencial na via. Entretanto, reanalisamos importantes diferenças e encontramos novos aspectos que podem implicar um funcionamento distinto do NER em diferentes organismos. Através da demonstração da heterogeneidade das estruturas gênicas e da variedade na arquitetura das proteínas dessa via, nossos resultados revelam diferenças importantes entre o NER humano e o de eucariotos evolutivamente distantes.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESporUniversidade Federal de Santa MariaCentro de Ciências Naturais e ExatasPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica ToxicológicaUFSMBrasilBioquímicaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessReparo de DNAVia NEREucariotosEstrutura gênicaArquitetura de domíniosDNA repairNER pathwayEukaryotesGene structureDomain architectureCNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICALacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotosOpen gaps in the evolution of the eukaryotic nucleotide excision repairinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisSchuch, André Passagliahttp://lattes.cnpq.br/4932611269622766Segatto, Ana Lúcia AnversaMenck, Carlos Frederico MartinsLoreto, Elgion Lucio da Silvahttp://lattes.cnpq.br/6281810289889181Feltrin, Rayana dos Santos200800000002600600600600600600d93539a4-7b55-44e5-9c20-52601682b4f70d165aaf-468f-4c81-9536-7401f2fcd2ed5ab3e05d-9397-4567-b75b-9751336f662fe9b02cbc-3861-426b-bb43-fb3b5c4151f8ab41f5b8-3dea-4caa-86ab-c37a1044a379reponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALDIS_PPGCBBT_2020_FELTRIN_RAYANA.pdfDIS_PPGCBBT_2020_FELTRIN_RAYANA.pdfDissertaçãoapplication/pdf11732417http://repositorio.ufsm.br/bitstream/1/22076/1/DIS_PPGCBBT_2020_FELTRIN_RAYANA.pdfb5df814977ed41ece327d94ec2cbb286MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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dc.title.por.fl_str_mv Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos
dc.title.alternative.eng.fl_str_mv Open gaps in the evolution of the eukaryotic nucleotide excision repair
title Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos
spellingShingle Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos
Feltrin, Rayana dos Santos
Reparo de DNA
Via NER
Eucariotos
Estrutura gênica
Arquitetura de domínios
DNA repair
NER pathway
Eukaryotes
Gene structure
Domain architecture
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
title_short Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos
title_full Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos
title_fullStr Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos
title_full_unstemmed Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos
title_sort Lacunas na evolução da via de reparo por excisão de nucleotídeos em eucariotos
author Feltrin, Rayana dos Santos
author_facet Feltrin, Rayana dos Santos
author_role author
dc.contributor.advisor1.fl_str_mv Schuch, André Passaglia
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/4932611269622766
dc.contributor.advisor-co1.fl_str_mv Segatto, Ana Lúcia Anversa
dc.contributor.referee1.fl_str_mv Menck, Carlos Frederico Martins
dc.contributor.referee2.fl_str_mv Loreto, Elgion Lucio da Silva
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/6281810289889181
dc.contributor.author.fl_str_mv Feltrin, Rayana dos Santos
contributor_str_mv Schuch, André Passaglia
Segatto, Ana Lúcia Anversa
Menck, Carlos Frederico Martins
Loreto, Elgion Lucio da Silva
dc.subject.por.fl_str_mv Reparo de DNA
Via NER
Eucariotos
Estrutura gênica
Arquitetura de domínios
topic Reparo de DNA
Via NER
Eucariotos
Estrutura gênica
Arquitetura de domínios
DNA repair
NER pathway
Eukaryotes
Gene structure
Domain architecture
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
dc.subject.eng.fl_str_mv DNA repair
NER pathway
Eukaryotes
Gene structure
Domain architecture
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
description Nucleotide excision repair (NER) is the most versatile DNA repair pathway as it removes different kinds of bulky lesions. Due to its essential role for genome integrity, it appeared early in the evolution of species. However, most published studies are focused on humans, mice, yeast or bacteria. Considering the large amount of information on genome databases, it is currently possible to retrieve sequences from NER components in many organisms. Therefore, we attempted to characterize the potential orthologs of 10 critical components of the human NER pathway in 12 eukaryotic species by using similarity and structural criteria through the use of bioinformatical tools. This approach has allowed us to characterize gene and protein structures comparatively, taking a glance at some evolutionary aspects of the NER pathway. We obtained significant search results for the majority of the proteins in most of the organisms studied, mainly for factors that play a pivotal role in the pathway. However, we revisited significant differences and found new aspects that may imply a distinct functioning of this pathway in different organisms. Through the demonstration of the heterogeneity of the gene structures and a variety in the protein architecture of the NER components evaluated, our results highlight important differences between human NER and evolutionarily distant eukaryotes.
publishDate 2020
dc.date.issued.fl_str_mv 2020-10-21
dc.date.accessioned.fl_str_mv 2021-08-26T17:58:39Z
dc.date.available.fl_str_mv 2021-08-26T17:58:39Z
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url http://repositorio.ufsm.br/handle/1/22076
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Centro de Ciências Naturais e Exatas
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dc.publisher.department.fl_str_mv Bioquímica
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
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