Doutorado em Genética e Biologia Molecular (ICB)
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Item Aplicações toxicogenômicas em cultura de células expostas a nanomateriais e populações humanas expostas a pesticidas(Universidade Federal de Goiás, 2017-09-04) Franco, Fernanda Craveiro; Silva, Daniela de Melo e; http://buscacv.cnpq.br/buscacv/#/espelho?nro_id_cnpq_cp_s=9895211901348365; Parise, Michelle Rocha; Silva, Claudio Carlos da; Vieira, Thais Cidália; Costa, Emília Oliveira Alves; Silva, Daniela de Melo eThe interaction of some compounds and DNA molecule can cause genotoxic changes. The tests used to evaluate genotoxicity have evolved over the years, and they have great efficiency. Currently, several traditional methodologies are used, such as the comet assay, and some more modern, based on molecular biology. Considering the importance of detecting the effects caused by exposure to potentially genotoxic agents, this thesis presents three chapters with different approaches to this topic. The first chapter aimed at evaluating published studies on the mutagenic, genotoxic and oxidative effects caused by occupational exposure to pesticides. For this, a systematic review of articles published between the years of 2011 and 2015 was carried out, focusing on these exposure conditions. The results showed that 44% of the studies addressed only men and 44% approached men and women, and 78% used rural workers as an exposed population. The most evaluated class of pesticide was organophosphorus. The studies were separated by methodologies of analysis used and all showed some type of alteration in the populations occupationally exposed to pesticides. The second chapter, published in the journal Environmental Science and Pollution Research, considered the dengue scene in the state of Goias and techniques of mosquitoes control, and sought to understand the genotoxic effects caused by exposure of endemic agents to pesticides used against Aedes aegypti, being the first study published with this group of workers. The main pesticides used were insecticides and larvicides and an increase in DNA damage was observed in the exposed population, without influence of the lifestyle factors. In the whole transcriptome assay the differential expression of genes related to various chronic diseases was observed. Finally, the third chapter was carried out in collaboration with the Institute of Experimental Medicine of the Czech Academy of Sciences, aiming the determination of cytotoxic and genotoxic effects caused by in vitro exposure to different types of metallic nanomaterials. In nanomaterials that showed cell viability reduction (cytotoxic), an increase in genotoxicity was also identified. In addition, three of the four non-cytotoxic nanomaterials evaluated showed genotoxic effects. Studies aimed at detecting the compounds genotoxic potential are extremely important for the regulatory definition and identification of risks caused by exposure. In this study, the toxicological and genotoxic effects of different compounds and mixtures were evaluated using traditional and modern techniques, in vitro or by human biomonitoring, seeking to understand and determine the risks involved in exposure to these substances.Item A história evolutiva de uma perereca Sul-Americana Scinax squalirostris (Lutz, 1925) (Anura, Hylidae): um resgate do passado e consequências futuras(Universidade Federal de Goiás, 2018-10-31) Jardim, Tatianne Piza Ferrari Abreu; Maciel, Natan Medeiros; http://lattes.cnpq.br/2116561844584292; Collevatti, Rosane Garcia; http://lattes.cnpq.br/9979596352166630; Maciel, Natan Medeiros; Silva, Daniela de Melo e; Lima, Natácia Evangelista de; Lima, Luciana Signorelli Faria; Machado, Iberê FarinaGeological events of the Neogene and the climatic fluctuations of the Quaternary played an important role in shaping the landscape and climate of South America therefore directly influencing the evolutionary history of the organisms of this area over the last million years. These changes led to the alternation between warm and humid, cold and dry periods. Such alternation dictated the dynamics of retraction and expansion of open and forest landscapes. Species associated to these environments evolved following this dynamic, which lead to alteration in genetic conformation, lineage differentiation and even speciation. As in the past, future changes inclimate can modify the landscape causing changes in the geographical distribution of species. In addition, predicted global warming may lead to a decline in genetic diversity as well as lead to extinction due to species' low ability to adapt to drastic and quick changes. In this thesis two regions of mitochondrial DNA (Cytb and 12S) and one nuclear (RAG-1) were used together with coalescing simulations, and ecological niche modelling to access the evolutionary history of a Scinax squalirostris (Lutz, 1925), a species associated to the South American grasslands. In the first chapter, we sought to understand how Neogene and Quaternary geological or climatic events, respectively, may have shaped the current disjunct distribution and the genetic diversity pattern of S. squalirostris. The populations of S. squalirostris were found to have high genetic diversity, with no sign of current gene flow, a high genetic differentiation, and a stable demographic history over time with scattered origin in southern Brazil. Coalescence events date from Pliocene-Pleistocene, with haplotype sharing among geographically distant populations, which indicates incomplete lineage sorting. The paleodistribution models suggests that S. squalirostris lineages were widely distributed during the last glacial maximum (LGM) but afterwards contracting and changing their area of occurrence. These results indicate that the current geographic distribution and genetic diversity of S. squalirostris is due to the contraction of an area widely distributed in the past, generated by the dynamics of retraction of grasslands in warmer periods due to the loss of areas suitable for their occurrence. In the second chapter, we tested the hypothesis that the current populations of S. squalirostris could represent distinct lineages with candidate species not previously described, due to the current disjunct distribution. Using molecular and morphometric data the formation of two groups was rescued. One of them consists in a candidate species to be described, which is a lineage restricted to the Central-West region of Brazil. The other one comprises of populations from the South and Southeast Brazil, Paraguay, Uruguay and Argentina. In the third chapter, ecological niche modelling, molecular techniques and simulations of genetic groups were used to verify how future climate changes could alter the genetic diversity and distribution of S. squalirostris. Through two climatic scenarios with different temperature changes to 2100 (scenario 4.5 RCP increases 1.8 ° C and stabilizes, and scenario 8.5 increases 3.7 ° C and continues to increase), ecological niche modelling analysis indicated a decrease of suitable areas in the Central-West and Southeast regions, with a displacement towards the South of Brazil entering the central region of Argentina towards more anthropized areas. Most of the Central West and Northern Southeast populations may be extinct due to the absence of climatic suitable areas for their occurrence and low genetic diversity. In addition, it was observed that Protections Areas (PAs) currently harbors a large part of the genetic diversity of S. squalirostris. Thus, PAs in areas that will be ideal for the occurrence of S. squalirostris will be able to maintain their high levels of genetic diversity, but with losses of genetic diversity in the Midwest and Southeast regions. This work indicates that future climate changes will negatively affect this species, since the appropriate areas for its occurrence will be reduced and displaced. The loss and changes in genetic clusters may lead to a possible loss of the evolutionary potential of S. squalirostris populations in responding to future climate changes, which could result in the extinction of some populations.Item Avaliação do dano ao DNA pelo ensaio cometa e análise dos pontos de variação dos genes CYP2E1, CYP1A1 e OGG1 em etilistas do município de Goiânia-GO(Universidade Federal de Goiás, 2018-05-28) Lopes, Mariana Paiva; Silva, Daniela de Melo e; http://lattes.cnpq.br/9895211901348365; Silva, Daniela de Melo e; http://lattes.cnpq.br/9895211901348365; Parise, Michelle Rocha; Nunes, Hugo Freire; Costa, Emília Oliveira Alves; Avelar, Juliana BoaventuraEthanol is considered the most consumed drug in the world, is part of several cultures. However, chronic ethanol consumption has become a social and public health problem, since it has serious health consequences and is a risk factor for several diseases and mortality. The CYP2E1 gene encodes an enzyme that is the main constituent of the microsomal oxidation system of ethanol. The CYP1A1 gene encodes an enzyme that, like CYP2E1, acts on the oxidative biotransformation of phase I substrates of the metabolism of xenobiotics such as ethanol. In addition, genes related to DNA repair such as OGG1 are also of great importance as they are involved in protecting the genome by helping to maintain the cellular functions of organisms. Problems in the repair process can interfere with aging and promote disease development. Genetic variations in these genes result in significant differences in enzyme activity. However, there is still no clear correlation between the functional significance of these variations in both ethanol metabolism and ethylene repair. In the present study, the variability of specific regions of the CYP2E1, CYP1A1 and OGG1 genes were analyzed in samples of alcoholics from a Psychosocial Care Center (CAPS) of the State of Goiás, in the city of Goiânia, and the results were compared with the data obtained by the 1000Genomas project. A study of the association between the polymorphism of these genes and the damage to the DNA in ethanol was carried out. Sequencing reactions and the comet assay were performed. There was no relation between the data of the polymorphism found with DNA damage. However, in the analysis of the DNA damage between the case and control groups, greater damage was observed in the alcoholics in relation to the control group. The genotypic frequencies adhered to that expected by the HardyWeinberg Equilibrium for all the polymorphism in the Brazilian samples. Based on the polymorphism of the CYP2E1 gene, 15 haplotypes were inferred. Of these, only 4 haplotypes were common in all populations. While based on the two polymorphism of the CYP1A1 and OGG1 genes, 3 haplotypes were inferred for each gene, all present in the Brazilian study population.Item Metabolismo do acetato entre membros do gênero paracoccidioides spp(Universidade Federal de Goiás, 2017-04-13) Mata, Fabiana Ribeiro da; Soares, Célia Maria de Almeida; http://lattes.cnpq.br/8539946335852637; Soares, Célia Maria de Almeida; Ricart, Carlos André Ornelas; Ulhoa, Cirano José; Bailão, Alexandre Melo; Brito, Wesley de AlmeidaMembers of the genus Paracoccidioides are known pathogens of humans that can be isolated from different infection sites. To investigate the expression rates of proteins expressed by different isolates, of the genus Paracoccidioides, including one isolate of P. lutzii (Pb01), and three isolates of P. brasiliensis (Pb03, Pb339 and PbEPM83) using sodium acetate, as carbon source, proteins quantities were determined using label-free and data independent LC-MSE. Statistical analysis provided the comparison of proteins profiles in the isolates. A total of 1160, 1211, 1280 and 1462 proteins were reproducibly identified, and relatively quantified in P. lutzii e P. brasiliensis isolates Pb03, Pb339 e PbEPM83, respectively. Notably, a total of 526, 435, 744 and 747 proteins were differentially expressed among P. lutzii and the P. brasiliensis isolates Pb03, Pb339 and PbEPM83, respectively with a fold change equal or higher than 1.5. The analysis revealed the reorganization of metabolism through the induction of proteins related to gluconeogenesis, stress response and amino acid degradation in the four isolates evaluated. The differences between the isolates were observed as follows: greater increases in the expression levels of proteins belonging to the cycle of glyoxalate, TCA and respiratory chain, ethanol production and β-oxidation were observed in the isolatesPPEPM83 and Pb01; Cyclic and cyclocyclic proteins of the methylcitrate were induced in Pb339. Proteomic profiles indicate that the four isolates reorganize the metabolism for the use of acetate as a carbon source.Item Avaliação de polimorfismos nos genes de reparo e detoxificação e a associação com o dano no DNA em etilistas(Universidade Federal de Goiás, 2017-07-06) Melo, Caroline Oliveira de Araújo; Silva, Daniela de Melo e; http://lattes.cnpq.br/9895211901348365; Parise, Michelle Rocha; Rodrigues, Flávia Melo; Avelar, Juliana Boaventura; Costa, Emília Oliveira AlvesAlcohol abuse is related to approximately 3.3 million annual deaths worldwide and is considered the first risk factor for the global burden of disease in countries of the Americas. Long-term abuse of alcohol induces numerous molecular and biochemical changes in alcohol-related tissues. It is believed that the toxic effects of alcohol are mediated by DNA damage by several mechanisms, such as by the induction of oxidative damage, DNA adducts, crosslinks and DNA strand breaks. In this sense, the aim of this study was to verify the frequency of polymorphisms in the repair and detoxification genes and the association with the DNA damage in alcoholics. The analysis of the obtained results showed a greater genotoxic damage in the alcoholics, when carrying out the Comet Assay. A point of variation was found in the GSTP1 gene and another point of variation in the XRCC1 gene. However, no statistically significant differences were observed between GSTM1 and GSTT1 genotypes and genetic damage. In this context, it can be concluded that the Comet Assay is a very effective and inexpensive method for the analysis of genotoxic damage.Item Análise de celulases e xilanases por fungo isolado a partir do bioma cerrado(Universidade Federal de Goiás, 2013-05-06) Pereira, Douglas Endrigo Perez; Faria, Fabrícia Paula de; Bataus, Luiz Artur Mendes; http://lattes.cnpq.br/5637230378599476; Bataus, Luiz Artur Mendes; Faria, Fabrícia Paula de; Jesuíno, Rosália Santos Amorim; Fonseca, Marcio José PoçasLignocellulosic biomass is constituted by cellulose, hemicellulose and lignin in the plant cell walls. The conversion of lignocellulose to fermentable sugars mainly depends on the action of a complex of enzymes that hydrolyze cellulose and hemicellulose. This study was to analyze the production of cellulases and xylanases by fungi isolated from soil and decaying material in Cerrado. Initially, the fungi were analyzed for cellulase production capacity among the fungal cellulase-producing fungus capable of producing the highest levels of cellulase was selected for the experiments of xylanase and cellulase production by submerged fermentation and biochemical analysis of the enzyme secreted. Among the isolated fungi, fungus called IFBMD01 was that higher activity of cellulase in the supernatant when cultivated with wheat bran as carbon source. This was identified as Aspergillus cf niger. The enzymes studied with their respective results were: FPase with better production time of 7 days, showing activity of 0.10 U / mL, optimum pH 5.5, optimum temperature of 60 ° C; CMCase with better time production 6 days, showing activity of 8.19 U / mL, pH optimum of 5, optimum temperature of 70 º C; Avicelase with better production time of 9 days, showing activity of 0.01 U / mL, pH optimum of 5.5 and optimum temperature of 60 ° C; xylanase, with better production time 3 days, showing activity of 35.5 U / mL, and the optimum pH of 5 and the optimum temperature of 50 ° C, the β-Glycosidase, with higher production on the sixth day showing activity of 0.98 U / mL, with the optimum pH 5 and optimum temperature of 60 ° C. The activity of β-glucosidase showing in the culture supernatant was influenced by the ions Mn2 +, NH4, K +, Mg2 +, Ca2 +, Ba2 +, Al3 +, Na +, and Co2+, as well as EDTA, glucose, xylose and cellobiose. In the culture supernatant of the fungus A. niger IFBMD01 grown on FT for 3 and 6 days protein bands were visualized with activity against xylan and CMC molecular weight be 30 to be 66 kDa.Item Investigações genéticas em doenças raras: uma contribuição positiva das tecnologias genômicas(Universidade Federal de Goiás, 2017-08-09) Reis, Fabiana Gonçalves dos; Cruz, Aparecido Divino da; http://lattes.cnpq.br/7868817504129985; Silva, Daniela de Melo e; http://lattes.cnpq.br/9895211901348365; Silva, Daniela de Melo e; Minasi, Lysa Bernardes; Gigonzac, Thaís Cidália Vieira; Paccez, Juliano Domiraci; Costa, Emília Oliveira AlvesNeurological disorders are a group of conditions that manifest early in the development of the child, so that delayed neuropsychomotor development (ADNPM) and intellectual disability (ID) can impair cognitive, language, motor and social behavior. The etiology of ID is quite heterogeneous and prenatal, perinatal and postnatal factors are associated with an increased risk of this deficiency. However, 30 to 50% of the cases remain with the unknown etiology. In this context, the main objective of this study was to identify submicroscopic genomic alterations (<5Mb) by means of microarray chromosomal analysis (CMA) in patients with clinical indication of ADNPM and/or ID, sent by attending physicians of the state public health network of Goiás. We analyzed 149 cases of both sexes. Of the total number of patients, 47 had the diagnosis clarified using cytogenetics by G banding. Of 102 patients with an incomplete diagnosis, 72 agreed to participate in the present study and, therefore, performed the CMA. The elucidation of the diagnosis by CMA was possible in 22 patients. Among the results obtained, three rare cases were selected to compose this thesis. The first case is from a patient in whom a de novo microduplication of 0.45 Mb in the 5q35.2q35.3 region containing the NSD1 gene was identified. The effect of the dosing of this gene has been related to Sotos Syndrome and its inverted phenotype. The second case shows the molecular detection of an absent allele on the X chromosome and the presence of 28 CGG repeats in FMR1 gene in the present allele. The CMA showed that the patient had a de novo microdeletion of 4.176 Mb in the Xq27.3-q28 region that affected 34 genes, including five genes (TMEM185A, TMEM257, FMR1, IDS, and FMR2) that were directly correlated with ID phenotypes and neurological disorders. The third case is a de novo microdeletion of 1.59 Mb in the 1p32.3 region involving the DHCR24 gene, which causes a gene dosage effect influencing the activation of enzymes that cause desmosterolosis, which is a desmosterol conversion disorder in cholesterol. Thus, the results of this thesis showed the relevance of the use of the CMA technology to diagnose patients with clinical signs of ADNPM and/or ID that presented karyotype without alterations, evidencing the importance of this technology for public health.Item Tamanho, montagem de novo e anotação do genoma de Dipteryx alata (Leguminosae)(Universidade Federal de Goiás, 2017-04-24) Taquary, Adriana Maria Antunes; Telles, Mariana Pires de Campos; http://lattes.cnpq.br/4648436798023532; Telles, Mariana Pires de Campos; http://lattes.cnpq.br/4648436798023532; Borba, Tereza; Almeida, Luciane; Novaes, Evandro; Soares, Thannya NascimentoIn recent years there has been a rapid increase in the availability and quality of sequencing data and with this an explosion of projects of sequencing of the genomes of plants occurred. In this scenario, genomic analyzes have been characterized as efficient to generate genetic information on a large scale, including for non-model species. Dipteryx alata is a non-model tree species endemic to the Cerrado biome belonging to the Leguminosae family. The objectives of this work were to estimate the number of chromosomes and the size of the genome of D. alata, and also assemble and annotate sequences of the genomes organelles and nuclear of the species using Illumina sequencing data. The size of the genome of D. alata was estimated as 1C = 0.825 pg, which corresponds to a haploid genome of 807.2 MB with 2n = 16 chromosomes. Were assembled 275,709 nuclear genomic sequences with N50 equal to 1598, which corresponds to 355MB and 44% of the whole genome. In the nuclear sequences, 21,981 microsatellite regions were annotated, of which 49.3% had dinucleotide motifs, 42.7% trinucleotide motifs and 4% tetranucleotide motifs. Transposable elements (TEs) were found in 39.29% of the sequences analyzed, corresponding to 421,701 TEs. LTR retrotransposons (gypsy and copy) were the most abundant TEs in nuclear sequences. Were annotated 1,431 RNA genes non-translated into proteins, being 176 rRNAs, 189 tRNAs, 477 snRNAs, 8 snoRNAs, 466 miRNAs and 115 lncRNAs. Were annotated also 62,200 protein coding genes with an average size of 1,156 bp. The estimated number of mRNAs transcribed by the set of annotated nuclear genes was 160,450, of which 131,228 showed significant similarity with known sequences and 84,793 were classified functionally in the Gene Ontology terms. A total of 736,787 SNPs and 90,803 InDels were discovered in the nuclear sequences. A mean of 1 SNP was identified for each 189 bp of the genome and the ratio between the transition (Ts) and transversion (Tv) mutations was 1.58. A percentage of 46.5% of the SNPs occurs in the genic context and the effects of the SNPs were annotated mainly in exons and intergenic regions. Were assembled 110 KB of chloroplastid sequences with N50 of 2,384 bp and 327 KB of mitochondrial sequences with N50 of 1,784 bp. Were annotated genes of 3 rRNA, 13 tRNA, 6 miRNA and 20 lncRNA for the chloroplast and genes of 4 rRNA, 26 tRNA, 7 miRNA and 54 lncRNA for the mitochondria. For the chloroplast were predicted 20 protein coding genes with a mean size of 2,374 bp and for mitochondria were predicted 176 genes with a mean size of 1,279 bp. The estimated number of mRNAs transcribed by this gene set was 63 and 525 for chloroplast and mitochondria respectively. Were annotated 39 microsatellite regions and 4 TEs in the chloroplastid sequences and 158 microsatellite regions and 26 TEs in the mitochondrial sequences. This work, which can be considered one of the first genomic studies for Cerrado species, represents a great advance in the knowledge on the structure and organization of the D. alata genome. The obtained results open the way for further genetic and genomic investigation for the species.Item Filogeografia e história demográfica de tabebuia serratifolia e tabebuia ochracea (bignoniaceae), duas espécies arbóreas neotropicais(Universidade Federal de Goiás, 2015-12-09) Vitorino, Luciana Cristina; Collevatti, Rosane Garcia; http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4784443D2There is strong evidence that the Neotropical vegetation has been influenced by climate changes at the end of the Tertiary and Quaternary. The response of vegetation to the cold weather and dry these periods, consistent with the occurrence of the last glacial maximum, still remains in debate. It is suggested that the areas currently occupied by the Cerrado and seasonal forests (SDTFs) are remnants of a continuous vegetation that existed in the past. From the perspective of that species widely distributed in savannas and Brazilian SDTFs could help unravel the role of climate change Pleistocene on the current distribution pattern of genetic diversity in these vegetation types, we sampled 17 populations of Tabebuia serratifolia in SDTFs and 24 populations Tabebuia ochracea in savannas and sequenced intergenic non-coding regions of chloroplast (psbA-trnH, trnG-trnS e trnC-ycf6) as well as the nuclear region ITS (nrDNA). Later, we used coalescent analysis, Ecological Niche Modeling techniques (ENM) and simulations of demographic hypothesis for these species in an attempt to broaden the understanding of the changes undergone by neotropical landscape during the last ice age cycles. The sampled populations for both species showed high genetic diversity for both markers (hcpDNA = 0.8731 and hnrDNA = 0.7723 - T. serratifolia and hcpDNA = 0.927 and hnrDNA = 0.637 - T. ochracea), and large structure (Fst(cpDNA) = 0.528, P < 0.001 and Fst(ITS) = 0.742, P < 0.001 - T. serratifolia and Fst(cpDNA) = 0.742, P < 0.001 and Fst(ITS) = 0.544, P < 0.001 - T. ochracea). The coalescing analysis showed the time to the most recent common ancestor between haplotypes of the sampled populations, oldest to T. serratifolia (~ 3.4 Ma - 95% CI 1.9 - 6.8), which for T. ochracea (~ 1.9 Ma - 95% CI 0.1 - 2.3). The two species show standard recent population expansion and the niche modeling revealed for the T. serratifolia a higher potential distribution area during Holoceno medium while for T. ochracea the highest suitability area was predicted for maximum glacial last (LGM - 21ka), going in favor the hypothesis that the savannas and STDFs have submitted in the past, a wider distribution than currently known.