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dc.contributor.authorZolet, Andreia Carina Turchettopt_BR
dc.contributor.authorMaraschin, Felipe dos Santospt_BR
dc.contributor.authorMorais, Guilherme Loss dept_BR
dc.contributor.authorCagliari, Alexandropt_BR
dc.contributor.authorAndrade, Claudia Marlise Balbinottipt_BR
dc.contributor.authorMargis-Pinheiro, Márciapt_BR
dc.contributor.authorMargis, Rogeriopt_BR
dc.date.accessioned2015-02-11T02:18:09Zpt_BR
dc.date.issued2011pt_BR
dc.identifier.issn1471-2148pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/109967pt_BR
dc.description.abstractBackground: Triacylglycerides (TAGs) are a class of neutral lipids that represent the most important storage form of energy for eukaryotic cells. DGAT (acyl-CoA: diacylglycerol acyltransferase; EC 2.3.1.20) is a transmembrane enzyme that acts in the final and committed step of TAG synthesis, and it has been proposed to be the rate-limiting enzyme in plant storage lipid accumulation. In fact, two different enzymes identified in several eukaryotic species, DGAT1 and DGAT2, are the main enzymes responsible for TAG synthesis. These enzymes do not share high DNA or protein sequence similarities, and it has been suggested that they play non-redundant roles in different tissues and in some species in TAG synthesis. Despite a number of previous studies on the DGAT1 and DGAT2 genes, which have emphasized their importance as potential obesity treatment targets to increase triacylglycerol accumulation, little is known about their evolutionary timeline in eukaryotes. The goal of this study was to examine the evolutionary relationship of the DGAT1 and DGAT2 genes across eukaryotic organisms in order to infer their origin. Results: We have conducted a broad survey of fully sequenced genomes, including representatives of Amoebozoa, yeasts, fungi, algae, musses, plants, vertebrate and invertebrate species, for the presence of DGAT1 and DGAT2 gene homologs. We found that the DGAT1 and DGAT2 genes are nearly ubiquitous in eukaryotes and are readily identifiable in all the major eukaryotic groups and genomes examined. Phylogenetic analyses of the DGAT1 and DGAT2 amino acid sequences revealed evolutionary partitioning of the DGAT protein family into two major DGAT1 and DGAT2 clades. Protein secondary structure and hydrophobic-transmembrane analysis also showed differences between these enzymes. The analysis also revealed that the MGAT2 and AWAT genes may have arisen from DGAT2 duplication events. Conclusions: In this study, we identified several DGAT1 and DGAT2 homologs in eukaryote taxa. Overall, the data show that DGAT1 and DGAT2 are present in most eukaryotic organisms and belong to two different gene families. The phylogenetic and evolutionary analyses revealed that DGAT1 and DGAT2 evolved separately, with functional convergence, despite their wide molecular and structural divergence.en
dc.format.mimetypeapplication/pdf
dc.language.isoengpt_BR
dc.relation.ispartofBMC Evolutionary Biology. London. Vol. 11 (Sept. 2011), [art.] 263pt_BR
dc.rightsOpen Accessen
dc.subjectFilogenéticapt_BR
dc.subjectTriglicerídeospt_BR
dc.subjectEnzimaspt_BR
dc.titleEvolutionary view of acyl-CoA diacylglycerol acyltransferase (DGAT), a key enzyme in neutral lipid biosynthesispt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000827074pt_BR
dc.type.originEstrangeiropt_BR


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