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1.
J Eukaryot Microbiol ; 63(3): 326-39, 2016 05.
Artigo em Inglês | MEDLINE | ID: mdl-26566594

RESUMO

Euglenids are an ancient lineage that may have existed as early as 2 billion years ago. A mere 65 years ago, Melvin Calvin and Andrew A. Benson performed experiments on Euglena gracilis and elucidated the series of reactions by which carbon was fixed and reduced during photosynthesis. However, the evolutionary history of this pathway (Calvin-Benson cycle) in euglenids was more complex than Calvin and Benson could have imagined. The chloroplast present today in euglenophytes arose from a secondary endosymbiosis between a phagotrophic euglenid and a prasinophyte green alga. A long period of evolutionary time existed before this secondary endosymbiotic event took place, which allowed for other endosymbiotic events or gene transfers to occur prior to the establishment of the green chloroplast. This research revealed the evolutionary history of the major enzymes of the Calvin-Benson cycle throughout the euglenid lineage and showed that the majority of genes for Calvin-Benson cycle enzymes shared an ancestry with red algae and/or chromophytes suggesting they may have been transferred to the nucleus prior to the acquisition of the green chloroplast.


Assuntos
Evolução Biológica , Euglênidos/enzimologia , Euglênidos/genética , Fotossíntese/fisiologia , Aldose-Cetose Isomerases/classificação , Aldose-Cetose Isomerases/genética , Aldose-Cetose Isomerases/metabolismo , Teorema de Bayes , Clorófitas/enzimologia , Clorófitas/genética , Clorófitas/fisiologia , Cloroplastos/genética , Enzimas/classificação , Enzimas/genética , Enzimas/metabolismo , Euglênidos/metabolismo , Frutose-Bifosfatase/classificação , Frutose-Bifosfatase/genética , Frutose-Bifosfatase/metabolismo , Transferência Genética Horizontal , Gliceraldeído-3-Fosfato Desidrogenases/classificação , Gliceraldeído-3-Fosfato Desidrogenases/genética , Gliceraldeído-3-Fosfato Desidrogenases/metabolismo , Monoéster Fosfórico Hidrolases/classificação , Monoéster Fosfórico Hidrolases/genética , Monoéster Fosfórico Hidrolases/metabolismo , Fotossíntese/genética , Filogenia , Rodófitas/enzimologia , Simbiose , Triose-Fosfato Isomerase/classificação , Triose-Fosfato Isomerase/genética , Triose-Fosfato Isomerase/metabolismo
2.
BMC Evol Biol ; 14: 25, 2014 Feb 11.
Artigo em Inglês | MEDLINE | ID: mdl-24517416

RESUMO

BACKGROUND: Methionine adenosyltransferase (MAT) is a ubiquitous essential enzyme that, in eukaryotes, occurs in two relatively divergent paralogues: MAT and MATX. MATX has a punctate distribution across the tree of eukaryotes and, except for a few cases, is mutually exclusive with MAT. This phylogenetic pattern could have arisen by either differential loss of old paralogues or the spread of one of these paralogues by horizontal gene transfer. Our aim was to map the distribution of MAT/MATX genes within the Euglenida in order to more comprehensively characterize the evolutionary history of MATX. RESULTS: We generated 26 new sequences from 23 different lineages of euglenids and one prasinophyte alga Pyramimonas parkeae. MATX was present only in photoautotrophic euglenids. The mixotroph Rapaza viridis and the prasinophyte alga Pyramimonas parkeae, which harbors chloroplasts that are most closely related to the chloroplasts in photoautotrophic euglenids, both possessed only the MAT paralogue. We found both the MAT and MATX paralogues in two photoautotrophic species (Phacus orbicularis and Monomorphina pyrum). The significant conflict between eukaryotic phylogenies inferred from MATX and SSU rDNA data represents strong evidence that MATX paralogues have undergone horizontal gene transfer across the tree of eukaryotes. CONCLUSIONS: Our results suggest that MATX entered the euglenid lineage in a single horizontal gene transfer event that took place after the secondary endosymbiotic origin of the euglenid chloroplast. The origin of the MATX paralogue is unclear, and it cannot be excluded that it arose by a gene duplication event before the most recent common ancestor of eukaryotes.


Assuntos
Clorófitas/enzimologia , Euglênidos/enzimologia , Evolução Molecular , Metionina Adenosiltransferase/genética , Proteínas de Protozoários/genética , Clorófitas/genética , Clorófitas/fisiologia , Cloroplastos/genética , Euglênidos/classificação , Euglênidos/genética , Euglênidos/fisiologia , Transferência Genética Horizontal , Dados de Sequência Molecular , Filogenia , Simbiose
3.
J Eukaryot Microbiol ; 55(5): 374-81, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-19017057

RESUMO

S-adenosylmethionine is one of the most important metabolites in living cells and is synthesized in a single reaction catalyzed by methionine adenosyltransferase (MAT). At the sequence and structural level, this enzyme is one of the most conserved proteins known. Here we show that some representatives of three distantly related eukaryotic lineages--dinoflagellates, haptophytes, and euglenids--possess a highly divergent type of MAT, which we call MATX. Even though MATX contains all the sites known to be involved in catalysis and the association of monomers, it also has four insertions throughout the protein that are not observed in other MAT homologs. The phylogenetic distribution and affinities of MATX suggest that it originated in a single eukaryotic lineage and was spread via multiple events of eukaryote-to-eukaryote lateral gene transfer. We suggest a tentative model in which the origin of MATX is connected with the progression of secondary endosymbiosis.


Assuntos
Dinoflagellida/enzimologia , Euglênidos/enzimologia , Eucariotos/enzimologia , Metionina Adenosiltransferase/genética , Sequência de Aminoácidos , Animais , Domínio Catalítico , Dinoflagellida/genética , Euglênidos/genética , Eucariotos/genética , Evolução Molecular , Modelos Biológicos , Dados de Sequência Molecular , Filogenia , Estrutura Terciária de Proteína , Homologia de Sequência de Aminoácidos
4.
J Eukaryot Microbiol ; 55(3): 170-7, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18460154

RESUMO

Two different length cDNAs encoding triosephosphate isomerase (TIM) were identified in the two trophic modes of euglenoids, the phototrophic Euglena gracilis and Euglena intermedia and the saprotrophic Astasia longa. Sequence analyses and presequence prediction indicated that the shorter cDNA encodes a cytosolic TIM and the longer cDNA encodes a plastid TIM (pTIM). The typical presequence of the putative A. longa pTIM and the high sequence similarity between A. longa pTIM and E. gracilis pTIM imply that A. longa pTIM is targeted to plastids. Therefore, although the plastids of A. longa have lost the ability of photosynthesis, they might retain other TIM-related function(s), such as glycolysis and the synthesis of isopentenyl diphosphate or fatty acids. Including the TIM sequences obtained by us from chlorophytes and rhodophytes, our phylogenetic analyses indicated that euglenoid TIMs group neither with TIMs of kinetoplastids, which share the nearest common ancestor with euglenoids, nor are closely related to TIMs of chlorophytes, which are considered to be the donors of euglenoid plastids through secondary endosymbiosis. Instead, they group with TIMs of rhodophytes. In addition, our amino acid sequence alignment and structure modeling showed that TIMs of euglenoids and rhodophytes share a unique 2-aa insertion within their loop-4 areas. Therefore, either tim convergent evolution or lateral gene transfer (more probably) might have occurred between euglenoids and rhodophytes after the divergence of euglenoids with kinetoplastids.


Assuntos
Proteínas de Algas/genética , Euglênidos/enzimologia , Filogenia , Proteínas de Protozoários/genética , Triose-Fosfato Isomerase/genética , Proteínas de Algas/química , Proteínas de Algas/metabolismo , Sequência de Aminoácidos , Animais , Euglênidos/química , Euglênidos/classificação , Euglênidos/genética , Evolução Molecular , Fungos/genética , Dados de Sequência Molecular , Plantas/genética , Proteínas de Protozoários/química , Proteínas de Protozoários/metabolismo , Rodófitas/genética , Alinhamento de Sequência , Triose-Fosfato Isomerase/química , Triose-Fosfato Isomerase/metabolismo
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