Evolutionary view of acyl-CoA diacylglycerol acyltransferase (DGAT), a key enzyme in neutral lipid biosynthesis

被引:163
|
作者
Turchetto-Zolet, Andreia C. [1 ,2 ]
Maraschin, Felipe S. [1 ]
de Morais, Guilherme L. [2 ]
Cagliari, Alexandro [1 ]
Andrade, Claudia M. B. [2 ]
Margis-Pinheiro, Marcia [1 ]
Margis, Rogerio [1 ,2 ,3 ]
机构
[1] Univ Fed Rio Grande do Sul, Dept Genet, Programa Posgrad Genet & Biol Mol, BR-90046900 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Ctr Biotecnol, BR-90046900 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Dept Biofis, BR-90046900 Porto Alegre, RS, Brazil
来源
BMC EVOLUTIONARY BIOLOGY | 2011年 / 11卷
关键词
FATTY-ACID PRODUCTION; MONOACYLGLYCEROL ACYLTRANSFERASE; DEVELOPING SEEDS; WAX-ESTER; TRIACYLGLYCEROL BIOSYNTHESIS; FUNCTIONAL-CHARACTERIZATION; OIL CONTENT; CLONING; GENE; IDENTIFICATION;
D O I
10.1186/1471-2148-11-263
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: 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.
引用
收藏
页数:14
相关论文
共 50 条
  • [41] In vivo efficacy of acyl CoA: Diacylglycerol acyltransferase (DGAT) 1 inhibition in rodent models of postprandial hyperlipidemia
    King, Andrew J.
    Segreti, Jason A.
    Larson, Kelly J.
    Souers, Andrew J.
    Kym, Philip R.
    Reilly, Regina M.
    Collins, Christine A.
    Voorbach, Martin J.
    Zhao, Gang
    Mittelstadt, Scott W.
    Cox, Bryan F.
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 637 (1-3) : 155 - 161
  • [42] Identification and characterization of DGA2, an acyltransferase of the DGAT1 acyl-CoA:diacylglycerol acyltransferase family in the oleaginous yeast Yarrowia lipolytica. New insights into the storage lipid metabolism of oleaginous yeasts
    Athanasios Beopoulos
    Ramdane Haddouche
    Philomene Kabran
    Thierry Dulermo
    Thierry Chardot
    Jean-Marc Nicaud
    Applied Microbiology and Biotechnology, 2012, 93 : 1523 - 1537
  • [43] The microsomal cardiolipin remodeling enzyme acyl-CoA lysocardiolipin acyltransferase is an acyltransferase of multiple anionic lysophospholipids
    Zhao, Yang
    Chen, Yan-Qun
    Li, Shuyu
    Konrad, Robert J.
    Cao, Guoqing
    JOURNAL OF LIPID RESEARCH, 2009, 50 (05) : 945 - 956
  • [44] Overexpression of Two New Acyl-CoA:Diacylglycerol Acyltransferase 2-Like Acyl-CoA:Sterol Acyltransferases Enhanced Squalene Accumulation in Aurantiochytrium limacinum
    Rau, E-Ming
    Bartosova, Zdenka
    Kristiansen, Kare Andre
    Aasen, Inga Marie
    Bruheim, Per
    Ertesvag, Helga
    FRONTIERS IN MICROBIOLOGY, 2022, 13
  • [45] Identification and characterization of DGA2, an acyltransferase of the DGAT1 acyl-CoA:diacylglycerol acyltransferase family in the oleaginous yeast Yarrowia lipolytica. New insights into the storage lipid metabolism of oleaginous yeasts
    Beopoulos, Athanasios
    Haddouche, Ramdane
    Kabran, Philomene
    Dulermo, Thierry
    Chardot, Thierry
    Nicaud, Jean-Marc
    APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2012, 93 (04) : 1523 - 1537
  • [46] Discovery of triazolopyridines as potent and selective acyl-CoA: Diacylglycerol acyltranferase 1 (DGAT1) inhibitors
    Sun, Chongqing
    Huang, Yanting
    Tuerdi, Huji
    Chao, Hannguang
    Peterson, Tara
    Dong, Jessica
    Chu, Ching-Hsuen
    Ma, Zhengping
    Chen, Luping
    Seethala, Ramakrishna
    Harvey, Susan
    Godonis, Helen
    Rooney, Suzanne
    Devenny, James
    Pelleymounter, Maryann
    Cai, Hong
    Fura, Aberra
    Ewing, William
    Poss, Michael
    Cheng, Dong
    Lawrence, R. Michael
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [47] Molecular dynamics simulation studies of human DGAT1 and its substrates, acyl-CoA and diacylglycerol
    Lee, Hwayoung
    Zhou, Ming
    Im, Wonpil
    BIOPHYSICAL JOURNAL, 2022, 121 (03) : 525A - 526A
  • [48] Role of Cysteine Residues in Thiol Modification of Acyl-CoA:Diacylglycerol Acyltransferase 2 from Yeast
    Liu, Qin
    Siloto, Rodrigo M. P.
    Weselake, Randall J.
    BIOCHEMISTRY, 2010, 49 (15) : 3237 - 3245
  • [49] DGAT 1 (Acyl CoA:diacylglycerol acyltransferase 1) catalyzes the formation of many types of retinyl ester in mice
    Burri, Betty Jane
    Neidlinger, Terry Ray
    FASEB JOURNAL, 2007, 21 (05): : A59 - A60
  • [50] Kinetic improvement of an algal diacylglycerol acyltransferase 1 via fusion with an acyl-CoA binding protein
    Xu, Yang
    Caldo, Kristian Mark P.
    Falarz, Lucas
    Jayawardhane, Kethmi
    Chen, Guanqun
    PLANT JOURNAL, 2020, 102 (04): : 856 - 871