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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Acetyl-CoA acyltransferase 2

mitochondrial 3-oxoacyl-CoA thiolase, ACAA2, Acetyl-Coenzyme A acyltransferase 2
mitochondrial matrix protein with acetyl-Coenzyme A acyltransferase 2 activity [RGD, Feb 2006] (from NCBI)
Top mentioned proteins: ACID, PPAR, HAD, Lipoprotein Lipase, V1a
Papers on mitochondrial 3-oxoacyl-CoA thiolase
Influence of Delipation on the Energy Metabolism in Pig Parthenogenetically Activated Embryos.
Li et al., Nanjing, China. In Reprod Domest Anim, Oct 2015
This study was designed not only to measure the effect of delipation on the developmental viability of pig parthenogenetically activated (PA) embryos, but also to evaluate the changes of mitochondria DNA (mtDNA), reactive oxygen species (ROS) level, adenosine triphosphate (ATP) content and gene (Acsl3, Acadsb, Acaa2, Glut1) expression level at different stages after delipation.
Dimethylsulfoxide and conjugated linoleic acids affect bovine embryo development in vitro.
Wrenzycki et al., Hannover, Germany. In Reprod Fertil Dev, 2013
Messenger RNA analysis of target gene transcripts (IGF1R, IGFBP2, IGFBP4, CPT2, ACAA1, ACAA2, FASN, SCD) via RT-qPCR was performed in single blastocysts.
Mechanisms of nanosized titanium dioxide-induced testicular oxidative stress and apoptosis in male mice.
Hong et al., Suzhou, China. In Part Fibre Toxicol, 2013
Furthermore, exposure to TiO₂ NPs resulted in the up-regulation of caspase-3, Nrbp2, and cytochrome c expression, and caused down-regulation of SOD, CAT, GPx, GST, GR, Cyp1b1, Car3, Bcl-2, Acaa2, and Axud1 expression in mouse testis.
An approach to identify SNPs in the gene encoding acetyl-CoA acetyltransferase-2 (ACAT-2) and their proposed role in metabolic processes in pig.
Jeong et al., Cheju, South Korea. In Plos One, 2013
Its comprehensive relative expression, in silico non-synonymous single nucleotide polymorphism (nsSNP) analysis, as well as its annotation in terms of metabolic process with another protein from the same family, namely, acetyl-CoA acyltransferase-2 (ACAA2) was performed in Sus scrofa.
Polymorphisms in genes involved in fatty acid β-oxidation interact with dietary fat intakes to modulate the plasma TG response to a fish oil supplementation.
Vohl et al., Québec, Canada. In Nutrients, 2013
SNPs within RXRA, CPT1A, ACADVL, ACAA2, ABCD2, ACOX1 and ACAA1 genes were genotyped using TAQMAN methodology.
Regulation of fatty acid oxidation in mouse cumulus-oocyte complexes during maturation and modulation by PPAR agonists.
Robker et al., Adelaide, Australia. In Plos One, 2013
Rosiglitazone restored Acsl1, Cpt1b and Acaa2 levels in cumulus-oocyte complexes and increased oocyte mitochondrial membrane potential yet resulted in significantly fewer embryos reaching the morula and hatching blastocyst stages.
HIV-1 Vpr enhances PPARβ/δ-mediated transcription, increases PDK4 expression, and reduces PDC activity.
Kopp et al., Bethesda, United States. In Mol Endocrinol, 2013
Vpr induced a 1.3-fold increase in mRNA expression of both carnitine palmitoyltransferase I (CPT1) and acetyl-coenzyme A acyltransferase 2 (ACAA2) and doubled the activity of β-hydroxylacyl coenzyme A dehydrogenase (HADH).
[Research on differentially expressed genes related to substance and energy metabolism between healthy volunteers and splenasthenic syndrome patients with chronic superficial gastritis].
Ying-Fang et al., Guangzhou, China. In Zhongguo Zhong Xi Yi Jie He Za Zhi, 2013
Differentially expressed genes related to lipid metabolism included ACAA2 and CYP20A1, manifested as fatty acid catabolism and cholesterol transformation.
A single nucleotide polymorphism in the acetyl-coenzyme A acyltransferase 2 (ACAA2) gene is associated with milk yield in Chios sheep.
Miltiadou et al., Limassol, Cyprus. In J Dairy Sci, 2012
The objective of this work was to identify single nucleotide polymorphisms (SNP) in the ovine acetyl-coenzyme A acyltransferase 2 (ACAA2) gene and investigate their association with milk production traits.
Proteomic characterization of early changes induced by triiodothyronine in rat liver.
Chambery et al., Caserta, Italy. In J Proteome Res, 2011
Several enzymes of lipid metabolism (e.g., Acaa2, Acads, Hadh, and Echs1) were differentially regulated by T3.
Antigenically dominant proteins within the human liver mitochondrial proteome identified by monoclonal antibodies.
Sun et al., Beijing, China. In Sci China Life Sci, 2011
The proteins that were antigenically dominant were: acetyl-Coenzyme A acyltransferase 2 (mitochondrial 3-oxoacyl-Coenzyme A thiolase), aldehyde dehydrogenase 1 family member A1, carbamoyl phosphate synthetase 1, dihydrolipoamide S-acetyltransferase (E2 component of pyruvate dehydrogenase complex), enoyl coenzyme A hydratase 1, and hydroxysteroid (11-beta) dehydrogenase 1.
Hepatic gene expression profiles are altered by dietary unsalted korean fermented soybean (chongkukjang) consumption in mice with diet-induced obesity.
Cha et al., Chŏnju, South Korea. In J Nutr Metab, 2010
Several genes involved in fatty acid catabolism (Acaa2, Mgll, Phyh, Slc27a2, and Slc27a5) were normalized by Chongkukjang consumption.
Opposing effects of dietary sugar and saturated fat on cardiovascular risk factors and glucose metabolism in mitochondrially impaired mice.
Ristow et al., Jena, Germany. In Eur J Nutr, 2010
In contrast, a high-saturated fat/low-sugar diet protects mice with impaired mitochondrial metabolism from diet-induced obesity by increasing total energy expenditure and increasing expression of ACAA2, a rate-limiting enzyme of mitochondrial beta-oxidation, whereas no concomitant improvement of glucose metabolism was observed.
Proteomics analysis of cardiac muscle from rats with peroxisomal proliferator-activated receptor alpha (PPARalpha) stimulation.
Patricelli et al., Los Angeles, United States. In J Toxicol Sci, 2010
Fenofibrate increased the expression of ACAA2, DECR1, and ECH1 consistent with activation of PPARalpha.
Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data.
Da et al., United States. In Bmc Med Genet, 2009
For HDL-C, LPL was confirmed by 12 SNPs 8-45 kb downstream, CETP by two SNPs 0.5-11 kb upstream, and the LIPG-ACAA2 region by five SNPs inside this region.
Acetyl-Coenzyme A acyltransferase 2 attenuates the apoptotic effects of BNIP3 in two human cell lines.
Lu et al., Shanghai, China. In Biochim Biophys Acta, 2008
ACAA2 is a functional BNIP3 binding partner and provide a possible linkage between fatty acid metabolism and apoptosis of cells.
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