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1.
Mol Biochem Parasitol ; 214: 27-35, 2017 06.
Article in English | MEDLINE | ID: mdl-28347672

ABSTRACT

Schistosoma mansoni is the parasite responsible for schistosomiasis, a disease that affects about 218 million people worldwide. Currently, both direct treatment and disease control initiatives rely on chemotherapy using a single drug, praziquantel. Concerns over the possibility of resistance developing to praziquantel, have stimulated efforts to develop new drugs for the treatment of schistosomiasis. Schistosomes do not have the de novo purine biosynthetic pathway, and instead depend entirely on the purine salvage pathway to supply its need for purines. The purine salvage pathway has been reported as a potential target for developing new drugs against schistosomiasis. Adenylosuccinate lyase (SmADSL) is an enzyme in this pathway, which cleaves adenylosuccinate (ADS) into adenosine 5'-monophosphate (AMP) and fumarate. SmADSL kinetic characterization was performed by isothermal titration calorimetry (ITC) using both ADS and SAICAR as substrates. Structures of SmADSL in Apo form and in complex with AMP were elucidated by x-ray crystallography revealing a highly conserved tetrameric structure required for their function since the active sites are formed from residues of three different subunits. The active sites are also highly conserved between species and it is difficult to identify a potent species-specific inhibitor for the development of new therapeutic agents. In contrast, several mutagenesis studies have demonstrated the importance of dimeric interface residues in the stability of the quaternary structure of the enzyme. The lower conservation of these residues between SmADSL and human ADSL could be used to lead the development of anti-schistosomiasis drugs based on disruption of subunit interfaces. These structures and kinetics data add another layer of information to Schistosoma mansoni purine salvage pathway.


Subject(s)
Adenylosuccinate Lyase/chemistry , Adenylosuccinate Lyase/metabolism , Schistosoma mansoni/enzymology , Adenosine Monophosphate/metabolism , Adenylosuccinate Lyase/genetics , Animals , Catalytic Domain , Conserved Sequence , Crystallography, X-Ray , Fumarates/metabolism , Kinetics , Models, Molecular , Protein Binding , Protein Conformation , Protein Multimerization , Protein Stability
2.
Genet Mol Res ; 14(4): 14823-30, 2015 Nov 23.
Article in English | MEDLINE | ID: mdl-26600543

ABSTRACT

In this study, meat quality traits were compared between Chinese lard- and European lean-type pigs. The association between expression of four genes (ADSL, GARS-AIRS-GART, DGAT1, and DECR1) and meat quality traits was also investigated. Meat quality traits were found to differ significantly between pig breeds. Meat color parameter values (a* and b*) and intramuscular fat content in Anqingliubai were significantly higher than those in Landrace (P < 0.01). Meat pH at 1 and 24 h following slaughter was significantly higher in Landrace than in Wei pigs, and meat inosine monophosphate (IMP) content was significantly higher in Landrace than in Wei and Anqingliubai pigs (both P < 0.01). Expression levels of ADSL, GARS-AIRS-GART, and DGAT1 were higher in longissimus lumborum muscle than in heart or liver tissues. ADSL and GARS-AIRS-GART expression levels were correlated with meat IMP content and pH levels. The results of this study will contribute to the understanding of meat quality traits in Chinese lard- and European lean-type pigs.


Subject(s)
Adenylosuccinate Lyase/genetics , Carbon-Nitrogen Ligases/genetics , Diacylglycerol O-Acyltransferase/genetics , Red Meat , Adenylosuccinate Lyase/metabolism , Animals , Breeding , Carbon-Nitrogen Ligases/metabolism , Diacylglycerol O-Acyltransferase/metabolism , Liver/metabolism , Muscle, Skeletal/metabolism , Myocardium/metabolism , Phenotype , Swine
3.
Genet Mol Res ; 14(1): 2031-40, 2015 Mar 20.
Article in English | MEDLINE | ID: mdl-25867349

ABSTRACT

Adenylosuccinate lyase (ADSL) and lipoprotein lipase (LPL) are key enzymes in the metabolism of inosine monophosphate (IMP) and fat mass, which are important factors in meat quality evaluation. In this study, we selected 50 hens from the ISA B-line layers and Guangxi Yellow chickens, slaughtered the chickens at 120 days old, and analyzed polymorphisms in the ADSL and LPL genes using the high-resolution melting curve method. Blood lipid parameters, intramuscular fat (IMF), and IMP content were higher (P < 0.05) in Guangxi Yellow chickens than in ISA B-line layers, while LPL activity was lower (P < 0.05). In exon 2 of the ADSL gene, a C3484T mutation was identified. In both breeds, the CC genotype showed the highest IMP, and IMP was the lowest in the TT genotype. In the 5ꞌ regulatory region of the LPL gene, a C293T mutation was identified. In both breeds, the CC genotype showed the lowest LPL and IMF, while IMF was the highest in the TT genotype. The percentages of individuals with the TT type in the ADSL gene, which was associated with the lowest IMP, were 16.0 and 52.0% in Guangxi chickens and ISA layers, respectively. The percentages of individuals with the CC type of the LPL gene, which was associated with the lowest LPL and IMF, were 28.0 and 44.0%, respectively. The ADSL and LPL gene mutations are correlated with differences in meat quality in different chicken breeds, and high-resolution melting curve is an effective prediction technology for these mutations.


Subject(s)
Adenylosuccinate Lyase/genetics , Chickens/genetics , Lipoprotein Lipase/genetics , Meat/analysis , Nucleic Acid Denaturation , Poultry , Adenylosuccinate Lyase/analysis , Animals , Body Weight/genetics , Chickens/blood , China , Genetic Association Studies , Lipoprotein Lipase/analysis , Lipoprotein Lipase/blood , Meat/standards , Polymorphism, Single Nucleotide
4.
J Pediatr ; 150(1): 57-61.e2, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17188615

ABSTRACT

OBJECTIVE: To characterize a new lethal fetal and early postnatal variant of adenylosuccinate lyase (ADSL) deficiency. STUDY DESIGN: This was a retrospective analysis of 6 patients with very early presentation of ADSL deficiency. RESULTS: Most of the 6 patients had impaired intrauterine growth, microcephaly, fetal hypokinesia, and a lack of fetal heart rate variability. Postnatally, they shared severe muscular hypotonia necessitating mechanical ventilation, intractable seizures, and early death. All 6 patients had biochemical evidence of severe (type 1) disease and low residual ADSL activities. All were compound heterozygous for mutations that, based on expression studies, have a pronounced effect on ADSL activity and/or stability. CONCLUSIONS: ADSL deficiency may present with prenatal growth restriction, fetal and neonatal hypokinesia, and rapidly fatal neonatal encephalopathy. This clinical presentation is associated with genotypes resulting in very low residual enzyme activity.


Subject(s)
Adenylosuccinate Lyase/deficiency , Fetal Death/etiology , Purine-Pyrimidine Metabolism, Inborn Errors/enzymology , Adenylosuccinate Lyase/genetics , DNA/genetics , Fatal Outcome , Female , Fetal Death/enzymology , Follow-Up Studies , Gene Expression , Genetic Predisposition to Disease , Humans , Infant, Newborn , Male , Mutation , Pregnancy , Purine-Pyrimidine Metabolism, Inborn Errors/complications , Purine-Pyrimidine Metabolism, Inborn Errors/genetics , Retrospective Studies
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