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1.
Genet Mol Res ; 15(3)2016 Aug 12.
Article in English | MEDLINE | ID: mdl-27525932

ABSTRACT

The Chinese fire-bellied newt, Cynops orientalis, belonging to Amphibia, Caudata, Salamandridae is a species endemic to China. The liver, which is an important digestive gland and the largest amphibian organ, has various functions, including detoxification, glycogen storage, protein synthesis, and hormone production. However, the newt liver has rarely been studied at the molecular level. We performed histomorphology and high-throughput proteomic analysis of the Chinese fire-bellied newt liver, using hematoxylin and eosin (H&E) staining and two-dimensional electrophoresis coupled with mass spectrometry. The H&E staining showed that the newt liver nuclei are large and round, are located in the lateral cytoplasm, and contain a large quantity of lipid droplets. Melanins were abundantly present throughout the hepatic parenchyma. The proteome analysis showed a total of 545 proteins detected in the newt liver. Furthermore, a gene ontology analysis suggested that these proteins were associated with metabolism, immune response, cellular homeostasis, etc. Among these, proteins with metabolic functions were found to be the most abundant and highly expressed. This supports the role of the liver as the metabolic center. The proteomic results provide new insights into the aspects of the liver proteomes of the Chinese fire-bellied newt. The identification of a more global liver proteome in the newt may provide a basis for characterizing and comparing the liver proteomes from other amphibian species.


Subject(s)
Amphibian Proteins/metabolism , Liver/metabolism , Proteome/metabolism , Salamandridae/metabolism , Animals , Gene Ontology , Liver/cytology , Male , Molecular Sequence Annotation
2.
Genet Mol Res ; 15(2)2016 Jun 03.
Article in English | MEDLINE | ID: mdl-27323143

ABSTRACT

The aim of this study was to investigate the association between four single nucleotide polymorphisms in NR3C1 (Tth111I, BclI, ER22/23EK, and N363S), which encode the glucocorticoid receptor, and asthma susceptibility in patients from the Henan Province of China. Three hundred and twenty-eight patients with asthma and 60 healthy volunteers were recruited to this study. The target SNPs were genotyped by polymerase chain reaction (PCR)-high resolution melting and PCR-restriction fragment length polymorphism. The frequencies of the AA (8.84%) and GG (30.79%) genotypes of Tth111I were higher, and that of the AG genotype was lower (60.37%), in the asthma patients compared to that seen in healthy controls (5.00, 26.67, and 68.33%, respectively). On the other hand, asthma patients showed higher frequencies of the AA genotype (78.05%) of N363S, and lower frequencies of the AG and GG genotypes (15.55 and 6.40%), compared to healthy volunteers (71.67, 18.33, and 10.00%, respectively). Neither of these differences were found to be statistically significant. Moreover, we observed no significant differences in the genotype or allele frequencies of the BclI and ER22/23EK SNPs between the patient and control groups. In conclusion, SNPs in NR3C1 were not significantly associated with asthma in patients from the Henan Province. Patients showed higher frequencies of the AA and GG genotypes of Tth111I and the AA genotype of the N363S SNP compared to healthy volunteers, although these differences were not significant.


Subject(s)
Asthma/genetics , Genetic Association Studies , Genetic Predisposition to Disease , Receptors, Glucocorticoid/genetics , Adolescent , Adult , Aged , Asian People , Asthma/pathology , China , Female , Gene Frequency , Genotype , Humans , Male , Middle Aged , Polymorphism, Single Nucleotide/genetics
3.
Genet Mol Res ; 13(3): 6350-5, 2014 Apr 16.
Article in English | MEDLINE | ID: mdl-24782217

ABSTRACT

We aimed to investigate the association of inflammation-related genes such as IL-10, IL-6 and IL-1B with risk of ischemic stroke. We included 426 cases with ischemic stroke and 426 health controls from Xinxiang, China. Genomic DNA was extracted from the buffy coat layer of collected blood with the TIANamp blood DNA kit. Diabetes, hypertension, obesity, and smoking habits were associated with risk of ischemic stroke. We found that individuals carrying the CC genotype of IL-1B rs1864169 had a higher risk of ischemic stroke when compared with the TT genotype (OR = 1.80, 95%CI = 1.16-2.80). The IL-6 rs1800796 TT genotype was associated with increased risk of ischemic stroke. We found that IL-1B rs1864169 and IL-6 rs1800796 polymorphisms may interact with diabetes, hypertension and obesity. Our study suggests that IL-6 rs1800796 and IL-1B rs1864169 polymorphisms are associated with ischemic stroke risk in the Chinese population.


Subject(s)
Brain Ischemia/genetics , Interleukin-10/genetics , Interleukin-1beta/genetics , Interleukin-6/genetics , Intracranial Thrombosis/genetics , Stroke/genetics , Adult , Asian People , Brain Ischemia/blood , Brain Ischemia/ethnology , Brain Ischemia/pathology , Case-Control Studies , Diabetes Mellitus/physiopathology , Female , Genotype , Humans , Hypertension/physiopathology , Interleukin-10/blood , Interleukin-1beta/blood , Interleukin-6/blood , Intracranial Thrombosis/blood , Intracranial Thrombosis/ethnology , Intracranial Thrombosis/pathology , Male , Middle Aged , Obesity/physiopathology , Polymorphism, Single Nucleotide , Risk Factors , Smoking/physiopathology , Stroke/blood , Stroke/ethnology , Stroke/pathology
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