Assuntos
Asma/genética , Glutationa Transferase/genética , Polimorfismo Genético , Adolescente , Adulto , Fatores Etários , Idoso , Asma/epidemiologia , Criança , Pré-Escolar , Feminino , Predisposição Genética para Doença , Genética Populacional/estatística & dados numéricos , Humanos , Masculino , Pessoa de Meia-Idade , Federação Russa/epidemiologia , Fatores SexuaisRESUMO
The genetic polymorphism of glutathione- S-transferase M1 (GSTM1) and glutathione- S-transferase T1 (GSTT1) genes and the cytochrome P4501A1 gene responsible for xenobiotic conjugating enzymes of the phase II and phase I detoxification system were studied by PCR-RFLP in the blood spots of 109 patients with atopic bronchial asthma and 90 healthy individuals. GSTM1 gene deletion (GSTM1(0/0)) was detected in 47.8% of individuals in the control group and in 76.1% of asthmatic patients. Individuals without the GSTM1 gene were at approximately 3.5--fold higher risk of developing asthma. The proportion of GSTT1(0/0) genotypes was significantly higher in the group of asthmatics (67.0%) than in controls (23.3%). The proportion of individuals with a deficiency in both GSTM1 and GSTT1 gene activity was more than four times higher in asthmatic patients than in the control group (54.1% and 12.2%, respectively). The frequency of the Ile-Val polymorphism of the CYP1A1 gene was similar in controls and asthmatic patients. This study shows the association of atopic bronchial asthma with GSTM1(0/0), GSTT1(0/0) genotypes.
Assuntos
Asma/genética , Glutationa Transferase/genética , Polimorfismo Genético , Adulto , Asma/enzimologia , Asma/etiologia , Criança , Pré-Escolar , Citocromo P-450 CYP1A1/genética , Predisposição Genética para Doença , Humanos , Fatores de RiscoRESUMO
The ratio between the normal (+) and null (0) alleles of the genes encoding glutatione S-transferases M1 (GSTM1) and T1 (GSTT1) were studied in normal individuals from northwestern Russia (control group) and in patients with bronchial asthma (BA). The frequency of the GSTM1 0/0 genotype in the population sample was statistically significantly lower (37.8%) than in the BA patients (82.1%; chi 2 = 16.8; P < 0.001; w chi 2 = 15.7; alpha = 0.01). For the GSTT1 gene, similar data were obtained. The frequency of the GSTT1 0/0 genotype in healthy donors was statistically significantly higher (16.3%) than in the BA patients (73.7%; chi 2 = 28.5; P < 0.001; w chi 2 = 23.22; alpha = 0.01). A significant preponderance of the compound homozygotes for the GSTM1 and GSTT1 null alleles among the BA patients was observed. The frequency of the GSTM1 0/0, GSTT1 0/0 individuals among the patients was 57.9%, while it was only 4.7% among the controls (chi 2 = 27.4; P < 0.001).
Assuntos
Asma/genética , Predisposição Genética para Doença , Alelos , Sequência de Bases , Estudos de Casos e Controles , Primers do DNA , Glutationa Transferase/genética , Humanos , Reação em Cadeia da PolimeraseRESUMO
The object of our investigation was an inbred LA strain of Drosophila melanogaster. This strain was selected during more than 700 generations for low male mating activity and was characterized by complex abnormalities and the remarkably high level of spontaneous mutability. The last property is determined by hobo system of hybrid dysgenesis. LA strain's hobo activity potential in H-E system of hybrid dysgenesis comprise 30-40%. It may be drastically increased up to 70-80% through LA-strain chromosome isogenization in dysgenic crosses. In genomes of independent isogenic LA substrains, numerous directional transpositions of hobo element take place. In spite of it, the retention of hobo element insertion sites inherent in original LA persist. The obtained data open up a new possibilities to study the genome instability mechanisms.
