IGF2, LEPR, POMC, PPARG, and PPARGC1 gene variants are associated with obesity-related risk phenotypes in Brazilian children and adolescents

Association studies of genetic variants and obesity and/or obesity-related risk factors have yielded contradictory results. The aim of the present study was to determine the possible association of five single-nucleotide polymorphisms (SNPs) located in the IGF2, LEPR, POMC, PPARG, and PPARGC1 genes with obesity or obesity-related risk phenotypes. This case-control study assessed overweight (n=192) and normal-weight (n=211) children and adolescents. The SNPs were analyzed using minisequencing assays, and variables and genotype distributions between the groups were compared using one-way analysis of variance and Pearson's chi-square or Fisher's exact tests. Logistic regression analysis adjusted for age and gender was used to calculate the odds ratios (ORs) for selected phenotype risks in each group. No difference in SNP distribution was observed between groups. In children, POMC rs28932472(C) was associated with lower diastolic blood pressure (P=0.001), higher low-density lipoprotein (LDL) cholesterol (P=0.014), and higher risk in overweight children of altered total cholesterol (OR=7.35, P=0.006). In adolescents, IGF2 rs680(A) was associated with higher glucose (P=0.012) and higher risk in overweight adolescents for altered insulin (OR=10.08, P=0.005) and homeostasis model of insulin resistance (HOMA-IR) (OR=6.34, P=0.010). PPARG rs1801282(G) conferred a higher risk of altered insulin (OR=12.31, P=0.003), and HOMA-IR (OR=7.47, P=0.005) in overweight adolescents. PARGC1 rs8192678(A) was associated with higher triacylglycerols (P=0.005), and LEPR rs1137101(A) was marginally associated with higher LDL cholesterol (P=0.017). LEPR rs1137101(A) conferred higher risk for altered insulin, and HOMA-IR in overweight adolescents. The associations observed in this population suggested increased risk for cardiovascular diseases and/or type 2 diabetes later in life for individuals carrying these alleles.

Characterization and regulation of glycine transport in Fusarium oxysporum var. lini

Glycine was transported in Fusarium oxysporum cells, grow on glycine as the sole source of carbon and nitrogen, by a facilitated diffusion transport system with a half-saturation constant(Ks) of 11 mM and a maximum velocity (Vmax) of 1.2 mM (g dry weight)-1 h-1 at pH 5.0 and 26 degrees Celsius. Under conditions of nitrogen starvation, the same system was present together with a high-affinity one(Ks) of about 47 muM and Vmax of about 60 muM (g dry weight)(-1) h-1)). The low-affinity system was more specific than the high-affinity system. Cells grown on gelatine showed the same behavior. In cells grown on glucose-gelatine medium, the low-affinity system was poorly expressed even after carbon and nitrogen starvation. Moreover, addition of glucose to cells grown on glycine and resuspended in mineral medium caused an increase of the glycine transport probably due to a boost in protein synthesis. This stimulation did not affect the Ks of the low-affinity system. These results demonstrate that, as is the case for other eukaryotic systems, F.oxysporum glycine transport is under control of nitrogen sources but its regulation by carbon sources appears to be more complex.

Novo metodo de pesquisa de fungos das micoses cutaneas superficiais. / A new diagnostic method for superficial cutaneous fungi

O trabalho apresenta novo metodo de colheita e coloracao, para fins de exame microscopico, de material de lesoes micoticas da superficie cutanea, possibilitando a identificacao das especies fungicas permitindo o acompanhamento das infeccoes sob tratamento e, podendo ser utilizado em pesquisas futuras. A tecnica envolve a fixacao da amostra do material em laminas com substancia aderente apropriada-transparente, sem cor, insoluvel em agua e inalteravel pelos reagentes usados e, a seguir, submetidas a coloracao histoquimica com PAS, que e corante especialmente adequado para o fim desejado