The increased incidence of malignant melanoma in obese individuals is due to impaired melanogenesis and melanocyte DNA repair.

Obese individuals have a higher incidence of malignant melanoma (MM). We here suggest that the higher incidence is caused by a reduction of melanogenesis and a decreased capacity of melanocytes DNA repair. These effects are caused by an increase in the haematic levels of melanocyte stimulating hormone (MSH) antagonists, namely of the protein attractin, the melanocyte concentrating hormone (MCH), the agouti related protein (ASRP) and perhaps also agouti protein (ASIP), determining a lower activity of circulating MSH and of melanocortotropin receptors (MCRs) 1 and 4. MCR1 is fundamental in melanocyte DNA repair and melanogenesis, and a reduction of its activity could well account for the increased incidence of MM. All these changes are ultimately caused by the leptin resistance normally present on obese individuals, that is a low effectiveness of leptin in spite of its high circulating level.

Synthetic aromatic compounds interfering with melanogenesis are responsible of the rising trend of malignant melanoma incidence.

The hypotheses is forwarded that the introduction in the environment of high concentrations of phenols and other aromatic compounds (AC) is one, perhaps the main cause of the continuously rising trend of malignant melanoma (MM) incidence. Two, non-mutually exclusive, possibilities could explain how AC may induce MM: (1) AC may act as inhibitors or alternative substrates of tyrosinase, the enzyme synthesizing melanin, thus impairing the melanocyte photoprotection. (2) AC may impair, directly or indirectly, the activity or synthesis of the melanocorticotropin receptor (MC1R), which photoprotects melanocytes from the UV rays (UVR) by stimulating the DNA repair system. Particularly suspected are sunscreens, as they contain high concentrations of a large variety of AC, three of which are known to be tyrosinase inhibitors. AC that may interfere with tyrosinase are also present in a large variety of medicines used orally or as creams, and in many industrial products with which man is frequently in contact.

Mosaicism may explain the evolution of social characters in haplodiploid Hymenoptera with female workers.

The role of haplodiploidy in the evolution of eusocial insects and why in Hymenoptera males do not perform any work is presently unknown. We show here that within-colony conflict caused by the coexistence of individuals of the same caste expressing the same character in different ways can be fundamental in the evolution of social characters in species that have already reached the eusocial condition. Mosaic colonies, composed by individuals expressing either the wild-type or a mutant phenotype, inevitably occurs during the evolution of advantageous social traits in insects. We simulated the evolution of an advantageous social trait increasing colony fitness in haplodiploid and diplodiploid species considering all possible conditions, i.e. dominance/recessivity of the allele determining the new social character, sex of the castes, and influence of mosaicism on the colony fitness. When mosaicism lowered colony fitness below that of the colony homogeneous for the wild type allele, the fixation of an advantageous social character was possible only in haplodiploids with female castes. When mosaicism caused smaller reductions in colony fitness, reaching frequencies of 90% was much faster in haplodiploids with female castes and dominant mutations. Our results suggest that the evolution of social characters is easier in haplodiploid than in diplodiploid species, provided that workers are females.

The main product of specialized tissues regulates cell life and may cause neoplastic transformation.

Many tissues and cells in vertebrates are highly specialized and devoted to a single function through the action of a single molecule, that we call the "main product" (MP) of the cell. The hypothesis here proposed is that these MPs control all aspects of the cell life, namely activity, division, differentiation and apoptosis. Evidences supporting this hypothesis are reported for the immune system, pancreatic beta-cells, melanocytes, connective tissues, thyroid cells, skin and erythroid cells. In all cases cell division and differentiation is promoted by a normal activity of the MP, while hyperactivity leads to cell apoptosis. Evidences are also provided that alterations of the activity of the MP may elicit pathological disorders; in particular mutations altering the structure of the MP may elicit tumoural transformation.

The exceptionally high rate of spontaneous mutations in the polymerase delta proofreading exonuclease-deficient Saccharomyces cerevisiae strain starved for adenine.

BACKGROUND: Mutagenesis induced in the yeast Saccharomyces cerevisiae by starvation for nutrilites is a well-documented phenomenon of an unknown mechanism. We have previously shown that the polymerase delta proofreading activity controls spontaneous mutagenesis in cells starved for histidine. To obtain further information, we compared the effect of adenine starvation on mutagenesis in wild-type cells and, in cells lacking the proofreading activity of polymerase delta (phenotype Exo-, mutation pol3-01). RESULTS: Ade+ revertants accumulated at a very high rate on adenine-free plates so that their frequency on day 16 after plating was 1.5 x 10(-4) for wild-type and 1.0 x 10(-2) for the Exo- strain. In the Exo- strain, all revertants arising under adenine starvation are suppressors of the original mutation, most possessed additional nutritional requirements, and 50% of them were temperature sensitive. CONCLUSIONS: Adenine starvation is highly mutagenic in yeast. The deficiency in the polymerase delta proofreading activity in strains with the pol3-01 mutation leads to a further 66-fold increase of the rate of mutations. Our data suggest that adenine starvation induces genome-wide hyper-mutagenesis in the Exo- strain.

The influence of colonial organization on thermotolerance and thermoresistance in Saccharomyces cerevisiae.

In this study we show that thermotolerance and thermoresistance of the yeast Saccharomyces cerevisae is enhanced when cells are in colonial condition. We also describe a method to select stable thermoresistant mutants which produce colonies from single plated cells at a temperature 2.5 degrees C higher than the maximum growth temperature of their parental strain.