reaction is catalyzed by methyltransferases, resulting in the production of carboxyl methyl esters. Carboxyl methyl esters are unstable and are readily hydrolyzed in neutral and basic pH conditions or by methylesterase to produce methanol. Interestingly, aspartame, which is a widely used synthetic non-nutritive sweetener, is a methyl ester of a dipeptide that is likely to convert to Clemizole hydrochloride web methanol with the participation of protein methylesterases. Based on the data above, methanol is a natural compound in normal, healthy humans and mammalians. Here, we identified MRGs as methanol gene targets using forward and reverse suppression subtractive hybridization cDNA libraries of HeLa cells that had been exposed to methanol. We showed that vegetable intake increases the methanol content in human plasma and MRG mRNA accumulation in human leukocytes. To approach the question of whether animal methanol is a metabolic waste product or whether methanol has specific function similar to the signaling function of methanol in plant life, we studied animal responses to digested and inhaled methanol. We showed that plant leaf wounding resulted in the emission of gaseous methanol, which increased methanol content in plasma of mice. Moreover, we identified MRGs as methanol gene targets and detected the up- or downregulation of MRGs in the brains of mice after breathing methanol and leaf vapors. We revealed a preference of the mice for the odor of methanol PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22189346 over other plant volatiles in a Y-maze setup and suggested that methanol may function as a crosskingdom signal. Results Identification of MRGs The experimental identification of animal MRGs includes serious challenges because of animal alcohol dehydrogenase, which is present mainly in hepatic cells and initiates methanol conversion into toxic formaldehyde and formic acid. Therefore, cell cultures lacking alcohol dehydrogenase activity had to be used to exclude genes involved in formaldehyde and formic acid detoxification from our analysis. To that end, we selected HeLa cells, which have been shown to have no ADH activity. To identify MRGs, forward and reverse SSH cDNA libraries of HeLa cells exposed to methanol were constructed. Of the 27 differentially expressed transcripts, 5 appeared to be more affected in intact cells, and 22 transcripts appeared to be upregulated following methanol treatment. The cloned expressed sequence tags of only the genes that were upregulated in response to methanol treatment were chosen for sequencing. The methanol-specific upregulation of the SSHidentified genes was validated by virtual northern blot analysis hybridized with -labeled probes prepared from randomly selected differential clones, which were identified by differential screening. We identified and selected four of the most abundant SSH-identified genes for further analysis. The first gene was glyceraldehyde 3-phosphate dehydrogenase, which has a role in glycolysis and nuclear functions, including transcription, RNA transport, DNA replication, and apoptosis. The second gene, hTax1 binding protein 1, encodes a cytoplasmic protein 
that inhibits TNF-induced apoptosis by mediating the anti-apoptotic activity of TNFAIP3 and that may also have a role in the proinflammatory cytokine IL-1 signaling cascade. The third gene, human sorting nexin family member 27, encodes a cytoplasmic protein that is involved in cellular endocytic trafficking and the T lymphocyte endocytic recycling pathway Methanol as a Cross-Kingdom Signal . The
