Arbuscular mycorrhizal symbiosis leads to differential regulation of genes and miRNAs associated with the cell wall and cuticle in tomato leaves. Mendoza-Soto, A.B, Rodríguez-Corral, A.Z., Castro-Martínez, C., López-Meyer, M. Instituto Politécnico Nacional, CIIDIR-Sinaloa, Depto. Biotecnología Agrícola. Blv. Juan de Dios Bátiz 250. Guasave, Sinaloa, México. CP 81000. Arbuscular mycorrhizal symbiosis is an association that provides nutritional benefits to plants. Furthermore, it induces a physiological state that allows plants to response in a more rapid and intense manner to a subsequent biotic attack, thus mycorrhizal plants become less susceptible to both root, as well as shoot pathogens. Our research aims to identify the molecular mechanisms related to the induction of systemic defense by mycorrhiza colonization. We identified genes responsive to the symbiosis related to the biogenesis of the cell wall, as well as its organization and modification. We observed a transcriptional induction of two cellulose synthase genes, an endoglucanase 1, a xyloglucan endotransglucosylase/hydrolase and a pectinesterase inhibitor. In contrast, a pectinesterase, and a NAD-dependent epimerase/hydrolase showed repression. Coinciding with the induction of two cellulose synthase genes, we also observed a higher accumulation of cellulose in leaves of mycorrhizal tomato plants. We identified two induced genes related to fatty acid metabolism; the enoyl reductase gene, and the long chain fatty acid CoA ligase gene. Also, we observed the repression of the 4-coumarate CoA ligase gene, which may be related to the biosynthesis of cuticle components. Regulatory mechanisms for the triggering of priming by mycorrhiza colonization may involve miRNAs along with other regulators. MicroRNAs (miRNAs) are 21-24 nt non-coding RNAs that regulate gene expression at the post-transcriptional level in plants. One objective of our research is to identify the possible role of miRNA as regulators of priming in leaves of mycorrhizal tomato. We observed a repression of miR164a-3p, miR164a-5p, and miR398b; these miRNAs are also related with cell wall. These results support the hypothesis that reinforcement of cell wall and cuticle could play a role in the priming mechanism triggered by mycorrhiza colonization by strengthen the first physical barriers for pathogens. Arbuscular mycorrhizal symbiosis leads to differential regulation of genes and miRNAs associated with the cell wall and cuticle in tomato leaves. Mendoza-Soto, A.B, Rodríguez-Corral, A.Z., Castro-Martínez, C., López-Meyer, M. Instituto Politécnico Nacional, CIIDIR-Sinaloa, Depto. Biotecnología Agrícola. Blv. Juan de Dios Bátiz 250. Guasave, Sinaloa, México. CP 81000. Arbuscular mycorrhizal symbiosis is an association that provides nutritional benefits to plants. Furthermore, it induces a physiological state that allows plants to response in a more rapid and intense manner to a subsequent biotic attack, thus mycorrhizal plants become less susceptible to both root, as well as shoot pathogens. Our research aims to identify the molecular mechanisms related to the induction of systemic defense by mycorrhiza colonization. We identified genes responsive to the symbiosis related to the biogenesis of the cell wall, as well as its organization and modification. We observed a transcriptional induction of two cellulose synthase genes, an endoglucanase 1, a xyloglucan endotransglucosylase/hydrolase and a pectinesterase inhibitor. In contrast, a pectinesterase, and a NAD-dependent epimerase/hydrolase showed repression. Coinciding with the induction of two cellulose synthase genes, we also observed a higher accumulation of cellulose in leaves of mycorrhizal tomato plants. We identified two induced genes related to fatty acid metabolism; the enoyl reductase gene, and the long chain fatty acid CoA ligase gene. Also, we observed the repression of the 4-coumarate CoA ligase gene, which may be related to the biosynthesis of cuticle components. Regulatory mechanisms for the triggering of priming by mycorrhiza colonization may involve miRNAs along with other regulators. MicroRNAs (miRNAs) are 21-24 nt non-coding RNAs that regulate gene expression at the post-transcriptional level in plants. One objective of our research is to identify the possible role of miRNA as regulators of priming in leaves of mycorrhizal tomato. We observed a repression of miR164a-3p, miR164a-5p, and miR398b; these miRNAs are also related with cell wall. These results support the hypothesis that reinforcement of cell wall and cuticle could play a role in the priming mechanism triggered by mycorrhiza colonization by strengthen the first physical barriers for pathogens.