IBAM   22618
INSTITUTO DE BIOLOGIA AGRICOLA DE MENDOZA
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Differential expression patterns within the grapevine stilbene synthase gene family revealed through their regulatory regions
Autor/es:
CHIALVA CONSTANZA; EICHLER ESTEFANÍA; LIJAVETZKY DIEGO; MICCONO MARÍA; PRIETO HUMBERTO; MUÑOZ CLAUDIO; CALDERÓN LUCIANO; CHIALVA CONSTANZA; EICHLER ESTEFANÍA; LIJAVETZKY DIEGO; MICCONO MARÍA; PRIETO HUMBERTO; MUÑOZ CLAUDIO; CALDERÓN LUCIANO
Lugar:
Bordeaux
Reunión:
Conferencia; XII International Conference on Grapevine Breeding and Genetics; 2018
Institución organizadora:
INRA
Resumen:
The analyses of the grapevine (Vitis vinifera L.) genome have revealed an unusually large and closely related stilbene synthase (VvSTS) gene family. Interestingly, despite the high sequence similarity among those genes, several studies have observed clear differences between their expression patterns. Here, we studied the transcriptional responses to different elicitors of severalVvSTSs in cellular suspension cultures. Primarily, we performed the in silico analysis of the VvSTS regulatory sequences and found the presence of several putative cis-regulatory elements. Then, we evaluated the effect of three treatments?naphtalene acetic acid, methyl jasmonate (MeJA), and ethylene?over the gene expression and found that the genes follow expression patterns probably specific to their sequences. According to this, we focused our study on their regulatory regions and adopted a novel and efficient transient expression assay to determine the activity of these promoters. The results demonstrated that variation in gene expression could be assessed through the analysis of VvSTS regulatory sequences under the effect of different stimuli such as MeJA and cyclodextrins. Furthermore, taking advantage of the lower sequence identity at the promoter level, this strategy accomplished a more accurate alternative to differentiate the members of a large multi-gene family such as STS. This work is expected to provide evidence of the specific expression functions of VvSTS promoters and may benefit future research in understanding the regulation of gene expression.