4.7 Article

Somatic embryogenesis is an effective strategy for dissecting chimerism phenomena in Vitis vinifera cv Nebbiolo

Journal

PLANT CELL REPORTS
Volume 40, Issue 1, Pages 205-211

Publisher

SPRINGER
DOI: 10.1007/s00299-020-02626-9

Keywords

Grapevine; Chimera; Single nucleotide variants (SNVs); TaqMan (R) genotyping assays

Categories

Funding

  1. GRAPEFIT project (Impronte molecolari e meccanismi fisiologici alla base dell'adattamento della vite a stress ambientali estremi) - Fondazione Cassa di Risparmio di Torino

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This study discussed the tendency of somatic embryogenesis to regenerate plants only from the L1 layer, emphasizing the importance of carefully considering this phenomenon in biotechnological improvement programmes in grapevines. The research successfully separated two genotypes associated with the L1 and L2 layers of the Vitis vinifera 'Nebbiolo' CVT185 clone using somatic embryogenesis technique.
Key Message The tendency of somatic embryogenesis to regenerate plants only from the L1 layer, associated with the spread of chimerism in grapevine, must be carefully considered in the framework of biotechnological improvement programmes. Grapevine is an important fruit crop with a high economic value linked to traditional genotypes that have been multiplied for centuries by vegetative propagation. In this way, somatic variations that can spontaneously occur within the shoot apical meristem are fixed in the whole plant and represent a source of intra-varietal variability. Previously identified inconsistencies in the allelic calls of single nucleotide variants (SNVs) suggested that theVitis vinifera'Nebbiolo' CVT185 clone is a potential periclinal chimera. We adopted the somatic embryogenesis technique to separate the two genotypes putatively associated with the L1 and L2 layers of CVT185 into different somaclones. Despite the recalcitrance of 'Nebbiolo' to the embryogenic process, 58 somaclones were regenerated and SNV genotyping assays attested that the genotype of all them differed from that of the mother plant and was only attributable to L1. The results confirmed that L2 has low or no competence for differentiating somatic embryos. After one year in the greenhouse, the somaclones showed no phenotypic alterations in comparison with the mother plant; however further analyses are needed to identify potential endogenous sources of variation. The tendency of somatic embryogenesis to regenerate plants only from L1 must be carefully considered in the framework of biotechnological improvement programmes in this species.

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