- Research article
- Open Access
Genetic chimerism of Vitis viniferacv. Chardonnay 96 is maintained through organogenesis but not somatic embryogenesis
© Bertsch et al; licensee BioMed Central Ltd. 2005
- Received: 25 April 2005
- Accepted: 29 September 2005
- Published: 29 September 2005
Grapevine can be a periclinal chimera plant which is composed at least of two distinct cell layers (L1, L2). When the cell layers of this plant are separated by passage through somatic embryogenesis, regenerated plants could show distinct DNA profiles and a novel phenotype which proved different from that of the parent plant.
Genetically Chardonnay clone 96 is a periclinal chimera plant in which is L1 and L2 cell layers are distinct. Plants obtained via organogenesis through meristematic bulks are shown to be composed of both cell layers. However, plants regenerated through somatic embryogenesis starting from anthers or nodal explants are composed only of L1 cells. These somaclones do not show phenotypic differences to the parental clone up to three years after regeneration. Interestingly, the only somaclone showing an atypical phenotype (asymmetric leave) shows a genotypic modification.
These results suggest that the phenotype of Chardonnay 96 does not result from an interaction between the two distinct cell layers L1 and L2. If phenotype conformity is further confirmed, somatic embryogenesis will result in true-to-type somaclones of Chardonnay 96 and would be well suitable for gene transfer.
- Somatic Embryogenesis
- Embryogenic Callus
- Shoot Organogenesis
- Berry Skin
- Wood Tissue
Improvement of grapevine rootstocks and scion varieties can be achieved through either inter-specific hybridization or clonal selection. Grapevine clonal selection consists in choosing in a variety one plant presenting desired characteristics. This selected plant is further propagated by vegetative multiplication known to maintain trueness-to-type. But clonal selection is restricted to the natural variability of a given cultivar, within the limits of the characteristics on which the trueness-to-type is based. Somatic embryogenesis could be an additional possibility for varietal improvement. A broader perspective of improvement of grapevine cultivars for characteristics such as resistance to pests and diseases has been opened by transgenic technologies which in most cases are based on somatic embryogenesis of grapevine  and shoot organogenesis . One question to be addressed is the phenotypic and genotypic variability of grapevine clones raised through somatic embryogenesis or shoot organogenesis. Recently, Desperriers et al.  presented results of a ten years observation of Vitis vinifera Gamay somaclones which showed variations in fertility as well as sugar content, size and level of maturity of the grapes. These observations illustrate that somaclones can differ from the original parent without changing the fundamental typicity of the wine. One possible origin of variability may be the separation of cell layers of the mother plant from which clones are grown.
The grapevine meristem is considered to be composed at least of two distinct cell layers L1 and L2 , which can produce a chimeric tissue structure. For example, Vitis vinifera cv. Pinot Meunier phenotype is due to the interaction of genetically distinct cell layers. When the cell layers of Pinot Meunier periclinal chimera were separated by passage through somatic embryogenesis, regenerated plants showed distinct DNA profiles which proved to be different from that of the parent plant. Regenerated somaclones also showed a novel phenotype .
About five hundred microsatellite markers of the grapevine genome are now available and widely as well as very efficiently used for identification of cultivars [6–8]. Riaz et al.  used microsatellite markers for the detection of reproducible intra-cultivar polymorphism in Vitis vinifera Chardonnay and Pinot noir. Furthermore, some of these microsatellite markers made it possible to differentiate the two cell layers L1 and L2 in some clones of both cultivars [9, 10].
A previous paper , showed that in the leaf tissue of Chardonnay 96 the microsatellite marker VMC 5g7 revealed two standard alleles (198:220 bp) and a variant allele (222 bp) previously defined by Riaz et al. . Wood tissues and roots only presented the two standard alleles with VMC 5g7. With a second microsatellite marker (VMC 6g10), two standard alleles (114:140 bp) and a mutant allele (142 bp) were detected in leaves. This mutant allele replaced one of the standard alleles in woods and roots (114:142 bp). In addition, we showed, that somaclones regenerated from anthers of a single inflorescence all derived from L1 cells exclusively.
In the present paper we report results of a wider genotypic analysis of somaclones regenerated either from anthers of different inflorescences or from nodal explants of Chardonnay 96. The same microsatellite markers were also used to compare the genotype of different clones obtained through shoot organogenesis. The genotypic identities (L1; L2) of the regenerated clones are in accordance with their respective phenotypic characteristics.
Genotypic analysis of various tissues of Chardonnay 96 mother clone
Genotypes of Chardonnay clone 96 at the VMC 5g7 and VMC 6c10 loci.
Locus alleles (bp)
L1 + L2
L1 + L2
Regeneration of plants through somatic embryogenesis or shoot organogenesis
Efficient plant growth was further obtained with a number of somaclones. The plants did not show any atypical phenotype in visual comparison with vegetatively propagated Chardonnay 96 grown in the growth chamber and the greenhouse. Except one somaclone (n° 21) originated from an anther-derived callus.
Genotypic analysis of Chardonnay 96 somaclones obtained from anthers and from nodal explants
Genotypes at the VMC 5g7 and VMC 6c10 loci of clones regenerated through embryogenesisor shoot organogenesis
Locus alleles (bp)
cell layer of origin
Primary (20) or secondary (6) somaclones
Leaves iv + gh
Primary somaclones (3)
Primary (5) or secondary (1) somaclones
Leaves iv + gh
Primary somaclone (1)
Leaves iv + gh
Primary somaclones (16)
L1 + L2
Phenotypic and genotypic analysis of somaclone n°21
Genotype of the somaclone 21 at the VMC 5g7 and VMC 6c10 loci
Locus alleles (bp)
Genotypic analysis of clones obtained through shoot organogenesis
Leaves from all 7 clones obtained through shoot organogenesis show the triallelic profile both for VMC 6c10 and VMC 5g7 (table 2). This suggests that plants obtained via organogenesis through meristematic bulks are derived from both L1 and L2 cell layers of the Chardonnay 96 tissues from which they grew.
Vitis viniferaChardonnay clone 96 is a periclinal chimera
In grapevine, apical meristems are composed of two or more cell layers forming the tunica in addition to a corpus [4, 12]. In the leaf tissue from Chardonnay 96, which is derived from both the outer tunica layer L1 and the inner cell layer L2, the microsatellite marker VMC 5g7 revealed the two standard alleles and a variant allele previously defined by Riaz et al. . Wood tissues and roots, which originate exclusively from the L2 layer, presented only the two standard alleles. The presence of a third allele in leaf suggests that Chardonnay is a periclinal chimera in which a mutant allele is present only in the L1 layer, as described by Riaz et al. . For the microsatellite marker VMC 6g10, a mutant allele was detected in leaves, wood tissue and roots. This mutant allele replaced one of the standard alleles in woods and roots, whereas in leaves the mutant allele was present simultaneously with the two standard alleles . These results suggest that the 2 bp-mutation resulting in the replacement of the VMC 6c10 140 bp allele by the 142 bp allele only occurred in L2. Riaz et al.  propose that the mutation most likely occurred in an L1 or L2 cell and then came to populate both layers of the meristem rather than two identical mutations appearing independently in the L1 and L2. Results reported by Riaz et al.  were based on visual interpretation of electrophoretic profiles of amplification products. We suggest that such observations could be biased by the DNA polymerase slippage. Our analyses with ABI PRISM allowed to differentiate between an allele and the different stutter bands, without ambiguity.
Somaclones develope only from L1 cells of Chardonnay 96
In the present study, we show that somaclones obtained not only from anthers from different inflorescences but also from nodal explants all derived from L1 cells. Embryogenic calli were composed exclusively of cells showing the genetic profile of L1 cells of the mother clone Chardonnay 96 (data not shown), suggesting that L2 cells could not multiply into callus at least in our culture conditions. On another hand, clones raised through shoot organogenesis are composed of cells showing the genetic profiles of both L1 and L2 cells of the mother clone. These observations suggest that the genetic chimerism of Chardonnay 96 is maintained through shoot organogenesis but not through somatic embryogenesis.
Anthers are the most widely used organ for initiation of grapevine somatic embryos. It has been shown that embryogenic cells derive from the anther filament. Both L1 and L2 cell layers seem to be competent to form embryogenic calli in some conditions, as reported for Pinot Meunier by Franks et al. . Filaments from anthers of Chardonnay 96 are composed of L1 and L2 cells (data not shown). But, in our conditions only L1 cells of Chardonnay 96 developed into embryos. A similar result was reported recently with Pinot gris from which only the L1 cell layer is competent to form embryogenic callus .
Phenotype variation of Chardonnay 96 somaclones
Embryogenesis might generate new grapevine phenotypes when the mother plant is a chimera of genetically distinct cell layers. For example, the separation of chimeric cell layers of Pinot Meunier through somatic embryogenesis generated plants that had distinct DNA profiles and had novel phenotypes which were different from those of the parent plants . The phenotype of all the somaclones we obtained from anthers has been observed for 2–3 years in a glasshouse: no visible modification was noticed (except for the somaclone n°21) in comparison to the mother clone Chardonnay 96. This phenotypic conformity suggests that the L2 genotype would not significantly participate in the phenotypic expression in the L1–L2 chimeric Chardonnay 96. More subtle variations in fruit setting and wine quality may be only detected in the future, when the somaclones will be grown in the vineyard. Variation of colour intensity, sugar content, size and level of maturity of the grapes has been reported for adult somaclones of Gamay after ten years observation . Though no genotypic analyses were done for the different Gamay somaclones, it can be hypothesised that this somaclonal variation is of epigenetic origin . The Chardonnay 96 mother clone shows the typical ampelographic traits of the cultivar Chardonnay with mature circular leaves undivided or with five lobes, petiolar sinus slightly open, often limited through veins at petiole end. Some adult leaves of somaclone 21 have an asymmetric shape, one half undivided or slightly lobed, the other half deeply lobed. Somaclone 21 probably arose from L1 cell(s) of Chardonnay 96 as all the other somaclones. We suggest that during an early cell division a mutation occurred in locus 6c10 which replaced the 140 bp allele by a 142 bp allele. The L2 cell layer of somaclone 21 originated from the diallelic mutated cell (114:142), whereas cells with the non mutated diallele (114:140) further multiplied giving the L1 cell layer of somaclone 21. This hypothesis is in accordance with the fact that the most frequently observed allelic size variation is the addition of one motif .
Regeneration via embryogenesis for Chardonnay 96 could result generally in a non chimeric plant and in an unchanged phenotype and would be well suited for gene transfer.
Vitis vinifera cv. Chardonnay clone 96, was obtained from ENTAV (Etablissement National Technique pour l'Amélioration de la Viticulture, Le Grau du Roi, France), the national repository for registered grape clones in France. Forced adult plants were maintained in a growth chamber at 25 ± 0.5°C, 70 ± 10 % RH with a 16 h – photoperiod.
Initiation of embryogenic calli from anthers
Anthers were dissected and grown as described by Mauro et al. . For long-term culture of embryogenic callus, subcultures were performed every three weeks on the MPM medium described by Perrin et al. . All the cultures were maintained at 25 ± 0.5°C, 70 ± 10 % RH with a 16 h – photoperiod, except the very first step -the culture of detached anthers- which was performed in the dark.
For production of secondary embryos, primary embryos were cut off and transferred onto half strength Murashige and Skoog medium (MS medium)  supplemented with 20 g.l-1 sucrose, 0.7% Bacto-agar, 2.5 μM 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.5 μM 6-benzylaminopurine (BA; N6-benzyladenine). Incubation was done at 25 ± 0.5°C in the dark, during 3 weeks. Then calli were subcultured every three weeks on MPM medium and maintained under the same conditions as previously described.
Initiation of embryogenic calli from nodal explants
Nodal explants were excised from plantlets grown in vitro and plated on half strength MS medium supplemented with 25 g.l-1 sucrose, 0.7 % Bacto-agar, 9 μM 2,4-D and 4.5 μM BA. Subculture was performed on half strength MS medium supplemented with 60 g.l-1 sucrose, 0.7 % Bacto-agar, 20 μM indole-3-acetic acid (IAA), 10 μM 2-naphtoxyacetic acid (NOA) and 1 μM BA. Embryogenic calli were obtained after several transfers onto this last medium. For long-term culture of embryogenic callus, subcultures were performed every three weeks on the same medium. All the cultures were maintained at 25 ± 0.5°C, 70 ± 10 % RH with a 16 h – photoperiod, except the callus initiation which was performed in the dark.
Regeneration and acclimatization of somaclones
Embryos were carefully excised and transferred onto half-strength MS medium containing 20 g.l-1 sucrose, 0.7 % agar and 0.4 μM BA. After two weeks at 25 ± 0.5°C and 16 h light, the growing embryos were individually transferred into tubes containing half-strength MS medium without plant growth factor. Plantlets with rootlets were transferred to soil and allowed to acclimatize in a growth chamber for about three weeks before transfer to a greenhouse.
Conformity of the different 3 years old somaclones were based on visual observation of leaf morphology and phyllotaxy compared to Chardonnay clone 96.
In vitro propagation of V. vinifera Chardonnay 96 was initiated on MS basal medium supplemented with 4.4 μM BA, 30 g.l-1 sucrose and 0.7 % Bacto agar. Meristematic bulks were initiated on IM medium of Mezzetti et al.  supplemented with 0.05 μM NAA (α-naphtalene-acetic acid) and increasing concentrations of BA : 4.4 μM for the first 30 days subculture, 8.8 μM for the second subculture and finally 13.2 μM. At each transplantation, the apical dome was eliminated.
In order to induce shoot organogenesis, thin slices were cut from the inner part of the meristematic bulks and transferred onto IM medium containing 13.2 μM BA. Growing shoots were transferred to rooting medium of Quoirin and Lepoivre  containing 4.9 μM indole-3-butyric acid (IBA) and 5.7 μM IAA . Growing plantlets were further propagated on hormone free MS medium with half strength macroelements.
Leaves were harvested from plants regenerated through somatic embryogenesis or shoot organogenesis: these plants were in vitro and greenhouse-grown somaclones and in vitro-grown clones from organogenesis. Leaves from greenhouse-grown plants of Chardonnay 96 mother clone were used as a control. Rootlets were taken from in vitro-grown plantlets. Wood tissue was obtained from the dormant canes after the bark and cambium were first scraped away. Berry skin, removed using a scalpel, was also analysed. About 80 mg tissue was ground in liquid nitrogen using a grinder (Retsch MM200) and total DNA was extracted with the Qiagen Dneasy Plant mini-kit (Qiagen, Hilden, Germany) as described by the supplier.
Amplification of microsatellites and polymorphism detection
DNA was analysed using two pairs of primers flanking two different microsatellite regions: VMC6c10 and VMC 5g7 (Vitis Microsatellites Consortium, Dr. Rosa Arroyo Garcia and Dr. Kirsten Wolff), respectively marked with the fluorophores HEX and FAM. Amplification reactions were performed in a total volume of 50 μl with 10 ng of template DNA, 0.35 μM of forward primer labelled either with 6-FAM or HEX fluorophore, 0.35 μM of non-labelled reverse primer, 200 μM dNTP (Invitrogen), 1.5 mM MgCl2, 1X PCR Buffer and 0.2 unit Platinium® Taq DNA Polymerase (Invitrogen). The PCR was carried out using a GeneAmp® PCR System 2700 thermocycler (Applied Biosystems). The cycling program consisted of the following steps: 2 min at 94°C followed by 35 cycles of 40 s at 92°C, 1 min at 57°C and 1 min at 72°C and a final extension step of 7 min at 72°C. The amplification products were separated by capillary electrophoresis and detected with an ABI PRISM 310 Genetic Analyser (Applied Biosystem), using HD400-ROX as an internal size standard. The PCR fragments were detected with the GeneScan™ analysis software version 3.1 and the alleles were scored using the Genotyper™ DNA fragment analysis software version 2.5.2 (Applied Biosystems).
The authors are grateful to Dr. Rosa Arroyo Garcia and Dr. Kirsten Wolff for the VMC 6c10 and VMC 5g7 primer sequences.
- Martinelli L, Mandolino G: Transgenic Grapes (Vitis species). Biotechnology in Agriculture and Forestry. 2003, 47: 325-338.View ArticleGoogle Scholar
- Mezzetti B, Pandolfini T, Navacchi O, Landi L: Genetic transformation of Vitis vinifera via organogenesis. BMC Biotechnology. 2002, 2: 1-10. 10.1186/1472-6750-2-18.View ArticleGoogle Scholar
- Desperrier JM, Berger JL, Bessis R, Fournioux JC, Labroche C: Création clonale dirigée par embryogenèse somatique. Bulletin de l'O.I.V. 2003, 76: 871-872.Google Scholar
- Thompson NM, Olmo HP: Cytohistological studies of cytochimeric and tetraploid grapes. Amer J Bot. 1963, 50: 901-906.View ArticleGoogle Scholar
- Franks T, Botta R, Thomas MR: Chimerism in grapevines: implications for cultivar identity, ancestry and genetic improvement. Theor Appl Genet. 2002, 104: 192-199. 10.1007/s001220100683.PubMedView ArticleGoogle Scholar
- Sefc KM, Lefort F, Grando MS, Scott K, Steinkellner H, Thomas MR: Microsatellite markers for grapevine: a state of the art. Molecular Biology and Biotechnology of Grapevine. Edited by: Roubelakis-Angelakis KA. Kluwer Publishers, Amsterdam; 2001:433-463. ISBN 0-7923-6949-1View ArticleGoogle Scholar
- This P, Jung A, Boccacci P, Borrego J, Botta R, Costantini L, Crespan M, Dangl GS, Eisenheld C, Ferreira-Monteiro F, Grando S, Ibanez J, Lacombe T, Laucou , Magalhaes R, Meredith CP, Milani N, Peterlunger E, Regner F, Zulini L, Maul E: Development of a standard set of microsatellite reference alleles for identification of grape cultivars. Theor Appl Genet. 2004, 109: 1448-1458. 10.1007/s00122-004-1760-3.PubMedView ArticleGoogle Scholar
- Merdinoglu D, Butterlin G, Bevilacqua L, Chiquet V, Adam-Blondon AF, Decroocq S: Development and characterization of a large set of microsatellite markers in grapevine (Vitis vinifera) suitable for multiplex PCR. Molecular Breeding. 2005.Google Scholar
- Riaz S, Garrison KE, Dangl GS, Boursiquot JM, Meredith CP: Genetic divergence and chimerism within ancient asexually propagated wine grape cultivars. J Amer Soc Hort Sci. 2002, 127: 508-514.Google Scholar
- Hocquigny S, Pelsy F, Dumas V, Kindt S, Heloir MC, Merdinoglu D: Diversification within grapevine cultivars goes through chimeric states. Genome. 2004, 47: 579-589. 10.1139/g04-006.PubMedView ArticleGoogle Scholar
- Bertsch C, Kieffer F, Triouleyre C, Butterlin G, Merdinoglu D, Walter B: Molecular profiling of Vitis vinifera Chardonnay obtained by somatic embryogenesis. J Int Sci Vigne Vin. 2003, 34: 223-227.Google Scholar
- Morrison J: Bud development in Vitis vinifera L. Bot Gaz. 1991, 152: 304-315. 10.1086/337894.View ArticleGoogle Scholar
- Henry RJ: Molecular and biochemical characterization of somaclonal variation. Somaclonal variation and induced mutations in crop improvement. Edited by: Jain SM, Brar DS, Ahloowalia BS. Kluwer Academic Publishers, Dordrecht, Boston, London; 1998:485-499.View ArticleGoogle Scholar
- Hocquigny S: La diversité génétique intra-variétale chez la vigne: caractérisation et origines. PhD thesis. Université Louis Pasteur, Strasbourg; 2003:138.Google Scholar
- Mauro M, Nef C, Fallot J: Stimulation of somatic embryogenesis and plant regeneration from anther culture of Vitis vinifera cv. Cabernet-Sauvignon. Plant Cell Reports. 1986, 5: 377-380. 10.1007/BF00268606.View ArticleGoogle Scholar
- Perrin M, Martin D, Joly D, Demangeat G, This P, Masson JE: Medium-dependent response of grapevine somatic embryogenic cells. Plant Science. 2001, 161: 107-116. 10.1016/S0168-9452(01)00385-5.View ArticleGoogle Scholar
- Murashige T, Skoog F: A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant. 1962, 15: 473-497.View ArticleGoogle Scholar
- Quoirin M, Lepoivre P: Improved media from in vitro culture of Prunus spp. Acta Horticulturae. 1997, 78: 437-442.Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.