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. 2020 Jul 31;9(8):971. doi: 10.3390/plants9080971

Table 1.

Transformation in Prunus persica L.

Genotype Method (Strain) Plasmid (Genes) Explant T.E. a (%) Main Advantage Main Disadvantage Reference
“14DR60” A. tumefaciens
(A281)
pGA472
(nptII)
Embryogenic callus, leaves,
and immature embryos
0 All three starting explants developed calli, which were able to grow in a medium containing the selective agents. Typically, long-term embryogenic
peach cultures produce few normal shoots.
Scorza et al. [15]
“Tennessee natural”
“PER 2D”
“Redhaven” A. tumefaciens
(tms328::Tn5)
pTiA6
(iaa, ipt)
Shoots 0 Demonstration of potential for using A. tumefaciens to transfer genes to peach. Shoots could not be regenerated from the transformed cells. Hammerschlag et al. [16]
Immature embryo axes n.s. Demonstration of regeneration of plants from embryo-derived callus infected with the shooty mutant strain of A. tumefaciens. Not reproduced in other laboratories. Smigocki and Hammerschlag [5]
“Lovell” Biolistic pBI505, pBI426
(nptII, gus)
Embryo calli, immature embryos, cotyledons, leaves, and shoot tips 0 Optimization of biolistic parameters for this species. Unsuccessful recovery of plants from the transformed embryogenic calli. Ye et al. [17]
“Miraflores” A. tumefaciens
(C58C1/pMP90)
pBin19-sgfp
(nptII, gfp)
Mature embryo axes 3.6 Mature seeds are available year-round. Not reproduced in other laboratories. Pérez-Clemente et al. [12]
“Bailey” A. tumefaciens
(LBA4404, EHA105, GV3101, CG937, CG1052, CG1059)
pLC101
(nptII, gfp)
Cotyledons, embryonic axis, hypocotyl slices, callus, internodes, and leaves 0 Comprehensive evaluation of factors affecting A. tumefaciens-mediated peach transformation.
Seed-derived internodes showed the highest transformation percentage compared to the other explants.
Rates of GFP transformation under the experimental conditions were low. Padilla et al. [18]
“Lady Nancy”
“Harrow Beauty”
KV930465 A. tumefaciens
(LBA4404, EHA105)
pBin19
(nptII, gus)
KV930408
KV930303
KV939455 A. tumefaciens
(LBA4404)
pBISNI, pGA482Ggi
(nptII, gus)
KV930478
KV930311
“Akatsuki” Electroporation pBI221, pE2113-GUS, PL-GUS
(gus)
Protoplasts from immature fruits mesocarp 0 The system can be applied for expression analysis of genes isolated from other Rosaceae species. The period suitable for protoplast isolation is limited to about 1 week. Honda and Moriguchi [19]
“O’Henry” A. tumefaciens
(GV3101, EHA105)
pBIN-m-gfp5-ER
(nptII, gfp)
Immature cotyledons 0.6 Very efficient regeneration protocol. Explants available for only a limited time each year (50 to 70 days post-bloom).
Not reproduced in other laboratories.
Prieto [13]
“Rich Lady”
“GF677” b A. tumefaciens
(GV2206)
hp-pBin19
(nptII)
Meristematic bulks 0.3 The first successful report of a peach rootstock genetic transformation using adult tissue as starting material. The efficiency of the procedure was relatively poor. Sabbadini et al. [14]
“Hansen 536” b A. tumefaciens
(EHA105)
pK7WG2-ihp35S-PPV194::eGFP
(nptII, gfp, PPV polyprotein hairpin)
Meristematic bulks 0 Uses adult tissues as source of explants. Shoot regeneration from transgenic calli was not obtained. Sabbadini et al. [20]
A. tumefaciens
(EHA105, LBA4404, GV3101)
pBISN1
(nptII, gus)
Leaves 0 Adult tissue available year-round. Only transient transformation was recorded. Zong et al. [21]
“Shantao” A. rhizogenes
(MSU440)
pMV2G + Ri Plasmid
(DsRED1) + (rol genes)
Leaves, hypocotyls, and shoots 27.8 c This protocol provides a way to evaluate gene functions, genetic engineering, and root-rhizosphere microorganism interaction in peach. Only transgenic hairy roots were regenerated. Transgenic shoots were not produced. Xu et al. [22]
“Shengli” 50.9 c
“Lvhuajiuhao” 30.7 c
“Shengli” pSAK277 (PpMYB10.1) Shoots n.s. c

a Transformation efficiency (number of transgenic shoots obtained per 100 explants). When not indicated, it was not specified (n.s.) by authors. b Prunus persica x Prunus amygdalus hybrids. c Efficiency of regeneration of transgenic hairy roots.