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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Here, we present two protocols to transform potato plants. The Agrobacterium tumefaciens transformation leads to a complete transgenic plant while the Agrobacterium rhizogenes produces transgenic hairy roots in a wild type shoot that can be self-propagated. We then detect promoter activity by GUS staining in the transformed roots.

Abstract

Agrobacterium sp. is one of the most widely used methods to obtain transgenic plants as it has the ability to transfer and integrate its own T-DNA into the plant's genome. Here, we present two transformation systems to genetically modify potato (Solanum tuberosum) plants. In A. tumefaciens transformation, leaves are infected, the transformed cells are selected and a new complete transformed plant is regenerated using phytohormones in 18 weeks. In A. rhizogenes transformation, stems are infected by injecting the bacteria with a needle, the new emerged transformed hairy roots are detected using a red fluorescent marker and the non-transformed roots are removed. In 5-6 weeks, the resulting plant is a composite of a wild type shoot with fully developed transformed hairy roots. To increase the biomass, the transformed hairy roots can be excised and self-propagated. We applied both Agrobacterium-mediated transformation methods to obtain roots expressing the GUS reporter gene driven by a suberin biosynthetic gene promoter. The GUS staining procedure is provided and allows the cell localization of the promoter induction. In both methods, the transformed potato roots showed GUS staining in the suberized endodermis and exodermis, and additionally, in A. rhizogenes transformed roots the GUS activity was also detected in the emergence of lateral roots. These results suggest that A. rhizogenes can be a fast alternative tool to study the genes that are expressed in roots.

Introduction

Aside from economic interest, the generation of transgenic plants has its own relevance in research to demonstrate the ultimate function of genes and to better understand plant physiology and development. The most widely used method for plant DNA insertion is Agrobacterium-mediated transformation. Agrobacterium tumefaciens is able to generate crown galls in the infected tissue of many plant species by the action of its tumour-inducing (Ti) plasmid. The plasmid contains a T-DNA region with a set of genes that will be integrated in the plant genome and induce tissue dedifferentiation1,2. The ex....

Protocol

The A. rhizogenes transformation protocol was adapted and modified from Horn et al.7 and the genotype tested was S. tuberosum ssp. tuberosum (cv. Désirée). The A. tumefaciens transformation protocol was adapted and modified from Banerjee et al.22 and the genotypes tested were S. tuberosum ssp. tuberosum (cv. Désirée) and S. tuberosum ssp. andigena. The main steps of both procedures a.......

Representative Results

Agrobacterium rhizogenes-mediated potato transformation

In this manuscript, the step-by-step procedure set up to obtain transformed root with A. rhizogenes is presented. Figure 1 presents an overview of the procedure, which altogether takes around 5-6 weeks (from injection of A. rhizogenes to obtaining fully developed hairy roots). Then, .......

Discussion

In potato, the most common system to obtain stable complete transgenic plants uses the transformation by Agrobacterium tumefaciens strains that require organogenesis using exogenous phytohormones. Although the Agrobacterium based protocols has the potential to integrate non-T-DNA vector sequence25, this methodology is still the easiest and less expensive available to transform potato plants. During last years, the interest in A. rhizogenes-mediated transformation has got.......

Acknowledgements

This work was supported by the Ministerio de Innovación y Ciencia (AGL2009-13745, FPI grant to PB), the Ministerio de Economía y Competitividad and FEDER funding (AGL2012-36725, AGL2015-67495-C2-1-R), and the University of Girona (PhD grant to SF, and grant SING11/1). The authors are grateful to Dr. Inge Broer (Institute for Land Use, University of Rostock, Rostock, Germany) and Dr. Salomé Prat (Centro Nacional de Biotecnología, Madrid, Spain) for providing the A. rhizogenes and the A. tumefaciens strain, respectively, and Dr. Marçal Soler and Dr. Anna Plasencia for the help and support received in initiating the A. rhizo....

Materials

NameCompanyCatalog NumberComments

Acetone

Panreac

1.310.071.21

Acetosyringone

Acros

115540050

Aquarium pump

Prodac

MP350

Autoclave

Ragpa Strelimatic

Bacteriological agar

Lab Conda

1800

BAP

Duchefa

B0904

Beef extract

Lab Conda

1700

Plant growing cabinet

Nuaire

Carbenicillin

Duchefa

C0109

Cefotaxime sodium

Duchefa

C0111

DMSO

Merck

1029310161

Ecotron infors

HT

29378

Ethanol

Merck

1,009,831,011

Falcon tube

Control tecnica

CFT011500

Ferricyanate

Sigma

101001081

Ferrocyanate

Sigma

100979088

Flask (8.06 cm diameter and 11.3 cm height) and plastic lid for in vitro culture

Apiglass

ref16

GA3

Sigma

G7645

Gamborg B5 media

Duchefa

G0210

Gelrite

Duchefa

G1101

Glucosa

Sigma

G5767

Kanamycin

Sigma

K1377

Leukopor tape

BSN Leukopor

BDF47467

Lupe

Wild-Heerbrugg

M420

Magnetic shaker

Agimatic

7000243

MES hydrate

Sigma

M2933-25G

MgSO4

Panreac

131404

Microscope

Olympus

Minufugue centrifugue 5415R

Eppendorf

Murashige and Skoog media

Duchefa

M0254.0050

Na2HPO4

Panreac

131679

NAA

Duchefa

N0903

NaCl

Panreac

131659

NaH2PO4

Sigma

58282

NightSea Stereo

SFA Moonting Adapter

Parafilm

Anorsa

PRFL-001-001

Peptone

Lab Conda

1616

Petri dishes (90 x 14)

Anorsa

200200

pHmetre

Crison

Phytotron

Inkoa

RFTI-R5485

Plant Agar

Duchefa

P1001

Refrigeratot

Liebherr Medline

Rifampicin

Duchefa

R0146

Spectinomycin

Sigma

59007

Spectrophotometer

Shimadzu

Square plates (120 x 120)

Deltalab

200204

Streptomycin

Sigma

S6501

Sucrose

Panreac

131621

Surgical blades

Swann-Morton

201

Surgical needle

NIPRO

015/0204

Triptone

Lab Conda

1612

Triton

Serva

37240

Unimax 1010 shaker

Heidolph

Vacuum

Dinko

x-GlcA (5-Bromo-4-chloro-3-indoxyl-beta-D-glucuronic acid, sodium salt anhydrous)

Biosynth

B-7398

Yeast extract

Lab Conda

1702.00

Zeatin riboside

Sigma

1001042850

References

  1. Gelvin, S. B. Traversing the Cell: Agrobacterium T-DNA's journey to the host genome. Frontiers in Plant Science. 3, 1-11 (2012).
  2. Lacroix, B., Citovsky, V. The roles of bacterial and host p....

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