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Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1. Chemical induction 2. Electroporation 3. Particle bombardment (Biolistics)

Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

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Page 1: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Direct DNA transfer

• Introduce DNA into cells; assay expression immediately or select for permanently transformed cells.

• Techniques:

1. Chemical induction

2. Electroporation

3. Particle bombardment (Biolistics)

Page 2: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Chemically-Induced Transformation

• Typically used on cells without walls• There are multiple protocols

Examples: 1. Put DNA inside artificial membrane vesicles

called liposomes, which will fuse with the plasma membrane of recipient cells, delivering the cargo.

2. Bind DNA with polycations that neutralize the charged, sugar-PO4 backbone, and condense the DNA. Some cell types will endocytose this complex.

3. Combine (1) and (2)

Page 3: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Electroporation• Use on cells without walls

(plant protoplasts or animal cells).

• High-voltage pulses cause pores to form transiently in cell membrane; DNA pulled in by electrophoresis and diffusion.

• Drawback - its more cumbersome to regenerate plants from single protoplasts than from the tissue transformations with Agrobacterium

Page 4: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Particle Bombardment

• Less limitations than electroporation• Can use on cells with walls• Can transform organelles!

• Method: 1. Precipitate DNA onto small tungsten or gold

particles.2. Accelerate particles to high speeds and aim them at

cells or tissues.3. Selective growth and regeneration of transgenic

plants as described for Agro-mediated transformation.

Page 5: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

DNA is bound to the microprojectiles, which impact the tissue or immobilized cells at high speeds.

J. Sanford & T. Klein, 1988

Original 22-caliber biolistic gun

Page 6: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

An Air Rifle for a DNA Gun – Circa 1990

A.Thompson, Bob ?, and D. Herrin

Page 7: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Repairing an organellar gene: ~ 1 x 107 cells of a mutant of Chlamydomonas that had a deletion in the atpB gene for photosynthesis was bombarded with the intact atpB gene. Then, the cells were transferred to minimal medium so that only photosynthetically competent cells could grow.

Control plate – cells were shot with tungsten particles without DNA

Page 8: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

The Helium Gas Gun – Circa 2000

Page 9: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

The Hand-Held Gas Gun

Purpose:Introduce DNA into cells that are below the top surface layer of tissues (penetrate into lower layers of a tissue)

One interesting use:Making DNA Vaccines in whole animals.

Page 10: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Transgenic Plants In Use on a Large Scale

• Herbicide-resistant plants

• Pest-resistant plants

• Vaccine plants (just starting to be used)

Page 11: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Herbicide-resistant plants

• Resistant to herbicide “Round-up” (glyphosate), which inhibits EPSP synthase.

• GEngineered plants contain a bacterial EPSP synthase, which is not inhibited by glyphosate.

• Advantages: better weed control, less tillage

• In use: soybeans (dicot), corn, rice, wheat

Page 12: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

The function of EPSP synthase is to combine the substrate shikimate-3-phosphate (S3P) with phosphoenolpyruvate (PEP) to form 5-enolpyruvylshikimate-3-phosphate (EPSP).

Page 13: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Pest-resistant plants

• Resistant to certain insects– Lepidopterans, Coleopterans

• Carry gene(s) for Bacillus thuringiensis (Bt) toxin

• Toxin proteins produced as a parasporal crystal – crystalline material has several

proteins– Cry and Cyt genes– encoded on a plasmid

• Advantage: less insecticide required, better yield

• corn, cotton, potatoes

A Transmission Electron Micrograph of negatively stained spores from Bt2-56 containing a filament (a), and a sac-like structure containing a spore (b) and parasporal body (c).

Cry5

Page 14: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Insecticide Usage on Bt and non-Bt Crops for 1999-2001

Page 15: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Vaccine plants

• pioneered by Charlie Arntzen • cheap vaccine-delivery system • plant produces protein(s) or DNA from the human

pathogen, and immunity is induced via food– potatoes, bananas

• being developed for a number of human and animal diseases, including measles, cholera, foot and mouth disease, and hepatitis B and C.

• Four plant vaccines were successful in phase I clinical trials.

C.J. Arntzen et al. (2005) Plant-derived Vaccines and Antibodies: Potential and

Limitations. Vaccine 23, 1753-1756.

Page 16: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction
Page 17: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

Concerns that have been raised about cultivating/consuming GM

crops (or GMOs)

1. They may be toxic or allergenic.

2. They may become established in the wild and outcompete other plants.

3. They may negatively affect insects or other organisms that use crops.

4. They may outcross to a nearby wild relative spreading the transgene into a wild population.

Page 18: Direct DNA transfer Introduce DNA into cells; assay expression immediately or select for permanently transformed cells. Techniques: 1.Chemical induction

References on regulation and eco-risk assessment vis-à-vis the

cultivation of GM crops

• Nap et al. (2003) Plant Journal 33, 1-18– Focuses on current status and regulations

• Conner et al. (2003) Plant Journal 33, 19-46– Focuses on ecological risk assessment

• GM Crops: A World View. Science, April 2008.