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Genetic Engineering of Plants. Must get DNA:into the cellsintegrated into the genome (unless using transient expression assays)expressed (everywhere or controlled) For (1) and (2), two main approaches for plants:Agrobacterium - mediated gene transferDirect gene transferFor (3), use promoter that will direct expression when and where wanted
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1. Making Transgenic Plants and Animals Why?
Study gene function and regulation
Making new organismic tools for other fields of research
Curing genetic diseases
Improving agriculture and related raw materials
New sources of bioengineered drugs (use plants instead of animals or bacteria) Metabolic engineering (2,4,5); marked (GFP) plants for population studies (2), increased food production or pest resistance (4)Metabolic engineering (2,4,5); marked (GFP) plants for population studies (2), increased food production or pest resistance (4)
3. Agrobacterium - mediated Gene Transfer Most common method of engineering dicots, but also used for monocots
Pioneered by J. Schell (Max-Planck Inst., Cologne)
Agrobacteria
soil bacteria, gram-negative, related to Rhizobia
species:
tumefaciens- causes crown galls on many dicots
rubi- causes small galls on a few dicots
rhizogenes- hairy root disease
radiobacter- avirulent J. Schell in race with Mary-Dell Chilton (CIBA-GEIGY)J. Schell in race with Mary-Dell Chilton (CIBA-GEIGY)
6. Note: pili used for attachment to plant cells, and conjugation to other bacteria.Note: pili used for attachment to plant cells, and conjugation to other bacteria.
7. Infection and tumorigenesis Infection occurs at wound sites
Involves recognition and chemotaxis of the bacterium toward wounded cells
galls are “real tumors”, can be removed and will grow indefinitely without hormones
genetic information must be transferred to plant cells
8. Tumor characteristics Synthesize a unique amino acid, called “opine”
octopine and nopaline - derived from arginine
agropine - derived from glutamate
Opine depends on the strain of A. tumefaciens
Opines are catabolized by the bacteria, which can use only the specific opine that it causes the plant to produce.
Has obvious advantages for the bacteria, what about the plant?
9. Elucidation of the TIP (tumor-inducing principle) It was recognized early that virulent strains could be cured of virulence, and that cured strains could regain virulence when exposed to virulent strains; suggested an extra- chromosomal element.
Large plasmids were found in A. tumefaciens and their presence correlated with virulence: called tumor-inducing or Ti plasmids.
10. Ti Plasmid Large (?200-kb)
Conjugative
~10% of plasmid transferred to plant cell after infection
Transferred DNA (called T-DNA) integrates semi-randomly into nuclear DNA
Ti plasmid also encodes:
enzymes involved in opine metabolism
proteins involved in mobilizing T-DNA (Vir genes)
13. Vir (virulent) genes On the Ti plasmid
Transfer the T-DNA to plant cell
Acetosyringone (AS) (a flavonoid) released by wounded plant cells activates vir genes.
virA,B,C,D,E,F,G (7 complementation groups, but some have multiple ORFs), span about 30 kb of Ti plasmid.
14. Vir gene functions (cont.) virA - transports AS into bacterium, activates virG post-translationally (by phosphoryl.)
virG - promotes transcription of other vir genes
virD2 - endonuclease/integrase that cuts T- DNA at the borders but only on one strand; attaches to the 5' end of the SS
virE2 - binds SS of T-DNA & can form channels in artificial membranes
virE1 - chaperone for virE2
virD2 & virE2 also have NLSs, gets T-DNA to the nucleus of plant cell
virB - operon of 11 proteins, gets T-DNA through bacterial membranes
17. VirE1 chaperones VirE2 in Agro. Cytoplasm, but complex can also bind the SS T-DNA. VirE2 may help the T-DNA cross the plant cell PM, as it can form a channel in artificial bilayers by itself.VirE1 chaperones VirE2 in Agro. Cytoplasm, but complex can also bind the SS T-DNA. VirE2 may help the T-DNA cross the plant cell PM, as it can form a channel in artificial bilayers by itself.
21. Leaf-disc transformation - after selection and regeneration with tissue culture, get plants with the introduced gene in every cell
Floral Dip – does not require tissue culture. Reproductive tissue is transformed and the resulting seeds are screened for drug-resistant growth. (Clough and Bent (1998) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant Journal 16, 735–743)
24. Chemically-Induced Transformation Usually use on cells without walls
Multiple protocols (examples):
Put DNA inside artificial membranes (liposomes), they will fuse with plasma membrane.
Bind DNA with polycations to neutralize charge, some cells endocytose the complex.
Combine (1) and (2)
32. Transgenic Plants In Use or About to be on a Large Scale Herbicide-resistant plants
Pest-resistant plants
Vaccine plants (just starting to be used)
33. Herbicide-resistant plants Resistant to herbicide “Round-up” (Glyphosate)
Contain bacterial EPSP synthase
Advantages: better weed control, less tillage
soybeans, corn, rice, wheat
35. Pest-resistant plants Resistant to certain insects
Lepidopterans, Coleopterans
Carry gene(s) for Bacillus thuringiensis (Bt) toxin
Toxin proteins produced as a parasporal crystal
Complex, composed of several proteins
Cry and Cyt genes
encoded on a plasmid
Advantage: less insecticide required, better yield
corn, cotton, potatoes
38. Concerns that have been raised about cultivating and consuming GM crops They may be toxic or allergenic.
They may become established in the wild and outcompete other plants.
They may negatively affect insects or other organisms that use crops.
They may outcross to a nearby wild relative spreading the transgene into a wild population.
39. References on release of GM crops into the environment 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