Biotechnology and plant breeding

See main article on Plant breeding.

See also Transgenic plants, Biotechnology, Genetic engineering.

The discovery around 1975 of methods to directly change DNA (usually called genetic engineering), and of ways to decode DNA sequences (usually referred to as DNA sequencing) ushered in a revolution in the biological sciences which is continuing, seemingly unabated, into the current century.

Rapid scientific progress fostered by these discoveries after 1975 quickly extended to plant genetics and plant breeding. Many new plant breeding techniques were invented, older methods were refined by the new experimental tools, and further powerful methods (such as the polymerase chain reaction (PCR) and automated DNA sequencing) were generated during the spectacular expansion of biotechnology.

For achieving useful practical outcomes in plant breeding, direct manipulation of DNA is complementary to the strengths of classical plant breeding, and the newer biotechnology methods do not displace classical plant breeding. But genetic engineering and other molecular biology tools allowed the creation of several new methods such as DNA fingerprinting (DNA markers) that accellerate the relatively slow process of classical breeding. DNA sequencing and gene sequence analysis applied to whole genomes, a scientific field now called genomics, eventually became both possible and practical, and in turn generated massive quantities of useful new knowledge that greatly assists scientific plant breeding.

Genetic engineering is used to generate transgenic plants, and also for the relatively new field of deliberate RNA silencing of plant genes (alternately referred to as cisgenics, or RNAi).

Genetic engineering together with genomics also underpins molecular-marker assisted breeding, which is valuable for speeding up classical breeding.

Genetic modification using direct DNA manipulation

Genetic modification of plants by DNA manipulation, usually just called Genetic Modification or "GM", is achieved by adding a specific gene or genes to a plant, or by silencing the expression of a gene with RNAi, to produce a desirable phenotype. The plants resulting from adding a new gene are often referred to as transgenic plants. It should be remembered that wide crosses (inter species crosses) used in classical breeding also create transgenic plants, and that gene silencing and formation of transgenic plants also occurs during natural evolution.

Plants in which RNAi is used to silence genes are now starting to be called cisgenic plants.

To genetically modify a plant, a genetic construct must be designed so that the gene to be added or knocked-out will be expressed by the plant. To do this, a promoter to drive transcription and a termination sequence to stop transcription of the new gene, and the gene of genes of interest must be introduced to the plant. A marker for the selection of transformed plants is also included. In the laboratory, antibiotic resistance is a commonly used marker: plants that have been successfully transformed will grow on media containing antibiotics; plants that have not been transformed will die. In some instances markers for selection are removed by backcrossing with the parent plant prior to commercial release.

The construct can be inserted in the plant genome by genetic recombination using the bacteria Agrobacterium tumefaciens or A. rhizogenes, or by direct methods like the gene gun or microinjection. Using plant viruses to insert genetic constructs into plants is also a possibility, but the technique is limited by the host range of the virus. For example, Cauliflower mosaic virus (CaMV) only infects cauliflower and related species. Another limitation of viral vectors is that the virus is not usually passed on the progeny, so every plant has to be inoculated.

Genetic modification via direct DNA manipulation can potentially produce a plant with the desired trait or traits faster than classical breeding because the majority of the plant's genome is not altered .

The majority of commercially released transgenic plants, are currently limited to plants that have introduced resistance to insect pests and herbicides. Insect resistance is achieved through incorporation of a gene from Bacillus thuringiensis (Bt) that encodes a protein that is toxic to some insects. For example, the cotton bollworm, a common cotton pest, feeds on Bt cotton it will ingest the toxin and die. Herbicides usually work by binding to certain plant enzymes and inhibiting their action. The enzymes that the herbicide inhibits are known as the herbicides target site. Herbicide resistance can be engineered into crops by expressing a version of target site protein that is not inhibited by the herbicide. This is the method used to produce glyphosate resistant crop plants (See Glyphosate).

Marker assisted breeding (MAS)

Marker assisted breeding refers to direct detection of small DNA subregions, such as restriction fragment length polymorphisms (RFLPs) or micro-satellites, with specific molecular tests of which the [[polymerase chain reaction] (PCR) is specially useful. An alternative term to genetic markers is DNA fingerprinting. While not actually a genetic engineering techniques themselves, they are now part of mainstream plant biotechnology, were invented using genetic engineering methods, and are heavily dependant on molecular biology insights.

DNA markers are useful for backcrossing major genes (such as those conferring pest-tolerance) into proven high performing cultivars . They can aid selection for traits that are not easily assayed in individual plants. Introduction of unwanted genes, genetically linked to the desired trait (linkage drag ) can be minimized, and the time needed to obtain a plant with a high percentage ( 98 to 99 percent) of the original desirable genetic background can be substantially reduced. . Such additional genes are a significant issue when classical breeding methods used to transfer major traits.

A good example illustrating the several advantages of marker assisted backcrossing was reported by Chinese scientists in 2000 working with rice, and improving bacterial blight resistance with the Xa21 gene. For this fine achievement Chen, Lin, Xu and Zhang used RFLP DNA markers to assist their breeding .

Twenty first century plant breeding

Template:Stub The scope of plant breeding continues to expand in the twenty first century. Genomics, marker-assisted breeding, and RNA interferance (RNAi, siRNA, cisgenics) are increasingly effective in accellerating commercial breeding, identifying the functions of physiologically relevant genes, and in allowing traits to be modified. Recent work with identifying wheat genes that infuence protein content illustrates how RNAi and marker assisted breeding come together in providing faster methods for crop improvement, although it needs to be borne in mind that improved protein quality and crop yield represent a trade-off.

Another technique known as in vitro gene shuffling allows rapid evolution of genes encoding new enzyme activities. This has been applied to create synthetic genes that can inactivate the herbicide glyphosate, but in principle could be used to create other novel trait for plants.

Modern plant breeding allows plants to be modified to express proteins such as a therapeutic monoclonal antibody used in the treatment of arthritis, or for treatment of diarrhea , which can save thousands, if not millions of childrens lives in the developing world. The term plant-made pharmaceuticals, refers to these therapeutic agents (pharmaceutical proteins) produced in live plants. The production of plant-based pharmaceuticals is an emerging area of modern crop biotechnology.

Plant genomics

In the twenty first century Genome science involving (chromosome sequence decoding and computer assisted dissection of gene functions and stucture) is increasingly used to assist plant breeders. One important approach is to compare gene arrangements in different species (comparative genomics) to take advantage of the greater ease of gene sequencing and faster progress with smaller more compact genomes such as those of Arabidopsis thaliana and Oryza sativa (rice), to provide clues for gene function and location in crop species with larger genomes.

A central repositary of plant gene sequences is accessible at The National Center for Biotechnology Information..

The fully completed plant genome sequences that are available include:

• Arabidopsis thaliana (thale cress) 5 chromosomes: 1, 2, 3, 4, 5, plastid, mitochondrion
• Medicago truncatula (barrel medic) 8 chromosomes: 1, 2, 3, 4, 5, 6, 7, 8 plastid, mitochondrion
• Oryza sativa (rice) 12 chromosomes: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, plastid , mitochondrion, mitochondrial plasmid B1, mitochondrial plasmid B2

A large number of genetic maps are also available at this resource.

PlantGDB is another project to develop plant species-specific genome databases and web-accessible tools for genome browsing.

Genome sequences at available for browsing through PlantGDB comprise the following:

• Arabidopsis thaliana (thale cress)
• Oryza sativa (rice)
• Zea mays
• Medicago truncatula (barrel medic)
• Lotus japonicus
• Populus trichocarpa (western balsam poplar)
• Lycopersicon esculentum (tomato)
• Glycine max (soybean)
• Brassica rapa (field mustard)
• Triticum aestivum (bread wheat)
• Sorghum bicolor (sorghum)

Biotechnology and safety assurance

The controversies about "GM food safety" have given impetus to detailed systematic investigation of any unexpected changes in crop and food compostion that may occuring during plant breeding. There has been extensive experimental testing of "GM" foods and feeds in animal feeding trials and in detailed analysis of unexpected changes and possible toxic compounds present in them. About 150 scientific publications on this work establish a strong weight of evidence that foods and animal created by biotechnology and passing through regulatory agency scrutiny are at least as scrutiny safe as the food from classical breeding.

An important study Safety of Genetically Engineered Foods: Approaches to Assessing Unintended Health Effects (2004) carried out by the US National Academy of Sciences considered the issue of unexpected outcomes in plant breeding and reported that:

Hazards associated with genetic modifications, specifically genetic engineering, do not fit into a simple dichotomy of genetic engineering versus nongenetic engineering breeding. Not only are many mechanisms common to both genetic engineering as a technique of genetic modification and conventional breeding, but also these techniques slightly overlap each other. Unintentional compositional changes in plants and animals are likely with all conventional and biotechnological breeding methods. The committee assessed the relative likelihood of compositional changes occurring from both genetic engineering and nongenetic engineering modification techniques and generated a continuum to express the potential for unintended compositional changes that reside in the specific products of the modification, regardless of whether the modification was intentional or not.

The National Academy report also commented, after considering a full range of plant breeding techniques, including genetic engineering, that

" ... induced mutagenesis is the most genetically disruptive and, consequently, most likely to display unintended effects from the widest potential range of phenotypic effects."

There has been further more recent research to establish the full profiles (fingerprints) of proteins and metabolites present in conventional crop varieties in comparisons with the profiles in crops created by modern biotechnology. This has involved investigation of the full profile of proteins (the protein "fingerprint") of a crop (an approach called proteomics) and characterisation the full metabolic profile of crops (an approach called metabolomics).

(The metabolic the profile itself is called the the metabolome. The protein profile is similarly called the proteome. These words copy the earlier coined word genomics which decribes the full gene profile of an organism.)

The metabolic fingerprinting and protein fingerprinting studies carried out so far confirm that the judgement made in the 2004 National Academy of Sciences report - that transgenic crops created by direct DNA have similar or less levels unexpected variations in their composition than do the varieties created by commonly used classical breeding methods - is valid.

General Bibliography

• Chrispeels, M.J.,and Sadava, D.E. 2003 Editors. Plants, Genes, and Crop Biotechnology. 2nd Edition. Jones and Bartlett/American Society of Plant Biologists ISBN 0-7637-1586-7
• Gepts, P. (2002). A Comparison between Crop Domestication, Classical Plant Breeding, and Genetic Engineering. Crop Science 42:1780–1790
• Fedoroff, N. V. and Brown, N. M. 2004 Mendel in the Kitchen: A Scientist's View of Genetically Modified Food. National Academy Press. ISBN 0-3090-9205-1
• news@nature.com. 1999 Are non-GM crops safe?

External links

• Making genetically engineered plants
• Adoption of Genetically Engineered Crops in the U.S.(1996-2006) ERS USDA
• ISAAA Briefs 34-2005: Global Status of Commercialized Biotech/GM Crops: 2005
• Biotech Crops Reduce Pesticide Use, Greenhouse Gas Emissions Planting of these crops generates additional US$27.5 billion in global farm income 2005
• 2006 Update of Impacts on US Agriculture of Biotechnology-Derived Crops Planted in 2005

[[Category:Biotechnology]