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  Section: Principles of Horticulture » Pollination and fertilization
 
 
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Mutations

 
     
 
Content
Pollination and fertilization
  Introductory principles
  Pollination
  The genetic code
  Cell Division
  Inheritance of characteristics
  Other breeding programmes
  Polyploids
  Triploids
  Mutations
  The Plant Varieties and Seeds Act, 1964
  Gene Banking

Figure 10.11 Chimaera (distinct genetical tissues) in variegated horseradish
Figure 10.11 Chimaera (distinct genetical tissues)
in variegated horseradish
Spontaneous changes in the content or arrangement of chromosomes (mutations), whether in the cells of the vegetative plant or in the reproductive cells, occur in nature at the rate of approximately one cell in one million. These changes to the plant DNA are one of the most important causes of new alleles leading to changes in the characteristics of the individual. Extreme chromosome alterations result in malformed and useless plants, but slight rearrangements may provide horticulturally desirable changes in flower colour or plant habit. Such desirable mutations have been seen in plants such as chrysanthemum, Dahlia and Streptocarpus . Mutation breeding also produces these variations, but using irradiation treatments with X-rays, gamma rays or mutagenic chemicals increases the mutation rate. In both situations (natural mutations and induced mutations), the mutation only becomes significant in the plant when the mutated cell originates in a meristem, where it proceeds to create a mass of novel genetic tissues (and organs). When a shoot with a different coloured flower or leaf arises, it is often referred to as a sport . A more extreme example of a mutation is a chimaera. This occurs when organs (and even whole plants) have two or more genetically distinct kinds of tissues existing together. This often results in variegation of the leaves, as seen in some Acer and Pelargonium species. Horticulturists use one form or other of vegetative propagation to preserve and increase the genetic novelty. These useful mutations may give rise to potential new cultivars in just one generation. (See Figure 10.11).


Recombinant DNA technology
For the plant breeder it has historically been difficult to predict whether the progeny from a breeding programme would show the desired characteristics. The term recombinant DNA technology refers to a modern method of breeding that enables novel sources of DNA to be integrated with greater certainty into a plant’s existing genotype. Two new techniques have appeared in the last few years that have enabled this major shift in breeding practice.

The first technique is marker-assisted breeding. Breeders are now able to analyze chromosome material and establish what DNA sequence is present on the chromosome. Some plant characters such as disease resistance are hard to evaluate in newly bred plants, as infection may be difficult to achieve under test conditions. Since the breeders are now able to recognize the chromosome DNA sequence for plant resistance, they can apply this knowledge by analyzing newly bred plants for this desirable character. Whilst
resistance to a disease may be complex, involving several genes acting together, the marker-assisted technique has proved a powerful form of assistance in this area.

The second technique is genetic modification (now known as GM), or genetic engineering. By this method, genes derived from other plant species can be incorporated into the species in question. The commonest technique involves the bacterium Agrobacterium tumifasciens. This organism causes crown gall disease on plants such as apple. The bacterium contains a circular piece of DNA (plasmid) that on entering plant cells can integrate its DNA into that of the infected plant cell. Breeders are able to develop strains of A. tumifasciens in large numbers. The new strains can be induced to accept, in their plastids, a desirable gene taken from other variants of the same plant species, or taken from other species. Wounded plants infected by a bacterial strain begin to multiply the newly acquired gene by integrating it into the cells of the plant. Tissues developing around the point of infection can then be used for micro-propagation of the new genetically-modified cultivar.

Confirmation of successful genetic change can be achieved most easily when the newly introduced gene is already linked in the bacterial plasmid by a marker gene. Two common kinds of marker were used initially, resistance to an antibiotic and resistance to a herbicide. In this way, the breeder was able to test whether incorporation of a desirable new character was successful by exposing it to the antibiotic or herbicide concerned. Alternative methods to the use of antibiotic markers have been sought. There seems little doubt that major advances in the quantity and quality of horticultural crops could follow GM methods of breeding. However, there are fears that such methods could result in deterioration of food quality or pose a threat to the environment.
 
     
 
 
     



     
 
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