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34 Biotechnological Approaches for Pest Management and Ecological Sustainability<br />

Application of Biotechnology in Biosystematics and Diagnostics<br />

Diagnosis and characterization of insect pests and their natural enemies through biosystematics<br />

can be exploited in pest management in the future. Characterization of natural<br />

enemies is particularly challenging in the tropics, where there is enormous diversity<br />

(Waage, 1991). Biochemical and molecular markers have proved to be quite useful in distinguishing<br />

between pest and nonpest forms. Biotechnological tools based on molecular<br />

markers offer a great promise for improving biosystematics, identifi cation of insect pests,<br />

and natural enemies across a range of taxonomic groups (Hawksworth, 1994), and can also<br />

be used for rapid diagnosis even by nontaxonomists in far-fl ung regions.<br />

Exploitation of Male-Sterility and Apomixis<br />

Genetic (GMS) or cytoplasmic (CMS) male-sterility leads to the suppression of production<br />

of viable pollen (Liedl and Anderson, 1993). Male-sterility has been observed in a wide<br />

variety of higher plants and is characterized by low levels of male-sterility or complete<br />

absence of pollen production. The male-sterility phenotype affects the pollen-producing<br />

organs because of a high energy requirement. The best known examples of this trait<br />

are the CMS observed in Z. mays, S. bicolor, Pennisetum glaucum (L.) R. Br., and Helianthus<br />

annus L. Both the GMS and CMS systems have been exploited for developing rice, maize,<br />

sorghum, and pearl millet hybrids (Williams and Levings, 1992). A general characteristic<br />

of CMS is the dysfunction of mitochondria in tapetal cells. Mitochondrial genomes encoding<br />

chimeric proteins are presumably present in all tissues of the plant. Mitochondrial<br />

dysfunction produced by a chimeric protein interferes with the organelle function, and<br />

affects pollen production. Biotechnological approaches can be used to transfer CMS from<br />

within a species or from one species into another.<br />

Apomixis resulting from the development of asexual embryos produces a large number<br />

of nucellar offsprings, which are genetically similar to the female parent (Sharma and<br />

Thorpe, 1995; Savidan, 2000). Obligate apomixis offers an opportunity to clone plants<br />

through seed propagation and gene manipulation, and could be used as a potent tool in<br />

plant breeding. It provides uniformity in seed propagation of rootstocks and true breeding<br />

of F 1 hybrids. Genetic manipulation of apomixes has the potential to result in production<br />

of stable and superior hybrids. Some apomictic cultivars have already been released for<br />

citrus, Kentucky grass, and buffalo grass. Development of cross compatible apomictic<br />

plants will allow for hybridization to break the barriers in gene transfer. This will also<br />

help to fi x heterosis and obtain nonsegregating populations from hybrids with a unique<br />

combination of characters from the parents. Genetic engineering of apomixes can be used<br />

for fi xing the genetic variability to produce crops with high productivity and better food<br />

quality. This system has been well studied in citrus, sorghum, maize, turf grass, and other<br />

crop plants. Introduction of apomictic genes into crops will have revolutionary implications<br />

for plant breeding and agriculture, where social and economic benefi ts will exceed those<br />

of the Green Revolution. However, the dangers associated with genetic uniformity could<br />

be exacerbated by inappropriate use of this technology, and therefore its application would<br />

have to be considered on a case-by-case basis.

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