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Redesigning Animal Agriculture

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tions underlying the desirable phenotypes<br />

of various production, reproduction and<br />

adaptation traits. Although hundreds of<br />

QTL are map ped in livestock species, very<br />

few causative mutations are identified. One<br />

notable exception is that of the DGAT1 locus<br />

contributing to fat composition in milk followed<br />

by functional confirmation of the<br />

effect of a missense mutation (Grisart et al.,<br />

2002, 2004). These are termed as the quantitative<br />

trait nucleotides (QTN) signifying the<br />

actual nucleotide affecting the quantitative<br />

trait of interest.<br />

Another tool that needs to be exploited<br />

is the field of comparative genomics, or<br />

comparative analyses of genomes. This is<br />

one of the ways of dissecting the genetic<br />

basis of pheno typic variation across species.<br />

The power of this tool is enhanced by<br />

the availability of whole genome sequences<br />

for the livestock species. These comparative<br />

studies can direct research to species-specific<br />

chromosomal regions that could not be<br />

revealed by focusing on studying individual<br />

genomes. Womack (2005) remarked that<br />

identification of QTL for disease resistance<br />

in livestock is the next big frontier, leading<br />

to the understanding of host–pathogen<br />

interaction and subsequent improvement of<br />

both animal and human health. In the tropics,<br />

however, resistance not only to endemic<br />

diseases but also to natural tropical stressors<br />

such as ticks, endo-parasites and heat is<br />

Precision <strong>Animal</strong> Breeding 73<br />

Table 5.2. Map status and genomic resource for livestock species (Source: Womack, 2005).<br />

Cow Pig Sheep Horse Buffalo Goat<br />

Chromosome<br />

Mapped markers<br />

60 38 54 64 50 60<br />

Synteny 1800 1000 250 500 60 –<br />

Linkage 2500 2700 1500 480 – 350<br />

Cytogenic 300 300 850 450 300 350<br />

RH<br />

Resources<br />

3200 3000 300 800 30 –<br />

EST sequence 450k 300k 20k 30k – –<br />

cDNA libraries 80 100 12 15 – –<br />

BAC libraries 3 5 3 3 – –<br />

Microarrays 3 2 – – – –<br />

Whole genome sequence 6× * – – – –<br />

Note:<br />

*Whole genome sequencing of pig genome begun in 2005<br />

essential to achieve desired production and<br />

health targets of farm animals.<br />

QTL mapping<br />

While the information on molecular genetic<br />

markers has revolutionized the biological<br />

research in animals, there have been equally<br />

important developments in statistical methods,<br />

aided by the availability of increased computing<br />

power. Detection of QTL requires accurate<br />

phenotypes for traits of interest from preferably<br />

a structured population of animals, genotypic<br />

data on those animals followed by statistical<br />

analyses correlating phenotypic and genotypic<br />

data. Traditional animal breeding relied on the<br />

performance recording for selection decisions.<br />

Later developments emphasized the importance<br />

of pedigree recording. This enables animal<br />

breeders to exploit the recent advances<br />

in molecular genetics assisting them in the<br />

mapping of genes affecting traits of economic<br />

importance. The recent developments in polymorphic<br />

DNA markers (microsatelites) as well<br />

as SNPs led to the onus on statistical developments<br />

in analysing this information.<br />

A comprehensive review of the development<br />

of statistical methods dealing with<br />

QTL analysis was given by Rocha et al.<br />

(2002). A summary of this review and important<br />

references are given in Table 5.3.

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