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Etude de la portabilité de marqueurs microsatellites issus d'EST de ...

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Bibliography – Organization of genetic resources<br />

information is avai<strong>la</strong>ble, it can be used to <strong>de</strong>sign PCR-based STS primers. To date, STS<br />

has been used to analyze the genetic diversity for several agricultural crops, such as in<br />

Hor<strong>de</strong>um (Chen et al. 2005). To assess the genetic diversity among China’s cultivated<br />

barley, sequence tagged site (STS) marker analysis was carried out to characterize 109<br />

morphologically distinctive accessions originating from five Chinese eco-geographical<br />

zones. Fourteen polymorphic STS markers representing at least one on each chromosome<br />

were chosen for the analysis. They revealed a total of 47 alleles, with an average of 3.36<br />

alleles per locus (range 2–8). The result suggested that the STS diversity in different zones<br />

was quite different from the morphology diversity, and indicated that the STS variation<br />

was partitioned into 17% among the zone and 83% within the zone (Chen et al. 2005).<br />

3.4.4.7 Single Nucleoti<strong>de</strong> Polymorphisms (SNPs)<br />

Single Nucleoti<strong>de</strong> Polymorphism or SNP is a DNA sequence variation, occurring when a<br />

single nucleoti<strong>de</strong> (a<strong>de</strong>nine (A), thymine (T), cytosine (C) or guanine (G)) is altered in the<br />

genome (i. e. substituted, <strong>de</strong>leted or ad<strong>de</strong>d). It is estimated that there is probably one SNP<br />

locus every 500 to 1,000 bp between two individuals randomly sampled in the same<br />

species. This <strong>la</strong>rge abundance suggests that SNPs markers can be useful for numerous<br />

genetic applications. For example, SNPs were approved as an effective mean of<br />

characterizing the range of DNA variation at a genomic scale in Arabidopsis thaliana and<br />

to build up a core collection (McKhann et al. 2004). Since SNPs appeared recently, only<br />

few studies used this method for genetic diversity estimation in cereals and they were<br />

focused on genes of interest. For example, in 2003, Yanagisawa et al. investigated a single<br />

nucleoti<strong>de</strong> polymorphism (SNP) in the Wx-D1 gene of wheat by using a <strong>de</strong>rived cleaved<br />

amplified polymorphic sequence (dCAPS) marker, and showed that the SNP in the Wx-D1<br />

gene was responsible for the waxy character. Furthermore, this type of marker was also<br />

<strong>de</strong>monstrated to be a very useful tool to study linkage disequilibrium in common wheat<br />

(Ravel et al. 2005) as well as in barley (Potokina et al. 2006).<br />

3.4.4.8 Expressed Sequence Tag (EST)<br />

An Expressed Sequence Tag or EST is a short sub-sequence of a transcribed<br />

protein-coding or non-protein-coding DNA sequence. ESTs can be <strong>de</strong>rived in PCR-based<br />

markers, which can <strong>de</strong>tect length and sequence polymorphisms carried by the expressed<br />

regions of p<strong>la</strong>nt genomes. This involves the <strong>de</strong>signing of primers separated by an<br />

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