Evaluation of the simple sequence repeat (SSR) genotyping of Elaeis oleifera germplasm / Wan Nurhayati Wan Hanafi
Special attention has been given to the second species of oil palm, Elaeis oleifera as it possess several interesting agronomic traits such as slow growth, higher oil unsaturation and disease resistance. Studying the variability of E. oleifera germplasm is therefore very important as it serves as a...
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| Main Author: | |
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| Format: | Book Section |
| Language: | English |
| Published: |
Institute of Graduate Studies, UiTM
2018
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| Online Access: | http://ir.uitm.edu.my/id/eprint/22095/1/ABS_WAN%20NURHAYATI%20WAN%20HANAFI%20TDRA%20VOL%2014%20IGS%2018.pdf http://ir.uitm.edu.my/id/eprint/22095/ |
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| Summary: | Special attention has been given to the second species of oil palm, Elaeis oleifera as it possess several interesting agronomic traits such as slow growth, higher oil unsaturation and disease resistance. Studying the variability of E. oleifera germplasm is therefore very important as it serves as a tool to select source of genetic diversity for the oil palm conservation programme. The objectives of this study were 1) to identify the polymorphic E. oleifera gSSRs for E. oleifera, 2) to measure the information content of E. oleifera gSSRs, 3) to unravel the genetic diversity of E. oleifera germplasm, 4) to determine the genetic differentiation of E. oleifera germplasm and 5) to assess the genetic structure of E. oleifera germplasm. MPOB has developed a collection of simple sequence repeats (SSRs) from E. oleifera genome. Initially, optimization of PCR conditions for analysis of the oleifera samples using E. oleifera gSSRs was carried out. A total of 316 E. oleifera gSSRs were tested to evaluate their usefulness to assess the genetic diversity and population structure of E. oleifera populations. The PCR conditions were optimized while keeping the original DNA concentration, annealing temperature (TA) and other reagent constant. Out of 316 E. oleifera gSSRs screened, 270 produced amplicons and of these numbers, 140 were polymorphic and potentially useful for diversity analysis. The modified PCR condition increases the success of amplifying E. oleifera gSSRs in the E. oleifera DNA samples analyzed. The PCR methods together with the polymorphic E. oleifera gSSRs were applied in genotyping the entire E. oleifera populations. A set of 21 polymorphic E. oleifera gSSRs was analyzed on a total of 214 E. oleifera genomic DNA belonging to eight germplasm originated from four countries in Central and South America (Columbia, Panama, Costa Rica and Honduras)… |
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