Issue |
BIO Web Conf.
Volume 123, 2024
The 1st International Seminar on Tropical Bioresources Advancement and Technology (ISOTOBAT 2024)
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Article Number | 01028 | |
Number of page(s) | 7 | |
Section | Agriculture, Animal Sciences, Agroforestry, and Agromaritime Innovation | |
DOI | https://doi.org/10.1051/bioconf/202412301028 | |
Published online | 30 August 2024 |
Simple sequence repeats (SSRs) discovery and characterization from Phoenix dactylifera genome
1 Department of Silviculture, Faculty of Forestry and Environment, IPB University, Bogor, West Java, Indonesia
2 Center for Standard Testing of Palm Plant Instruments (BSIP Palma), Manado, North Sulawesi, Indonesia
3 Department of Forestry, Faculty of Agriculture, Bengkulu University, Bengkulu, Bengkulu, Indonesia
* Corresponding author: mroiyanripb1@gmail.com
The date palm is a palm plant belonging to the Arecaceae family. Date palms have several benefits, such as leaves used in various religious ceremonies, tree trunks as firewood, and fruit with various health benefits. In addition, date palm flowers undergo cross-pollination, are dioecious, and consist of 18 chromosomes, resulting in a heterozygous genetic constitution that can lead to high genetic diversity. The development of Next Generation Sequencing technology can detect genetic diversity using whole genome sequencing approaches. Therefore, this study aims to discover and develop SSR markers using an in-silico approach from Phoenix dactylifera genome data. Genome data from male Phoenix dactylifera leaf tissue was obtained from NCBI with GenBank assembly accession: GCA_009389715.1. Quality analysis of de novo assembly using Busco Analysis result in single-copy completeness of 76.7%, duplicated completeness of 19.0%, fragmented completeness of 2.8%, and missing completeness of 1.5%. A total of 36,764 genes and 29,239 protein-coding genes were found. SSRs were identified and extracted using the Microsatellite (MISA) program, resulting in the distribution of dinucleotide SSR motifs (68.37%), trinucleotide (24.22%), tetranucleotide (6.36%), pentanucleotide (0.59%), and heptanucleotide (0.47%). Based on these perfect SSRs, 15 primer pairs were designed. The SSR markers developed will be expected to help further research on the genetic diversity of P. dactylifera.
© The Authors, published by EDP Sciences, 2024
This is an Open Access article distributed under the terms of the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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