Uncu Ayşe Özgür, Gultekin Visam, Allmer Jens, Frary Anne, Doganlar Sami
Izmir Inst. of Technology, Dep. of Molecular Biology & Genetics Urla, Izmir, 35430, Turkey.
Plant Genome. 2015 Jul;8(2):eplantgenome2014.11.0087. doi: 10.3835/plantgenome2014.11.0087.
Sesame (Sesamum indicum L. syn. Sesamum orientale L.) is an orphan crop species with most molecular genetic research work done in the last decade. In this study, we used a pyrosequencing approach for the development of genomic simple-sequence repeat (SSR) markers in sesame. Our approach proved successful in identifying 19,816 nonredundant SSRs, 5727 of which were identified in a contig assembly that covers 19.29% of the sesame genome. Mononucleotide repeats were the most abundant SSR type identified in the sesame genome (48.5% of all SSRs), followed by dinucleotide SSRs (45.0%). Adenine-thymine-rich motifs were predominant, representing 81.7, 51.7, 66.5, and 22.1% of the mononucleotide, dinucleotide, trinucleotide, and tetranucleotide SSRs, respectively. As a result of this work, we introduce 933 experimentally validated sesame specific markers, 849 of which are also applicable in Sesamum mulayanum (syn. Sesamum orientale var. malabaricum Nar.), the wild progenitor of cultivated sesame. Using a subset of the newly identified SSR markers, we analyzed molecular genetic diversity and population structure of a collection of world accessions. Results of the two analyses almost overlapped and suggested correlation between genetic similarity and geographical proximity. Indeed, a pattern of gene flow among sesame diversity centers was apparent, with levels of variability in some regions similar to that seen in the domestication origin of the crop. Taken together with the high rate of genomic marker transferability detected between S. indicum and S. mulayanum, our results represent additional molecular genetic evidence for designating the two taxa as cultivated and wild forms of the same species.
芝麻(Sesamum indicum L. 同义词Sesamum orientale L.)是一种孤儿作物物种,在过去十年中开展了大多数分子遗传学研究工作。在本研究中,我们采用焦磷酸测序方法开发芝麻基因组简单序列重复(SSR)标记。我们的方法成功鉴定出19816个非冗余SSR,其中5727个在一个覆盖芝麻基因组19.29%的重叠群组装中被鉴定出来。单核苷酸重复是芝麻基因组中鉴定出的最丰富的SSR类型(占所有SSR的48.5%),其次是二核苷酸SSR(45.0%)。富含腺嘌呤 - 胸腺嘧啶的基序占主导地位,分别占单核苷酸、二核苷酸、三核苷酸和四核苷酸SSR的81.7%、51.7%、66.5%和22.1%。作为这项工作的成果,我们引入了933个经过实验验证的芝麻特异性标记,其中849个也适用于栽培芝麻的野生祖先多花芝麻(Sesamum mulayanum,同义词Sesamum orientale var. malabaricum Nar.)。使用新鉴定的SSR标记的一个子集,我们分析了一组世界种质的分子遗传多样性和群体结构。这两项分析的结果几乎重叠,并表明遗传相似性与地理距离之间存在相关性。事实上,芝麻多样性中心之间的基因流动模式很明显,一些地区的变异水平与该作物驯化起源地的情况相似。结合在印度芝麻和多花芝麻之间检测到的高基因组标记可转移性,我们的结果为将这两个分类群指定为同一物种的栽培和野生形式提供了额外的分子遗传学证据。