椰子基因组新SSR标记的挖掘与验证。

IF 3.6 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Reina Esther S Caro, Jesmar Cagayan, Roanne R Gardoce, Anand Noel C Manohar, Alma O Canama-Salinas, Ramon L Rivera, Darlon V Lantican, Hayde F Galvez, Consorcia E Reaño
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引用次数: 5

摘要

背景:过去,在椰子中开发简单序列重复(SSR)标记是通过微卫星探测细菌人工染色体(BAC)克隆或利用先前开发的近缘基因组SSR标记来实现的。这些椰子ssr在已发表的文献和在线数据库中都是公开的;然而,数量是相当有限的。在这里,我们利用当地建立的椰子全基因组SSR预测生物信息学管道,生成了大量的椰子SSR标记。结果:从椰子‘Catigan Green Dwarf’(CATD)基因组中获得了7139个新的SSR标记。根据基序过滤、组群分布、产物大小排除和PCR在CATD基因组组装中的成功,选择了131个标记子集进行合成。还使用OligoAnalyzer工具使用以下所需参数:%GC, 40-60%;发夹回路的最小ΔG值为-0.3 kcal/mol;自二聚体最小ΔG值,-0.9 kcal/mol;异二聚体的最小ΔG值为-0.9 kcal/mol。利用‘Catigan Green Dwarf’(CATD)、‘Laguna Tall’(LAGT)、‘West African Tall’(WAT)和SYNVAR (LAGT × WAT)基因型,成功合成、优化和扩增了131个新的椰子SSR标记。在131个SSR标记中,有113个在分析的椰子基因型中存在多态性。结论:新型SSR标记的开发将为椰子数量性状位点定位、遗传多样性和群体结构评价、杂种性检测以及其他标记辅助植物育种应用提供宝贵资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mining and validation of novel simple sequence repeat (SSR) markers derived from coconut (Cocos nucifera L.) genome assembly.

Mining and validation of novel simple sequence repeat (SSR) markers derived from coconut (Cocos nucifera L.) genome assembly.

Mining and validation of novel simple sequence repeat (SSR) markers derived from coconut (Cocos nucifera L.) genome assembly.

Mining and validation of novel simple sequence repeat (SSR) markers derived from coconut (Cocos nucifera L.) genome assembly.

Background: In the past, simple sequence repeat (SSR) marker development in coconut is achieved through microsatellite probing in bacterial artificial chromosome (BAC) clones or using previously developed SSR markers from closely related genomes. These coconut SSRs are publicly available in published literatures and online databases; however, the number is quite limited. Here, we used a locally established, coconut genome-wide SSR prediction bioinformatics pipeline to generate a vast amount of coconut SSR markers.

Results: A total of 7139 novel SSR markers were derived from the genome assembly of coconut 'Catigan Green Dwarf' (CATD). A subset of the markers, amounting to 131, were selected for synthesis based on motif filtering, contig distribution, product size exclusion, and success of in silico PCR in the CATD genome assembly. The OligoAnalyzer tool was also employed using the following desired parameters: %GC, 40-60%; minimum ΔG value for hairpin loop, -0.3 kcal/mol; minimum ΔG value for self-dimer, -0.9 kcal/mol; and minimum ΔG value for heterodimer, -0.9 kcal/mol. We have successfully synthesized, optimized, and amplified 131 novel SSR markers in coconut using 'Catigan Green Dwarf' (CATD), 'Laguna Tall' (LAGT), 'West African Tall' (WAT), and SYNVAR (LAGT × WAT) genotypes. Of the 131 SSR markers, 113 were polymorphic among the analyzed coconut genotypes.

Conclusion: The development of novel SSR markers for coconut will serve as a valuable resource for mapping of quantitative trait loci (QTLs), assessment of genetic diversity and population structure, hybridity testing, and other marker-assisted plant breeding applications.

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