Abstract

Cabbage (Brassica oleracea L. var. capitata) accounts for a critical vegetable crop belonging to Brassicaceae family, and it has been extensively planted worldwide. Simple sequence repeats (SSRs), the markers with high polymorphism and co-dominance degrees, offer a crucial genetic research resource. The current work identified totally 64,546 perfect and 93,724 imperfect SSR motifs in the genome of the cabbage ‘TO1000.’ Then, we divided SSRs based on the respective overall length and repeat number into different linkage groups. Later, we characterized cabbage genomes from the perspectives of motif length, motif-type classified and SSR level, and compared them across cruciferous genomes. Furthermore, a large set of 64,546 primer pairs were successfully identified, which generated altogether 1,113 SSR primers, including 916 (82.3%) exhibiting repeated and stable amplification. In addition, there were 32 informative SSR markers screened, which might decide 32 cabbage genotypes for their genetic diversity, with level of polymorphism information of 0.14–0.88. Cultivars were efficiently identified by the new strategy designating manual diagram for identifying cultivars. Lastly, 32 cabbage accessions were clearly separately by five Bol-SSR markers. Besides, we verified whether such SSRs were available and transferable in 10 Brassicaceae relatives. Based on the above findings, those genomic SSR markers identified in the present work may facilitate cabbage research, which lay a certain foundation for further gene tagging and genetic linkage analyses, like marker-assisted selection, genetic mapping, as well as comparative genomic analysis.

Highlights

  • Molecular markers used for research change from enzyme-based to DNA-based ones at present; numerous DNA markers systems are constructed. (Zhang et al, 2016; Ikten et al, 2019)

  • Simple sequence repeats (SSRs) markers have been deemed as the promising candidates to conduct genetic mapping and diversity analyses on crop species because they are specific and highly conserved (Yang et al, 2015)

  • Functional markers were employed in the genetic diversity analysis, to identify the cultivars among 32 different genotypes of cabbage and in the availability analysis across 10 relatives in the cruciferous crops

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Summary

Introduction

Molecular markers used for research change from enzyme-based to DNA-based ones at present; numerous DNA markers systems are constructed. (Zhang et al, 2016; Ikten et al, 2019). The emergence of next-generation sequencing (NGS) technology has reduced the time and cost necessary to carry out whole-genome sequencing (WGS) for plant species (Portis et al, 2018). Genomes make it possible for the development of numerous SSR markers for assessing genetic variations in germplasms and cultivars, identifying quantitative trait loci and genes for the control of traits with economic importance, develop molecular genetics and physical maps and assist in breeding for crop improvement (Cui et al, 2017; Xue et al, 2018). With the exception of Chinese cabbage, eggplant and cucumber, research on key vegetable species like cabbage in this field is lacking

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