Identifying Molecular Markers for Ficus erecta Thunb. Based on Complete Plastome Sequences of Korean Figs (Ficus L., Moraceae)

被引:1
|
作者
Jung, Joonhyung [1 ]
Kim, Tae-Hee [2 ]
Kwon, Seog Woo [1 ]
Park, Hyun Ji [3 ]
Choi, In Suk [4 ]
Kim, Joo-Hwan [1 ]
机构
[1] Gachon Univ, Dept Life Sci, Seongnam 13120, South Korea
[2] Korea Natl Arboretum, Div Forest Biodivers, Pochon 11186, South Korea
[3] CHA Adv Res Inst, Ctr Consumer Hlth Res 1, Seongnam 13488, South Korea
[4] CMG Pharmaceut Co Ltd, Res Inst 2, Seongnam 13488, South Korea
来源
DIVERSITY-BASEL | 2024年 / 16卷 / 03期
关键词
Korean figs; plastid genome (plastome); molecular markers; RAPD MARKERS; ORGANIZATION; MULBERRY;
D O I
10.3390/d16030129
中图分类号
X176 [生物多样性保护];
学科分类号
090705 ;
摘要
Plastome sequences are crucial in plant studies due to their role in examining genomic evolution, understanding phylogenetic relationships, and developing molecular markers. Despite the collection of information about Korean figs, their genomic data remain underexplored. We utilize next-generation sequencing and PCR techniques to investigate genomic data and to develop and validate molecular markers. In this study, we characterize the complete plastomes of Korean figs: F. erecta, F. erecta var. sieboldii, F. sarmentosa var. nipponica, and F. sarmentosa var. thunbergii, which range in length from 160,276 to 160,603 bp. These genomes comprise 78 plastid protein-coding genes, 30 tRNA, and four rRNA, with the exception of one pseudogene, infA. We discovered that F. erecta and F. erecta var. sieboldii share identical plastome sequences. Phylogenomic analysis indicates the monophyly of Ficus, although the relationships among its subgenera remain unclear. We discovered that Ficus possesses 467 molecular diagnostic characters in its plastid protein-coding genes compared to other Moraceae groups, and F. erecta exhibits 33 molecular diagnostic characters. Single nucleotide polymorphisms in ndhD, petA, and rbcL were effectively used to develop molecular markers for distinguishing F. erecta from other figs. Additionally, we provided a straightforward PCR protocol for utilizing these newly developed molecular markers.
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页数:12
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