Affiliation(s)
1. Graduate School of Environmental and Life Science, Okayama University, 1-1-1 Tsushima Naka, Kita-ku, Okayama 700-8530, Japan
2. Faculty of Agronomy, College of Agriculture and Forestry, Hue University, No. 102 Phung Hung Street, Hue City 47000, Vietnam
3. Faculty of Humanities, Hirosaki University, 1 Bunkyo, Hirosaki, Aomori 036-8560, Japan
ABSTRACT
Random amplified polymorphic
DNA (RAPD) has been used widely in diversity studies, including population
structure and phylogenetics at all taxonomic levels. However, there is a
problem in stability and repeatability of RAPD in some cases. Therefore,
conversion of RAPD markers into new type of PCR-based marker to overcome low
levels of repeatability of RAPD marker is needed. The aim of this study was to develop
sequence-tagged site (STS) markers by designing specific primers based on RAPD
marker sequences to provide the potential markers for analyzing genetic
diversity of melon germplasm. Eight RAPD-STS markers were successfully converted from RAPD
markers and have two polymorphism types:
A20 and B99 showed different sizes of fragment; A22,
A31, A57, B15, B71 and C00 showed presence/absence polymorphism in melon
germsplasm. The applicability of new RAPD-STS markers has been demonstrated by
comparing genotype analysis of 41 melon accessions using RAPD and RAPD-STS
markers. Both of RAPD markers and RAPD-STS markers divided them into two major
clusters. However, the RAPD-STS markers were more polymorphic than RAPD markers
(polymorphic index content (PIC) values were 0.346 and 0.274, respectively).
Mantel’s test showed significant correlation (r = 0.896, P < 0.01) between RAPD-STS
dendrogram and RAPD
dendrogram. Furthermore, RAPD-STS markers could give
more information in population structure and identify admixture individuals by
using STRUCTURE software. Eight RAPD-STS markers developed in this study are
useful for genetic diversity analysis and population studies in melon.
KEYWORDS
RAPD, STS, Cucumis melo L., genetic diversity, marker.
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